Butanes
Clostridium acetobutylicum
Clostridium beijerinckii
Nitrosamines
Phospholipase D
1-Propanol
Clostridium
Acetone
Biofuels
1-Octanol
Glucuronates
Fermentation
Alcohol Dehydrogenase
Phosphatidic Acids
Cotinine
Metabolic Engineering
Oxygen Radioisotopes
Alcohol-induced biphasic inhibition of myosin subfragment 1 K-EDTA-ATPase. (1/210)
Butanol-induced inhibition of K-EDTA-ATPase of myosin subfragment 1 proceeded by biphasic kinetics, consisting of rapid and slow inactivations. The extent of the rapid inactivation, which was estimated by extrapolating the process of slow inactivation to zero time of the incubation period, was saturated with butanol concentration. Recovery of activity by dilution in the rapid phase indicates that the rapid process is reversible. The slow inactivation was concomitant with a partial denaturation of the 50 kDa domain of S1, which was detected by limited tryptic digestion. Other alcohols (methanol, ethanol, propanol and hexanol) also inhibited the K-EDTA-ATPase in the rapid phase. The Ki decreased with an increase in the number of methylene groups of alcohol. When K-EDTA-ATPase activity in the rapid phase was plotted against viscosity, surface tension or dielectric constant, the curves were different for each of the various alcohol solutions. The rapid inactivation appears to be caused by a binding of the alkyl group to S1, rather than by solvent effects. The kinetics of rapid butanol inhibitions indicate that butanol reduces the maximum activity of ATPase but enhances an apparent affinity of S1 with ATP. These indications suggest that alcohol stabilizes S1.KATP intermediate. The rapid K-EDTA-ATPase inhibition was observed at the same alcohol concentration where S1 Mg-ATPase was activated. (+info)Lysophosphatidic acid increases intracellular H2O2 by phospholipase D and RhoA in rat-2 fibroblasts. (2/210)
We have investigated the possible roles of phospholipase D (PLD) and RhoA in the production of intracellular H2O2 and actin polymerization in response to lysophosphatidic acid (LPA) in Rat-2 fibroblasts. LPA increased intracellular H2O2, with a maximal increase at 30 min, which was blocked by the catalase from Aspergillus niger. The LPA-stimulated production of H2O2 was inhibited by 1-butanol or PKC-downregulation, but not by 2-butanol. Purified phosphatidic acid (PA) also increased intracellular H2O2 and the increase was inhibited by the catalase. The role of RhoA was studied by the scrape-loading of C3 transferase into the cells. The C3 toxin, which inhibited stress fiber formation stimulated by LPA, blocked the H2O2 production in response to LPA or PA, but had no inhibitory effect on the activation of PLD by LPA. Exogenous H2O2 increased F-actin content by stress fiber formation. In addition, catalase inhibited actin polymerization activated by LPA, PA, or H2O2, indicated the role of H2O2 in actin polymerization. These results suggest that LPA increased intracellular H2O2 by the activation of PLD and RhoA, and that intracellular H2O2 was required for the LPA-stimulated stress fiber formation. (+info)beta-glycosidase from the hyperthermophilic archaeon Sulfolobus solfataricus: structure and activity in the presence of alcohols. (3/210)
beta-Glycosidase from the extreme thermophilic archaeon Sulfolobus solfataricus is a tetrameric protein with a molecular mass of 240 kDa, stable in the presence of detergents, and with a maximal activity at temperatures above 95 degrees C. Understanding the structure-activity relationships of the enzyme under different conditions is of fundamental importance for both theoretical and applicative purposes. In this paper we report the effect of methanol, ethanol, 1-propanol, and 1-butanol on the activity of S. solfataricus beta-glycosidase expressed in Escherichia coli. The alcohols stimulated the enzyme activity, with 1-butanol producing its maximum effect at a lower concentration than the other alcohols. The structure of the enzyme was studied in the presence of 1-butanol by circular dichroism, and Fourier-transform infrared and fluorescence spectroscopies. Circular dichroism and steady-state fluorescence measurements revealed that at low temperatures the presence of the alcohol produced no significant changes in the tertiary structure of the enzyme. However, time-resolved fluorescence data showed that the alcohol modifies the protein microenvironment, leading to a more flexible enzyme structure, which is probably responsible for the enhanced enzymatic activity. (+info)Diversity in butane monooxygenases among butane-grown bacteria. (4/210)
Butane monooxygenases of butane-grown Pseudomonas butanovora, Mycobacterium vaccae JOB5, and an environmental isolate, CF8, were compared at the physiological level. The presence of butane monooxygenases in these bacteria was indicated by the following results. (i) O(2) was required for butane degradation. (ii) 1-Butanol was produced during butane degradation. (iii) Acetylene inhibited both butane oxidation and 1-butanol production. The responses to the known monooxygenase inactivator, ethylene, and inhibitor, allyl thiourea (ATU), discriminated butane degradation among the three bacteria. Ethylene irreversibly inactivated butane oxidation by P. butanovora but not by M. vaccae or CF8. In contrast, butane oxidation by only CF8 was strongly inhibited by ATU. In all three strains of butane-grown bacteria, specific polypeptides were labeled in the presence of [(14)C]acetylene. The [(14)C]acetylene labeling patterns were different among the three bacteria. Exposure of lactate-grown CF8 and P. butanovora and glucose-grown M. vaccae to butane induced butane oxidation activity as well as the specific acetylene-binding polypeptides. Ammonia was oxidized by all three bacteria. P. butanovora oxidized ammonia to hydroxylamine, while CF8 and M. vaccae produced nitrite. All three bacteria oxidized ethylene to ethylene oxide. Methane oxidation was not detected by any of the bacteria. The results indicate the presence of three distinct butane monooxygenases in butane-grown P. butanovora, M. vaccae, and CF8. (+info)Short-chain alcohols promote an early stage of membrane hemifusion. (5/210)
Hemifusion, the linkage of contacting lipid monolayers of two membranes before the opening of a fusion pore, is hypothesized to proceed through the formation of a stalk intermediate, a local and strongly bent connection between membranes. When the monolayers' propensity to bend does not support the stalk (e.g., as it is when lysophosphatidylcholine is added), hemifusion is inhibited. In contrast, short-chain alcohols, reported to affect monolayer bending in a manner similar to that of lysophosphatidylcholine, were here found to promote hemifusion between fluorescently labeled liposomes and planar lipid bilayers. Single hemifusion events were detected by fluorescence microscopy. Methanol or ethanol (1.2-1.6 w/w %) added to the same compartment of the planar bilayer chamber as liposomes caused a 5-50 times increase in the number of hemifusion events. Alcohol-induced hemifusion was inhibited by lysophosphatidylcholine. Promotion of membrane hemifusion by short-chain alcohol was also observed for cell-cell fusion mediated by influenza virus hemagglutinin (HA). Alcohol promoted a fusion stage subsequent to the low pH-dependent activation of HA. We propose that binding of short-chain alcohol to the surface of membranes promotes hemifusion by facilitating the transient breakage of the continuity of each of the contacting monolayers, which is required for their subsequent merger in the stalk intermediate. (+info)Trp-Lys-Tyr-Met-Val-D-Met is a chemoattractant for human phagocytic cells. (6/210)
Trp-Lys-Tyr-Met-Val-D-Met (WKYMVm) is a synthetic peptide that stimulates phosphoinositide (PI) hydrolysis in human leukocytes. The peptide binds to a unique cell surface receptor(s). Recently we had demonstrated that human neutrophils, monocytes, and B lymphocytes express this peptide-specific receptor and that stimulation of human leukocytes with the peptide leads to activation of the oxidative respiratory system and the bactericidal activity of neutrophils or monocytes. In this study we showed that the peptide induces chemotaxis of phagocytic leukocytes and studied the signaling pathway leading to chemotaxis in human monocytes. The peptide-induced monocyte chemotaxis is pertussis toxin (PTX)-sensitive. This fact correlates with the peptide's stimulation of PI hydrolysis and intracellular Ca2+ ([Ca2+]i) release, which is also PTX-sensitive. We demonstrate that the peptide-specific receptor is different from receptor(s) for monocyte chemoattractant protein-1 (MCP-1). We also show that intracellular signaling of WKYMVm leading to monocyte chemotaxis is different from that of MCP-1. The peptide-mediated monocyte chemotaxis is insensitive to protein kinase C (PKC) inhibitor (GF109203X) and butan-1-ol, ruling out PKC and phospholipase D participation in this process. On the other hand, a tyrosine kinase inhibitor (genistein) and RhoA inhibitor (C3 transferase) curtailed the peptide-induced chemotaxis in a concentration-dependent manner, implying the involvement of tyrosine kinase and RhoA, respectively. Treatment of human monocytes with the peptide stimulates tyrosine phosphorylation of several cellular proteins, including p125FAK and Pyk2 and translocation of RhoA from the cytosol to the membrane. We conclude that WKYMVm induces chemotaxis of human phagocytic leukocytes via unique receptors and signaling. (+info)Ethanol increases superoxide anion production stimulated with 4beta-phorbol 12-myristate 13-acetate in human polymorphonuclear leukocytes. Involvement of protein kinase C. (7/210)
Stimulation of human polymorphonuclear leukocytes (PMNs) with PMA initiates a cascade of events leading to the production and release of superoxide anion (O-2), a major component in anti-bacterial defense. Generation of O-2 by PMA-stimulated PMNs occurs through the translocation and activation of protein kinase C (PKC). In this study, using freshly isolated PMNs, we examined the effect of ethanol on this response to PMA. Our results show that the basal production of O-2 was not affected by ethanol. In contrast, the response induced by PMA was potentiated by ethanol. This potentiation was observed even at high doses of PMA (200 nM) which alone had stimulated the O-2 response maximally. This enhanced response was not due to an increase of PMA uptake by PMNs. The maximal effect was obtained when the cells were preincubated with 80 mM of ethanol before PMA stimulation. Measurement of PKC activity in the cytosolic and membrane fractions showed that pretreatment of PMNs with ethanol increased twofold the PMA-stimulated PKC activity in the membrane fraction. Furthermore, Western blot analysis verified that this increase in PKC activity in the membrane fraction was linked to an increase in the translocation of PKC-alpha and -beta isoforms to the membrane. These results suggest that ethanol potentiates PMA-induced O-2 production through increasing PKC translocation and activity in PMNs. (+info)General anesthetic action at an internal protein site involving the S4-S5 cytoplasmic loop of a neuronal K(+) channel. (8/210)
The structural bases of general anesthetic action on a neuronal K(+) channel were investigated using the series of homologous 1-alkanols, electrophysiology, and mutational analysis. Domain swapping between dShaw2 (alkanol-sensitive) and hKv3.4 (alkanol-resistant) and site-directed mutagenesis demonstrated that a 13-amino acid cytoplasmic loop (S4-S5) determines the selective inhibition of native dShaw2 channels by 1-alkanols. The S4-S5 loop may contribute to a receptor for both 1-alkanols and the inactivation particle, because the enhanced 1-alkanol sensitivity of hKv3.4 channels hosting S4-S5 mutations correlates directly with disrupted channel inactivation. Evidence of a discrete protein site was also obtained from the analysis of the relationship between potency and alkyl chain length, which begins to level off after 1-hexanol. Rapid application to the cytoplasmic side of inside-out membrane patches shows that the interaction between dShaw2 channels and 1-alkanols equilibrates in <200 ms. By contrast, the equilibration time is >1000-fold slower when the drug is applied externally to outside-out membrane patches. The data strongly favor a mechanism of inhibition involving a discrete internal site for 1-alkanols in dShaw2 K(+) channels. A new working hypothesis proposes that 1-alkanols lock dShaw2 channels in their closed conformation by a direct interaction at a crevice formed by the S4-S5 loop. (+info)Butanols are a family of alcohols with four carbon atoms and a chemical formula of C4H9OH. They are commonly used as solvents, intermediates in chemical synthesis, and fuel additives. The most common butanol is n-butanol (normal butanol), which has a straight chain of four carbon atoms. Other forms include secondary butanols (such as isobutanol) and tertiary butanols (such as tert-butanol). These compounds have different physical and chemical properties due to the differences in their molecular structure, but they all share the common characteristic of being alcohols with four carbon atoms.
1-Butanol, also known as n-butanol or butyl alcohol, is a primary alcohol with a chemical formula of C4H9OH. It is a colorless liquid that is used as a solvent and in the manufacture of other chemicals. 1-Butanol has a wide range of applications including use as a paint thinner, in the production of rubber, and as a fuel additive. It is also found naturally in some foods and beverages.
In medical terms, 1-butanol may be used as an ingredient in topical medications or as a solvent for various pharmaceutical preparations. However, it is not typically used as a therapeutic agent on its own. Exposure to high levels of 1-butanol can cause irritation to the eyes, skin, and respiratory tract, and prolonged exposure may lead to more serious health effects.
Butanes are a group of flammable, colorless gases that are often used as fuel or in the production of other chemicals. They have the chemical formula C4H10 and are composed of four carbon atoms and ten hydrogen atoms. Butanes are commonly found in natural gas and crude oil, and they can be extracted through a process called distillation.
There are two main types of butane: n-butane and isobutane. N-butane has a straight chain of four carbon atoms, while isobutane has a branched chain with one carbon atom branching off the main chain. Both forms of butane are used as fuel for lighters, stoves, and torches, and they are also used as refrigerants and in the production of aerosols.
Butanes are highly flammable and can be dangerous if not handled properly. They should be stored in a cool, well-ventilated area away from sources of ignition, and they should never be used near an open flame or other source of heat. Ingesting or inhaling butane can be harmful and can cause symptoms such as dizziness, nausea, and vomiting. If you suspect that you have been exposed to butane, it is important to seek medical attention immediately.
'Clostridium acetobutylicum' is a gram-positive, spore-forming, rod-shaped bacterium that is commonly found in soil and aquatic environments. It is a species of the genus Clostridium, which includes many bacteria capable of producing industrial chemicals through fermentation.
'Clostridium acetobutylicum' is particularly known for its ability to produce acetic acid and butyric acid, as well as solvents such as acetone and butanol, during the process of anaerobic respiration. This makes it a potential candidate for biotechnological applications in the production of biofuels and other industrial chemicals.
However, like many Clostridium species, 'Clostridium acetobutylicum' can also produce toxins and cause infections in humans and animals under certain circumstances. Therefore, it is important to handle this organism with care and follow appropriate safety protocols when working with it in a laboratory setting.
'Clostridium beijerinckii' is a species of gram-positive, spore-forming, rod-shaped bacteria found in various environments such as soil, aquatic sediments, and the intestinal tracts of animals. It is named after the Dutch microbiologist Martinus Willem Beijerinck.
This bacterium is capable of fermenting a wide range of organic compounds and producing a variety of metabolic end-products, including butanol, acetone, and ethanol. 'Clostridium beijerinckii' has attracted interest in biotechnology due to its potential for the production of biofuels and industrial chemicals through fermentation processes.
However, it is also known to cause food spoilage and, under certain circumstances, can produce harmful metabolites that may pose a risk to human health. Therefore, proper handling and safety precautions are necessary when working with this bacterium in laboratory or industrial settings.
Nitrosamines are a type of chemical compound that are formed by the reaction between nitrous acid (or any nitrogen oxide) and secondary amines. They are often found in certain types of food, such as cured meats and cheeses, as well as in tobacco products and cosmetics.
Nitrosamines have been classified as probable human carcinogens by the International Agency for Research on Cancer (IARC). Exposure to high levels of nitrosamines has been linked to an increased risk of cancer, particularly in the digestive tract. They can also cause DNA damage and interfere with the normal functioning of cells.
In the medical field, nitrosamines have been a topic of concern due to their potential presence as contaminants in certain medications. For example, some drugs that contain nitrofurantoin, a medication used to treat urinary tract infections, have been found to contain low levels of nitrosamines. While the risk associated with these low levels is not well understood, efforts are underway to minimize the presence of nitrosamines in medications and other products.
"Pentanols" is not a recognized medical term. However, in chemistry, pentanols refer to a group of alcohols containing five carbon atoms. The general formula for pentanols is C5H12O, and they have various subcategories such as primary, secondary, and tertiary pentanols, depending on the type of hydroxyl (-OH) group attachment to the carbon chain.
In a medical context, alcohols like methanol and ethanol can be toxic and cause various health issues. However, there is no specific medical relevance associated with "pentanols" as a group. If you have any further questions or need information about a specific chemical compound, please let me know!
Phospholipase D is an enzyme that catalyzes the hydrolysis of phosphatidylcholine and other glycerophospholipids to produce phosphatidic acid and a corresponding alcohol. This reaction plays a crucial role in various cellular processes, including signal transduction, membrane trafficking, and lipid metabolism. There are several isoforms of Phospholipase D identified in different tissues and organisms, each with distinct regulatory mechanisms and functions. The enzyme's activity can be modulated by various factors such as calcium ions, protein kinases, and G proteins, making it a critical component in the regulation of cellular homeostasis.
1-Propanol is a primary alcohol with the chemical formula CH3CH2CH2OH. It is also known as n-propanol or propan-1-ol. It is a colorless, flammable liquid that is used as a solvent and in the production of other chemicals. 1-Propanol has a wide range of applications including as a disinfectant, an intermediate in the synthesis of other chemicals, and as a component in various industrial and consumer products such as cosmetics, cleaning agents, and pharmaceuticals. It is also used as a fuel additive to increase the octane rating of gasoline.
'Clostridium' is a genus of gram-positive, rod-shaped bacteria that are widely distributed in nature, including in soil, water, and the gastrointestinal tracts of animals and humans. Many species of Clostridium are anaerobic, meaning they can grow and reproduce in environments with little or no oxygen. Some species of Clostridium are capable of producing toxins that can cause serious and sometimes life-threatening illnesses in humans and animals.
Some notable species of Clostridium include:
* Clostridium tetani, which causes tetanus (also known as lockjaw)
* Clostridium botulinum, which produces botulinum toxin, the most potent neurotoxin known and the cause of botulism
* Clostridium difficile, which can cause severe diarrhea and colitis, particularly in people who have recently taken antibiotics
* Clostridium perfringens, which can cause food poisoning and gas gangrene.
It is important to note that not all species of Clostridium are harmful, and some are even beneficial, such as those used in the production of certain fermented foods like sauerkraut and natto. However, due to their ability to produce toxins and cause illness, it is important to handle and dispose of materials contaminated with Clostridium species carefully, especially in healthcare settings.
Acetone is a colorless, volatile, and flammable liquid organic compound with the chemical formula (CH3)2CO. It is the simplest and smallest ketone, and its molecules consist of a carbonyl group linked to two methyl groups. Acetone occurs naturally in the human body and is produced as a byproduct of normal metabolic processes, particularly during fat burning.
In clinical settings, acetone can be measured in breath or blood to assess metabolic status, such as in cases of diabetic ketoacidosis, where an excess production of acetone and other ketones occurs due to insulin deficiency and high levels of fatty acid breakdown. High concentrations of acetone can lead to a sweet, fruity odor on the breath, often described as "fruity acetone" or "acetone breath."
Biofuels are defined as fuels derived from organic materials such as plants, algae, and animal waste. These fuels can be produced through various processes, including fermentation, esterification, and transesterification. The most common types of biofuels include biodiesel, ethanol, and biogas.
Biodiesel is a type of fuel that is produced from vegetable oils or animal fats through a process called transesterification. It can be used in diesel engines with little or no modification and can significantly reduce greenhouse gas emissions compared to traditional fossil fuels.
Ethanol is a type of alcohol that is produced through the fermentation of sugars found in crops such as corn, sugarcane, and switchgrass. It is typically blended with gasoline to create a fuel known as E85, which contains 85% ethanol and 15% gasoline.
Biogas is a type of fuel that is produced through the anaerobic digestion of organic materials such as food waste, sewage sludge, and agricultural waste. It is composed primarily of methane and carbon dioxide and can be used to generate electricity or heat.
Overall, biofuels offer a renewable and more sustainable alternative to traditional fossil fuels, helping to reduce greenhouse gas emissions and decrease dependence on non-renewable resources.
Hexanols are a class of organic compounds that contain a hexanol functional group, which is a hydroxyl group (-OH) attached to a linear or branched carbon chain containing six carbon atoms. They can be either primary, secondary, or tertiary alcohols depending on the position of the hydroxyl group in relation to the carbon chain. Hexanols are used in various applications such as in the production of flavors, fragrances, and industrial chemicals.
1-Octanol is a fatty alcohol with the chemical formula C8H17OH. It is a colorless oily liquid that is slightly soluble in water and miscible with most organic solvents. 1-Octanol is used as an intermediate in the synthesis of other chemicals, including pharmaceuticals, agrochemicals, and fragrances.
In medical terminology, 1-octanol may be used as a reference standard for measuring the partition coefficient of drugs between octanol and water, which can help predict their distribution and elimination in the body. This value is known as the octanol-water partition coefficient (Kow) and is an important parameter in pharmacokinetics and drug design.
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.
Fermentation is a metabolic process in which an organism converts carbohydrates into alcohol or organic acids using enzymes. In the absence of oxygen, certain bacteria, yeasts, and fungi convert sugars into carbon dioxide, hydrogen, and various end products, such as alcohol, lactic acid, or acetic acid. This process is commonly used in food production, such as in making bread, wine, and beer, as well as in industrial applications for the production of biofuels and chemicals.
Alcohol dehydrogenase (ADH) is a group of enzymes responsible for catalyzing the oxidation of alcohols to aldehydes or ketones, and reducing equivalents such as NAD+ to NADH. In humans, ADH plays a crucial role in the metabolism of ethanol, converting it into acetaldehyde, which is then further metabolized by aldehyde dehydrogenase (ALDH) into acetate. This process helps to detoxify and eliminate ethanol from the body. Additionally, ADH enzymes are also involved in the metabolism of other alcohols, such as methanol and ethylene glycol, which can be toxic if allowed to accumulate in the body.
Phosphatidic acids (PAs) are a type of phospholipid that are essential components of cell membranes. They are composed of a glycerol backbone linked to two fatty acid chains and a phosphate group. The phosphate group is esterified to another molecule, usually either serine, inositol, or choline, forming different types of phosphatidic acids.
PAs are particularly important as they serve as key regulators of many cellular processes, including signal transduction, membrane trafficking, and autophagy. They can act as signaling molecules by binding to and activating specific proteins, such as the enzyme phospholipase D, which generates second messengers involved in various signaling pathways.
PAs are also important intermediates in the synthesis of other phospholipids, such as phosphatidylcholine, phosphatidylethanolamine, and phosphatidylinositol. They are produced by the enzyme diacylglycerol kinase (DGK), which adds a phosphate group to diacylglycerol (DAG) to form PA.
Abnormal levels of PAs have been implicated in various diseases, including cancer, diabetes, and neurological disorders. Therefore, understanding the regulation and function of PAs is an active area of research with potential therapeutic implications.
Cotinine is the major metabolite of nicotine, which is formed in the body after exposure to tobacco smoke or other sources of nicotine. It is often used as a biomarker for nicotine exposure and can be measured in various biological samples such as blood, urine, saliva, and hair. Cotinine has a longer half-life than nicotine, making it a more reliable indicator of long-term exposure to tobacco smoke or nicotine products.
Metabolic engineering is a branch of biotechnology that involves the modification and manipulation of metabolic pathways in organisms to enhance their production of specific metabolites or to alter their flow of energy and carbon. This field combines principles from genetics, molecular biology, biochemistry, and chemical engineering to design and construct novel metabolic pathways or modify existing ones with the goal of optimizing the production of valuable compounds or improving the properties of organisms for various applications.
Examples of metabolic engineering include the modification of microorganisms to produce biofuels, pharmaceuticals, or industrial chemicals; the enhancement of crop yields and nutritional value in agriculture; and the development of novel bioremediation strategies for environmental pollution control. The ultimate goal of metabolic engineering is to create organisms that can efficiently and sustainably produce valuable products while minimizing waste and reducing the impact on the environment.
Oxygen radioisotopes are unstable isotopes of the element oxygen that emit radiation as they decay to a more stable form. These isotopes can be used in medical imaging and treatment, such as positron emission tomography (PET) scans. Common oxygen radioisotopes used in medicine include oxygen-15 and oxygen-18. Oxygen-15 has a very short half-life of about 2 minutes, while oxygen-18 has a longer half-life of about 2 hours. These isotopes can be incorporated into molecules such as water or carbon dioxide, which can then be used to study blood flow, metabolism and other physiological processes in the body.
Carcinogens are agents (substances or mixtures of substances) that can cause cancer. They may be naturally occurring or man-made. Carcinogens can increase the risk of cancer by altering cellular DNA, disrupting cellular function, or promoting cell growth. Examples of carcinogens include certain chemicals found in tobacco smoke, asbestos, UV radiation from the sun, and some viruses.
It's important to note that not all exposures to carcinogens will result in cancer, and the risk typically depends on factors such as the level and duration of exposure, individual genetic susceptibility, and lifestyle choices. The International Agency for Research on Cancer (IARC) classifies carcinogens into different groups based on the strength of evidence linking them to cancer:
Group 1: Carcinogenic to humans
Group 2A: Probably carcinogenic to humans
Group 2B: Possibly carcinogenic to humans
Group 3: Not classifiable as to its carcinogenicity to humans
Group 4: Probably not carcinogenic to humans
This information is based on medical research and may be subject to change as new studies become available. Always consult a healthcare professional for medical advice.
1-Butanol
2-Methyl-1-butanol
2-Ethyl-1-butanol
3,3-Dimethyl-1-butanol
2,2-Dimethyl-1-butanol
2-Butanol
Butanol fuel
Butanol
Acetone-butanol-ethanol fermentation
Comparison of psychoactive alcohols in alcoholic drinks
Monobutyl phthalate
Primary alcohol
Cofactor engineering
Triethylborane
Tert-Butyl alcohol
Dibutyl phthalate
Artificial photosynthesis
Solar fuel
Electrochemical reduction of carbon dioxide
1-Chlorobutane
Levopropoxyphene
Protein detection
Werner Urland
Industrial microbiology
Isobutanol
Methoxymethyl ether
Anastrepha suspensa
Valinol
Alcohol (drug)
Tobacco-specific nitrosamines
1-Butanol - Wikipedia
1-Butanol, 3-methyl-, benzoate
NNAL (4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol) Factsheet | National Biomonitoring Program | CDC
1-Butanol - n-Butanol, Butyl alcohol
4-(Tetrahydro-2-furanyloxy)-1-butanol | C8H16O3 | ChemSpider
4-{[1-(5-Chloro-2-thienyl)ethyl]amino}-2-butanol | C10H16ClNOS | ChemSpider
1-(2-Furyl)-1-butanol supplier - CAS 4208-62-2 - EC-000.1529
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1-Butanol crystalline
1-Butanol for UV, IR, HPLC
3-METHYL-1-BUTANOL [Isoamyl Alcohol] - Crescendo
R)-(-)-2-Amino-1-butanol - Chemlyte solutions
EWG Tap Water Database | West Deptford Twp Water Department
13325-10-5 | MFCD00008230 | 1-Butanol, 4-amino
Azeotropic Data of 1-Butanol + Cyclohexane from Dortmund Data Bank
4 Chloro 1 Butanol Manufacturers, Suppliers, Exporters, Importers in India
Xylose utilization stimulates mitochondrial production of isobutanol and 2-methyl-1-butanol in Saccharomyces cerevisiae<...
S)-(+)-sec-Butanol, 99%, Thermo Scientific Chemicals, Quantity: 1 g | Fisher Scientific
EP 2799416 B1 20161012 - METHOD OF PRODUCING 1-(2-t-BUTYL CYCLOHEXYLOXY)-2-BUTANOL
View of Vapour phase Guerbet condensation of ethanol to 1-butanol on CsX zeolite | Catalysis and petrochemistry
High Purity Primary Solvents | Fujifilm [Philippines]
Molecules | Free Full-Text | Characterization of a (2R,3R)-2,3-Butanediol Dehydrogenase from Rhodococcus erythropolis WZ010
Kitagawa 190U Ethyl cellosolve, Methyl cellosolve Detector Tube 5-500 ppm; 1-Butanol, Butyl cellosolve, Diacetone alcohol,more
ArboCat Virus: Murray Valley encephalitis (MVEV)
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2-Methyl-1-butanol: CAS # 137-32-6 Compound Information and Applications for GC (Gas Chromatography) and LC (Liquid...
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Butan-2-1
- Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. (wikipedia.org)
Butyl10
- The largest use of 1-butanol is as an industrial intermediate, particularly for the manufacture of butyl acetate (itself an artificial flavorant and industrial solvent). (wikipedia.org)
- A variety of butanol derivatives are used as solvents, e.g. butoxyethanol or butyl acetate. (wikipedia.org)
- The market for butanols (excluding butan-1-ol (n-butyl alcohol)) in Australia and Oceania rose modestly to $X in 2022, growing by 4.2% against the previous year. (indexbox.io)
- In value terms, butanols (excluding butan-1-ol (n-butyl alcohol)) production expanded slightly to $X in 2022 estimated in export price. (indexbox.io)
- In 2022, after seven years of growth, there was significant decline in overseas shipments of butanols (excluding butan-1-ol (n-butyl alcohol)), when their volume decreased by -59.6% to X tons. (indexbox.io)
- In value terms, butanols (excluding butan-1-ol (n-butyl alcohol)) exports fell rapidly to $X in 2022. (indexbox.io)
- Australia was also the fastest-growing in terms of the butanols (excluding butan-1-ol (n-butyl alcohol)) exports, with a CAGR of +23.3% from 2012 to 2022. (indexbox.io)
- In value terms, Australia ($X) also remains the largest butanols (excluding butan-1-ol (n-butyl alcohol)) supplier in Australia and Oceania. (indexbox.io)
- For the third consecutive year, Australia and Oceania recorded growth in overseas purchases of butanols (excluding butan-1-ol (n-butyl alcohol)), which increased by 3.4% to X tons in 2022. (indexbox.io)
- 1.1 This specification covers n-butyl alcohol (butanol). (astm.org)
Ethanol9
- 1-Butanol occurs naturally as a minor product of the ethanol fermentation of sugars and other saccharides and is present in many foods and drinks. (wikipedia.org)
- Butanol at 85 percent strength can be used in cars designed for gasoline without any change to the engine (unlike 85% ethanol), and it provides more energy for a given volume than ethanol, almost as much as gasoline. (wikipedia.org)
- Therefore, a vehicle using butanol would return fuel consumption more comparable to gasoline than ethanol. (wikipedia.org)
- Vapour-liquid equilibrium of CO(2) + [0.00871 glycerol + 0.99129 (ethanol or 1-propanol or 1-butanol)] mixtures was measured at the temperatures of 313.15 K and 333.15 K, and close to the critical line, at pressures up to 12 MPa. (unl.pt)
- Background: Branched-chain higher alcohols (BCHAs), including isobutanol and 2-methyl-1-butanol, are promising advanced biofuels, superior to ethanol due to their higher energy density and better compatibility with existing gasoline infrastructure. (illinois.edu)
- Like Ethanol, Butanol is a biomas-based renewable fuel that can be produced by alcoholic fermentation of sugar beet, sugar can, corn, wheat (bio-Butanol), although petro-Butanol also exists, i.e. (bfh.ch)
- Butanol, a four-carbon alcohol, is a candidate alternative fuel, with properties closer to gasoline than Ethanol. (bfh.ch)
- The biorefineries producing cellulosic ethanol from wood or agricultural residues can be retrofitted to enable the production of butanol, which is actually practiced in US. (bfh.ch)
- Biologically produced alcohols , most commonly ethanol, and less commonly propanol and butanol , are produced by the action of microorganisms and enzymes through the fermentation of sugars or starches (easiest), or cellulose (which is more difficult).The IEA estimates that ethanol production used 20% of sugar supplies and 13% of corn supplies in 2021. (wikipedia.org)
Isomers1
- Two of its isomers, n-Butanol (1-butanol) and iso-Butanol can be considered for use in spark ignition (SI) engines. (bfh.ch)
Tert-butanol1
- Differently from this pattern, XP Bond® adhesive system (Dentsply Caulk, Milford, MA, USA) 12 , which contains tert-butanol as solvent, is a two-step etch-and-rinse adhesive which is marketed as being a good adhesive agent even in over-wet or dry dentin conditions. (bvsalud.org)
Alcohols2
- Butan-1-ol is one of the "fusel alcohols" (from the German for "bad liquor"), which include alcohols that have more than two carbon atoms and have significant solubility in water. (wikipedia.org)
- The oxygen content of Butanol has similar advantages, like with other alcohols: tendency of less CO & HC, but possibility of increasing NO x (depending on engine parameters setting). (bfh.ch)
Formula1
- 1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C4H9OH and a linear structure. (wikipedia.org)
Isobutanol2
- We then increased the flux through these pathways by making gene deletions of BAT1, ALD6, and PHO13, to develop a strain (YZy197) that produces as much as 4 g/L of BCHAs (3.10 ±- 0.18 g isobutanol/L and 0.91 ±- 0.02 g 2-methyl-1-butanol/L) from xylose. (illinois.edu)
- This represents approximately a 28-fold improvement on the highest isobutanol titers obtained from xylose previously reported in yeast and the first report of 2-methyl-1-butanol produced from xylose. (illinois.edu)
Solvent1
- 1-Butanol is used as an ingredient in processed and artificial flavorings, and for the extraction of lipid-free protein from egg yolk, natural flavouring materials and vegetable oils, the manufacture of hop extract for beermaking, and as a solvent in removing pigments from moist curd leaf protein concentrate. (wikipedia.org)
C4H9OH1
- Inelastic Neutron Scattering spectrum of 1-Butanol crystalline, C4H9OH, measured on the TOSCA instrument. (stfc.ac.uk)
Alcohol1
- Butanol, a four-carbon alcohol, is considered in the last years as an interesting alternative fuel, both for Diesel and for Gasoline application. (bfh.ch)
Biofuel1
- Butanol is considered as a potential biofuel (butanol fuel). (wikipedia.org)
Metabolite2
- DMB and its predicted metabolite, DMBut, were detected in the liver and serum, suggesting systemic effects, and both significantly reduced arthritis severity and circulating IL-1β and IL-6, but not circulating anti-CII antibodies, compared to untreated CIA mice. (acrabstracts.org)
- RESULTS: Among individuals who did not currently use tobacco (148 cases/163 controls), two acrolein metabolites, two acrylonitrile metabolites, one propylene oxide metabolite and one 1,3-butadiene metabolite were significantly associated with incident ESCC (adjusted ORs between 1.8 and 4.3). (cdc.gov)
Chloroform1
- The aqueous and 50% ethanolic extracts of A. catechu stem bark were prepared and 50% ethanolic extract was further fractioned by successively partitioning with petroleum ether, chloroform and n-butanol. (nih.gov)
Assay3
- Differences in Detection of DNA Adducts in the 32P-Postlabelling Assay After Either 1-Butanol Extraction or Nuclease Pl Treatment. (epa.gov)
- In the above assay, n-butanol fraction exhibited anti-HIV-1 activity with an IC50 of 1.7 ± 0.12 μg/ml. (nih.gov)
- The n-butanol fraction interfered with the Tat-mediated Long Terminal Repeat transactivation in TZM-bl cells, mRNA quantitation (qRT-PCR) and electrophoretic mobility shift assay (EMSA). (nih.gov)
Microorganisms1
- Research in the past few decades showed results of other microorganisms that can produce butanol through fermentation. (wikipedia.org)
Gasoline1
- 1-Butanol has been proposed as a substitute for diesel fuel and gasoline. (wikipedia.org)
Ethyl1
- and those of SN wine were 1-butanol, 1-hexanol, 2-butenoic acid ethyl ester, and 3-methyl-1-butanol. (unboundmedicine.com)
Methylnitrosamino3
- NNAL is a product formed after 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) enters the body. (cdc.gov)
- We collected preshift and postshift urine samples on 114 NP casino dealers to determine whether levels of ETS biomarkers (Cotinine (COT) and 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL)) in their urine would increase over an 8-hour work shift. (cdc.gov)
- METHODS: We measured 2 metabolites, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and its glucuronides (NNAl-Gluc) in the urine of males who were either current CS or WPS, and their wives exposed to either cigarette or waterpipe smoke in a sample of 46 subjects from rural Egypt. (who.int)
Amino1
- E 1 SO 4 transport activity surpassed GSH-stimulated levels in the presence of tripeptides in which Cys was substituted with the hydrophobic amino acids Leu, Phe, and homo-Phe. (aspetjournals.org)
Emissions2
- Butanol can also be added to diesel fuel to reduce soot emissions. (wikipedia.org)
- In the research project DiBut (with support of BfE and BAFU) addition of Butanol to Diesel fuel is investigated from the points of view of engine combustion, of influences on exhaust aftertreatment systems and of non-legislated emissions of cars in transient operation. (bfh.ch)
Yield1
- According to the present invention, 1-(2-t-butylcyclohexyloxy)-2-butanol having a woody or amber-like fragrance as a perfume material and excellent fragrance notes can be obtained in a high purity because of a small remaining amount of a reaction intermediate and in a high yield. (epo.org)
Secretion3
- Stimulation of BMDMs with LPS in the presence of DMB or DMBut significantly reduced secretion of IL-1β and IL-6. (acrabstracts.org)
- The effect of n-butanol fraction on the induction of pro-inflammatory cytokines secretion in Vk2/E6E7 cells and transepithelial resistance in Caco-2 and HEC-1A cells was investigated. (nih.gov)
- The n-butanol fraction did not cause an enhanced secretion of pro-inflammatory cytokines in Vk2/E6E7 cells. (nih.gov)
Methyl6
- Field Evaluation of Synthetic Lure (3-methyl-1-butanol) When Compared to Non Odor-Baited Control in Capturing Anopheles Mosquitoes in Varying Land-Use Sites in Madagascar. (pivotworks.org)
- and recommended 3-methyl-1-butanol as a compound to increase An. (pivotworks.org)
- In this study, we evaluate the role of the synthetic compound, 3-methyl-1-butanol in combination with field produced CO(2) in attracting Anopheles mosquitoes in varying land-use sites in Madagascar. (pivotworks.org)
- To test the role of 3-methyl-1-butanol in luring Anopheles mosquitoes, two traps were set in each land-use site (village, agricultural sites, and forested habitats affiliated with each village). (pivotworks.org)
- While 3-methyl-1-butanol baited traps did capture An. (pivotworks.org)
- Our findings suggest that trapping mosquitoes near livestock in malaria endemic regions, such as Madagascar, may be more successful at capturing Anopheles mosquitoes than the proposed 3-1-methyl-butanol lure. (pivotworks.org)
Corn1
- 1-Butanol is also formed during deep frying of corn oil, cottonseed oil, trilinolein, and triolein. (wikipedia.org)
Diesel3
Propylene1
- A second method for producing butanol involves the Reppe reaction of propylene with CO and water: CH3CH=CH2 + H2O + 2 CO → CH3CH2CH2CH2OH + CO2 In former times, butanol was prepared from crotonaldehyde, which can be obtained from acetaldehyde. (wikipedia.org)
Fermentation3
- Butanol can also be produced by fermentation of biomass by bacteria. (wikipedia.org)
- Prior to the 1950s, Clostridium acetobutylicum was used in industrial fermentation to produce butanol. (wikipedia.org)
- Butan-1-ol occurs naturally as a result of carbohydrate fermentation in a number of alcoholic beverages, including beer, grape brandies, wine, and whisky. (wikipedia.org)
Biomarker1
- NNAL saliva and urine biomarker for SHSe (table 1). (cdc.gov)
Https1
- Butanol can be produced via furan hydrogenation over Pd or Pt catalyst at high temperature and high pressure.https://pubs.rsc.org/en/content/articlehtml/2014/gc/c3gc41183d Constituting 85% of its use, 1-butanol is mainly used in the production of varnishes. (wikipedia.org)
Acid1
- 3-Hydroxy Benzoic Acid (98-99%), 4 Chloro 1 Butanol. (needsinfo.com)
Protein4
- The human multidrug resistance protein 1 (MRP1) is a primary active transporter of reduced (GSH) and oxidized glutathione, as well as GSH-, glucuronate-, and sulfate-conjugated organic anions. (aspetjournals.org)
- To evaluate the structural features of GSH required for interaction with the protein, we investigated the ability of a series of GSH analogs to enhance GSH stimulatable transport of [ 3 H]estrone 3-sulfate (E 1 SO 4 ). (aspetjournals.org)
- The active n-butanol fraction was evaluated for its inhibition against HIV-1 reverse transcriptase, integrase, protease, pro-viral genome integration and viral Tat protein mediated transactivation. (nih.gov)
- The results presented here show a potential anti-HIV-1 activity of A. catechu mediated by the inhibition of the functions of the viral protein and Tat. (nih.gov)
Higher1
- Clostridium produces much higher yields of butanol. (wikipedia.org)
Table1
- Methods for the determination of benzidine in biological samples are summarized in Table 7-1. (cdc.gov)
Method1
- and [2] a perfume composition containing 1-(2-t-butylcyclohexyloxy)-2-butanol obtained by the foregoing method. (epo.org)
Production1
- Thus, we investigated modulation of TMAO production as a therapeutic target in CIA using the choline TMA lyase inhibitors 3,3-diemthyl-1-butanol (DMB) and fluoromethylcholine (FMC). (acrabstracts.org)
Analysis3
- γ-Glu-Leu-Gly was 1.6-fold more effective than GSH in stimulating E 1 SO 4 uptake, and kinetic analysis indicated this was due to an increased V max . (aspetjournals.org)
- [ 1 ] Given that an element of intoxication is involved in many motor vehicle collisions, the vital role toxicologic analysis plays in modern death investigation becomes clear. (medscape.com)
- METHODS: We performed multiple regression analysis of longitudinal measures of urinary biomarkers of alkaloids, tobacco-specific nitrosamines, polycyclic aromatic hydrocarbons, volatile organic compounds (VOC), and metals to examine the sample-to-sample consistency in Waves 1 and 2 of the Population Assessment of Tobacco and Health Study including demographic characteristics and use behavior variables of persons who smoked exclusively. (cdc.gov)
Inhibition1
- The n-butanol fraction showed a dose-dependent inhibition against HIV-1NL4.3 infection of the peripheral blood lymphocytes and against HIV-1BaL(R-5-tropic) as well as two different primary viral isolates of HIV-1 infection of TZM-bl cells. (nih.gov)
Found1
- [ 1 , 2 ] This figure only accounts for deaths caused by intoxication and does not include cases in which an intoxicant was found that did not cause death. (medscape.com)
Term1
- The unmodified term butanol usually refers to the straight chain isomer. (wikipedia.org)