beta-Aminoethyl Isothiourea
Cysteamine
A mercaptoethylamine compound that is endogenously derived from the COENZYME A degradative pathway. The fact that cysteamine is readily transported into LYSOSOMES where it reacts with CYSTINE to form cysteine-cysteamine disulfide and CYSTEINE has led to its use in CYSTINE DEPLETING AGENTS for the treatment of CYSTINOSIS.
Dithiothreitol
Glutathione
Hydrogen-Ion Concentration
Oxidation-Reduction
A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471).
Dithionitrobenzoic Acid
Disulfides
Action of partially thiolated polynucleotides on the DNA polymerase alpha from regenerating rat liver. (1/4324)
The effects of partially thiolated polynucleotides on the DNA polymerase alpha from regenerating rat liver were investigated. The enzyme was isolated from the nuclear fraction essentially according to the method of Baril et al.; it was characterized as the alpha polymerase on the basis of its response to synthetic templates and its inhibition with N-ethylmaleimide. Although polycytidylic acid had no effect on the DNA polymerase alpha either as a template or as an inhibitor, partially thiolated polycytidylic acid (MPC) was found to be a potent inhibitor, its activity being directly related to its extent of thiolation (percentage of 5-mercaptocytidylate units in the polymer). In comparison, the DNA polymerase beta which was purified from normal rat liver nuclear fraction, was much less sensitive to inhibition by MPC. Analysis of the inhibition of the alpha polymerase by the method of Lineweaver and Burk showed that the inhibitory action of MPC was competitively reversible with the DNA template, but the binding of the 7.2%-thiolated MPC to the enzyme was much stronger than that of the template (Ki/Km less than 0.03). Polyuridylic acid as such showed some inhibitory activity which increased on partial thiolation, but the 8.4%-thiolated polyuridylic acid was less active than the 7.2% MPC. When MPC was annealed with polyinosinic acid, it lost 80% of its inhibitory activity in the double-stranded configuration. However, 1 to 2%-thiolated DNA isolates were significantly more potent inhibitors than were comparable (1.2%-thiolated) MPC and showed competitive reversibility with the unmodified (but "activated") DNA template. These results indicate that the inhibitory activities of partially thiolated polynucleotides depend not only on the percentage of 5-mercapto groups but also on the configuration, base composition, and other specific structural properties. (+info)Sulfhydryl compounds in melanocytes of yellow (Ay/a), nonagouti (a/a), and agouti (A/A) mice. (2/4324)
CLEFFMANN (1953, 1963a,b) has reported that yellow but not black melanocytes of agouti (A/A) rabbits contained reducing sulfhydryl compounds. We have attempted to repeat CLEFFMANN's observations in mouse melanocytes of the lethal yellow (Ay/a), nonagouti (a/a) and agouti (A/A) genotypes. Our results contradict those of CLEFFMANN and reveal that yellow and black melanocytes, regardless of genotype, possess equivalent amounts of histochemically detectable sulfhydryl compounds. These results do not support the hypothesis that agouti-locus genes act by controlling the sulfhydryl metabolism of pigment cells. (+info)Kinetics of oxidation of aliphatic and aromatic thiols by myeloperoxidase compounds I and II. (3/4324)
Myeloperoxidase (MPO) is the most abundant protein in neutrophils and plays a central role in microbial killing and inflammatory tissue damage. Because most of the non-steroidal anti-inflammatory drugs and other drugs contain a thiol group, it is necessary to understand how these substrates are oxidized by MPO. We have performed transient kinetic measurements to study the oxidation of 14 aliphatic and aromatic mono- and dithiols by the MPO intermediates, Compound I (k3) and Compound II (k4), using sequential mixing stopped-flow techniques. The one-electron reduction of Compound I by aromatic thiols (e.g. methimidazole, 2-mercaptopurine and 6-mercaptopurine) varied by less than a factor of seven (between 1.39 +/- 0.12 x 10(5) M(-1) s(-1) and 9.16 +/- 1.63 x 10(5) M(-1) s(-1)), whereas reduction by aliphatic thiols was demonstrated to depend on their overall net charge and hydrophobic character and not on the percentage of thiol deprotonation or redox potential. Cysteamine, cysteine methyl ester, cysteine ethyl ester and alpha-lipoic acid showed k3 values comparable to aromatic thiols, whereas a free carboxy group (e.g. cysteine, N-acetylcysteine, glutathione) diminished k3 dramatically. The one-electron reduction of Compound II was far more constrained by the nature of the substrate. Reduction by methimidazole, 2-mercaptopurine and 6-mercaptopurine showed second-order rate constants (k4) of 1.33 +/- 0.08 x 10(5) M(-1) s(-1), 5.25 +/- 0.07 x 10(5) M(-1) s(-1) and 3.03 +/- 0.07 x 10(3) M(-1) s(-1). Even at high concentrations cysteine, penicillamine and glutathione could not reduce Compound II, whereas cysteamine (4.27 +/- 0.05 x 10(3) M(-1) s(-1)), cysteine methyl ester (8.14 +/- 0.08 x 10(3) M(-1) s(-1)), cysteine ethyl ester (3.76 +/- 0.17 x 10(3) M(-1) s(-1)) and alpha-lipoic acid (4.78 +/- 0.07 x 10(4) M(-1) s(-1)) were demonstrated to reduce Compound II and thus could be expected to be oxidized by MPO without co-substrates. (+info)Thiol-dependent degradation of protoporphyrin IX by plant peroxidases. (4/4324)
Protoporphyrin IX (PP) is the last porphyrin intermediate in common between heme and chlorophyll biosynthesis. This pigment normally does not accumulate in plants because its highly photodynamic nature makes it toxic. While the steps leading to heme and chlorophylls are well characterized, relatively little is known of the metabolic fate of excess PP in plants. We have discovered that plant peroxidases can rapidly degrade this pigment in the presence of thiol-containing substrates such as glutathione and cysteine. This thiol-dependent degradation of PP by horseradish peroxidase consumes oxygen and is inhibited by ascorbic acid. (+info)Selenium redox biochemistry of zinc-sulfur coordination sites in proteins and enzymes. (5/4324)
Selenium has been increasingly recognized as an essential element in biology and medicine. Its biochemistry resembles that of sulfur, yet differs from it by virtue of both redox potentials and stabilities of its oxidation states. Selenium can substitute for the more ubiquitous sulfur of cysteine and as such plays an important role in more than a dozen selenoproteins. We have chosen to examine zinc-sulfur centers as possible targets of selenium redox biochemistry. Selenium compounds release zinc from zinc/thiolate-coordination environments, thereby affecting the cellular thiol redox state and the distribution of zinc and likely of other metal ions. Aromatic selenium compounds are excellent spectroscopic probes of the otherwise relatively unstable functional selenium groups. Zinc-coordinated thiolates, e.g., metallothionein (MT), and uncoordinated thiolates, e.g., glutathione, react with benzeneseleninic acid (oxidation state +2), benzeneselenenyl chloride (oxidation state 0) and selenocystamine (oxidation state -1). Benzeneseleninic acid and benzeneselenenyl chloride react very rapidly with MT and titrate substoichiometrically and with a 1:1 stoichiometry, respectively. Selenium compounds also catalyze the release of zinc from MT in peroxidation and thiol/disulfide-interchange reactions. The selenoenzyme glutathione peroxidase catalytically oxidizes MT and releases zinc in the presence of t-butyl hydroperoxide, suggesting that this type of redox chemistry may be employed in biology for the control of metal metabolism. Moreover, selenium compounds are likely targets for zinc/thiolate coordination centers in vivo, because the reactions are only partially suppressed by excess glutathione. This specificity and the potential to undergo catalytic reactions at low concentrations suggests that zinc release is a significant aspect of the therapeutic antioxidant actions of selenium compounds in antiinflammatory and anticarcinogenic agents. (+info)Alloxan in vivo does not only exert deleterious effects on pancreatic B cells. (6/4324)
The aim of the experiment was to investigate the mechanism of harmful alloxan action in vivo. 75 mg/kg b.w. of this diabetogenic agent were administered to fasting rats. Two minutes later the animals were decapitated. It was observed that alloxan caused a distinct rise in blood insulin and glucose levels with a concomitant drop of free fatty acids. The amount of sulfhydryl groups in the liver of alloxan-treated rats was decreased and glutathione peroxidase activity was substantially higher. These results indicate that some changes observed in alloxan-induced diabetes can not only be the consequence of B cells damage by alloxan but may also be the result of its direct influence on other tissues. It was also observed that glucose given 20 min before alloxan injection only partially protected against the deleterious effects of alloxan. (+info)Formation of 4-hydroxy-2-nonenal-modified proteins in ischemic rat heart. (7/4324)
4-Hydroxy-2-nonenal (HNE) is a major lipid peroxidation product formed during oxidative stress. Because of its reactivity with nucleophilic compounds, particularly metabolites and proteins containing thiol groups, HNE is cytotoxic. The aim of this study was to assess the extent and time course for the formation of HNE-modified proteins during ischemia and ischemia plus reperfusion in isolated rat hearts. With an antibody to HNE-Cys/His/Lys and densitometry of Western blots, we quantified the amount of HNE-protein adduct in the heart. By taking biopsies from single hearts (n = 5) at various times (0, 5, 10, 15, 20, 35, and 40 min) after onset of zero-flow global ischemia, we showed a progressive, time-dependent increase (which peaked after 30 min) in HNE-mediated modification of a discrete number of proteins. In studies with individual hearts (n = 4/group), control aerobic perfusion (70 min) resulted in a very low level (296 arbitrary units) of HNE-protein adduct formation; by contrast, after 30-min ischemia HNE-adduct content increased by >50-fold (15,356 units, P < 0.05). In other studies (n = 4/group), administration of N-(2-mercaptopropionyl)glycine (MPG, 1 mM) to the heart for 5 min immediately before 30-min ischemia reduced HNE-protein adduct formation during ischemia by approximately 75%. In studies (n = 4/group) that included reperfusion of hearts after 5, 10, 15, or 30 min of ischemia, there was no further increase in the extent of HNE-protein adduct formation over that seen with ischemia alone. Similarly, in experiments with MPG, reperfusion did not significantly influence the tissue content of HNE-protein adduct. Western immunoblot results were confirmed in studies using in situ immunofluorescent localization of HNE-protein in cryosections. In conclusion, ischemia causes a major increase in HNE-protein adduct that would be expected to reflect a toxic sequence of events that might act to compromise tissue survival during ischemia and recovery on reperfusion. (+info)Differential protein S-thiolation of glyceraldehyde-3-phosphate dehydrogenase isoenzymes influences sensitivity to oxidative stress. (8/4324)
The irreversible oxidation of cysteine residues can be prevented by protein S-thiolation, in which protein -SH groups form mixed disulfides with low-molecular-weight thiols such as glutathione. We report here the identification of glyceraldehyde-3-phosphate dehydrogenase as the major target of protein S-thiolation following treatment with hydrogen peroxide in the yeast Saccharomyces cerevisiae. Our studies reveal that this process is tightly regulated, since, surprisingly, despite a high degree of sequence homology (98% similarity and 96% identity), the Tdh3 but not the Tdh2 isoenzyme was S-thiolated. The glyceraldehyde-3-phosphate dehydrogenase enzyme activity of both the Tdh2 and Tdh3 isoenzymes was decreased following exposure to H2O2, but only Tdh3 activity was restored within a 2-h recovery period. This indicates that the inhibition of the S-thiolated Tdh3 polypeptide was readily reversible. Moreover, mutants lacking TDH3 were sensitive to a challenge with a lethal dose of H2O2, indicating that the S-thiolated Tdh3 polypeptide is required for survival during conditions of oxidative stress. In contrast, a requirement for the nonthiolated Tdh2 polypeptide was found during exposure to continuous low levels of oxidants, conditions where the Tdh3 polypeptide would be S-thiolated and hence inactivated. We propose a model in which both enzymes are required during conditions of oxidative stress but play complementary roles depending on their ability to undergo S-thiolation. (+info)
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Isosorbide mononitrate
Sulfhydryl-containing compounds. The metabolism of organic nitrates to nitric oxide is dependent on the presence of sulfhydryl ... Concomitant administration of other exogenous sources of sulfhydryl groups such as methionine and captopril may produce a ...
Neutron capture therapy of cancer
Tumor-binding sulfhydryl boron compounds". Journal of Medicinal Chemistry. 10 (4): 714-7. doi:10.1021/jm00316a042. PMID 6037065 ... Second, gadolinium compounds, such as Gd-DTPA (gadopentetate dimeglumine Magnevist®), have been used routinely as contrast ... Ono K (August 2016). "An analysis of the structure of the compound biological effectiveness factor". Journal of Radiation ... 1 and a compound biological effectiveness (CBE) factor for BPA in skin of 2.5. A relative biological effectiveness (RBE) or CBE ...
Thiol S-methyltransferase
Bremer J; Greenberg DM (1961). "Enzymic methylation of foreign sulfhydryl compounds". Biochim. Biophys. Acta. 46 (2): 217-224. ...
Tiopronin
Jaffe IA (March 1986). "Adverse effects profile of sulfhydryl compounds in man". The American Journal of Medicine. 80 (3): 471- ... which are broadly similar to those of D-penicillamine and other compounds containing active sulfhydryl groups. Its ... In 2016 Imprimis Pharmaceuticals introduced a lower cost version marketed as a compounded drug. It may also be used for ... Portal: Medicine (Chemical articles with multiple compound IDs, Multiple chemicals in an infobox that need indexing, Chemical ...
Thiosalicylic acid
... is an organosulfur compound containing carboxyl and sulfhydryl functional groups. Its molecular formula is ... Chemical articles with multiple compound IDs, Multiple chemicals in an infobox that need indexing, Articles without InChI ...
Sulfate transporter
"In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias". Pediatric ...
Johanna Budwig
Budwig believed sulphydryl compounds were important to cellular metabolism and cellular respiration. Budwig researched the ... theory that a low oxygen environment would develop in the absence of sulphydryl groups and/or fatty acid partners that would ... a researcher at the German Federal Health Office she noted many cancer drugs being evaluated in the 1950s contained sulphydryl ...
Cell cycle
The pattern of resistance and sensitivity correlates with the level of sulfhydryl compounds in the cell. Sulfhydryls are ...
MPGES-2
The activity of PTGES2 is thought to be increased in the presence of sulfhydryl compounds, in particular dithiothreitol. The ...
Cinitapride
... prostaglandins and sulfhydryl compounds". Pharmacology. 54 (4): 193-202. doi:10.1159/000139487. PMID 9211565. Alarcón de la ...
Meralluride
Kunin, Calvin A. (September 10, 1976). "Effect of organic mercurials and sulfhydryl compounds on the urease activity of Proteus ... Studies in the late 1970s showed the compound had antimicrobial effect against Proteus bacteria responsible for urinary tract ... Studies from Japan showed the compound caused ventricular fibrillation in a high percentage of animals when compared to ...
2-Iminothiolane
... reacts with primary amines efficiently at pH 7 to 9, creating amidine compounds with a sulfhydryl group. Thus ... It is a thiolating reagent that reacts with primary amine groups, such as those of amino acids, to form sulfhydryl groups. ... Chemical articles with multiple compound IDs, Multiple chemicals in an infobox that need indexing, Chemical articles with ... 2-Iminothiolane is a cyclic thioimidate compound also known as Traut's reagent. ...
Iproniazid
... did not deplete sulfhydryl-group containing compounds. The isopropyl radical formed as a result of the metabolism of iproniazid ... In contrast, the compounds cobalt chloride, piperonyl butoxide and alpha-naphthylisothiocyanate inhibit microsomal enzymes ... Alkylating agents have the capability to bind to chemical groups such as amino, phosphate hydroxyl, imidazole and sulfhydryl ... Rat models and other animal models have shown that cytochrome P450 enzymes convert isopropyl hydrazine to alkylating compounds ...
Mesna
... is an organosulfur compound. It works by altering the breakdown products of cyclophosphamide and ifosfamide found in the ... Mesna assists to detoxify these metabolites by reaction of its sulfhydryl group with α,β-unsaturated carbonyl containing ... Mesna reduces the toxicity of urotoxic compounds that may form after chemotherapy administration. Mesna is a water-soluble ... This conjugation reaction inactivates the urotoxic compounds to harmless metabolites. The metabolites are then excreted in the ...
Louis Rapkine
He pursued biochemical research on the metabolic and developmental roles of sulfhydryl compounds, working initially with ... Rapkine, L. (1938). "Sulfhydryl groups and enzymic oxido-reduction". Biochemical Journal. 32 (10): 1729-1739. doi:10.1042/ ...
Margaret Kelly (pharmacologist)
Her studies with laboratory animals showed that sulfhydryl compounds may protect against toxicity from x-irradiation and ... alkylating agents by a distribution pattern which causes more of a protective compound to accumulate in the sensitive tissues ...
Methacrylonitrile
For example, via epoxide hydratase (EH) or via interactions with a sulfhydryl compound, which leads to the formation of a ... Methacrylonitrile (or 2-Methylprop-2-enenitrile), MeAN in short, is a chemical compound that is an unsaturated aliphatic ... "unsaturated compounds formed by a burning cigarette. Anal. Proc. 21, 135 Farooqui, M. Y. H. and M. M. Mumtaz (1991). " ...
Acetylcholine
Organic mercurial compounds, such as methylmercury, have a high affinity for sulfhydryl groups, which causes dysfunction of the ... In 1926, Loewi and E. Navratil deduced that the compound is probably acetylcholine, as vagusstoff and synthetic acetylcholine ... Acetylcholine is synthesized in certain neurons by the enzyme choline acetyltransferase from the compounds choline and acetyl- ... muscarine is a compound found in the mushroom Amanita muscaria; nicotine is found in tobacco. Nicotinic acetylcholine receptors ...
Moexipril
A divergence of structure-activity relationships for non-sulfhydryl and sulfhydryl types". Journal of Medicinal Chemistry. 29 ( ... and is metabolized in the liver to form the pharmacologically active compound moexiprilat. Formation of moexiprilat is caused ... "Synthesis of novel angiotensin converting enzyme inhibitor quinapril and related compounds. ...
Branched-chain amino acid aminotransferase
... sulfhydryl, or Cu2+ or Co2+ reagents/compounds Enzyme catalyzes reaction best with branched chain amino acids (in order from ... In Cucumis melo (melon), BCATs have been found to play a role in developing aroma volatile compounds that give melons their ... As fermentation proceeds, these α-ketoacids degrade into a class of compounds known as methyl-branched volatiles that include ... The branched-chain amino acid aminotransferases help to produce compounds like isovaleric acid, isobutyric acid, 2- and 3- ...
Thiophenol
... s also describes a class of compounds formally derived from thiophenol itself. All have a sulfhydryl group (-SH) ... The prefix thio- implies a sulfur-containing compound and when used before a root word name for a compound which would normally ... Thiophenol is an organosulfur compound with the formula C6H5SH, sometimes abbreviated as PhSH. This foul-smelling colorless ... There are several methods of synthesis for thiophenol and related compounds, although thiophenol itself is usually purchased ...
Arsenic biochemistry
However, the monomethylated compound was shown to be more reactive and more toxic than the inorganic arsenic compounds to human ... Enzymes and receptors that contain thiol or sulfhydryl functional groups are actively targeted by arsenite (III) metabolites. ... This compound is then converted to a mono-methylated arsenic (III) compound using Glutathione S-Transferase Omega-1 (GSTO1). ... Representative organoarsenic compounds found in nature. Arsenobetaine, one of the most common arsenic compound in nature. Also ...
Miguel Ondetti
He settled on using a sulfhydryl group which binds strongly to zinc. Ondetti had discovered Captopril, an ACE inhibitor with ... U.S. Patent 3,740,385 "N-Terminal Derivatives of Secretin", filed May 1970, issued June 1973 U.S. Patent 4,199,512 "Compounds ... "Compounds for alleviating angiotensin related hypertension", filed February 1978, issued July 1982 U.S. Patent 4,722,810 " ... His group tried thousands of compounds from the Squibb library, but none yielded satisfying results. After reading literature ...
Glutathione S-transferase
... of GSH-via a sulfhydryl group-to electrophilic centers on a wide variety of substrates in order to make the compounds more ... However, some endogenous compounds, e.g., bilirubin, can inhibit the activity of GSTs. In mammals, GST isoforms have cell ... The compounds targeted in this manner by GSTs encompass a diverse range of environmental or otherwise exogenous toxins, ... Because the GST protein has a strong binding affinity for GSH, beads coated with the compound can be added to the protein ...
Bioprospecting
The mechanism of action of an isolated compound can also be misidentified if a single assay is used because some compounds ... For example, the sulfhydryl-scavenging assay used to detect histone acetyltransferase inhibition can give a false positive ... to include reference compounds (ie. pure chemical compounds for which accurate bioactivity and toxicity data are available), to ... Using just a single assay, especially a single in vitro assay, gives a very incomplete picture of an extract or compound's ...
Propanethiol
... is an organic compound with the molecular formula C3H8S. It belongs to the group of thiols. It is a colorless ... except that sulfur-containing sulfhydryl group (-SH) replaces the oxygen-containing hydroxyl group in the molecule. ... Propanethiol is chemically classified among the thiols, which are organic compounds with molecular formulas and structural ... 21, 1962, Preparation of Organic Sulfur Compounds (Webarchive template wayback links, Articles without InChI source, Articles ...
Thiol
The term sulfhydryl- or mercapto- is used as a prefix, e.g. mercaptopurine. Many thiols have strong odors resembling that of ... These compounds are detectable by the human nose at concentrations of only 10 parts per billion. Human sweat contains (R)/(S)-3 ... Sulfhydryl groups in the active site of an enzyme can form noncovalent bonds with the enzyme's substrate as well, contributing ... The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group. Thiols are ...
1-Butanethiol
... is a very noxious and caustic chemical compound, and at sufficiently high concentrations, it produces serious ... except that the sulfur-containing sulfhydryl group (-SH) replaces the oxygen-containing hydroxyl group (-OH) in the molecule. 1 ... which are organic compounds with molecular formulas and structural formulas similar to alcohols, ...
Helenalin
The double bond in the carbonyl group can undergo a Michael addition with a thiol group, also called a sulfhydryl group. ... For this reason the compound or its derivatives may have potential medical applications. Helenalin belongs to the group of ... Depending on the dose of helenalin, thiol-bearing compounds such as glutathione may provide some protection to cells from ... Most of these derivatives occur naturally, such as the compound dihydrohelenalin, but there are also some semi-synthetic ...
Quantitative proteomics
... reactive iodacetyl function group which labels sulfhydryl-(-SH) groups (iodoTMT) and (3) reactive alkoxyamine functional group ... which provides covalent labeling of carbonyl-containing compounds (aminoxyTMT). A key benefit of isobaric labeling over other ...
Molybdopterin
InChI Key HPEUEJRPDGMIMY-UHFFFAOYSA-N Structure, synthesis, empirical formula for the di-sulfhydryl. Archived 2016-06-04 at the ... Webarchive template wayback links, CS1 maint: uses authors parameter, Chemical articles with multiple compound IDs, Multiple ... Lassner, Erik (1999). Tungsten: Properties, Chemistry, Technology of the Element, Alloys and Chemical Compounds. Springer. pp. ...
Enzyme inhibitor
The residues modified are those with side chains containing nucleophiles such as hydroxyl or sulfhydryl groups; these include ... A common treatment for erectile dysfunction is sildenafil (Viagra). This compound is a potent inhibitor of cGMP specific ... In many cases, allosteric, substrate competitive compounds result in conformational changes to the enzyme that change the ... Cohen JA, Oosterbaan RA, Berends F (1967). "[81] Organophosphorus compounds". Enzyme Structure. Methods in Enzymology. Vol. 11 ...
Hypochlorous acid
... some sulfhydryl function can be restored. One sulfhydryl-containing amino acid can scavenge up to four molecules of HClO. ... The resulting compound is a chlorohydrin. The polar chlorine disrupts lipid bilayers and could increase permeability. When ... could completely inactivate proteins containing sulfhydryl groups. This is because HClO oxidises sulfhydryl groups, leading to ... Its compounds will be called hypochlorites.) Unangst, P. C. "Hypochlorous Acid" in Encyclopedia of Reagents for Organic ...
Acute inhalation injury
Phosgene directly reacts with amine, sulfhydryl, and alcohol groups, adversely affecting cell macromolecules and metabolism. ... is also used as an industrial reagent and building block in synthesis of pharmaceuticals and other organic compounds. Because ...
Cyanase
Denaturation, renaturation, and role of sulfhydryls and oligomeric structure in catalytic activity". The Journal of Biological ... supplying energetic Nitrogen compounds to the organism. The activity of cyanase is heavily dependent on the present of ...
Dough conditioner
Di Carlo, F.J.; Schultz, A.S.; McManus, D.K. (1951). "The assimilation of nucleic acid derivatives and related compounds by ... Dehydroascorbic acid and potassium bromate are oxidants, acting on sulfhydryl groups and disulfide bonds in wheat dough, in ...
4-Amino-2-methyl-1-naphthol
Vitamin K function of the compound was first noted in 1940. Oral lethal dose for the HCl salt in rats is 0.7 g/kg. 4-Amino-2- ... Heisler CR, Yang, HY (1966). "Non-stoichiometric sulfhydryl loss with vitamin K5". Biochemical and Biophysical Research ... 1940). "Parenteral administration of a watersoluble compound with vitamin K activity: 4-amino-2-methyl-1-naphthol hydrochloride ... Chemical articles with multiple compound IDs, Chemicals using indexlabels, Chemical articles with multiple CAS registry numbers ...
Ellman's reagent
Thiols react with this compound, cleaving the disulfide bond to give 2-nitro-5-thiobenzoate (TNB−), which ionizes to the TNB2− ... Quantitation of sulfhydryls DTNB, Ellman's reagent (uses incorrect absorbance coefficient) (Articles without KEGG source, ECHA ... Riener CK, Kada G, Gruber HJ (2002). "Quick measurement of protein sulfhydryls with Ellman's reagent and with 4,4'- ... Riener, Christian K.; Kada, Gerald; Gruber, Hermann J. (2002-07-01). "Quick measurement of protein sulfhydryls with Ellman's ...
Hypothiocyanite
... is the anion [OSCN]− and the conjugate base of hypothiocyanous acid (HOSCN). It is an organic compound part of ... Thomas EL, Aune TM (May 1978). "Lactoperoxidase, peroxide, thiocyanate antimicrobial system: correlation of sulfhydryl ... Initially, this particular lactoperoxidase-catalyzed compound was originally discovered while viewing the specific environment ... against bacteria is reported to be caused by sulfhydryl (SH) oxidation. The oxidation of -SH groups in the bacterial ...
Captopril
... was developed from this peptide after it was found via QSAR-based modification that the terminal sulfhydryl moiety of ... Proline derivatives and related compounds, methods for their manufacturing and their use as a medicinal product]", published ... is consistent with the observation that animal screening models indicate putative antidepressant activity for this compound, ...
List of MeSH codes (D27)
... chromogenic compounds MeSH D27.720.233.348 - fluorescent dyes MeSH D27.720.233.674 - food coloring agents MeSH D27.720.269.189 ... sulfhydryl reagents MeSH D27.720.470.410.750 - thiobarbituric acid reactive substances MeSH D27.720.470.420 - ion exchange ... chromogenic compounds MeSH D27.720.470.410.210 - cross-linking reagents MeSH D27.720.470.410.360 - intercalating agents MeSH ...
Potassium arsenite
Additionally, arsenite containing compounds have also been labeled carcinogens. The carcinogenicity of potassium arsenite ... The toxicity of potassium arsenite arises from arsenic's high affinity for sulfhydryl groups. The formation of these arsenite- ... Potassium arsenite (KAsO2) is an inorganic compound that exists in two forms, potassium meta-arsenite (KAsO2) and potassium ... Thus, exposure to potassium arsenite and other arsenite containing compounds results in the production of damaging oxygen free ...
Phthalaldehyde
The compound was first described in 1887 when it was prepared from α,α,α',α'-tetrachloro-ortho-xylene. A more modern synthesis ... OPA is used in a very sensitive fluorescent reagent for assaying amines or sulfhydryls in solution, notably contained in ... This pale yellow solid is a building block in the synthesis of heterocyclic compounds and a reagent in the analysis of amino ... Phthalaldehyde (sometimes also o-phthalaldehyde or ortho-phthalaldehyde, OPA) is the chemical compound with the formula C6H4( ...
Nitrogen dioxide poisoning
... to the sulfhydryl form glutathione (GSH), which is a critical molecule in resisting oxidative stress and maintaining the ... on non-polar compounds that contain an electrophilic carbon and nitrogen. These inhibition mechanisms generates free radicals ... Inorganic nitrogen compounds, Nitrogen oxides, Hazardous air pollutants, Smog, Free radicals, Food additives, Toxic effects of ...
Acetylcysteine
The thiol (sulfhydryl) group confers antioxidant effects and is able to reduce free radicals. N-acetyl-L-cysteine is soluble in ... "L-Cysteine, N-acetyl- - Compound Summary". PubChem. National Center for Biotechnology Information. 25 March 2005. ... US3091569A, Leonard, Sheffner Aaron, "Mucolytic-nu-acylated sulfhydryl compositions and process for treating animal mucus", ... issued 28 May 1963 US patent 3091569, Aaron Leonard Sheffner, "Mucolytic-N-acylated sulfhydryl compositions and process for ...
Cyclophosphamide
A small proportion of aldophosphamide freely diffuses into cells, where it is decomposed into two compounds, phosphoramide ... a sulfhydryl donor which binds and detoxifies acrolein. Intermittent dosing of cyclophosphamide decreases cumulative drug dose ... Chloroethyl compounds, World Health Organization essential medicines, Wikipedia medicine articles ready to translate). ... Brock and his team synthesised and screened more than 1,000 candidate oxazaphosphorine compounds. They converted the base ...
Urease
The breakdown of this intermediate is then helped by a sulfhydryl group of a cysteine located near the active site. A hydrogen ... and related compounds". Canadian Journal of Biochemistry. 58 (12): 1335-1344. doi:10.1139/o80-181. PMID 6788353. Zimmer M (Apr ...
Chemotherapy
Derivatives of these compounds include epirubicin and idarubicin. Other clinically used drugs in the anthracycline group are ... They impair cell function by forming covalent bonds with the amino, carboxyl, sulfhydryl, and phosphate groups in biologically ... The first modern chemotherapeutic agent was arsphenamine, an arsenic compound discovered in 1907 and used to treat syphilis. ... Liu YQ, Yang L, Tian X (2007). "Podophyllotoxin: current perspectives". Current Bioactive Compounds. 3 (1): 37-66. doi:10.1016/ ...
Perchloromethyl mercaptan
The compound slowly hydrolyzes: CSCl4 + 2 H2O → CO2 + 4 HCl + 1⁄8 S8 The compound is corrosive to most metals. It reacts with ... sulfhydryl, amino and carboxyl groups. This results in an inactivation of key enzymes. A second general pathway reaction is the ... Organosulfur compounds, Trichloromethyl compounds, Pulmonary agents, Foul-smelling chemicals). ... Perchloromethyl mercaptan is the organosulfur compound with the formula CCl3SCl. It is mainly used as an intermediate for the ...
Urine test strip
However, as these compounds are derived from the acetoacetic acid their existence can be assumed and a separate test is not ... Those medicines that contain sulfhydryl groups, such as mercaptoethane sulphonate Na (Mesna) and captopril and L-DOPA can give ... The three ketone compounds appear in different proportions in the urine, although these proportions are relatively constant in ... Bilirubin is a highly pigmented compound that is a by-product of haemoglobin degradation. The haemoglobin that is released ...
Cyanogen bromide
... and synthesize other compounds. The compound is classified as a pseudohalogen. The carbon atom in cyanogen bromide is bonded to ... However, if the adjacent amino acid to methionine has a hydroxyl or sulfhydryl group, this group can react with the imine to ... Bromine compounds, Cyano compounds, Nonmetal halides, Blood agents, Lachrymatory agents, Pseudohalogens). ... Cyanogen bromide is the inorganic compound with the formula (CN)Br or BrCN. It is a colorless solid that is widely used to ...
巯基乙酸正丁酯-Sulfhydryl compounds-Qingdao Open Sesame Mining Co., Ltd.
Aerobic benzoyl-CoA catabolic pathway in Azoarcus evansii: studies on the non-oxygenolytic ring cleavage enzyme
Advanced Search Results - Public Health Image Library(PHIL)
Morphogenesis - 2nd Edition
NIOSHTIC-2 Search Results - Full View
Mercury compounds reacting with sulfhydryl groups inhibit a variety of enzymes. Chronic occupational exposure to mercury ... Occupational-exposure; Environmental-exposure; Lead-compounds; Cadmium-compounds; Mercury-compounds; Arsenic-compounds; Acute- ... Organic compounds of mercury are used in agriculture and have environmental and occupational impacts. ...
Clinical reliability of non-organoleptic oral malodour measurements
TPMT gene: MedlinePlus Genetics
... specific chemical reaction called S-methylation of a group of molecules known as aromatic and heterocyclic sulphydryl compounds ... Once inside the body, thiopurine drugs are converted to toxic compounds that kill immune system cells in the bone marrow. The ... Without enough of this enzyme, the body cannot "turn off" thiopurine drugs by metabolizing them into inactive compounds. The ... TPMT enzyme "turns off" thiopurine drugs by metabolizing them to inactive, nontoxic compounds. ...
Etymologia: Granulicatella - Volume 24, Number 9-September 2018 - Emerging Infectious Diseases journal - CDC
Molecular Biology (BMBB) - Research output
- [email protected]
Mesnex (mesna) dosing, indications, interactions, adverse effects, and more
Thiols as mechanistic probes for catalysis by the free radical enzyme galactose oxidase<...
Biblio | College of Agricultural Sciences
Renal Artery Stenosis Medication: Angiotensin-converting enzyme inhibitors, Angiotensin II receptor antagonists, HMG-CoA...
Parent compound of this class of medications. Sulfhydryl group associated with proteinuria and neutropenia when used at high ... Initial compound in class to gain approval. Useful for treatment of hypertension and heart failure in patients who are ... One of many compounds with comparable efficacy and adverse effect profiles. Inhibits HMG-CoA reductase, which, in turn, ... Many alternative compounds exist with few significant clinical differences. Nonpeptide angiotensin II receptor antagonist that ...
SciELO - Brazil - Mercury distribution in different tissues and trophic levels of fish from a tropical reservoir, Brazil...
Water-soluble Hg compounds attach to sulfhydryl bonds present in the amino acids cysteine and methionine. However, those two ... Experimental study of trophic contamination of Salmo gairdneri by two mercury compounds (HCl2 and CH3HgCl)-analysis at the ... Therefore, mainly liposoluble complexes (and, consequently, lipo-soluble Hg compounds) may be attached to the gonads. ...
The EPA National Library Catalog | EPA National Library Network | US EPA
A number of sulfhydryl-containing compounds reduce the toxic effects of antimony, suggesting that it may bind to cellular ... The most stable valence states of antimony are Sb(3+) and Sb(5+). Numerous inorganic and organic compounds of antimony are ... Most of the common antimony compounds are slightly to readily soluble in water. Antimony is thought to exert its toxic effects ... sulfhydryl groups. Antimony has been reported to increase the activity of heme oxygenase, to increase the action of thyroid ...
JCM | Free Full-Text | The Role of Antioxidants on Wound Healing: A Review of the Current Evidence
4) Conclusions: this review offers a map of the research on some of the antioxidant compounds with potential for use as wound ... Curcumin, NAC, quercetin and chitosan are the antioxidant compounds that shown some initial evidence of efficacy, but more ... Seven compounds with antioxidant activity were identified (Curcumin, N-acetyl cysteine, Chitosan, Gallic Acid, Edaravone, ... Crocin, Safranal and Quercetin) and 46 studies reporting the effects on the healing process of these antioxidants compounds ...
Saadi ABDUL VAHAB - Professor - Biotechnology
Erowid.org: Erowid Reference 3884 : The effects of some psychopharmcological agents on heat stress-induced changes in the...
Jorge Castro Ribeiro - Fingerprint
- Universidade NOVA de Lisboa
Munita, R.<...
Produção científica</span>
Dr Budwig's Cancer - The Problem and the Solution (Book Extract)
Everybody knows the sulfur-containing protein compound of the sulfhydryl group can be detected in all breathing tissues. ... these were medications for cancer therapy with the sulfhydryl group (sulfur-containing protein compounds). Everywhere I saw ... or 12 carbon compounds respectively. The unsaturated vital fatty acids really start in the chain with 18 carbon compounds. ... The carbon compounds are heavy matter, even in the fatty acid. If two people reach out to each other with two arms, then they ...
Oxidative stress and pro-apoptotic conditions in a rodent model of Wilson's disease<...
Division of General Surgery - Research output
- Research Profiles at Washington University School of Medicine
Ellman's Reagent | Reducing Reagents | Cross-Linking & Modification | Protein Research
Protein oxidation and antioxidants in myocardial infarction - Fingerprint - Manipal Academy of Higher Education, Manipal,...
Chemical Compounds1
- In the healthcare setting, "alcohol" refers to two water-soluble chemical compounds-ethyl alcohol and isopropyl alcohol-that have generally underrated germicidal characteristics 482 . (cdc.gov)
Thiol7
- Coenzyme M (commonly known by its salt form, Mesna) is a synthetic sulfhydryl (thiol) compound and is used for prophylaxis of Ifosfamide and cyclophosphamide induced hemorrhagic cystitis. (drugbank.com)
- Measure peptide cysteines or other free, reduced sulfhydryls (-SH groups) in solution using this thiol-reactive, colored compound (Amax 412nm). (fishersci.com)
- The term thiol refers to compounds containing sulfur. (balkanmedicaljournal.org)
- Thiol-containing compounds are found in all body cells and are indispensable for life. (balkanmedicaljournal.org)
- The more highly reduced form a thiol-containing compound has, the more stronger antioxidative activity it exerts. (balkanmedicaljournal.org)
- In this article, antioxidant and antioxidative effects of garlic and some thiol-containing compounds are reviewed. (balkanmedicaljournal.org)
- Paclitaxel analogues with a thiol group in place of the hydroxyl group on the C-13 side chain constitute an interesting avenue of research for the study of new taxoid compounds. (ewha.ac.kr)
Cysteine3
- In 1961, Frenkel and Hirsch described strains of streptococci isolated from cases of bacterial endocarditis that grew only in the presence of other bacteria, around which they formed satellite colonies, or in media enriched with sulfhydryl compounds, such as cysteine. (cdc.gov)
- Ellman's Reagent (5,5′-dithio-bis-[2-nitrobenzoic acid]) is used to estimate sulfhydryl groups in a sample by comparing to a standard curve of a sulfhydryl-containing compound such as cysteine. (meltingpointathens.com)
- Many people consume inadequate amounts of sulfur-containing compounds, such as methionine and cysteine. (humannaturellc.com)
Water-soluble2
- Ellman's reagent is a versatile, water-soluble compound for quantifying free sulfhydryl groups in solution. (gbiosciences.com)
- In 1959, Ellman introduced 5,5′-dithio-bis-(2-nitrobenzoic acid), also known as DTNB, as a versatile water-soluble compound for quantitating free sulfhydryl groups in solution. (meltingpointathens.com)
Sulfur5
- At this time, 1951, many applications had been submitted to me for approval, or to be more precise, these were medications for cancer therapy with the sulfhydryl group (sulfur-containing protein compounds). (healingcancernaturally.com)
- Everybody knows the sulfur-containing protein compound of the sulfhydryl group can be detected in all breathing tissues. (healingcancernaturally.com)
- The figures below show the boiling and melting point for organic sulfur compounds as sulfides, disulfides, thiols (mercaptans) and thiophenes , together with the molecular structures of the different compounds. (engineeringtoolbox.com)
- Biotics Research's MSM provides a supplemental source of methylsulfonylmethane, an organic sulfur containing compound. (humannaturellc.com)
- MSM (methylsulfonylmethane) is a natural compound found in plants and animals, MSM is a normal oxidation product of dimethyl sulfoxide (DMSO), and is a part of the natural global sulfur cycle. (humannaturellc.com)
Glutathione2
- A number of enzymes in carbohydrate and lipid metabolism depend upon glutathione and other sulfhydryl compounds such as coenzyme A for their activity. (erowid.org)
- Glutathione dihydrogenase acts on the reabsorbed portion and produces free sulfhydryl groups. (drugbank.com)
Sulphur compounds2
- Measurement of volatile sulphur compounds (VSC) by portable sulphur monitors (Halimeter, OralChroma) is a common practice for diagnosis of oral malodour. (nih.gov)
- rather it occurs in an interplay between the positive electrically-charged sulphur compounds in the protein, and some kind of fatty substance that we cannot detect, because no verifications for it are available. (healingcancernaturally.com)
Substances1
- Antimetabolites are structural analogues of naturally occurring compounds and function as fraudulent substances for vital biochemical reactions. (medicinalplants.us)
Organic2
Intracellular1
- Additionally, intracellular sulfhydryl groups are necessary for the catalytic function of numerous enzymes. (humannaturellc.com)
Thiols1
- Protein thiols, GSH, other low-molecular-weight thiols, and the seleno-compound ebselen react, in a nonstoichiometric manner, with both peptide and protein peroxides. (ku.dk)
Reacts4
- It reacts with a free sulfhydryl group to yield a mixed disulfide and 2-nitro-5-thiobenzoic acid (NTB), a measurable yellow colored product at 412nm. (gbiosciences.com)
- A solution of this compound produces a measurable yellow-colored product when it reacts with sulfhydryls. (meltingpointathens.com)
- DTNB reacts with a free sulfhydryl group to yield a mixed disulfide and 2-nitro-5-thiobenzoic acid (TNB). (meltingpointathens.com)
- DTNB (Ellman's Reagent) (5,5-dithio-bis-(2-nitrobenzoic acid) Thermo Scientific Pierce Ellman's Reagent (DTNB) reacts with sulfhydryl groups to yield a colored product, providing a reliable method to measure reduced cysteines and other free sulfhydryls in solution. (meltingpointathens.com)
Assay2
- Ellman's reagent is very useful as a free sulfhydryl assay reagent due to its high specificity for -SH groups at neutral pH, high molar extinction coefficient and short reaction time. (gbiosciences.com)
- Ellman's assay is a useful tool that can be used to determine the sulfhydryl concentration of unknown solutions. (meltingpointathens.com)
Oxidation Reaction1
- Dihydrolipoic acid has two sulfhydryl groups and it can undergo further oxidation reaction forming lipoic acid. (balkanmedicaljournal.org)
DTNB1
- The target of DTNB in this reaction is the conjugate base (R-S-) of a free sulfhydryl group. (meltingpointathens.com)
Enzymes2
- Mercury compounds reacting with sulfhydryl groups inhibit a variety of enzymes. (cdc.gov)
- It also maintains several enzymes in their active sulfhydryl form. (erowid.org)
Bacteria2
Toxic4
- Once inside the body, thiopurine drugs are converted to toxic compounds that kill immune system cells in the bone marrow. (medlineplus.gov)
- A number of sulfhydryl-containing compounds reduce the toxic effects of antimony, suggesting that it may bind to cellular sulfhydryl groups. (epa.gov)
- These free sulfhydryl groups bind acrolein in the bladder, allowing effective excretion and prevention of toxic effects. (drugbank.com)
- Those compounds were irradiated in the presence of two non-cancer cell lines and were found equally toxic only upon irradiation and not in the dark. (bvsalud.org)
Cyclophosphamide1
- Alkylating agents, such as the platinum compounds and cyclophosphamide, prevent cell division primarily by cross-linking strands of DNA. (oncohemakey.com)
412nm1
- Alternatively, sulfhydryl groups can be assayed using the extinction coefficient of TNB (14,150M-1 cm-1 at 412nm). (meltingpointathens.com)
Molecules1
- This enzyme carries out a specific chemical reaction called S-methylation of a group of molecules known as aromatic and heterocyclic sulphydryl compounds. (medlineplus.gov)
Group3
- Sulfhydryl group associated with proteinuria and neutropenia when used at high doses. (medscape.com)
- Through official channels I had the right to ask the companies questions relative to how they wanted to substantiate how this substance (sulfhydryl group) could help with cancer. (healingcancernaturally.com)
- However another partner must be present in the interplay with this sulfhydryl group, because the self-active oxygen consumption in the living system is executed in a zig zag curve. (healingcancernaturally.com)
Medications2
- Parent compound of this class of medications. (medscape.com)
- In this situation I noticed the sulfhydryl groups in my appraisal of the medications for cancer therapy. (healingcancernaturally.com)
Hypersensitivity1
- The taxanes and platinum compounds are the most likely to cause hypersensitivity. (oncohemakey.com)
Boiling temperature1
- It is not known whether these compounds are stable at the 1 atm boiling temperature or not. (engineeringtoolbox.com)
Clinical2
- Many alternative compounds exist with few significant clinical differences. (medscape.com)
- In the same decade, bleomycin, etoposide, and doxorubicin came into clinical use, and derivative compounds such as carboplatin, vinorelbine, and idarubicin were developed for their ability to achieve similar antitumor effects but with less hematologic toxicity. (oncohemakey.com)
Drugs2
- The TPMT enzyme "turns off" thiopurine drugs by metabolizing them to inactive, nontoxic compounds. (medlineplus.gov)
- Without enough of this enzyme, the body cannot "turn off" thiopurine drugs by metabolizing them into inactive compounds. (medlineplus.gov)
Adverse1
- One of many compounds with comparable efficacy and adverse effect profiles. (medscape.com)
Activity1
- Mechanism of action of gliotoxin: elimination of activity by sulfhydryl compounds. (wikidata.org)
Found1
- Moving to in vitro experiments, irradiation was found to slightly enhance the death of the cells in the majority of the compounds. (bvsalud.org)
Common1
- Most of the common antimony compounds are slightly to readily soluble in water. (epa.gov)