Results 241 to 250 of about 3,705,484 (314)
Some of the next articles are maybe not open access.
Molecular Pharmacology, 1985
The rate of loss of the sulfhydryl group, determined with the Ellman reagent, was used to derive second order rate constants for the reaction of a series of organic nitrates with a series of sulfhydryl compounds.
R. Yeates, H. Laufen, M. Leitold
semanticscholar +1 more source
The rate of loss of the sulfhydryl group, determined with the Ellman reagent, was used to derive second order rate constants for the reaction of a series of organic nitrates with a series of sulfhydryl compounds.
R. Yeates, H. Laufen, M. Leitold
semanticscholar +1 more source
Reaction of malformin with sulfhydryl compounds
Phytochemistry, 1970Abstract Malformin reacts with the sulfhydryl compounds, cysteine and β-mercaptoethanol, to form an insoluble 1:1 addition product. This reaction may explain the ability of thiol compounds to inhibit the activity of malformin and suggests reaction of malformin with thiol compounds in vivo .
Shinobu Iriuchijima, Roy W. Curtis
openaire +1 more source
Food Chemistry
Herein, we made 3D MXene-AuNPs by in situ growth of gold nanoparticles (AuNPs) on the surface of MXene by chemical reduction method, and then introduced three sulfhydryl (-SH) compounds as functionalized modifiers attached to the AuNPs to form a highly ...
Yuanyuan Chen +8 more
semanticscholar +1 more source
Herein, we made 3D MXene-AuNPs by in situ growth of gold nanoparticles (AuNPs) on the surface of MXene by chemical reduction method, and then introduced three sulfhydryl (-SH) compounds as functionalized modifiers attached to the AuNPs to form a highly ...
Yuanyuan Chen +8 more
semanticscholar +1 more source
Sulfhydryl Compounds as Thermosensitizers
1988The cytotoxic effects of a number of widely used chemotherapeutic agents have been reported to be enhanced by heat (Hahn 1979; Hahn and Li 1982). The exact mechanism of this enhancement is not fully understood and might differ with the various compounds. Thermosensitization by sulfhydryl compounds in vitro has been observed by Kapp and Hahn (1979).
openaire +2 more sources
Protection of sulfhydryl compounds against ionizing radiation
Biochimica et Biophysica Acta, 1963Cysteamine was shown to provide strong protection against x-ray inactivation of papain and of a small molecular compound, CoA, in solutions. The mechanism involved modification of their -SH groups. It is concluded that results are compatible with the hypothesis that the protection afforded by sulfhydryl compounds in vivo may be due in part to blocking ...
A, PIHL, T, SANNER
openaire +2 more sources
Role of Sulfhydryls in the Hepatotoxicity of Organic and Metallic Compounds
Toxicological Sciences, 1985Endogenous sulfhydryl compounds serve a critical role in maintaining the function and viability of living systems. Glutathione (GSH) is the most abundant of these nonprotein thiols. During the past decade it has been demonstrated that sulfhydryls such as GSH also serve an important role in protecting vital nucleophilic sites in the liver from ...
C D, Klaassen +5 more
openaire +2 more sources
Alteration of lymphocyte response by sulfhydryl and disulfide compounds
Biochemical Pharmacology, 1979Abstract The effects on the proliferative response of human lymphocytes of the sulfhydryl agents d -penicillamine and 5-thiopyridoxine, some analogues of these agents, and their respective disulfides were investigated. The sulfhydryl agents inhibited the proliferation of mitogen-stimulated lymphocytes and suppressed the mixed lymphocyte reaction ...
P F, Merryman, J, Nowakowski, I A, Jaffe
openaire +2 more sources
Products of the reaction of peroxyacetyl nitrate with sulfhydryl compounds
Archives of Biochemistry and Biophysics, 1969Abstract Peroxyacetyl nitrate reacts with reduced glutathione producing oxidized glutathione and S -acetyl glutathione. Reaction of peroxyacetyl nitrate with reduced coenzyme A results in the formation of coenzyme A disulfide, accounting for 35–45% of the reacted sulfhydryl. The remaining products can be separated by ion exchange chromatography and
J B, Mudd, T T, McManus
openaire +2 more sources
Role of sulfhydryl compounds in the Bactericidal effect of metronidazole
Biochemical Pharmacology, 1983The bactericidal effect of metronidazole on Escherichia coli and Bacteroides fragilis can be partially reversed by cysteamine under conditions that lead to the formation of an adduct, the thioether, 4-(2-aminoethyl)thio-2-methylimidazole-1-ethanol (4-ATME). This adduct, which is not mutagenic for the Ames histidine auxotrophs of Salmonella typhimurium,
T C, Yeung, P, Goldman
openaire +2 more sources