Sulfhydryl Compounds
"Sulfhydryl Compounds" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Compounds containing the -SH radical.
Descriptor ID |
D013438
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MeSH Number(s) |
D02.886.489
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Concept/Terms |
Sulfhydryl Compounds- Sulfhydryl Compounds
- Compounds, Sulfhydryl
- Thiols
- Mercaptans
- Mercapto Compounds
- Compounds, Mercapto
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Below are MeSH descriptors whose meaning is more general than "Sulfhydryl Compounds".
Below are MeSH descriptors whose meaning is more specific than "Sulfhydryl Compounds".
This graph shows the total number of publications written about "Sulfhydryl Compounds" by people in this website by year, and whether "Sulfhydryl Compounds" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2005 | 1 | 0 | 1 | 2008 | 2 | 0 | 2 | 2010 | 2 | 0 | 2 | 2011 | 1 | 0 | 1 | 2012 | 1 | 0 | 1 | 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sulfhydryl Compounds" by people in Profiles.
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Qi J, Motwani P, Gheewala M, Brennan C, Wolfe JC, Shih WC. Surface-enhanced Raman spectroscopy with monolithic nanoporous gold disk substrates. Nanoscale. 2013 May 21; 5(10):4105-9.
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Wang Y, Gibney PA, West JD, Morano KA. The yeast Hsp70 Ssa1 is a sensor for activation of the heat shock response by thiol-reactive compounds. Mol Biol Cell. 2012 Sep; 23(17):3290-8.
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De Mori G, Fu Z, Viola E, Cai X, Ercolani C, Donzello MP, Kadish KM. Tetra-2,3-pyrazinoporphyrazines with externally appended thienyl rings: synthesis, UV-visible spectra, electrochemical behavior, and photoactivity for the generation of singlet oxygen. Inorg Chem. 2011 Sep 05; 50(17):8225-37.
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West JD, Stamm CE, Kingsley PJ. Structure-activity comparison of the cytotoxic properties of diethyl maleate and related molecules: identification of diethyl acetylenedicarboxylate as a thiol cross-linking agent. Chem Res Toxicol. 2011 Jan 14; 24(1):81-8.
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Yost JM, Alfie RJ, Tarsis EM, Chong I, Coltart DM. Direct carbon-carbon bond formation via soft enolization: aldol addition of a-halogenated thioesters. Chem Commun (Camb). 2011 Jan 07; 47(1):571-2.
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Tarsis E, Gromova A, Lim D, Zhou G, Coltart DM. Overcoming the limitations of the Morita-Baylis-Hillman reaction: a rapid and general synthesis of alpha-alkenyl-beta'-hydroxy thioesters. Org Lett. 2008 Nov 06; 10(21):4819-22.
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Trott A, West JD, Klaic L, Westerheide SD, Silverman RB, Morimoto RI, Morano KA. Activation of heat shock and antioxidant responses by the natural product celastrol: transcriptional signatures of a thiol-targeted molecule. Mol Biol Cell. 2008 Mar; 19(3):1104-12.
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Teng X, Degterev A, Jagtap P, Xing X, Choi S, Denu R, Yuan J, Cuny GD. Structure-activity relationship study of novel necroptosis inhibitors. Bioorg Med Chem Lett. 2005 Nov 15; 15(22):5039-44.
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