Glucosides are glycosides that contain glucose as the sugar component, often forming part of the plant's defense mechanism and can have various pharmacological effects when extracted and used medically.
Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed)
A type of MONOTERPENES, derived from geraniol. They have the general form of cyclopentanopyran, but in some cases, one of the rings is broken as in the case of secoiridoid. They are different from the similarly named iridals (TRITERPENES).
Thirteen-carbon butene cyclohexene degradation products formed by the cleavage of CAROTENOIDS. They contribute to the flavor of some FRUIT. Ionone should not be confused with the similarly named ionol.
A subclass of iridoid compounds that include a glucoside moiety, usually found at the C-1 position.
The Madder plant family of the order Rubiales, subclass Asteridae, class Magnoliopsida includes important medicinal plants that provide QUININE; IPECAC; and COFFEE. They have opposite leaves and interpetiolar stipules.
A group of FLAVONOIDS derived from FLAVONOLS, which lack the ketone oxygen at the 4-position. They are glycosylated versions of cyanidin, pelargonidin or delphinidin. The conjugated bonds result in blue, red, and purple colors in flowers of plants.
Thioglucosides are organic compounds primarily found in plants, characterized by the functional group consisting of a sulfur atom linked to a glucose molecule through a sulfur-carbon bond.
An exocellulase with specificity for a variety of beta-D-glycoside substrates. It catalyzes the hydrolysis of terminal non-reducing residues in beta-D-glucosides with release of GLUCOSE.
A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin.
The above-ground plant without the roots.
Enzymes that catalyze the transfer of glucose from a nucleoside diphosphate glucose to an acceptor molecule which is frequently another carbohydrate. EC 2.4.1.-.
A cyanogenic glycoside found in the seeds of Rosaceae.
Concentrated pharmaceutical preparations of plants obtained by removing active constituents with a suitable solvent, which is evaporated away, and adjusting the residue to a prescribed standard.
A plant genus of the family VERBENACEAE. Members contain verbenachalcone (dimeric dihydrochalcone), iridoids, and phenylethanoids.
Expanded structures, usually green, of vascular plants, characteristically consisting of a bladelike expansion attached to a stem, and functioning as the principal organ of photosynthesis and transpiration. (American Heritage Dictionary, 2d ed)
The spurge family of flowering plants, in the order Euphorbiales, contains some 7,500 species in 275 genera. The family consists of annual and perennial herbs and woody shrubs or trees.
The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds.
A mass spectrometric technique that is used for the analysis of a wide range of biomolecules, such as glycoalkaloids, glycoproteins, polysaccharides, and peptides. Positive and negative fast atom bombardment spectra are recorded on a mass spectrometer fitted with an atom gun with xenon as the customary beam. The mass spectra obtained contain molecular weight recognition as well as sequence information.
Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING).
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
3-Phenylchromones. Isomeric form of FLAVONOIDS in which the benzene group is attached to the 3 position of the benzopyran ring instead of the 2 position.
Cyclohexane ring substituted by one or more ketones in any position.
A plant genus of the family POLYGONACEAE. Members contain chrysophanic acid, rhein, EMODIN, and other ANTHRAQUINONES. The roots were formerly used as PURGATIVES.
Purifying or cleansing agents, usually salts of long-chain aliphatic bases or acids, that exert cleansing (oil-dissolving) and antimicrobial effects through a surface action that depends on possessing both hydrophilic and hydrophobic properties.
Hydrogen cyanide (HCN); A toxic liquid or colorless gas. It is found in the smoke of various tobacco products and released by combustion of nitrogen-containing organic materials.
A plant genus of the family ASTERACEAE. Members contain bidensyneosides (polyacetylene glucosides).
The rose plant family in the order ROSALES and class Magnoliopsida. They are generally woody plants. A number of the species of this family contain cyanogenic compounds.
The figwort plant family of the order Lamiales. The family is characterized by bisexual flowers with tubular corollas (fused petals) that are bilaterally symmetrical (two-lips) and have four stamens in most, two of which are usually shorter.
The yam plant family, of the order Liliales, has thick roots or tubers and net-veined, heart-shaped leaves that sometimes are lobed.
Herbaceous biennial plants and their edible bulbs, belonging to the Liliaceae.
A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.
Picrates are salts of picric acid, an explosive organic compound previously used as a yellow dye and antiseptic, which are now primarily used in chemical research and industrial applications. Please note that picrates should be handled with care due to their potential explosiveness when heated or subjected to friction.
Plants whose roots, leaves, seeds, bark, or other constituent parts possess therapeutic, tonic, purgative, curative or other pharmacologic attributes, when administered to man or animals.
A group of 3-hydroxy-4-keto-FLAVONOIDS.
Thioglycosides are organic compounds consisting of a glycosyl group linked to a sulfur atom, often used in medicinal chemistry as antimicrobial, antiviral, and antifungal agents, or as enzyme inhibitors.
A group of phenyl benzopyrans named for having structures like FLAVONES.
A plant genus of the family MALVACEAE, order Malvales, subclass Dilleniida. The common name of 'Mallow' may sometimes get confused with other plants.
A plant genus of the family CUPRESSACEAE. The species are slow growing coniferous evergreen trees or shrubs.
Compounds with a core of 10 carbons generally formed via the mevalonate pathway from the combination of 3,3-dimethylallyl pyrophosphate and isopentenyl pyrophosphate. They are cyclized and oxidized in a variety of ways. Due to the low molecular weight many of them exist in the form of essential oils (OILS, VOLATILE).
A class of phenolic acids related to chlorogenic acid, p-coumaric acid, vanillic acid, etc., which are found in plant tissues. It is involved in plant growth regulation.
5,7,4'-trihydroxy-flavone, one of the FLAVONES.
A plant genus of the family EUPHORBIACEAE that is perennial with conspicuous, almost palmate leaves like those of RICINUS but more deeply parted into five to nine lobes. It is a source of a starch after removal of the cyanogenic glucosides. The common name of Arrowroot is also used with Maranta (MARANTACEAE). The common name of yuca is also used for YUCCA.
5,7,3',4'-tetrahydroxy-flavone, one of the FLAVONES.
Root-like underground horizontal stem of plants that produces shoots above and roots below. Distinguished from true roots which don't have buds and nodes. Similar to true roots in being underground and thickened by storage deposits.
A plant genus of the family ASTERACEAE. Members contain SESQUITERPENES. The common name of sweet coltsfoot is similar to the common name for TUSSILAGO.
The process of cleaving a chemical compound by the addition of a molecule of water.
The fleshy or dry ripened ovary of a plant, enclosing the seed or seeds.
A key intermediate in carbohydrate metabolism. Serves as a precursor of glycogen, can be metabolized into UDPgalactose and UDPglucuronic acid which can then be incorporated into polysaccharides as galactose and glucuronic acid. Also serves as a precursor of sucrose lipopolysaccharides, and glycosphingolipids.
Methylglycosides are glycosides with a methanol group (CH3-) replacing the hydrogen atom on the glycosidic oxygen, which can be found in various natural sources and have potential applications as sweetening agents or in pharmaceuticals.
A plant genus of the family OLEACEAE. Members contain secoiridoid glucosides and this is the source of oil of jasmine.
A plant species of the genus SOLANUM, family SOLANACEAE. The fruit is a large, egg-shaped berry, varying in color from dark purple to red, yellowish, or white. The leaves are large and ovate. The flowers are pendant, violet, and two inches across.
'Pyrans' are heterocyclic organic compounds containing a six-membered ring with one oxygen atom and five carbon atoms, which can be found in various natural substances and synthesized compounds, and may have potential applications in medicinal chemistry.
Organic compounds containing the -CN radical. The concept is distinguished from CYANIDES, which denotes inorganic salts of HYDROGEN CYANIDE.
A plant family of the order Lamiales. The leaves are usually opposite and the flowers usually have four sepals, four petals, two stamens, and two fused carpels that form a single superior ovary.
Methylglucosides are a type of sugar alcohols, specifically methylated glucose derivatives, which are used as sweetening agents, excipients, and solvents in pharmaceutical and cosmetic products due to their low toxicity and good solubility in water.
Enzymes that hydrolyze O-glucosyl-compounds. (Enzyme Nomenclature, 1992) EC 3.2.1.-.
A group of degraded TRITERPENES in which the four terminal carbons of the C17 side chain have been removed, and the remaining portion often forming C17 furans.
Triterpenes are a class of naturally occurring compounds consisting of six isoprene units arranged to form a 30-carbon skeleton, often found in plants and some animals, with various bioactivities including anti-inflammatory, antiviral, and cytotoxic properties.
The characteristic three-dimensional shape of a molecule.
A plant family of the order Santalales, subclass Rosidae, class Magnoliopsida. They are root parasites lacking CHLOROPHYLL.
A monocot family within the order Liliales. This family is divided by some botanists into other families such as Convallariaceae, Hyacinthaceae and Amaryllidaceae. Amaryllidaceae, which have inferior ovaries, includes CRINUM; GALANTHUS; LYCORIS; and NARCISSUS and are known for AMARYLLIDACEAE ALKALOIDS.
Arbutin is a natural derivative of hydroquinone, found in the leaves of some plant species, which exhibits skin lightening properties by inhibiting tyrosinase activity and reducing melanin production.
Chromatography on thin layers of adsorbents rather than in columns. The adsorbent can be alumina, silica gel, silicates, charcoals, or cellulose. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Parts of plants that usually grow vertically upwards towards the light and support the leaves, buds, and reproductive structures. (From Concise Dictionary of Biology, 1990)
A group of compounds which can be described as benzo-pyrano-furano-benzenes which can be formed from ISOFLAVONES by internal coupling of the B ring to the 4-ketone position. Members include medicarpin, phaseolin, and pisatin which are found in FABACEAE.
A plant genus of the family LILIACEAE that contains curculin and cycloartane saponins.
Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
Triterpenes that derive from LANOSTEROL by a shift of the C19 methyl to the C9 position. They are found in seeds and roots of CUCURBITACEAE and other plants and are noted for intense bitterness.
SESQUITERPENES cyclized into two adjoining cyclohexane rings but with a different configuration from the ARTEMISININS.
A plant genus of the family FABACEAE. This genus was formerly known as Tetragonolobus. The common name of lotus is also used for NYMPHAEA and NELUMBO.
Uridine Diphosphate (UDP) sugars are nucleotide sugars that serve as essential glycosyl donors in the biosynthesis of various glycoconjugates, including proteoglycans and glycoproteins.
Hydrocarbons with more than one triple bond; or an oxidized form of POLYENES. They can react with SULFUR to form THIOPHENES.
The extent to which the active ingredient of a drug dosage form becomes available at the site of drug action or in a biological medium believed to reflect accessibility to a site of action.
A plant family of the order Malvales, subclass Dilleniidae, class Magnoliopsida. The leaves of Sterculiaceae are alternate and simple or palmately compound. Flowers have three to five sepals and five or no petals.
A family of glycosidases that hydrolyse crystalline CELLULOSE into soluble sugar molecules. Within this family there are a variety of enzyme subtypes with differing substrate specificities that must work together to bring about complete cellulose hydrolysis. They are found in structures called CELLULOSOMES.
A plant genus of the family Paeoniaceae, order Dilleniales, subclass Dilleniidae, class Magnoliopsida. These perennial herbs are up to 2 m (6') tall. Leaves are alternate and are divided into three lobes, each lobe being further divided into three smaller lobes. The large flowers are symmetrical, bisexual, have 5 sepals, 5 petals (sometimes 10), and many stamens.
A plant genus of the family Plantaginaceae. Members contain bis-sesquiterpene and iridoid glucosides.
A plant genus of the family LAMIACEAE that contains cyasterone, ajugasterone, 20-hydroxyecdysone, 8-acetylharpagide (an iridoid glycoside).
Mildly aromatic herb in the Allium genus used in SPICES.
A beverage prepared from SOYBEANS.
Spectrophotometry in the infrared region, usually for the purpose of chemical analysis through measurement of absorption spectra associated with rotational and vibrational energy levels of molecules. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
A plant genus of the family Apiaceae. The seeds are used as flavoring.
A group of FLAVONOIDS characterized with a 4-ketone.
A plant genus of the family LAMIACEAE best known for the thyme spice added to foods.
A plant genus of the family MENISPERMACEAE. Members contain sinomenine, caffeine, 1,7-dimethylxanthine, and other ALKALOIDS.
A plant genus of the family Gentianaceae whose members contain SECOIRIDOIDS and have been used in TRADITIONAL MEDICINE for suppressing INFLAMMATION.
Derivatives of GLUCURONIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that include the 6-carboxy glucose structure.
Hydroxycinnamic acid and its derivatives. Act as activators of the indoleacetic acid oxidizing system, thereby producing a decrease in the endogenous level of bound indoleacetic acid in plants.
A plant genus of the family COMBRETACEAE. Triterpenes and combretastatin have been identified in members of this genus.
The ability of a substance to be dissolved, i.e. to form a solution with another substance. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
The mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).
A plant family of the order Dilleniales, subclass Dilleniidae, class Magnoliopsida.
A potent mycotoxin produced in feedstuffs by several species of the genus FUSARIUM. It elicits a severe inflammatory reaction in animals and has teratogenic effects.
A class of dibenzylbutane derivatives which occurs in higher plants and in fluids (bile, serum, urine, etc.) in man and other animals. These compounds, which have a potential anti-cancer role, can be synthesized in vitro by human fecal flora. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)

Single cell studies of enzymatic hydrolysis of a tetramethylrhodamine labeled triglucoside in yeast. (1/1610)

Several hundred molecules of enzyme reaction products were detected in a single spheroplast from yeast cells incubated with a tetramethylrhodamine (TMR) labeled triglucoside, alpha-d-Glc(1-->2)alpha-d-Glc(1-->3)alpha-d-Glc-O(CH2)8CONHCH2- CH2NH- COTMR. Product detection was accomplished using capillary electrophoresis and laser induced fluorescence following the introduction of a single spheroplast into the separation capillary. The in vivo enzymatic hydrolysis of the TMR-trisaccharide involves at least two enzymes, limited by processing alpha-glucosidase I, producing TMR-disaccharide, TMR-monosaccharide, and the free TMR-linking arm. Hydrolysis was reduced by preincubation of the cells with the processing enzyme inhibitor castanospermine. Confocal laser scanning microscopy studies confirmed the uptake and internalization of fluorescent substrate. This single cell analysis methodology can be applied for the in vivo assay of any enzyme with a fluorescent substrate.  (+info)

Determination of the anomeric configurations of Corbicula ceramide di- and trihexoside by chromium trioxide oxidation. (2/1610)

The anomeric configurations of Corbicula ceramide dihexoside and ceramide trihexoside were determined by chromium trioxide oxidation and the structures of these lipids were shown to be Man-beta(1 leads to 4)-Glc-beta(1 leads to 1)-ceramide and Man-alpha(1 leads to 4)-Man-beta(1 leads to 4)-Glc-beta(1 leads to 1)-ceramide. These results are compatible with those obtained by enzymic hydrolysis reported previously.  (+info)

Antioxidative and chelating activities of phenylpropanoid glycosides from Pedicularis striata. (3/1610)

AIM: To study the antioxidative and iron chelating activities of phenylpropanoid glycosides (PPG) isolated from a Chinese herb Pedicularis striata. METHODS: Antioxidative effects of PPG on lipid peroxidation induced by FeSO4-edetic acid in linoleic acid were measured by thiobarbituric acid method. Chelating activities of PPG for Fe2+ were tested by differential spectrum method. RESULTS: The reaction rates (A532.min-1) of lipid peroxidation were 0.0046 in the control, 0.0021 in verbascoside group, and 0.0008 in isoverbascoside group. The chelating activity of isoverbascoside was 2-fold stronger than that of verbascoside. Permethyl verbascoside showed neither antioxidative nor chelating activities. CONCLUSION: The inhibitory effects of PPG with phenolic hydroxy groups on lipid peroxidation are owing to their chelating properties. Under physiological condition PPG-Fe2+ chelates are sufficiently stable. Thus PPG are able to inhibit the Fe(2+)-dependent lipid peroxidation in vivo through chelating Fe2+ and exhibit their therapeutic potential by the same mechanism in vitro.  (+info)

Reduction of serum cholesterol and hypercholesterolemic atherosclerosis in rabbits by secoisolariciresinol diglucoside isolated from flaxseed. (4/1610)

BACKGROUND: Secoisolariciresinol diglucoside (SDG) is a plant lignan isolated from flaxseed. Lignans are platelet-activating factor-receptor antagonists that would inhibit the production of oxygen radicals by polymorphonuclear leukocytes. SDG is an antioxidant. Antioxidants studied thus far are known to reduce hypercholesterolemic atherosclerosis. The objective of this study was to determine the effect of SDG on various blood lipid and aortic tissue oxidative stress parameters and on the development of atherosclerosis in rabbits fed a high-cholesterol diet. METHODS AND RESULTS: Rabbits were assigned to 4 groups: group 1, control; group 2, SDG control (15 mg. kg body wt-1. d-1 PO); group 3, 1% cholesterol diet; and group 4, same as group 3 but with added SDG (15 mg. kg body wt-1. d-1 PO). Blood samples were collected before (time 0) and after 4 and 8 weeks of experimental diets for measurement of serum triglycerides, total cholesterol (TC), and LDL, HDL, and VLDL cholesterol (LDL-C, HDL-C, and VLDL-C). The aorta was removed at the end of the protocol for assessment of atherosclerotic plaques; malondialdehyde, an aortic tissue lipid peroxidation product; and aortic tissue chemiluminescence, a marker for antioxidant reserve. Serum TC, LDL-C, and the ratios LDL-C/HDL-C and TC/HDL-C increased in groups 3 and 4 compared with time 0, the increase being smaller in group 4 than in group 3. Serum HDL-C decreased in group 3 and increased in group 4 compared with time 0, but changes were lower in group 3 than in group 4. SDG reduced TC and LDL-C by 33% and 35%, respectively, at week 8 but increased HDL-C significantly, by>140%, as early as week 4. It also decreased TC/LDL-C and LDL-C/HDL-C ratios by approximately 64%. There was an increase in aortic malondialdehyde and chemiluminescence in group 3, and they were lower in group 4 than in group 3. SDG reduced hypercholesterolemic atherosclerosis by 73%. CONCLUSIONS: These results suggest that SDG reduced hypercholesterolemic atherosclerosis and that this effect was associated with a decrease in serum cholesterol, LDL-C, and lipid peroxidation product and an increase in HDL-C and antioxidant reserve.  (+info)

Comparative study of carbohydrate-protein complexes. II. Determination of hydroxylysine and its glycosides in human skin and scar collagens by an improved method. (5/1610)

A modification of the existing methods for measuring hydroxylysine, galactosylhydroxylysine, and glucosylgalactosylhydroxylysine is described. The method is based on analysis with an automated amino acid analyzer using a conventional separation system for basic amino acids. The prior removal of acidic and neutral amino acids was necessary. This was achieved by passing an alkaline hydrolysate of collagen through a column of Amberlite CG-120, Type II (H+) and washing the column with 8% aqueous pyridine. A basic fraction containing the hydroxylysine compounds was then recovered from the column by elution with 3 M NH4OH. Model experiments showed that hydroxylysine and its glycosides could be analyzed with an hour and that recoveries exceeded 90%. This method was applied to human tissues to investigate whether the dermal scar is different in collagen composition from normal skin. With the limited number of samples analyzed, the data suggested that long-standing scar tissues reverted to a composition similar to that of normal skin. The composition of hydroxylysine-linked carbohydrate units is also discussed on the basis of the age-related change.  (+info)

Latency of some glycosidases of rat liver lysosomes. (6/1610)

The latency of the alpha-glucosidase activity of intact rat liver lysosomes was studied by using four substrates (glycogen, maltose, p-nitrophenyl, alpha-glucoside, alpha-fluoroglucoside) at a range of substrate concentrations. The results indicate that the entire lysosome population is impermeable to glycogen and maltose, but a proportion of lysosomes are permeable to alpha-fluoroglucoside and a still higher proportion permeable to p-nitrophenyl alpha-glucoside. Incubation at 37 degrees C in an osmotically protected buffer of of pH 5.0 caused lysosomes to become permeable to previously impermeant substrates and ultimately to release their alpha-glucosidase into the medium. The latencies of lysosomal beta-glucosidase and beta-galactosidase were examined by using p-nitrophenyl beta-glucoside and beta-galactoside as substrates. The results indicate permeability properties to these substrates similar to that to p-nitrophenyl alpha-glucoside. On incubation in an osmotically protected buffer of pH 5, lysosomes progressively released their beta-galactosidase in soluble form, but beta-glucosidase remained attached to sedimentable material. Lysosomal beta-glucosidase was inhibited by 0.1% Triton X-100; alpha-glucosidase and beta-galactosidase were not inhibited.  (+info)

Elucidation of a PTS-carbohydrate chemotactic signal pathway in Escherichia coli using a time-resolved behavioral assay. (7/1610)

Chemotaxis of Escherichia coli toward phosphotransferase systems (PTSs)-carbohydrates requires phosphoenolpyruvate-dependent PTSs as well as the chemotaxis response regulator CheY and its kinase, CheA. Responses initiated by flash photorelease of a PTS substrates D-glucose and its nonmetabolizable analog methyl alpha-D-glucopyranoside were measured with 33-ms time resolution using computer-assisted motion analysis. This, together with chemotactic mutants, has allowed us to map out and characterize the PTS chemotactic signal pathway. The responses were absent in mutants lacking the general PTS enzymes EI or HPr, elevated in PTS transport mutants, retarded in mutants lacking CheZ, a catalyst of CheY autodephosphorylation, and severely reduced in mutants with impaired methyl-accepting chemotaxis protein (MCP) signaling activity. Response kinetics were comparable to those triggered by MCP attractant ligands over most of the response range, the most rapid being 11.7 +/- 3.1 s-1. The response threshold was <10 nM for glucose. Responses to methyl alpha-D-glucopyranoside had a higher threshold, commensurate with a lower PTS affinity, but were otherwise kinetically indistinguishable. These facts provide evidence for a single pathway in which the PTS chemotactic signal is relayed rapidly to MCP-CheW-CheA signaling complexes that effect subsequent amplification and slower CheY dephosphorylation. The high sensitivity indicates that this signal is generated by transport-induced dephosphorylation of the PTS rather than phosphoenolpyruvate consumption.  (+info)

Effects of endotoxin on surfactant protein A and D stimulation of NO production by alveolar macrophages. (8/1610)

Surfactant protein (SP) A and SP-D affect numerous functions of immune cells including enhancing phagocytosis of bacteria and production of reactive species. Previous studies have shown that SP-A and SP-D bind to a variety of bacteria and to the lipopolysaccharide (LPS) components of their cell walls. In addition, purified preparations of SPs often contain endotoxin. The goals of this study were 1) to evaluate the effects of SP-A and SP-D and complexes of SPs and LPS on the production of nitric oxide metabolites by rat alveolar macrophages and 2) to evaluate methods for the removal of endotoxin with optimal recovery of SP. Incubation of SP-A or SP-D with polymyxin, 100 mM N-octyl-beta-D-glucopyranoside, and 2 mM EDTA followed by dialysis was the most effective method of those tested for reducing endotoxin levels. Commonly used storage buffers for SP-D, but not for SP-A, inhibited the detection of endotoxin. There was a correlation between the endotoxin content of the SP-A and SP-D preparations and their ability to stimulate production of nitrite by alveolar macrophages. SP-A and SP-D treated as described above to remove endotoxin did not stimulate nitrite production. These studies suggest that the functions of SP-A and SP-D are affected by endotoxin and illustrate the importance of monitoring SP preparations for endotoxin contamination.  (+info)

Glucosides are chemical compounds that consist of a glycosidic bond between a sugar molecule (typically glucose) and another non-sugar molecule, which can be an alcohol, phenol, or steroid. They occur naturally in various plants and some microorganisms.

Glucosides are not medical terms per se, but they do have significance in pharmacology and toxicology because some of them may release the sugar portion upon hydrolysis, yielding aglycone, which can have physiological effects when ingested or absorbed into the body. Some glucosides are used as medications or dietary supplements due to their therapeutic properties, while others can be toxic if consumed in large quantities.

Glycosides are organic compounds that consist of a glycone (a sugar component) linked to a non-sugar component, known as an aglycone, via a glycosidic bond. They can be found in various plants, microorganisms, and some animals. Depending on the nature of the aglycone, glycosides can be classified into different types, such as anthraquinone glycosides, cardiac glycosides, and saponin glycosides.

These compounds have diverse biological activities and pharmacological effects. For instance:

* Cardiac glycosides, like digoxin and digitoxin, are used in the treatment of heart failure and certain cardiac arrhythmias due to their positive inotropic (contractility-enhancing) and negative chronotropic (heart rate-slowing) effects on the heart.
* Saponin glycosides have potent detergent properties and can cause hemolysis (rupture of red blood cells). They are used in various industries, including cosmetics and food processing, and have potential applications in drug delivery systems.
* Some glycosides, like amygdalin found in apricot kernels and bitter almonds, can release cyanide upon hydrolysis, making them potentially toxic.

It is important to note that while some glycosides have therapeutic uses, others can be harmful or even lethal if ingested or otherwise introduced into the body in large quantities.

Iridoids are a type of naturally occurring compounds that are widely distributed in the plant kingdom. They are characterized by the presence of a cyclopentanoid structure fused to a monoterpene unit. Iridoids have a wide range of biological activities, including anti-inflammatory, analgesic, and antioxidant effects. Some iridoids also have potential therapeutic benefits in the treatment of various diseases, such as cancer and neurodegenerative disorders.

In a medical context, iridoids may be mentioned in relation to their presence in certain medicinal plants or herbs used in traditional medicine, or in research investigating their potential pharmacological properties. However, it is important to note that the use of iridoid-containing plants or supplements should only be done under the guidance of a qualified healthcare professional, as with any medical treatment.

I'm sorry for any confusion, but "Norisoprenoids" is not a widely recognized or established term in medicine or medical chemistry. It appears to be a term used primarily in the field of plant metabolism and natural products chemistry, referring to a class of compounds that are derived from the degradation of carotenoids (a type of isoprenoid) and have lost one or more methyl groups.

If you're asking about this term in a different context or if there's specific medical relevance you have in mind, could you please provide more details? I'd be happy to help further if I can.

Iridoid glucosides are a type of plant-based compounds that are characterized by their iridoid structure, which is a cyclic organic compound containing a cyclopentane ring fused to a six-membered unsaturated carbocycle. These compounds are often found in plants as glycosides, meaning they are combined with a sugar molecule such as glucose.

Iridoid glucosides have been identified in a variety of plant families, including the Lamiaceae (mint family), Scrophulariaceae (figwort family), and Rubiaceae (coffee family). Some examples of iridoid glucosides include geniposide, which is found in the fruit of the gardenia plant, and aucubin, which is found in the leaves of the eucommia tree.

Iridoid glucosides have been studied for their potential medicinal properties, including anti-inflammatory, antioxidant, and antimicrobial effects. However, more research is needed to fully understand their mechanisms of action and potential therapeutic uses.

Rubiaceae is not a medical term, but a taxonomic category in botany. It refers to the family of flowering plants that includes more than 13,500 species, distributed across approximately 600 genera. Some well-known members of this family include coffee (Coffea arabica), gardenias (Gardenia jasminoides), and madder (Rubia tinctorum).

In a medical context, certain plants from the Rubiaceae family have been used in traditional medicine for various purposes. For example:

* Coffee (Coffea arabica) beans are used to prepare caffeinated beverages that can help with alertness and concentration.
* Gardenia fruits and flowers have been used in traditional Chinese medicine to treat anxiety, insomnia, and inflammation.
* Madder root (Rubia tinctorum) has been used as a dye and in traditional medicine to treat skin conditions and digestive disorders.

However, it's important to note that the medicinal use of plants from this family should be based on scientific evidence and under the guidance of healthcare professionals, as some of these plants can have side effects or interact with medications.

Anthocyanins are a type of plant pigment that belong to the flavonoid group. They are responsible for providing colors ranging from red, purple, and blue to black in various fruits, vegetables, flowers, and leaves. Anthocyanins have been studied extensively due to their potential health benefits, which include antioxidant, anti-inflammatory, and anti-cancer properties. They also play a role in protecting plants from environmental stressors such as UV radiation, pathogens, and extreme temperatures. Chemically, anthocyanins are water-soluble compounds that can form complex structures with other molecules, leading to variations in their color expression depending on pH levels.

Thioglucosides are organic compounds that contain a sulfur atom bonded to a glucose molecule and another group, usually a methane or phenyl group. They are found in certain plants, particularly in the Brassicaceae family (which includes vegetables like broccoli, brussels sprouts, and cabbage) and in the Liliaceae family (which includes onions and garlic). These compounds are responsible for the characteristic flavors and odors of these plants. They have been studied for their potential health benefits, including anti-cancer and antimicrobial properties. However, they can also be toxic in high concentrations.

Beta-glucosidase is an enzyme that breaks down certain types of complex sugars, specifically those that contain a beta-glycosidic bond. This enzyme is found in various organisms, including humans, and plays a role in the digestion of some carbohydrates, such as cellulose and other plant-based materials.

In the human body, beta-glucosidase is produced by the lysosomes, which are membrane-bound organelles found within cells that help break down and recycle various biological molecules. Beta-glucosidase is involved in the breakdown of glycolipids and gangliosides, which are complex lipids that contain sugar molecules.

Deficiencies in beta-glucosidase activity can lead to certain genetic disorders, such as Gaucher disease, in which there is an accumulation of glucocerebrosidase, a type of glycolipid, within the lysosomes. This can result in various symptoms, including enlargement of the liver and spleen, anemia, and bone pain.

Quercetin is a type of flavonoid antioxidant that is found in plant foods, including leafy greens, tomatoes, berries, and broccoli. It has been studied for its potential health benefits, such as reducing inflammation, protecting against damage to cells, and helping to reduce the risk of heart disease and cancer. Quercetin is also known for its ability to stabilize mast cells and prevent the release of histamine, making it a popular natural remedy for allergies. It is available in supplement form, but it is always recommended to consult with a healthcare provider before starting any new supplement regimen.

Aerial parts of plants refer to the above-ground portions of a plant, including leaves, stems, flowers, and fruits. These parts are often used in medicine, either in their entirety or as isolated extracts, to take advantage of their medicinal properties. The specific components of aerial parts that are used in medicine can vary depending on the plant species and the desired therapeutic effects. For example, the leaves of some plants may contain active compounds that have anti-inflammatory or analgesic properties, while the flowers of others may be rich in antioxidants or compounds with sedative effects. In general, aerial parts of plants are used in herbal medicine to treat a wide range of conditions, including respiratory, digestive, and nervous system disorders, as well as skin conditions and infections.

Glucosyltransferases (GTs) are a group of enzymes that catalyze the transfer of a glucose molecule from an activated donor to an acceptor molecule, resulting in the formation of a glycosidic bond. These enzymes play crucial roles in various biological processes, including the biosynthesis of complex carbohydrates, cell wall synthesis, and protein glycosylation. In some cases, GTs can also contribute to bacterial pathogenesis by facilitating the attachment of bacteria to host tissues through the formation of glucans, which are polymers of glucose molecules.

GTs can be classified into several families based on their sequence similarities and catalytic mechanisms. The donor substrates for GTs are typically activated sugars such as UDP-glucose, TDP-glucose, or GDP-glucose, which serve as the source of the glucose moiety that is transferred to the acceptor molecule. The acceptor can be a wide range of molecules, including other sugars, proteins, lipids, or small molecules.

In the context of human health and disease, GTs have been implicated in various pathological conditions, such as cancer, inflammation, and microbial infections. For example, some GTs can modify proteins on the surface of cancer cells, leading to increased cell proliferation, migration, and invasion. Additionally, GTs can contribute to bacterial resistance to antibiotics by modifying the structure of bacterial cell walls or by producing biofilms that protect bacteria from host immune responses and antimicrobial agents.

Overall, Glucosyltransferases are essential enzymes involved in various biological processes, and their dysregulation has been associated with several human diseases. Therefore, understanding the structure, function, and regulation of GTs is crucial for developing novel therapeutic strategies to target these enzymes and treat related pathological conditions.

Amygdalin is a naturally occurring compound found in the seeds of some fruits, such as apricots, and in certain nuts, including almonds. It is also known as "laetrile" and has been promoted as an alternative treatment for cancer. However, its effectiveness as a cancer treatment is not supported by scientific evidence, and it can have serious side effects, including cyanide poisoning. The use of amygdalin as a medical treatment is not approved by regulatory agencies in many countries, including the United States and Canada.

A plant extract is a preparation containing chemical constituents that have been extracted from a plant using a solvent. The resulting extract may contain a single compound or a mixture of several compounds, depending on the extraction process and the specific plant material used. These extracts are often used in various industries including pharmaceuticals, nutraceuticals, cosmetics, and food and beverage, due to their potential therapeutic or beneficial properties. The composition of plant extracts can vary widely, and it is important to ensure their quality, safety, and efficacy before use in any application.

I'm sorry for any confusion, but "Verbena" is not a medical term. It is the name of a genus of plants commonly known as vervain, which have been used in various traditional medicines and herbal remedies. However, it is not a term used in modern conventional medicine.

I believe there may be a slight misunderstanding in your question. "Plant leaves" are not a medical term, but rather a general biological term referring to a specific organ found in plants.

Leaves are organs that are typically flat and broad, and they are the primary site of photosynthesis in most plants. They are usually green due to the presence of chlorophyll, which is essential for capturing sunlight and converting it into chemical energy through photosynthesis.

While leaves do not have a direct medical definition, understanding their structure and function can be important in various medical fields, such as pharmacognosy (the study of medicinal plants) or environmental health. For example, certain plant leaves may contain bioactive compounds that have therapeutic potential, while others may produce allergens or toxins that can impact human health.

Euphorbiaceae is not a medical term, but a taxonomic category in botany. It refers to the spurge family, which is a large family of flowering plants that includes around 300 genera and 7,500 species. Some members of this family have medicinal uses, but others are toxic or invasive. Therefore, it is important to use caution when handling or consuming any plant material from this family.

Molecular structure, in the context of biochemistry and molecular biology, refers to the arrangement and organization of atoms and chemical bonds within a molecule. It describes the three-dimensional layout of the constituent elements, including their spatial relationships, bond lengths, and angles. Understanding molecular structure is crucial for elucidating the functions and reactivities of biological macromolecules such as proteins, nucleic acids, lipids, and carbohydrates. Various experimental techniques, like X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and cryo-electron microscopy (cryo-EM), are employed to determine molecular structures at atomic resolution, providing valuable insights into their biological roles and potential therapeutic targets.

Fast Atom Bombardment (FAB) Mass Spectrometry is a technique used for determining the mass of ions in a sample. In FAB-MS, the sample is mixed with a matrix material and then bombarded with a beam of fast atoms, usually xenon or cesium. This bombardment leads to the formation of ions from the sample which can then be detected and measured using a mass analyzer. The resulting mass spectrum provides information about the molecular weight and structure of the sample molecules. FAB-MS is particularly useful for the analysis of large, thermally labile, or polar molecules that may not ionize well by other methods.

Magnetic Resonance Spectroscopy (MRS) is a non-invasive diagnostic technique that provides information about the biochemical composition of tissues, including their metabolic state. It is often used in conjunction with Magnetic Resonance Imaging (MRI) to analyze various metabolites within body tissues, such as the brain, heart, liver, and muscles.

During MRS, a strong magnetic field, radio waves, and a computer are used to produce detailed images and data about the concentration of specific metabolites in the targeted tissue or organ. This technique can help detect abnormalities related to energy metabolism, neurotransmitter levels, pH balance, and other biochemical processes, which can be useful for diagnosing and monitoring various medical conditions, including cancer, neurological disorders, and metabolic diseases.

There are different types of MRS, such as Proton (^1^H) MRS, Phosphorus-31 (^31^P) MRS, and Carbon-13 (^13^C) MRS, each focusing on specific elements or metabolites within the body. The choice of MRS technique depends on the clinical question being addressed and the type of information needed for diagnosis or monitoring purposes.

High-performance liquid chromatography (HPLC) is a type of chromatography that separates and analyzes compounds based on their interactions with a stationary phase and a mobile phase under high pressure. The mobile phase, which can be a gas or liquid, carries the sample mixture through a column containing the stationary phase.

In HPLC, the mobile phase is a liquid, and it is pumped through the column at high pressures (up to several hundred atmospheres) to achieve faster separation times and better resolution than other types of liquid chromatography. The stationary phase can be a solid or a liquid supported on a solid, and it interacts differently with each component in the sample mixture, causing them to separate as they travel through the column.

HPLC is widely used in analytical chemistry, pharmaceuticals, biotechnology, and other fields to separate, identify, and quantify compounds present in complex mixtures. It can be used to analyze a wide range of substances, including drugs, hormones, vitamins, pigments, flavors, and pollutants. HPLC is also used in the preparation of pure samples for further study or use.

Isoflavones are a type of plant-derived compounds called phytoestrogens, which have a chemical structure similar to human estrogen. They are found in various plants, particularly in soybeans and soy products. Isoflavones can act as weak estrogens or anti-estrogens in the body, depending on the levels of natural hormones present. These compounds have been studied for their potential health benefits, including reducing menopausal symptoms, improving cardiovascular health, and preventing certain types of cancer. However, more research is needed to fully understand their effects and safety.

Cyclohexanones are organic compounds that consist of a cyclohexane ring (a six-carbon saturated ring) with a ketone functional group (-CO-) attached to it. The general structure is C6H11CO. They can be found in various natural sources, including essential oils and certain plants, but many cyclohexanones are also synthesized for use in the chemical industry.

Cyclohexanones are important intermediates in the production of various chemicals, such as nylon and other synthetic fibers, resins, and perfumes. One of the most common cyclohexanones is cyclohexanone itself, which is a colorless liquid with an odor reminiscent of peppermint or acetone. It is used in the production of adipic acid, a precursor to nylon.

Like other ketones, cyclohexanones can undergo various chemical reactions, such as reduction, oxidation, and condensation. However, due to the cyclic structure of cyclohexanones, they also exhibit unique reactivity patterns that are exploited in organic synthesis.

In medical terms, "Rheum" is not a specific disease or condition. Instead, it is a term that was historically used to refer to a variety of disorders characterized by inflammation and pain in the musculoskeletal system, particularly in the joints. These disorders were often associated with symptoms such as stiffness, swelling, and warmth in the affected areas.

Over time, the term "rheumatic diseases" has become more commonly used to describe this group of conditions. Rheumatic diseases now encompass a wide range of disorders that affect the joints, muscles, tendons, ligaments, bones, and other connective tissues. Examples include rheumatoid arthritis, osteoarthritis, lupus, gout, and many others.

It's important to note that while "rheum" is an outdated term in modern medical nomenclature, it still holds historical significance and is sometimes used in the names of certain medical conditions or concepts, such as "rheumatology," which is the medical specialty focused on the diagnosis and management of rheumatic diseases.

Detergents are cleaning agents that are often used to remove dirt, grease, and stains from various surfaces. They contain one or more surfactants, which are compounds that lower the surface tension between two substances, such as water and oil, allowing them to mix more easily. This makes it possible for detergents to lift and suspend dirt particles in water so they can be rinsed away.

Detergents may also contain other ingredients, such as builders, which help to enhance the cleaning power of the surfactants by softening hard water or removing mineral deposits. Some detergents may also include fragrances, colorants, and other additives to improve their appearance or performance.

In a medical context, detergents are sometimes used as disinfectants or antiseptics, as they can help to kill bacteria, viruses, and other microorganisms on surfaces. However, it is important to note that not all detergents are effective against all types of microorganisms, and some may even be toxic or harmful if used improperly.

It is always important to follow the manufacturer's instructions when using any cleaning product, including detergents, to ensure that they are used safely and effectively.

Hydrogen Cyanide (HCN) is a chemical compound with the formula H-C≡N. It is a colorless, extremely poisonous and flammable liquid that has a bitter almond-like odor in its pure form. However, not everyone can detect its odor, as some people lack the ability to smell it, which makes it even more dangerous. It is soluble in water and alcohol, and its aqueous solution is called hydrocyanic acid or prussic acid.

Hydrogen Cyanide is rapidly absorbed by inhalation, ingestion, or skin contact, and it inhibits the enzyme cytochrome c oxidase, which is essential for cellular respiration. This leads to rapid death due to hypoxia (lack of oxygen) at the cellular level. It is used industrially in large quantities as a pesticide, fumigant, and chemical intermediate, but it also has significant potential for use as a chemical weapon.

In the medical field, Hydrogen Cyanide poisoning can be treated with high-concentration oxygen, sodium nitrite, and sodium thiosulfate, which help to restore the function of cytochrome c oxidase and enhance the elimination of cyanide from the body.

"Bidens" is a genus of flowering plants in the family Asteraceae, also known as the daisy or composite family. The name "Bidens" comes from the Latin words "bi," meaning two, and "dens," meaning teeth, referring to the characteristic pair of pointed bracts at the base of each flower. These plants are often called "beggar's ticks" or "stickseeds" because the small, barbed seeds cling to fur, feathers, and clothing, aiding in their dispersal.

There is no medical definition for "Bidens" as it does not refer to any medical condition, disease, or treatment. It is purely a taxonomic term used in botany to classify a group of plants with similar characteristics.

Rosaceae is not a medical term but a taxonomic category in biology, specifically an family of flowering plants. However, many physicians and dermatologists are familiar with some members of this family because they cause several common skin conditions.

Rosaceae refers to a family of plants that include roses, strawberries, blackberries, and many other ornamental and edible plants. Some genera within this family contain species known to cause various dermatologic conditions in humans, particularly affecting the face.

The most well-known skin disorders associated with Rosaceae are:

1. Acne rosacea (or rosacea): A chronic inflammatory skin condition primarily affecting the central face, characterized by flushing, persistent erythema (redness), telangiectasia (dilated blood vessels), papules, pustules, and sometimes rhinophyma (enlarged, bulbous nose).
2. Erythematotelangiectatic rosacea: A subtype of rosacea characterized by persistent central facial erythema, flushing, and telangiectasia without papules or pustules.
3. Phymatous rosacea: A subtype of rosacea characterized by thickening skin, irregular surface nodularities, and enlargement, particularly of the nose (rhinophyma).
4. Ocular rosacea: Inflammation of the eyes and eyelids associated with rosacea, causing symptoms like dryness, grittiness, foreign body sensation, burning, stinging, itching, watering, redness, and occasional blurry vision.

While not a medical term itself, Rosaceae is an essential concept in dermatology due to the skin conditions it encompasses.

Scrophulariaceae is a family of plants commonly known as the Figwort or Snapdragon family. It was once a large and diverse group, but many of its members have been reclassified into different families in recent years based on molecular evidence. The family still includes a number of well-known garden plants such as foxgloves (Digitalis), snapdragons (Antirrhinum), and penstemons (Penstemon).

The plants in Scrophulariaceae are typically herbaceous, although some are shrubs or small trees. They are characterized by their two-lipped flowers, with the upper lip usually forming a hood and the lower lip often having three lobes. The stamens and style are often enclosed within the flower and only emerge when it is fully open.

Scrophulariaceae has been reported to contain various chemical compounds with potential medicinal properties, such as cardiac glycosides in Digitalis species, which have been used to treat heart conditions. However, it's important to note that the use of these plants for medicinal purposes should only be done under the guidance and supervision of a qualified healthcare professional, as they can also contain toxic compounds that may cause harm if not used correctly.

Dioscoreaceae is a family of flowering plants that includes around 750 species, mostly native to tropical and warm temperate regions. It is also known as the yam family. The plants in this family are primarily herbaceous or climbing vines, although some are small trees or shrubs. They have simple, alternate leaves and produce small flowers that are typically greenish-white or yellowish in color.

The most economically important member of Dioscoreaceae is the sweet potato (Ipomoea batatas), which is not a true yam but is a close relative. True yams, on the other hand, are the starchy, tuberous roots of several species of Dioscorea, including D. alata, D. esculenta, and D. rotundata. Yams are an important food crop in many parts of the world, particularly in Africa and Asia.

Overall, Dioscoreaceae is a diverse family of plants that includes a number of economically and culturally significant species.

I'm sorry for any confusion, but "onions" are not a medical term. They are a type of vegetable, specifically a variety of bulb vegetables, known scientifically as Allium cepa. Onions are widely used in cooking and have been cultivated for centuries for their unique, pungent flavor and potential health benefits. If you have any questions about onions in a culinary or nutritional context, I'd be happy to try to help answer those!

Rutin is a flavonoid, a type of plant pigment that is found in various plants and foods including citrus fruits, buckwheat, and asparagus. It has antioxidant properties and is known to help strengthen blood vessels and reduce inflammation. In medical terms, rutin may be mentioned in the context of discussing treatments for conditions related to these effects, such as varicose veins or hemorrhoids. However, it's important to note that while rutin has potential health benefits, more research is needed to fully understand its effects and proper dosages.

I am not a medical expert, but I can provide some information that may be helpful. "Picrates" is not a term commonly used in medical definitions. Instead, it is a term used in chemistry to refer to salts of picric acid (2,4,6-trinitrophenol), which was once used as a yellow dye and explosive.

Picric acid has been used historically in some medical applications, such as a component in certain topical antiseptics and in histological staining procedures. However, its use in modern medicine is quite limited due to its high sensitivity to impact, heat, and friction, which makes it potentially dangerous to handle.

Therefore, it's important to note that "picrates" is not a medical term per se but rather a chemical one, and any medical application of picric acid or its salts would be highly specialized and unlikely to be encountered in most healthcare settings.

Medicinal plants are defined as those plants that contain naturally occurring chemical compounds which can be used for therapeutic purposes, either directly or indirectly. These plants have been used for centuries in various traditional systems of medicine, such as Ayurveda, Chinese medicine, and Native American medicine, to prevent or treat various health conditions.

Medicinal plants contain a wide variety of bioactive compounds, including alkaloids, flavonoids, tannins, terpenes, and saponins, among others. These compounds have been found to possess various pharmacological properties, such as anti-inflammatory, analgesic, antimicrobial, antioxidant, and anticancer activities.

Medicinal plants can be used in various forms, including whole plant material, extracts, essential oils, and isolated compounds. They can be administered through different routes, such as oral, topical, or respiratory, depending on the desired therapeutic effect.

It is important to note that while medicinal plants have been used safely and effectively for centuries, they should be used with caution and under the guidance of a healthcare professional. Some medicinal plants can interact with prescription medications or have adverse effects if used inappropriately.

Flavonols are a type of flavonoid, which is a class of plant and fungal metabolites. They are characterized by the presence of a 3-hydroxyflavone skeleton. Flavonols are found in a variety of plants and are known for their antioxidant properties. Some common dietary sources of flavonols include onions, kale, broccoli, apples, tea, and red wine. They have been studied for their potential health benefits, including reducing the risk of chronic diseases such as cancer and cardiovascular disease. Flavonols are also known to have anti-inflammatory, neuroprotective, and antimicrobial properties.

Thioglycosides are organic compounds that contain a sulfur atom (sulfur-sulfur bond) linked to a glycosyl group. They are structurally similar to glycosides, but instead of having an oxygen atom linking the sugar moiety to the aglycone, they have a sulfur atom. Thioglycosides are often used in glycobiology research as inhibitors of glycosidases or as substrates for glycosyltransferases. They also have applications in the pharmaceutical industry as anti-microbial and anti-cancer agents.

Flavonoids are a type of plant compounds with antioxidant properties that are beneficial to health. They are found in various fruits, vegetables, grains, and wine. Flavonoids have been studied for their potential to prevent chronic diseases such as heart disease and cancer due to their ability to reduce inflammation and oxidative stress.

There are several subclasses of flavonoids, including:

1. Flavanols: Found in tea, chocolate, grapes, and berries. They have been shown to improve blood flow and lower blood pressure.
2. Flavones: Found in parsley, celery, and citrus fruits. They have anti-inflammatory and antioxidant properties.
3. Flavanonols: Found in citrus fruits, onions, and tea. They have been shown to improve blood flow and reduce inflammation.
4. Isoflavones: Found in soybeans and legumes. They have estrogen-like effects and may help prevent hormone-related cancers.
5. Anthocyanidins: Found in berries, grapes, and other fruits. They have antioxidant properties and may help improve vision and memory.

It is important to note that while flavonoids have potential health benefits, they should not be used as a substitute for medical treatment or a healthy lifestyle. It is always best to consult with a healthcare professional before starting any new supplement regimen.

I'm sorry for any confusion, but "Malva" is not a commonly used medical term. It is the name of a genus of plants that includes mallows, which have been used in traditional medicine for various purposes such as treating skin inflammation and digestive issues. However, it is not a standard term in modern clinical or pathological settings. If you have any specific concerns related to health or medical conditions, it would be best to consult with a healthcare professional.

"Juniperus" is not a medical term itself, but it refers to a genus of evergreen coniferous trees and shrubs that belong to the cypress family (Cupressaceae). There are around 50-70 species in this genus, which are native to the northern hemisphere.

Juniperus species have been used in traditional medicine for various purposes, such as treating digestive disorders, skin conditions, and respiratory ailments. The essential oil extracted from some Juniperus species contains compounds that have antimicrobial, anti-inflammatory, and analgesic properties. However, it's important to note that the use of juniper in modern medicine is limited, and its efficacy and safety for specific medical conditions are not well-established.

Therefore, if you're considering using juniper or any of its preparations for medicinal purposes, it's recommended to consult a healthcare professional first to ensure its safe and appropriate use.

Monoterpenes are a class of terpenes that consist of two isoprene units and have the molecular formula C10H16. They are major components of many essential oils found in plants, giving them their characteristic fragrances and flavors. Monoterpenes can be further classified into various subgroups based on their structural features, such as acyclic (e.g., myrcene), monocyclic (e.g., limonene), and bicyclic (e.g., pinene) compounds. In the medical field, monoterpenes have been studied for their potential therapeutic properties, including anti-inflammatory, antimicrobial, and anticancer activities. However, more research is needed to fully understand their mechanisms of action and clinical applications.

Caffeic acids are a type of phenolic compounds that contain a catechol structure and a carboxylic acid group. They are found in various plants, including coffee, tea, fruits, and vegetables. The most common caffeic acid is caffeic acid itself, which is abundant in coffee. Caffeic acids have been studied for their potential health benefits, such as antioxidant, anti-inflammatory, and anticancer activities. However, more research is needed to fully understand their effects on human health.

Apigenin is a flavonoid, which is a type of plant pigment that is responsible for the color of many fruits and vegetables. It is found in various plants such as chamomile, parsley, celery, and citrus fruits. Apigenin has been studied for its potential health benefits, including anti-cancer, anti-inflammatory, and neuroprotective effects. However, more research is needed to confirm these potential benefits and determine the safe and effective dosage for human use.

"Manihot" is a botanical term that refers to a genus of plants in the Euphorbiaceae family, also known as the spurge family. The most well-known species in this genus is Manihot esculenta, which is commonly called cassava or yuca. Cassava is a staple food crop in many tropical and subtropical regions of the world, providing carbohydrates and calories for millions of people.

The roots of the cassava plant are rich in starch and can be eaten after being cooked or processed to remove toxic compounds. Cassava is an important source of dietary energy in many parts of Africa, Latin America, and Asia. In addition to its use as a food crop, some species of Manihot have also been used in traditional medicine for various purposes, although more research is needed to confirm their effectiveness and safety.

Luteolin is a flavonoid, which is a type of plant pigment that has various beneficial effects on human health. It can be found in various fruits, vegetables, and herbs such as artichokes, peppers, celery, broccoli, peppermint, rosemary, and chamomile tea.

Luteolin has been shown to have anti-inflammatory, antioxidant, and anticancer properties in laboratory studies. It works by inhibiting the activity of certain enzymes and receptors that play a role in inflammation and cancer development. However, more research is needed to determine its effectiveness and safety as a treatment for various medical conditions.

A rhizome is not typically used as a medical term, but it is a term borrowed from botany that has been adopted in some areas of medicine, particularly in psychiatry and psychotherapy.

In its original botanical sense, a rhizome is a horizontal stem of a plant that grows underground, often sending out roots and shoots from its nodes. This growth pattern is contrasted with that of a root system, which grows downward, and a stem system, which grows upward.

In psychiatry and psychotherapy, the term "rhizome" has been used as a metaphor to describe a non-hierarchical and decentralized approach to understanding mental processes and subjectivity. The rhizome model emphasizes the complexity, multiplicity, and interconnectedness of these processes, and rejects simplistic or reductionist explanations that focus on a single cause or origin. Instead, it encourages a more holistic and dynamic view of mental life, one that is open to multiple perspectives and interpretations.

It's important to note that the use of the term "rhizome" in this context is metaphorical and not medical in the strict sense. It is a way of thinking about mental processes and subjectivity that has been influenced by poststructuralist and feminist theories, among others.

"Petasites" is a genus name in botany, which refers to a group of flowering plants in the family Asteraceae. While it may not have a direct medical definition, some species within this genus have been used in traditional medicine. For instance, Petasites hybridus (also known as butterbur) has been used in herbal medicine for treating migraines, allergies, and asthma. However, it's important to note that the use of these plants should be under the guidance of a healthcare professional, as they can have side effects and interact with certain medications.

Hydrolysis is a chemical process, not a medical one. However, it is relevant to medicine and biology.

Hydrolysis is the breakdown of a chemical compound due to its reaction with water, often resulting in the formation of two or more simpler compounds. In the context of physiology and medicine, hydrolysis is a crucial process in various biological reactions, such as the digestion of food molecules like proteins, carbohydrates, and fats. Enzymes called hydrolases catalyze these hydrolysis reactions to speed up the breakdown process in the body.

I'm sorry for any confusion, but "fruit" is not a medical term per se. It is a common term used to describe the part of a plant that develops from the ovary after flowering and contains seeds. However, in a nutritional or dietary context, "fruits" are often referred to as foods that are typically sweet and juicy, and come from plants' flowers. They are rich in fiber, vitamins, and minerals, making them an essential part of a healthy diet. But in a strict medical sense, there isn't a specific definition for "fruit."

Uridine Diphosphate Glucose (UDP-glucose) is a nucleotide sugar that plays a crucial role in the synthesis and metabolism of carbohydrates in the body. It is formed from uridine triphosphate (UTP) and glucose-1-phosphate through the action of the enzyme UDP-glucose pyrophosphorylase.

UDP-glucose serves as a key intermediate in various biochemical pathways, including glycogen synthesis, where it donates glucose molecules to form glycogen, a large polymeric storage form of glucose found primarily in the liver and muscles. It is also involved in the biosynthesis of other carbohydrate-containing compounds such as proteoglycans and glycolipids.

Moreover, UDP-glucose is an essential substrate for the enzyme glucosyltransferase, which is responsible for adding glucose molecules to various acceptor molecules during the process of glycosylation. This post-translational modification is critical for the proper folding and functioning of many proteins.

Overall, UDP-glucose is a vital metabolic intermediate that plays a central role in carbohydrate metabolism and protein function.

Methylglycosides are not a recognized medical term or concept. However, in chemistry, methylglycosides refer to glycosidic compounds in which the glycosidic linkage is formed between a hemiacetal or hemiketal of a monosaccharide and a methanol molecule. These compounds are not typically associated with medical definitions or applications, but rather fall under the broader categories of organic chemistry or biochemistry.

"Jasminum" is the botanical name for a genus of shrubs and vines that belong to the family Oleaceae. There are around 200 species in this genus, including many well-known ornamental plants that are cultivated for their fragrant flowers. However, it's important to note that "Jasminum" is not a medical term and does not have a specific medical definition.

While some Jasminum species have been used in traditional medicine in various cultures, there is limited scientific evidence to support their effectiveness or safety. Therefore, it's essential to consult with a healthcare professional before using any plant or herbal remedy for medicinal purposes.

'Solanum melongena' is the scientific name for a plant species more commonly known as eggplant or aubergine. It belongs to the Solanaceae family, which also includes tomatoes, bell peppers, and potatoes. The eggplant fruit is widely consumed and used in various cuisines around the world.

While 'Solanum melongena' is a horticultural term related to the plant species, it does not have a direct medical definition. However, eggplants do have some nutritional and potential medicinal properties. They are low in calories and contain vitamins, minerals, and dietary fiber. Some studies suggest that eggplants may have antioxidant and anti-inflammatory properties due to their phenolic compounds. Nonetheless, it is essential to consult medical professionals or healthcare providers for advice on medicinal applications rather than relying on information about the plant's scientific name alone.

"Pyrans" is not a term commonly used in medical definitions. It is a chemical term that refers to a class of heterocyclic compounds containing a six-membered ring with one oxygen atom and five carbon atoms. The name "pyran" comes from the fact that it contains a pyroline unit (two double-bonded carbons) and a ketone group (a carbon double-bonded to an oxygen).

While pyrans are not directly related to medical definitions, some of their derivatives have been studied for potential medicinal applications. For example, certain pyran derivatives have shown anti-inflammatory, antiviral, and anticancer activities in laboratory experiments. However, more research is needed before these compounds can be considered as potential therapeutic agents.

Nitriles, in a medical context, refer to a class of organic compounds that contain a cyano group (-CN) bonded to a carbon atom. They are widely used in the chemical industry and can be found in various materials, including certain plastics and rubber products.

In some cases, nitriles can pose health risks if ingested, inhaled, or come into contact with the skin. Short-term exposure to high levels of nitriles can cause irritation to the eyes, nose, throat, and respiratory tract. Prolonged or repeated exposure may lead to more severe health effects, such as damage to the nervous system, liver, and kidneys.

However, it's worth noting that the medical use of nitriles is not very common. Some nitrile gloves are used in healthcare settings due to their resistance to many chemicals and because they can provide a better barrier against infectious materials compared to latex or vinyl gloves. But beyond this application, nitriles themselves are not typically used as medications or therapeutic agents.

"Oleaceae" is not a medical term, but a taxonomic category in botany. It refers to the family of plants that includes olive trees, ash trees, and lilacs, among others. These plants produce various compounds with potential medicinal properties, such as oleuropein from olive leaves, which has been studied for its antioxidant and anti-inflammatory effects. However, "Oleaceae" itself does not have a specific medical definition.

Methylglucosides are not a medical term, but rather a chemical term referring to a type of compound known as glycosides, where a methanol molecule is linked to a glucose molecule. They do not have a specific medical relevance, but they can be used in various industrial and laboratory applications, including as sweetening agents or intermediates in chemical reactions.

However, if you meant "Methylglucamine," it is a related term that has medical significance. Methylglucamine is an organic compound used as an excipient (an inactive substance that serves as a vehicle or medium for a drug) in some pharmaceutical formulations. It is often used as a solubilizing agent to improve the solubility and absorption of certain drugs, particularly those that are poorly soluble in water. Methylglucamine is generally considered safe and non-toxic, although it can cause gastrointestinal symptoms such as diarrhea or nausea in some individuals if taken in large amounts.

Glucosidases are a group of enzymes that catalyze the hydrolysis of glycosidic bonds, specifically at the non-reducing end of an oligo- or poly saccharide, releasing a single sugar molecule, such as glucose. They play important roles in various biological processes, including digestion of carbohydrates and the breakdown of complex glycans in glycoproteins and glycolipids.

In the context of digestion, glucosidases are produced by the pancreas and intestinal brush border cells to help break down dietary polysaccharides (e.g., starch) into monosaccharides (glucose), which can then be absorbed by the body for energy production or storage.

There are several types of glucosidases, including:

1. α-Glucosidase: This enzyme is responsible for cleaving α-(1→4) and α-(1→6) glycosidic bonds in oligosaccharides and disaccharides, such as maltose, maltotriose, and isomaltose.
2. β-Glucosidase: This enzyme hydrolyzes β-(1→4) glycosidic bonds in cellobiose and other oligosaccharides derived from plant cell walls.
3. Lactase (β-Galactosidase): Although not a glucosidase itself, lactase is often included in this group because it hydrolyzes the β-(1→4) glycosidic bond between glucose and galactose in lactose, yielding free glucose and galactose.

Deficiencies or inhibition of these enzymes can lead to various medical conditions, such as congenital sucrase-isomaltase deficiency (an α-glucosidase deficiency), lactose intolerance (a lactase deficiency), and Gaucher's disease (a β-glucocerebrosidase deficiency).

Limonin is not a medical term, but a chemical compound found in various plants, including citrus fruits. It is a type of limonoid, which is a class of naturally occurring compounds that are known for their bitter taste and potential health benefits. Specifically, limonin is found in the seeds and membranes of citrus fruits such as oranges, lemons, and grapefruits.

Limonin has been studied for its potential medicinal properties, including its antioxidant, anti-inflammatory, and chemopreventive effects. However, more research is needed to fully understand its mechanisms of action and potential health benefits in humans. It's important to note that while limonin may have potential health benefits, it should not be used as a substitute for medical treatment or advice from a healthcare professional.

Triterpenes are a type of natural compound that are composed of six isoprene units and have the molecular formula C30H48. They are synthesized through the mevalonate pathway in plants, fungi, and some insects, and can be found in a wide variety of natural sources, including fruits, vegetables, and medicinal plants.

Triterpenes have diverse structures and biological activities, including anti-inflammatory, antiviral, and cytotoxic effects. Some triterpenes are also used in traditional medicine, such as glycyrrhizin from licorice root and betulinic acid from the bark of birch trees.

Triterpenes can be further classified into various subgroups based on their carbon skeletons, including squalene, lanostane, dammarane, and ursane derivatives. Some triterpenes are also modified through various biochemical reactions to form saponins, steroids, and other compounds with important biological activities.

Molecular conformation, also known as spatial arrangement or configuration, refers to the specific three-dimensional shape and orientation of atoms that make up a molecule. It describes the precise manner in which bonds between atoms are arranged around a molecular framework, taking into account factors such as bond lengths, bond angles, and torsional angles.

Conformational isomers, or conformers, are different spatial arrangements of the same molecule that can interconvert without breaking chemical bonds. These isomers may have varying energies, stability, and reactivity, which can significantly impact a molecule's biological activity and function. Understanding molecular conformation is crucial in fields such as drug design, where small changes in conformation can lead to substantial differences in how a drug interacts with its target.

Balanophoraceae is a family of parasitic flowering plants that are found primarily in tropical regions. These plants do not have chlorophyll and therefore cannot produce their own food through photosynthesis. Instead, they obtain nutrients by parasitizing the roots of other plants. The plants in this family have a unique life cycle, beginning as small, inconspicuous structures that grow on the roots of host plants. Over time, these structures develop into larger, fleshy organs called "haustoria" that penetrate the host plant's tissues and establish a connection to its vascular system.

The haustoria then begin to absorb nutrients from the host plant, which allow the Balanophoraceae plant to grow and develop. Eventually, the parasitic plant produces flowers and fruits, which are dispersed by animals or wind. The seeds of these plants germinate on the roots of new host plants, beginning the life cycle anew.

Balanophoraceae includes a number of genera, including Balanophhora, Dactylanthus, and Langsdorffia. These plants have unusual morphology and reproductive structures, which can make them difficult to classify and study. Nonetheless, they are an important component of many tropical ecosystems, and their unique biology has attracted the interest of scientists for centuries.

I'm sorry for any confusion, but "Liliaceae" is not a medical term. It is a taxonomic category in botany, specifically it is the family name for plants that include lilies, tulips, and related species. In a medical context, you might be referring to the specific plant species themselves, or possibly the allergic reactions some people can have to the pollen of these plants. If you have any more specific questions about botanical terms in a medical context, I'd be happy to try and help further.

Arbutin is a natural compound found in the leaves of some plants, such as bearberry (Arctostaphylos uva-ursi), cranberry, and blueberry. It is a glycoside of hydroquinone, which means it consists of a molecule of hydroquinone attached to a sugar molecule.

Arbutin has been used in some skincare products as a skin-lightening agent because it inhibits the production of melanin, the pigment that gives skin its color. When applied to the skin, arbutin is broken down into hydroquinone, which has been shown to have skin-lightening effects by interfering with the enzyme tyrosinase, which is involved in melanin production.

However, it's important to note that the use of hydroquinone in skincare products is controversial due to concerns about its potential toxicity and side effects, such as skin irritation and discoloration. Therefore, arbutin may be a safer alternative for those looking for a natural skin-lightening ingredient, but more research is needed to confirm its safety and effectiveness.

Thin-layer chromatography (TLC) is a type of chromatography used to separate, identify, and quantify the components of a mixture. In TLC, the sample is applied as a small spot onto a thin layer of adsorbent material, such as silica gel or alumina, which is coated on a flat, rigid support like a glass plate. The plate is then placed in a developing chamber containing a mobile phase, typically a mixture of solvents.

As the mobile phase moves up the plate by capillary action, it interacts with the stationary phase and the components of the sample. Different components of the mixture travel at different rates due to their varying interactions with the stationary and mobile phases, resulting in distinct spots on the plate. The distance each component travels can be measured and compared to known standards to identify and quantify the components of the mixture.

TLC is a simple, rapid, and cost-effective technique that is widely used in various fields, including forensics, pharmaceuticals, and research laboratories. It allows for the separation and analysis of complex mixtures with high resolution and sensitivity, making it an essential tool in many analytical applications.

A plant stem is not typically defined in a medical context, but rather in the field of botany. However, I can certainly provide a general biological definition for you.

In plants, stems are organs that serve primarily as support structures, holding leaves, flowers, and fruits aloft where they can receive sunlight and exchange gases. They also act as conduits, transporting water, nutrients, and sugars made during photosynthesis between the roots and shoots of a plant.

The stem is usually composed of three main tissue systems: dermal, vascular, and ground. The dermal tissue system forms the outermost layer(s) of the stem, providing protection and sometimes participating in gas exchange. The vascular tissue system contains the xylem (which transports water and nutrients upward) and phloem (which transports sugars and other organic compounds downward). The ground tissue system, located between the dermal and vascular tissues, is responsible for food storage and support.

While not a direct medical definition, understanding the structure and function of plant stems can be relevant in fields such as nutrition, agriculture, and environmental science, which have implications for human health.

Pterocarpans are a type of chemical compound known as flavonoids, which are found naturally in plants. They are specifically classified as a subgroup of pterocarpanoids and have a characteristic chemical structure consisting of two benzene rings joined by a heterocyclic pyran ring.

Pterocarpans are produced through the phenylpropanoid pathway, which is a metabolic route used by plants to synthesize various compounds with diverse biological activities. These compounds have been found to possess a range of pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer effects.

Some examples of pterocarpans include medicarpin, maackiain, and glyceollins. They are commonly found in leguminous plants such as soybeans, kudzu, and red clover. In recent years, there has been growing interest in the potential therapeutic applications of pterocarpans due to their diverse biological activities.

Curculigo is a genus of plants in the family Hypoxidaceae. It includes several species of small, perennial herbs that are native to tropical and subtropical regions of Asia, Africa, and Australia. Some species of Curculigo have been used in traditional medicine for their supposed medicinal properties. For example, Curculigo orchioides (also known as Xian Mao) has been used in Traditional Chinese Medicine for its alleged aphrodisiac effects and to treat kidney deficiency and impotence. However, it's important to note that the scientific evidence supporting these claims is limited, and more research is needed before any definitive conclusions can be drawn about the medicinal value of Curculigo.

Therefore, there is no medical definition for 'Curculigo' as it is a plant genus and not a medical term or condition.

Phenols, also known as phenolic acids or phenol derivatives, are a class of chemical compounds consisting of a hydroxyl group (-OH) attached to an aromatic hydrocarbon ring. In the context of medicine and biology, phenols are often referred to as a type of antioxidant that can be found in various foods and plants.

Phenols have the ability to neutralize free radicals, which are unstable molecules that can cause damage to cells and contribute to the development of chronic diseases such as cancer, heart disease, and neurodegenerative disorders. Some common examples of phenolic compounds include gallic acid, caffeic acid, ferulic acid, and ellagic acid, among many others.

Phenols can also have various pharmacological activities, including anti-inflammatory, antimicrobial, and analgesic effects. However, some phenolic compounds can also be toxic or irritating to the body in high concentrations, so their use as therapeutic agents must be carefully monitored and controlled.

Cucurbitacins are a type of triterpenoid compound that are naturally occurring in some plants, particularly in the Cucurbitaceae family which includes pumpkins, cucumbers, and melons. These compounds have a bitter taste and are known for their potential medicinal properties, including anti-inflammatory, cytotoxic, and antifeedant activities. However, they can also be toxic to humans and animals in high concentrations. Cucurbitacins have been studied for their potential therapeutic benefits in various medical fields, such as oncology, where they have been shown to inhibit the growth of certain types of cancer cells.

Eudesmane is a subclass of sesquiterpenes, which are organic compounds consisting of three isoprene units and having the molecular formula C15H24. Sesquiterpenes are derived from farnesyl pyrophosphate (FPP) in the mevalonate pathway and are biosynthesized through a series of enzymatic reactions.

Eudesmane sesquiterpenes are characterized by a unique carbon skeleton with a cyclohexane ring fused to a bicyclic system consisting of a cyclopentane and a cyclobutane ring. They can be found in various plants, fungi, and insects, and some eudesmane derivatives have been shown to possess biological activities such as anti-inflammatory, antimicrobial, and cytotoxic properties.

Eudesmane sesquiterpenes can exist in different forms, including alcohols, aldehydes, ketones, and esters, depending on the functional groups attached to the carbon skeleton. Some examples of eudesmane sesquiterpenes include α-eudesmol, β-eudesmol, and eudesma-1,4-diene.

I'm sorry for any confusion, but the term "Lotus" does not have a specific medical definition in the context of human health or medicine. The lotus is a flowering plant that is often used as a symbol in various cultural and spiritual contexts, but it does not directly relate to medical terminology. If you have any questions related to medical topics, I'd be happy to help answer those!

Uridine diphosphate sugars (UDP-sugars) are nucleotide sugars that play a crucial role in the biosynthesis of glycans, which are complex carbohydrates found on the surface of many cell types. UDP-sugars consist of a uridine diphosphate molecule linked to a sugar moiety, such as glucose, galactose, or xylose. These molecules serve as activated donor substrates for glycosyltransferases, enzymes that catalyze the transfer of sugar residues to acceptor molecules, including proteins and other carbohydrates. UDP-sugars are essential for various biological processes, such as cell recognition, signaling, and protein folding. Dysregulation of UDP-sugar metabolism has been implicated in several diseases, including cancer and congenital disorders of glycosylation.

Polyacetylenes are a type of chemical compound that naturally occur in certain plants, including members of the families Asteraceae (daisies, sunflowers) and Apiaceae (carrots, parsley). They are characterized by alternating double bonds along their carbon chain, which can give them unique chemical properties. Some polyacetylenes have been found to have potential medicinal benefits, such as anti-inflammatory and anticancer effects. However, they can also be toxic in high concentrations. It's important to note that the term "polyacetylenes" refers to a broad class of compounds, and individual members may have different properties and effects.

Biological availability is a term used in pharmacology and toxicology that refers to the degree and rate at which a drug or other substance is absorbed into the bloodstream and becomes available at the site of action in the body. It is a measure of the amount of the substance that reaches the systemic circulation unchanged, after administration by any route (such as oral, intravenous, etc.).

The biological availability (F) of a drug can be calculated using the area under the curve (AUC) of the plasma concentration-time profile after extravascular and intravenous dosing, according to the following formula:

F = (AUCex/AUCiv) x (Doseiv/Doseex)

where AUCex is the AUC after extravascular dosing, AUCiv is the AUC after intravenous dosing, Doseiv is the intravenous dose, and Doseex is the extravascular dose.

Biological availability is an important consideration in drug development and therapy, as it can affect the drug's efficacy, safety, and dosage regimen. Drugs with low biological availability may require higher doses to achieve the desired therapeutic effect, while drugs with high biological availability may have a more rapid onset of action and require lower doses to avoid toxicity.

Sterculiaceae is a former family of flowering plants that is now classified as a subfamily (Sterculioideae) within the family Malvaceae, according to the Angiosperm Phylogeny Group IV system. This group includes several genera of trees and shrubs, many of which have tropical distributions. Some well-known members of this subfamily include Sterculia, Cola, and Ficus (which contains various fig tree species). These plants are characterized by their typically large, simple leaves and showy flowers with numerous stamens. The fruits of Sterculiaceae are diverse in form, ranging from capsules to berries or schizocarps.

Cellulases are a group of enzymes that break down cellulose, which is a complex carbohydrate and the main structural component of plant cell walls. These enzymes are produced by various organisms, including bacteria, fungi, and protozoa. They play an important role in the natural decomposition process and have various industrial applications, such as in the production of biofuels, paper, and textiles.

Cellulases work by hydrolyzing the beta-1,4 glycosidic bonds between the glucose molecules that make up cellulose, breaking it down into simpler sugars like glucose. This process is known as saccharification. The specific type of cellulase enzyme determines where on the cellulose molecule it will cleave the bond.

There are three main types of cellulases: endoglucanases, exoglucanases, and beta-glucosidases. Endoglucanases randomly attack internal bonds in the amorphous regions of cellulose, creating new chain ends for exoglucanases to act on. Exoglucanases (also known as cellobiohydrolases) cleave cellobiose units from the ends of the cellulose chains, releasing cellobiose or glucose. Beta-glucosidases convert cellobiose into two molecules of glucose, which can then be further metabolized by the organism.

In summary, cellulases are a group of enzymes that break down cellulose into simpler sugars through hydrolysis. They have various industrial applications and play an essential role in natural decomposition processes.

"Paeonia" is the botanical name for a genus of plants that includes peonies. It is not a medical term with a specific definition in the context of medicine. However, some peony species have been used in traditional medicine for various purposes, such as treating inflammation and menstrual disorders. The roots and bark of Paeonia suffruticosa (also known as moutan cortex) have been used in Traditional Chinese Medicine (TCM).

In a medical context, if someone is referring to "Paeonia," they are most likely talking about the plant or its extracts. Always consult with a healthcare professional before using any plant or herbal remedy for medicinal purposes.

I'm sorry for any confusion, but "Veronica" is not a medical term. It is a name of Latin origin, and in popular culture, it might refer to a character in various movies, books, or other non-medical contexts. If you have a different question or need information on a medical topic, please don't hesitate to ask!

I apologize for any confusion, but "Ajuga" is not a medical term. It is actually the name of a genus of plants in the mint family, also known as bugleweed. These plants have been used in traditional medicine to treat various conditions such as anxiety, sleep disorders, and skin irritations. However, it's important to note that the use of herbal remedies should always be discussed with a healthcare provider beforehand, as they can interact with other medications or have unintended side effects.

I apologize for any confusion, but "shallots" is not a term with a widely accepted medical definition. It is a culinary term that refers to a type of onion (Allium cepa L. var. aggregatum) characterized by their small size and clustered bulbs. They are often used in cooking for their mild flavor. If you have any questions related to medicine or health, I would be happy to try to help answer those!

Soy milk is not a medical term, but it is a common term used to describe a plant-based milk alternative made from soybeans. Here's a brief description:

Soy milk is a beverage produced by soaking and grinding soybeans, then filtering the resulting mixture to remove solid particles. It is often consumed as a dairy substitute by individuals who are lactose intolerant or have milk allergies. Soy milk contains protein, carbohydrates, and fat, similar to cow's milk, but its nutritional profile may vary depending on the manufacturing process. Some brands of soy milk are fortified with calcium, vitamins B12, D, and riboflavin (B2) to resemble the nutritional content of cow's milk.

Please note that while soy milk can be a healthy alternative for many people, it may not be suitable for everyone, especially those with soy allergies or sensitivities. If you have any concerns about incorporating soy milk into your diet, consult a healthcare professional or a registered dietitian.

Spectrophotometry, Infrared is a scientific analytical technique used to measure the absorption or transmission of infrared light by a sample. It involves the use of an infrared spectrophotometer, which directs infrared radiation through a sample and measures the intensity of the radiation that is transmitted or absorbed by the sample at different wavelengths within the infrared region of the electromagnetic spectrum.

Infrared spectroscopy can be used to identify and quantify functional groups and chemical bonds present in a sample, as well as to study the molecular structure and composition of materials. The resulting infrared spectrum provides a unique "fingerprint" of the sample, which can be compared with reference spectra to aid in identification and characterization.

Infrared spectrophotometry is widely used in various fields such as chemistry, biology, pharmaceuticals, forensics, and materials science for qualitative and quantitative analysis of samples.

Stereoisomerism is a type of isomerism (structural arrangement of atoms) in which molecules have the same molecular formula and sequence of bonded atoms, but differ in the three-dimensional orientation of their atoms in space. This occurs when the molecule contains asymmetric carbon atoms or other rigid structures that prevent free rotation, leading to distinct spatial arrangements of groups of atoms around a central point. Stereoisomers can have different chemical and physical properties, such as optical activity, boiling points, and reactivities, due to differences in their shape and the way they interact with other molecules.

There are two main types of stereoisomerism: enantiomers (mirror-image isomers) and diastereomers (non-mirror-image isomers). Enantiomers are pairs of stereoisomers that are mirror images of each other, but cannot be superimposed on one another. Diastereomers, on the other hand, are non-mirror-image stereoisomers that have different physical and chemical properties.

Stereoisomerism is an important concept in chemistry and biology, as it can affect the biological activity of molecules, such as drugs and natural products. For example, some enantiomers of a drug may be active, while others are inactive or even toxic. Therefore, understanding stereoisomerism is crucial for designing and synthesizing effective and safe drugs.

"Carum" is a genus name that refers to a group of plants in the family Apiaceae, also known as the carrot or parsley family. One of the most well-known species in this genus is Carum carvi, which is commonly known as caraway. Caraway is an herb that is native to Europe and Western Asia, and its seeds are used as a spice in cooking and baking. The seeds have a pungent, aromatic flavor and are often used to add flavor to breads, cakes, cheeses, and other dishes.

Carum plants are typically biennial or perennial herbs that grow to be about 1-2 feet tall. They have feathery leaves and small white or pink flowers that bloom in umbels. The seeds are small and crescent-shaped, with a brown or grayish color.

Caraway seeds contain several compounds that contribute to their flavor and aroma, including carvone, limonene, and anethole. Carvone is the primary compound responsible for the distinctive taste and smell of caraway seeds. In addition to their use as a spice, caraway seeds have also been used in traditional medicine to treat various ailments, such as digestive problems and respiratory issues. However, there is limited scientific evidence to support these uses.

Flavanones are a type of flavonoid, which is a class of plant pigments widely found in fruits, vegetables, and other plants. Flavanones are known for their antioxidant properties and potential health benefits. They are typically found in citrus fruits such as oranges, lemons, and grapefruits. Some common flavanones include hesperetin, naringenin, and eriodictyol. These compounds have been studied for their potential effects on cardiovascular health, cancer prevention, and neuroprotection, although more research is needed to fully understand their mechanisms of action and therapeutic potential.

I'm sorry for any confusion, but the term "Thymus Plant" refers to a type of plant and does not have a medical definition. The Thymus plant belongs to the mint family and is commonly used as an herb in cooking. It is known for its small, fragrant leaves and is often used to add flavor to dishes. In some cases, the essential oil from the thymus plant may be used in medicinal products, such as throat lozenges or mouthwashes, due to its antiseptic properties. However, a "Thymus plant" itself does not have a medical definition. If you have any questions about medicinal plants or herbs, I'd be happy to try and help answer those for you!

Sinomenium is not a medical term itself, but it is the name of a plant species (Sinomenium acutum) that has been used in traditional Chinese medicine. The dried root of this plant contains several alkaloids, among which sinomenine is the most prominent and well-studied one.

Sinomenine is an isoquinoline alkaloid with anti-inflammatory, analgesic, and immunomodulatory properties. It has been used in traditional Chinese medicine to treat various conditions such as rheumatoid arthritis, joint pain, and allergies.

In modern medical research, sinomenine has been investigated for its potential therapeutic effects on a range of diseases, including autoimmune disorders, neurodegenerative diseases, and cancer. However, more studies are needed to establish its safety and efficacy in clinical settings.

"Gentiana" is a term that refers to a genus of plants in the family Gentianaceae. These plants are often characterized by their beautiful, trumpet-shaped flowers and are found primarily in the Northern Hemisphere, with some species located in tropical mountains in Africa and South America. The name "Gentiana" comes from the Illyrian king Genius, who is said to have discovered the medicinal properties of this plant.

In a medical context, certain species of Gentiana have been used in traditional medicine for their anti-inflammatory, antipyretic, and bitter digestive stimulant properties. For example, Gentiana lutea (yellow gentian) is commonly used in herbal medicine to treat digestive disorders such as loss of appetite, heartburn, and flatulence. However, it's important to note that the use of Gentiana in modern medicine is not well-studied, and more research is needed to establish its safety and efficacy.

It's worth noting that "Gentiana" is primarily a botanical term and is not commonly used as a medical diagnosis or treatment. If you have any health concerns, it's always best to consult with a qualified healthcare professional for advice.

Glucuronates are not a medical term per se, but they refer to salts or esters of glucuronic acid, a organic compound that is a derivative of glucose. In the context of medical and biological sciences, glucuronidation is a common detoxification process in which glucuronic acid is conjugated to a wide variety of molecules, including drugs, hormones, and environmental toxins, to make them more water-soluble and facilitate their excretion from the body through urine or bile.

The process of glucuronidation is catalyzed by enzymes called UDP-glucuronosyltransferases (UGTs), which are found in various tissues, including the liver, intestines, and kidneys. The resulting glucuronides can be excreted directly or further metabolized before excretion.

Therefore, "glucuronates" can refer to the chemical compounds that result from this process of conjugation with glucuronic acid, as well as the therapeutic potential of enhancing or inhibiting glucuronidation for various clinical applications.

Coumaric acids are a type of phenolic acid that are widely distributed in plants. They are found in various foods such as fruits, vegetables, and grains. The most common forms of coumaric acids are p-coumaric acid, o-coumaric acid, and m-coumaric acid.

Coumaric acids have been studied for their potential health benefits, including their antioxidant, anti-inflammatory, and antimicrobial properties. They may also play a role in preventing chronic diseases such as cancer and cardiovascular disease. However, more research is needed to fully understand the potential health benefits of coumaric acids.

It's worth noting that coumaric acids are not to be confused with warfarin (also known as Coumadin), a medication used as an anticoagulant. While both coumaric acids and warfarin contain a similar chemical structure, they have different effects on the body.

"Combretum" is a genus of flowering plants in the family Combretaceae, also known as the shrubs and small trees commonly found in tropical and subtropical regions around the world. These plants have various medicinal uses in different cultures. The active compounds in some species have been studied for potential anti-inflammatory, antimicrobial, and antimalarial properties. However, it's important to note that using herbal remedies can involve risks, and it's crucial to consult with a healthcare provider before starting any new treatment.

Solubility is a fundamental concept in pharmaceutical sciences and medicine, which refers to the maximum amount of a substance (solute) that can be dissolved in a given quantity of solvent (usually water) at a specific temperature and pressure. Solubility is typically expressed as mass of solute per volume or mass of solvent (e.g., grams per liter, milligrams per milliliter). The process of dissolving a solute in a solvent results in a homogeneous solution where the solute particles are dispersed uniformly throughout the solvent.

Understanding the solubility of drugs is crucial for their formulation, administration, and therapeutic effectiveness. Drugs with low solubility may not dissolve sufficiently to produce the desired pharmacological effect, while those with high solubility might lead to rapid absorption and short duration of action. Therefore, optimizing drug solubility through various techniques like particle size reduction, salt formation, or solubilization is an essential aspect of drug development and delivery.

I apologize for the confusion, but "Lamiaceae" is not a medical term. It is a taxonomic category in biology, specifically it is a family of flowering plants that includes many familiar herbs such as mint, rosemary, sage, basil, and lavender. These plants are often used in medicine, cooking, and for ornamental purposes. The Lamiaceae family is characterized by their square stems, opposite leaves, and two-lipped flowers.

Dilleniaceae is a family of flowering plants that includes around 30 genera and 600 species. These plants are primarily found in tropical and subtropical regions, with a few species occurring in temperate zones. The family is characterized by having five or often many sepals and petals, numerous stamens, and a superior ovary.

The plants in Dilleniaceae are quite diverse, ranging from small herbs to large trees. Some of the more well-known members of this family include the Indian rubber tree (Dillenia indica), the cape gooseberry (Physalis peruviana), and the mock orange (Philadelphus coronarius).

It's worth noting that while Dilleniaceae is a distinct family of plants, it has been subject to significant reclassification in recent years. Some botanists have proposed merging it with other families or splitting it into smaller groups, so its exact composition and boundaries may continue to evolve as more research is conducted.

T-2 toxin is a type B trichothecene mycotoxin, which is a secondary metabolite produced by certain Fusarium species of fungi. It is a low molecular weight sesquiterpene epoxide that is chemically stable and has a high toxicity profile. T-2 toxin can contaminate crops in the field or during storage, and it is often found in grains such as corn, wheat, barley, and oats.

T-2 toxin has a variety of adverse health effects, including nausea, vomiting, diarrhea, abdominal pain, immune suppression, skin irritation, and neurotoxicity. It is also known to have teratogenic and embryotoxic effects in animals, and it is considered a potential human carcinogen by some agencies.

Exposure to T-2 toxin can occur through ingestion, inhalation, or skin contact. Ingestion is the most common route of exposure, particularly in areas where contaminated grains are used as a food source. Inhalation exposure can occur during agricultural activities such as harvesting and processing contaminated crops. Skin contact with T-2 toxin can cause irritation and inflammation.

Prevention of T-2 toxin exposure involves good agricultural practices, including crop rotation, use of resistant varieties, and proper storage conditions. Monitoring of T-2 toxin levels in food and feed is also important to ensure that exposure limits are not exceeded.

Lignans are a type of plant compound that have antioxidant and estrogen properties. They are found in various plants such as seeds, grains, fruits, and vegetables. Once consumed, some lignans can be converted by intestinal bacteria into enterolactone and enterodiol, which can have weak estrogenic or anti-estrogenic effects in the body. These compounds have been studied for their potential health benefits, including reducing the risk of cancer and heart disease. However, more research is needed to fully understand their effects and potential health benefits.

Benzoyl-beta-D-glucoside is a compound found in the fern Pteris ensiformis. Phenol derivatives There are a number of glucosides ... A glucoside is a glycoside that is chemically derived from glucose. Glucosides are common in plants, but rare in animals. ... and in some cases the preparation of the synthetic glucoside effected. The simplest glucosides are the alkyl ethers which have ... The classification of glucosides is a matter of some intricacy. One method based on the chemical constitution of the non- ...
... may refer to: Catechin-3-O-glucoside Catechin-3'-O-glucoside Catechin-4'-O-glucoside Catechin-5-O-glucoside ... Catechin-7-O-glucoside This set index article lists chemical compounds articles associated with the same name. If an internal ...
... (AA-2G) is an ascorbic acid derivative that contains at least one glycosyl group. Ascorbyl glucoside is ... Ascorbyl glucosides such as AA-2G, like many other derivatives of the ascorbic acid, show antiscorbutic effects. It is also ... Ascorbyl glucoside exhibits superior stability and penetration ability compared to ascorbyl phosphate salts, but the rate of ... Ascorbyl glucoside is synthesized through a glycosylation process catalyzed by glycosyltransferase-class enzymes. Ascorbyl ...
Lauryl glucoside Octyl glucoside Fiume MM, Heldreth B, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler D, Marks JG Jr, ... Decyl glucoside was invented by Robert Prairie in 1934. Decyl glucoside is produced by the reaction of glucose from corn starch ... Safety assessment of decyl glucoside and other alkyl glucosides as used in cosmetics. Int J Toxicol. 2013 Sep-Oct;32(5 Suppl): ... Decyl glucoside is a mild non-ionic surfactant used in cosmetic formularies, including baby shampoo and in products for ...
Decyl glucoside Octyl glucoside n-Dodecyl β-D-glucopyranoside at Sigma-Aldrich "Lauryl glucoside". pubchem.ncbi.nlm.nih.gov. ... Lauryl glucoside is a surfactant used in cosmetics and laundry detergents. It is a glycoside produced from glucose and lauryl ... Glucosides, Non-ionic surfactants, All stub articles, Alcohol stubs, Heterocyclic compound stubs). ...
Decyl glucoside Lauryl glucoside Alkyl polyglycoside octyl thioglucoside octyl glucoside bound to proteins in the PDB Shinoda, ... Octyl glucoside (n-octyl-β-d-glucoside) is a nonionic surfactant frequently used to solubilise integral membrane proteins for ... Octyl glucoside has been proposed as a conditioning agent to prevent microbial colonization of contact lenses, due to its ... Keana, Jf; Roman, Rb (1978). "Improved synthesis of n-octyl-beta-D-glucoside: a nonionic detergent of considerable potential in ...
In enzymology, a beta-glucoside kinase (EC 2.7.1.85) is an enzyme that catalyzes the chemical reaction ATP + cellobiose ⇌ {\ ... This enzyme is also called beta-D-glucoside kinase (phosphorylating). Palmer RE, Anderson RL (1972). "Cellobiose metabolism in ... Phosphorylation of cellobiose with adenosine 5'-triphosphate by a -glucoside kinase". J. Biol. Chem. 247 (11): 3415-9. PMID ...
... (calycanthoside) is a constituent of Eleutherococcus senticosus that is classified as a coumarin. It is ... "Isofraxidin-7-glucoside , C17H20O10 , ChemSpider". www.chemspider.com. Retrieved 2022-11-15. v t e (CS1 maint: multiple names: ... a glucoside of isofraxidin. Anetai, Masaki; Yamagishi, Takashi; Kaneshima, Hiroyasu (1987). "Quantitative determination of ...
O-glucoside or marein, a chalconoid glucoside Quercetin 4'-O-glucoside or spiraeoside, a flavonol glucoside O-glucoside This ... 4'-O-glucoside may refer to: Hydrangenol 4'-O-glucoside, an isocoumarin glucoside Okanin 4'- ...
In enzymology, a glucoside 3-dehydrogenase (EC 1.1.99.13) is an enzyme that catalyzes the chemical reaction sucrose + acceptor ... Other names in common use include D-glucoside 3-dehydrogenase, D-aldohexopyranoside dehydrogenase, D-aldohexoside:cytochrome c ... oxidoreductase, D-glucoside 3-dehydrogenase, hexopyranoside-cytochrome c oxidoreductase, and D-aldohexoside:(acceptor) 3- ...
... is a flavan-3-ol glycoside formed from catechin. Catechin-7-O-glucoside can be isolated from the ... Catechin-7-O-glucoside can be found in paeoniae radix, the crude drug made from the roots of Chinese peony (Paeonia lactiflora ... Nonaka, Gen'ichiro; Ezakia, Emiko; Hayashia, Katsuya; Nishioka, Itsuo (1983). "Flavanol glucosides from rhubarb and ... reveals catechin-O-glucoside as the dominant compound". Food Chemistry. 139 (1-4): 35-43. doi:10.1016/j.foodchem.2013.01.117. ...
... is a benzoyl glucoside, a natural substance that can be found in Pteris ensiformis. Yung-Husan Chen; ... Fang-Rong Chang; Mei-Chin Lu; Pei-Wen Hsieh; Ming-Jiuan Wu; Ying-Chi Du; Yang-Chang Wu (2008). "New Benzoyl Glucosides and ... Glucosides, All stub articles, Aromatic compound stubs). ...
Catechin 5-O-glucoside is a flavanol glucoside. It can be found in rhubarb and in the bark of Rhaphiolepis umbellata. It can ... Catechin glucosides: occurrence, synthesis, and stability. Raab T, Barron D, Vera FA, Crespy V, Oliveira M and Williamson G, J ... Flavonoid glucosides, All stub articles, Aromatic compound stubs). ... Agric Food Chem., 2010 Feb 24, 58(4), pages 2138-2149, doi:10.1021/jf9034095 Flavanol glucosides from rhubarb and Rhaphiolepis ...
This compound has a better color stability at pH 5.5 than malvidin-3O-glucoside. When the pH was increased from 2.2 to 5.5, the ... Malvidin glucoside-ethyl-catechin is a flavanol-anthocyanin adduct. Flavanol-anthocyanin adducts are formed during wine ageing ... Malvidin glucoside-ethyl-catechin on Yeast Metabolome Database Atanasova, Vessela; Fulcrand, Hélène; Cheynier, Véronique; ... Pissarra, J.; Mateus, N.; Rivas-Gonzalo, J.; Santos Buelga, C.; Freitas, V. (2003). "Reaction Between Malvidin 3-Glucoside and ...
... is a flavonol glucoside. It can be found in Smilax china, and in the fern Asplenium rhizophyllum, and ... Xu, W.; Liu, J.; Li, C.; Wu, H. Z.; Liu, Y. W. (2008). "Kaempferol-7-O-β-d-glucoside (KG) isolated from Smilax china L. rhizome ... Amurensin is the tert-amyl alcohol derivative of kaempferol 7-O-glucoside. 6'''-O-acetyl amurensin is found in the leaves of ... Flavonol glucosides, All stub articles, Aromatic compound stubs). ...
Phenolic glucosides in bread containing flaxseed. C. Strandås, A. Kamal-Eldin, R. Andersson and P. Åman, Food Chemistry, Volume ... p-Coumaric acid glucoside is a hydroxycinnamic acid, an organic compound found in commercial breads containing flaxseed. ... Phenol glucosides, All stub articles, Aromatic compound stubs). ... 10.1016/j.foodchem.2008.02.088 p-Coumaric acid glucoside at www ...
... is anthocyanin. It is found in fruits and berries, in red Vitis vinifera grapes and red wine, in red ... Phenolic compounds in wine Peonidin 3-O-glucoside on www.phenol-explorer.eu Anthocyanins isolated from purple corn (Zea mays L ...
... is anthocyanin. It is found in fruits and berries, in red Vitis vinifera grapes and red wine. Phenolic ... compounds in wine Petunidin 3-O-glucoside on www.phenol-explorer.eu Archived 2013-02-13 at archive.today v t e (Webarchive ...
... beta-D-glucoside Thus, the two substrates of this enzyme are UDP-glucose and flavonol 3-O-beta-D-glucoside, whereas its two ... The systematic name of this enzyme class is UDP-glucose:flavonol-3-O-glucoside 2''-O-beta-D-glucosyltransferase. Jourdan PS, ... In enzymology, a flavonol-3-O-glucoside glucosyltransferase (EC 2.4.1.239) is an enzyme that catalyzes the chemical reaction ... products are UDP and flavonol 3-O-beta-D-glucosyl-(1→2)-beta-D-glucoside. This enzyme belongs to the family of ...
Not all β-glucoside PTS porters are in this class, as the PTS porter first described as the cellobiose β-glucoside porter is ... The IIC domains of the glucose and glucoside subfamilies are as distant from each other as they are from the Fru, Mtl and Lac ... The PTS Glucose-Glucoside (Glc) family (TC# 4.A.1) includes porters specific for glucose, glucosamine, N-acetylglucosamine and ... The PTS Glucose-Glucoside (Glc) Family (Transporter Classification Database, Saier Lab Group, UCSD) As of this edit, this ...
... beta-D-glucoside] Thus, the two substrates of this enzyme are UDP-L-rhamnose and flavonol 3-O-D-glucoside, whereas its two ... The systematic name of this enzyme class is UDP-L-rhamnose:flavonol-3-O-D-glucoside 6''-O-L-rhamnosyltransferase. Other names ... In enzymology, a flavonol-3-O-glucoside L-rhamnosyltransferase (EC 2.4.1.159) is an enzyme that catalyzes the chemical reaction ... flavonol 3-O-glucoside rhamnosyltransferase. This enzyme participates in flavonoid biosynthesis. Wiermann R (1982). "Formation ...
... is a glucoside of p-hydroxybenzoic acid. It can be found in mycorrhizal (Picea abies- ... Media related to 4-Hydroxybenzoic acid 4-O-glucoside at Wikimedia Commons 4-Hydroxybenzoic acid 4-O-glucoside at Phenol- ... Phenolic acid glucosides, All stub articles, Aromatic compound stubs). ...
... is a p-coumaroylated anthocyanin found in grape and wine. There are two forms with the ... Malvidin 3-O-(6″-p-coumaroyl-glucoside) at phenol-explorer.eu v t e (Chemical articles without CAS registry number, Articles ...
It is formed by the enzyme anthocyanin 3-O-glucoside 6″-O-hydroxycinnamoyltransferase from delphinidin 3-O-glucoside and p- ... Delphinidin 3-O-(6-p-coumaroyl)glucoside is a p-coumaroylated anthocyanin. It can be found in some red Vitis vinifera grape ... Delphinidin 3-(6-p-coumaroyl)glucoside synthesis reaction on www.kegg.jp v t e (Articles without UNII source, Articles with ... doi:10.1016/S0925-5214(03)00140-6. "Delphinidin 3-(6-p-coumaroyl)glucoside on www.phenol-explorer.eu". Archived from the ...
... beta-D-glucoside The enzyme is highly specific for cyanidin 3-O-glucosides and UDP-D-glucuronate. Sawada S, Suzuki H, Ichimaida ... anthocyanidin 3-glucoside 2'-O-beta-glucuronosyltransferase, BpUGAT, UDP-D-glucuronate:cyanidin-3-O-beta-glucoside 2-O-beta- ... Cyanidin-3-O-glucoside+2-O-glucuronosyltransferase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) ... Cyanidin-3-O-glucoside 2-O-glucuronosyltransferase (EC 2.4.1.254, BpUGT94B1, UDP-glucuronic acid:anthocyanin ...
The systematic name of this enzyme class is malonyl-CoA:pelargonidin-3-O-(6-caffeoyl-beta-D-glucoside)-5-O-beta- D-glucoside 6 ... 6-caffeoyl-beta-D-glucoside) 5-O-beta-D-glucoside, whereas its two products are CoA and 4'''-demalonylsalvianin. This enzyme ... 6-caffeoyl-beta-D-glucoside) 5-O-beta-D-glucoside ⇌ {\displaystyle \rightleftharpoons } CoA + 4'''-demalonylsalvianin Thus, the ... In enzymology, an anthocyanin 5-O-glucoside 6'''-O-malonyltransferase (EC 2.3.1.172) is an enzyme that catalyzes the chemical ...
6-O-malonyl-beta-D-glucoside) Thus, the two substrates of this enzyme are malonyl-CoA and flavonol 3-O-beta-D-glucoside, ... The systematic name of this enzyme class is malonyl-CoA:flavonol-3-O-beta-D-glucoside 6"-O-malonyltransferase. Other names in ... In enzymology, a flavonol-3-O-beta-glucoside O-malonyltransferase (EC 2.3.1.116) is an enzyme that catalyzes the chemical ... Matern U, Feser C, Hammer D (1983). "Further characterization and regulation of malonyl-coenzyme A: flavonoid glucoside ...
Anthocyanin 3-O-glucoside 6″-O-hydroxycinnamoyltransferase is an enzyme forming delphinidin 3-(6-p-coumaroyl)glucoside from ... Delphinidin 3-(6-p-coumaroyl)glucoside synthesis reaction on www.kegg.jp Yonekura-Sakakibara K, Tanaka Y, Fukuchi-Mizutani M, ... anthocyanin 3-O-glucoside-6"-O-acyltransferase from Perilla frutescens". Plant & Cell Physiology. 41 (4): 495-502. doi:10.1093/ ... delphinidin 3-O-glucoside (myrtillin) and p-coumaroyl-CoA. It is an enzyme in the anthocyanin biosynthesis pathway. It can be ...
6-O-malonyl-beta-D-glucoside) Thus, the two substrates of this enzyme are malonyl-CoA and biochanin A 7-O-beta-D-glucoside, ... flavone/flavonol 7-O-glucoside malonyltransferase, MAT-7, malonyl-coenzyme A:isoflavone 7-O-glucoside-6"-malonyltransferase, ... The systematic name of this enzyme class is malonyl-CoA:isoflavone-7-O-beta-D-glucoside 6"-O-malonyltransferase. Other names in ... In enzymology, an isoflavone-7-O-beta-glucoside 6"-O-malonyltransferase (EC 2.3.1.115) is an enzyme that catalyzes the chemical ...
... beta-D-glucoside] Thus, the two substrates of this enzyme are UDP-L-rhamnose and flavanone 7-O-glucoside, whereas its two ... In enzymology, a flavanone 7-O-glucoside 2"-O-beta-L-rhamnosyltransferase (EC 2.4.1.236) is an enzyme that catalyzes the ... The systematic name of this enzyme class is UDP-L-rhamnose:flavanone-7-O-glucoside 2''-O-beta-L-rhamnosyltransferase. Other ... Bar-Peled M, Lewinsohn E, Fluhr R, Gressel J (1991). "UDP-rhamnose:flavanone-7-O-glucoside-2''-O-rhamnosyltransferase ...
Benzoyl-beta-D-glucoside is a compound found in the fern Pteris ensiformis. Phenol derivatives There are a number of glucosides ... A glucoside is a glycoside that is chemically derived from glucose. Glucosides are common in plants, but rare in animals. ... and in some cases the preparation of the synthetic glucoside effected. The simplest glucosides are the alkyl ethers which have ... The classification of glucosides is a matter of some intricacy. One method based on the chemical constitution of the non- ...
... screening of new mycotoxin glucosides conducted by the authors and risk assessment research of mycotoxin glucosides). Chapter ... Home / Shop / Books / Science and Technology / Chemistry / Biochemistry / Glucosides: Sources, Applications, and New Research. ... Chapter 1. Mycotoxin Glucosides (Masked Mycotoxins). Hiroyuki Nakagawa (National Agriculture and Food Research Organization ( ... Chapter 3. Phase Behavior of n-Alkyl Glucosides in the Arid System Recent Developments and Experiment Notes. Shigesaburo ...
glucoside: Now Found - Search Error - Toll Free 1-800-877-8702, PayPal Available. ... "glucoside"] 0 Results found. - No Items Found, the search requires a exact word match or exact partial word match. please try ...
... glucoside? Find out what is the full meaning of cardiac+glucoside on Abbreviations.com! The Webs largest and most ... Weve got 0 shorthands for cardiac+glucoside ». Acronyms that contain the term cardiac+glucoside What does cardiac+glucoside ... Know the definition for cardiac+glucoside? Know the meaning of cardiac+glucoside? Dont keep it to yourself!. ... Couldnt find the right meaning of cardiac+glucoside?. Maybe you were looking for one of these abbreviations:. CARDA, CARDER, ...
Cetearyl glucoside is used as an emulsifier & texture enhancer in cosmetic formulas. It also lends skin-softening emollience. ...
Naturally occurring glucosides of benzyl alcohol, (±)-menthol, (+)-borneol, thymol, carvacrol and eugenol were synthesized by ... glucosides of volatiles; synthesis of glucosides; 1D and 2D NMR spectra; glucoside tetraacetates; GC-MS spectra ... Diastereomeric β-glucoside tetraacetates of (±)-menthol were well separated on the HP-101 column. The mass spectra of ... Naturally occurring glucosides of benzyl alcohol, (±)-menthol, (+)-borneol, thymol, carvacrol and eugenol were synthesized by ...
PubMed:The flavonol quercetin-3-glucoside inhibits cyanidin-3-glucoside absorption in vitro.. ... PubMed:Influence of glucose on cyanidin 3-glucoside absorption in rats.. PubMed:Urinary excretion of strawberry anthocyanins is ... PubMed:Protocatechuic acid is the major human metabolite of cyanidin-glucosides.. PubMed:Identification of anthocyanins in the ... PubMed:Dietary cyanidin 3-O-beta-D-glucoside-rich purple corn color prevents obesity and ameliorates hyperglycemia in mice.. ...
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Ascorbyl Glucoside is a water-soluble derivative of Vitamin C. Arriving in a serum form, the vitamin packed solution is stable ... Brighten the complexion with The Ordinary Ascorbyl Glucoside Solution 12%; a hydrating treatment that works to transform skin. ...
Disodium Coco-Glucoside Citrate: The foam produced by Disodium Coco-Glucoside Citrate is stable and rich. It is a global ... Disodium Coco-Glucoside Citrate: The foam produced by Disodium Coco-Glucoside Citrate is stable and rich. It is a global ... Disodium coco-glucoside citrate, 30%. It is an anionic mild surfactant that has emulsifying qualities, a rich and stable foam. ... Disodium coco glucoside citrate_The latest Qatar News,Qatar Technology,Qatar Indus ...
tetrahydroxystilbene-2-O-β-D-glucoside in antiaging and antiaging-related disease treatments," Oxidative Medicine and Cellular ... tetrahydroxystilbene-2-O-β-D-glucoside in the MPTP-induced mouse model of Parkinsons disease: involvement of reactive oxygen ... Tetrahydroxystilbene-2-O-beta-D-glucoside (THSG) is one of the most effective ingredients in the traditional Chinese edible ... tetrahydroxystilbene-2-O-β-D-glucoside against staurosporine-induced toxicity on cultured rat hippocampus neurons," ...
Preparation of Methyl 6‐O‐p‐Nitrobenzoyl‐β-D-glucoside. Preparation of Methyl 6‐O‐p‐Nitrobenzoyl‐β-D-glucoside. Title. ...
8-O-methylated benzoxazinoid glucoside biosynthesis, DIMBOA-glucoside activation, DIMBOA-glucoside biosynthesis, superpathway ... 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one glucoside, 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-D-glucoside, 2,4- ... Ligand DIMBOA-glucoside. Please wait a moment until all data is loaded. This message will disappear when all data is loaded. ... DIMBOA-beta-D-glucoside, DIMBOA beta-D-glucoside ... Links to other databases for DIMBOA-glucoside. top print hide ...
The following is a list of the most recent articles about Cetearyl Glucoside (and) ... Cetearyl Glucoside, (and) Cetearyl Alcohol does not contain ethyleneoxide, has a good biodegradability as well as skin affinity ... Prices of Cetearyl Glucoside (and) Cetearyl Alcohol If you want to buy Cetearyl Glucoside or Cetearyl Alcohol in bulk. Product ... The following is a list of the most recent articles about Cetearyl Glucoside (and) Cetearyl Alcohol : Cetearyl Glucoside is a ...
Shop BiopureTM Deoxynivalenol-3-Glucoside - 50 µg/mL, 5 mL now! Lets make the Worlds Food safer together. ...
C12-14 Alkyl glucoside CAS 110615-47-9. C12-14 Alkylglucoside is typically 50% aqueous or neutral. A viscous yellow liquid that ... C12 14 Alkyl glucoside CAS 110615 47 9_hiphopgalaxy.com , Nanomaterials, Chemical Product ...
Lee, J.S., Kim, Y.R., Song, I.G., Ha, S., Kim, Y.E., Baek, N., & Hong, E.K. (2015). Cyanidin-3-glucoside isolated from mulberry ... Lee, J. S., Kim, Y. R., Song, I. G., Ha, S., Kim, Y. E., Baek, N., Hong, E. K.Cyanidin-3-glucoside isolated from mulberry ... Lee, J. S., Kim, Y. R., Song, I. G., Ha, S., Kim, Y. E., Baek, N., Hong, E. K.Cyanidin-3-glucoside isolated from mulberry ... Cyanidin-3-glucoside isolated from mulberry fruit protects pancreatic β-cells against oxidative stress-induced apoptosis. * ...
X-Glucoside, 100 MG Home Biochemicals Substrates Galactosidase Substrates X-Glucoside, 100 MG ... X-Glucoside is a substrate for β-Glucosidase that, upon enzymatic action, renders an insoluble indigo-blue chromophore (615 nm ...
INDOFINE Chemical Company supplies HESPERETIN-7-O-GLUCOSIDE WITH HPLC for pharmaceutical, agricultural and life science ...
Decyl Glucoside Surfactant is a gentle foaming agent composed of cornstarch, glucose, & coconut oil. Wholesale pricing from ... Decyl Glucoside Naturally Derived Mild Surfactant. CTFA Name: Decyl Glucoside. INCI Name: Decyl Glucoside. Country of Origin: ... Decyl Glucoside Surfactant Natural $7.52. - $1,095.20. ALL NATURALbath bombsHAIRSKINUSA. Decyl Glucose in skin care products ... Decyl Glucoside is mild on the skin, easy to work with, and has great formability. You can use this in shampoos, foaming shower ...
The Lauryl Glucoside manufacturing plant project report provides detailed information about industry performance, business plan ... Lauryl Glucoside. Report Coverage. Detailed Process Flow: Unit Operations Involved, Quality Assurance Criteria, Technical Tests ... Lauryl glucoside is a naturally derived, versatile surfactant that has gained prominence in the realm of personal care and ... Lauryl glucoside offers numerous advantages, making it a sought-after ingredient in various applications. Its mild and gentle ...
MALTOOLIGOSYL GLUCOSIDE INCI: Maltooligosyl Glucoside. Obtenção: é um polissacárido de hidratos de carbono obtido naturalmente ... MACADAMIA OIL MADECASSOSIDE MADEIRA ROSA MAGNÉSIO MAGNOLOL MALAQUITA MALIC ACID MALTODEXTRINA MALTOOLIGOSYL GLUCOSIDE MANDARINA ... C10-18 TRIGLYCERIDES C12-16 ALCOHOLS C12-20 ALKYL GLUCOSIDE C14-22 ALCOHOLS C9-12 ALKANE CAESALPINA SPINOSA GUM CAESALPINIA ... DAMASK ROSE DARUTOSIDE DECYL GLUCOSIDE DECYL OLEATE DEHYDROACETIC ACID DEHYDROXANTHAN GUM DEODORANT NATURAL PERFUME DIAPER ...
It is a 7-O-glucoside of luteolin and can be found in dandelion coffee, in Ferula varia and F. foetida in Campanula ... luteolin-7-glucoside inhibits the reaction [lipopolysaccharide, E. coli O26-B6 results in increased expression of IL6 protein] ... luteolin-7-glucoside inhibits the reaction [lipopolysaccharide, E. coli O26-B6 results in increased expression of TNF protein] ...
Shop NIOD Modulating Glucosides at TGC™ - Enjoy Free Delivery & 5* Customer Service. ... Rosmarinyl Glucoside, Caffeyl Glucoside, Gallyl Glucoside, Tetrasodium Tetracarboxymethyl Naringeninchalcone, ... Modulating Glucosides by NIOD is a lightweight emulsion which uses the lastest skincare technology to target and disrupt ... For best results, apply Modulating Glucosides to clean, dry skin before heavier serums and allow the formula a couple of ...
"Glucosides" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Glucosides" by people in this website by year, and whether " ... Below are the most recent publications written about "Glucosides" by people in Profiles. ...
In this The Ordinary Glucoside Foaming Cleanser review, see how it can transform your skincare routine with its gentle and ... The Ordinary Glucoside Foaming Cleanser Review. The Ordinary Glucoside Foaming Cleanser is a clear, fragrance-free gel. It has ... The Ordinary Glucoside Foaming Cleanser Ingredients. There are only eight ingredients in Glucoside Foaming Cleanser. ... Where To Buy The Ordinary Glucoside Foaming Cleanser. You can purchase Glucoside Foaming Cleanser on The Ordinarys website, ...
NIOD Modulating Glucosides (MG) serum targets signs of skin sensitivity while respecting skin integrity and supporting ... Epigallocatechin Gallatyl Glucoside, Rosmarinyl Glucoside, Caffeyl Glucoside, Gallyl Glucoside, Tetrasodium Tetracarboxymethyl ... BIO-ACTIVE GLUCOSIDES. A complex for dermal balance that acts through multiple pathways to soothe skin immediately by targeting ... Modulating Glucosides is a concentrated emulsion to target signs of skin sensitivity, of discomfort and of irritation. This ...
Modulating Glucosides is a concentrated emulsion to target signs of skin sensitivity, of discomfort and of irritation. This ... In Nigeria, NIOD Modulating Glucosides (MG). Modulating Glucosides is a concentrated emulsion to target signs of skin ... SKU: NIODUMG01 Categories: Face, NIOD Skincare Tags: Face, Itch & Irritation, Modulating Glucosides, NIOD, Serum ... BIO-ACTIVE GLUCOSIDES. A complex for dermal balance that acts through multiple pathways to soothe skin immediately by targeting ...
  • Ascorbyl Glucoside is a water-soluble derivative of Vitamin C. Arriving in a serum form, the vitamin packed solution is stable and effective, whilst also being comfortable to use. (coggles.com)
  • Ascorbyl Glucoside Solution 12% offers a lightweight, water-based formula that helps reduce signs of aging by brightening and balancing uneven skin tone. (theordinary.com)
  • Ascorbyl Glucoside is a water-soluble derivative of vitamin C. It is much more stable in water but it is less potent than direct L-Ascorbic Acid. (theordinary.com)
  • Ascorbyl Glucoside: Offers enhanced brightening benefits. (lookyounglb.com)
  • Ascorbyl glucoside (AA-2G), also known as VC glucoside, is a derivative of VC. (sdlookchem.com)
  • Ascorbyl glucoside is mainly used in advanced cosmetics as skin lightening and whitening agents. (sdlookchem.com)
  • Ascorbyl glucoside is one of the whitening additives announced and approved by the Department of Health, and it is recognized as the most stable vitamin C derivative. (sdlookchem.com)
  • Ascorbyl glucoside not only has a good whitening effect, but also has stable chemical properties and is non-irritating to the skin. (sdlookchem.com)
  • Ascorbyl glucoside is not only made use of for whitening, yet additionally can lighten up boring skin, hold-up aging, and protect the skin in sun block items. (sdlookchem.com)
  • Ascorbyl Glucoside is utilized to lighten skin tone and decrease hyperpigmentation old places and blemishes. (sdlookchem.com)
  • After ascorbyl glucoside is exchanged vitamin C, it can greatly decrease the free radicals generated by ultraviolet radiation on the skin, considerably lower skin damage, and also contribute in shielding the skin in sunscreen products. (sdlookchem.com)
  • In cosmetics, ascorbyl glucoside is mostly used as a whitening ingredient like MAP. (sdlookchem.com)
  • As an experienced ascorbyl glucoside manufacturer and supplier, Look Chemical is committed to producing and selling high-quality Methionine. (sdlookchem.com)
  • And we can customize the production of ascorbyl glucoside of different specifications according to the needs of the customer market. (sdlookchem.com)
  • The Ordinary Ascorbyl Glucoside 12% uses a stabilized form of water-soluble Vitamin C that has been gently combined with moisturizing glucose. (wortheecosmetics.com)
  • Ascorbyl glucoside is widely accepted as the gold standard of Vitamin C derivatives, thanks to its superb stability and efficiency in brightening skin complexion and eliminating aging concerns. (wortheecosmetics.com)
  • It is an anionic mild surfactant that has emulsifying qualities, a rich and stable foam.Solid Content: 30 % Disodium Coco-Glucoside Citrate: The foam produced by Disodium Coco-Glucoside Citrate is stable and rich. (actionext.com)
  • Modulating Glucosides by NIOD is a lightweight emulsion which uses the lastest skincare technology to target and disrupt sensitivity. (thegroomingclinic.com)
  • For best results, apply Modulating Glucosides to clean, dry skin before heavier serums and allow the formula a couple of minutes to work its magic before continuing with the rest of your skincare regime. (thegroomingclinic.com)
  • Modulating Glucosides is a concentrated emulsion to target signs of skin sensitivity, of discomfort and of irritation. (niod.com)
  • Cetearyl Glucoside, (and) Cetearyl Alcohol does not contain ethyleneoxide, has a good biodegradability as well as skin affinity. (cookingmamacookoff.com)
  • Is a trusted global provider of Cetearyl Glucoside, (and) Cetearyl Alcohol. (cookingmamacookoff.com)
  • Prices of Cetearyl Glucoside (and) Cetearyl Alcohol If you want to buy Cetearyl Glucoside or Cetearyl Alcohol in bulk. (cookingmamacookoff.com)
  • We offer a variety of packaging options based on the quantity of Cetearyl Glucoside or Cetearyl Alcohol. (cookingmamacookoff.com)
  • Montanov™ 68, INCI Cetearyl Alcohol (and) Cetearyl Glucoside, is a unique non-ionic emulsifier of natural origin. (makeyourown.buzz)
  • In this study, we examined the cytoprotective effects of cyanidin-3-glucoside (C3G) isolated from mulberry fruit against pancreatic β-cell apoptosis caused by hydrogen peroxide (H2O2)-induced oxidative stress. (spandidos-publications.com)
  • In particular, a representative of the anthocyanins isolated from mulberry fruit, cyanidin-3-glucoside (C3G), is present in high quantities in mulberry fruit and is considered a phytotherapeutic agent due to its anti-oxidant properties ( 11 , 14 ). (spandidos-publications.com)
  • I have been testing it out and will share my thoughts on the face wash in this The Ordinary Glucoside Foaming Cleanser review. (abeautyedit.com)
  • The Ordinary Glucoside Foaming Cleanser is an affordable, vegan option for anyone looking for an effective yet gentle, water-based cleanser that you can easily incorporate into your skincare routine. (abeautyedit.com)
  • The Ordinary Glucoside Foaming Cleanser is The Ordinary's first water-based gel cleanser. (abeautyedit.com)
  • Because The Ordinary Squalane Cleanser is an oil-based cleanser, so Glucoside Foaming Cleanser is a complementary water-based cleanser that pairs well with Squalane Cleanser in a double cleanse. (abeautyedit.com)
  • You can use the Squalane Cleanser (or your favorite cleansing balm or cleansing oil) to remove makeup, dirt, and oil and Glucoside Foaming Cleanser to remove residual impurities and debris. (abeautyedit.com)
  • Glucoside Foaming Cleanser is also the perfect morning cleanse, as it gently cleanses your skin without stripping away its natural oils. (abeautyedit.com)
  • There are only eight ingredients in Glucoside Foaming Cleanser. (abeautyedit.com)
  • The Ordinary Glucoside Foaming Cleanser is a clear, fragrance-free gel. (abeautyedit.com)
  • In the evenings, I use this as part of a double cleanse for my combination skin: I start with The Ordinary Squalane Cleanser, which removes my makeup, dirt, oil, and sunscreen, and follow with The Ordinary Glucoside Foaming Cleanser, which finishes my cleansing routine with its thorough water-based cleansing agents. (abeautyedit.com)
  • Cetyl glucoside has a good skin affinity, is biodegradable and does not contain ethylene dioxide. (cookingmamacookoff.com)
  • Decyl Glucoside is a naturally derived, biodegradable, plant-based surfactant, made by reacting corn or potato starch, with glucose and a natural fatty alcohol derived from coconut oil. (shayandcompany.com)
  • In addition to being skin-friendly, lauryl glucoside is biodegradable and environmentally safe. (imarcgroup.com)
  • IMARC Group's report, titled "Lauryl Glucoside Manufacturing Plant Project Report 2024: Industry Trends, Plant Setup, Machinery, Raw Materials, Investment Opportunities, Cost and Revenue" provides a complete roadmap for setting up a lauryl glucoside manufacturing plant. (imarcgroup.com)
  • Lauryl glucoside is a naturally derived, versatile surfactant that has gained prominence in the realm of personal care and household products. (imarcgroup.com)
  • Lauryl glucoside possesses excellent foaming properties, making it a popular choice for formulating mild and gentle cleansers, shampoos, and body washes. (imarcgroup.com)
  • Lauryl glucoside offers numerous advantages, making it a sought-after ingredient in various applications. (imarcgroup.com)
  • The lauryl glucoside market is experiencing robust growth, driven by several key market drivers that underscore its significance in the personal care and cleaning industries. (imarcgroup.com)
  • As consumers prioritize sustainable choices, the need for products containing lauryl glucoside is on the rise. (imarcgroup.com)
  • Furthermore, the global emphasis on green cleaning and sustainable household products is fueling the adoption of lauryl glucoside in dishwashing liquids, laundry detergents, and all-purpose cleaners. (imarcgroup.com)
  • Lastly, regulatory initiatives promoting the use of environmentally safe surfactants further boost the adoption of lauryl glucoside in various applications. (imarcgroup.com)
  • These market drivers collectively position lauryl glucoside as a key ingredient in the shift toward eco-conscious and skin-friendly products. (imarcgroup.com)
  • The report provides insights into the landscape of the lauryl glucoside industry at the global level. (imarcgroup.com)
  • The report also provides a segment-wise and region-wise breakup of the global lauryl glucoside industry. (imarcgroup.com)
  • Additionally, it also provides the price analysis of feedstocks used in the manufacturing of lauryl glucoside, along with the industry profit margins. (imarcgroup.com)
  • The report also provides detailed information related to the process flow and various unit operations involved in a lauryl glucoside manufacturing plant. (imarcgroup.com)
  • Decyl Glucoside Surfactant is a gentle naturally derived foaming agent for skincare products. (shayandcompany.com)
  • Decyl Glucoside is a nonionic coconut-derived surfactant that works as either the primary or secondary surfactant in your formulas. (shayandcompany.com)
  • Due to its mildness and foaming properties, we recommend that you buy Decyl Glucoside as a primary or co-surfactant in shampoos, shower gels, and bubble baths, hand and face cleansers, and other applications where mildness without sacrificing performance is required. (shayandcompany.com)
  • We do also offer naturally derived Cocamidopropyl Betaine as a stand-alone liquid surfactant, or that can be paired along with Decyl Glucoside. (shayandcompany.com)
  • Decyl Glucoside is a mild non-ionic surfactant that's plant-derived from coconut and corn without the use of chemicals. (eco-max.com)
  • Decyl Glucoside is mild on the skin, easy to work with, and has great formability. (shayandcompany.com)
  • A group may also be constructed to include the cyanogenic glucosides, i.e. those containing prussic acid. (wikipedia.org)
  • Amygdalin-- A naturally occurring cyanogenic glucoside found in almonds and apricot pits. (cdc.gov)
  • Decyl Glucoside will be thicker at colder temperatures, so if you find your container difficult to work with, slightly warm it in warm water bath to loosen it up. (shayandcompany.com)
  • What is Decyl Glucoside? (eco-max.com)
  • Hesperetin-7- O -glucoside/ß-cyclodextrin Inclusion Complex Induces Acute Vasodilator Effect to Inhibit the Cold Sensation Response during Localized Cold-Stimulate Stress in Healthy Human Subjects: A Randomized, Double-Blind, Crossover, and Placebo-Controlled Study. (bvsalud.org)
  • Hesperetin dihydrochalcone 4'-glucoside, 1, and phloretin 4'-glucoside, 2, belong to a family of dihydrochalcone glycosides that exhibit flavorant properties. (cdc.gov)
  • Synthesis of Selected Naturally Occurring Glucosides of Volatile Compounds. (srce.hr)
  • 2004). 'Synthesis of Selected Naturally Occurring Glucosides of Volatile Compounds. (srce.hr)
  • Mastelić J, Jerković I, Vinković M, Džolić Z, Vikić-Topić D. Synthesis of Selected Naturally Occurring Glucosides of Volatile Compounds. (srce.hr)
  • X-Glucoside is a substrate for β-Glucosidase that, upon enzymatic action, renders an insoluble indigo-blue chromophore (615 nm. (agscientific.com)
  • We have many different kinds of packing which depend on C8-14 Alkyl glucoside quantity. (advanc3dmaterials.de)
  • A glucoside is a glycoside that is chemically derived from glucose. (wikipedia.org)
  • Glucose is produced when a glucoside is hydrolysed by purely chemical means, or decomposed by fermentation or enzymes. (wikipedia.org)
  • The simplest glucosides are the alkyl ethers which have been obtained by reacting hydrochloric acid on alcoholic glucose solutions. (wikipedia.org)
  • Haskap berry is a rich source of anthocyanins and (poly)phenols with a notable enrichment of cyanidin-3-O-β-glucoside (C3G), a potent anti-inflammatory agent. (researchgate.net)
  • Haskap (Lonicera caerulea L.) berry is enriched in anthocyanins, primarily cyanidin-3-O-β-glucoside (C3G). (researchgate.net)
  • This book reviews sources, applications and new research of glucosides. (novapublishers.com)
  • Phenol derivatives There are a number of glucosides found in natural phenols and polyphenols, as, for example, in the flavonoids chemical family. (wikipedia.org)
  • After ascorbic acid glucoside enters the human body, it will be converted into ascorbic acid, so it also has the effect of ascorbic acid. (sdlookchem.com)
  • Immunogen and coating antigen were prepared by conjugating hapten, 4-(3-oxo-3-(2,6-dihydroxy-4-glucoside phenyl)propyl) benzoic acid, to thyroglobulin and bovine serum albumin, respectively. (cdc.gov)
  • Benzoyl-beta-D-glucoside is a compound found in the fern Pteris ensiformis. (wikipedia.org)
  • It is a 7-O-glucoside of luteolin and can be found in dandelion coffee, in Ferula varia and F. foetida in Campanula persicifolia and C. rotundifolia and in Cynara scolymus (artichoke). (selfdecode.com)