| Weight | 99.158 g/mol |
|---|---|
| Formula | C4H5NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Methylthiazole (3581-89-3)
Score:
#44 in Medicinal chemistry
,
#2690 in Biochemistry
,
#6671 in Chemistry
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- Activity of rat cytosolic thioredoxin reductase is strongly decreased by trans-[bis(2-amino-5- methylthiazole)tetrachlororuthenate(III)]: first report of relevant thioredoxin reductase inhibition for a ruthenium compound. (Journal of Medicinal Chemistry, 2007)
- Electrochemical oxidation of substituted thiazoles: 2-amino-4-ethoxycarbonyl-5- methylthiazole and N-ethoxycarbonyl-N- (4-ethoxycarbonyl-5-methylthiazol-2-yl) thiourea (Electrochimica Acta, 1979)
- Synthesis and pharmacological evaluation of a novel series of 3-aryl-2-(2-substituted-4-methylthiazole-5-yl)thiazolidin-4-one as possible anti-inflammatory and antimicrobial agents (Bioorganic & Medicinal Chemistry Letters, 2012)
- Bifunctional ethyl 2-amino-4-methylthiazole-5-carboxylate derivatives: Synthesis and in vitro biological evaluation as antimicrobial and anticancer agents (European Journal of Medicinal Chemistry, 2014)
- Efficiency of alkoxyl radical product formation from 5-substituted 3-alkoxy-4-methylthiazole-2(3H)-thiones (Tetrahedron, 2010)
- Bacterial Metabolism of Thiamine III. METABOLISM OF THIAMINE TO 3-(2'-METHYL-4'-AMINO-5'-PYRIMIDYLMETHYL)-4-METHYLTHIAZOLE-5-ACETIC ACID (THIAMINE ACETIC ACID) BY A FLAVOPROTEIN ISOLATED FROM A SOIL MICROORGANISM (Journal of Biological Chemistry, 1970)
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SMILESCC1=CN=CS1
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InChIKeyRLYUNPNLXMSXAX-UHFFFAOYSA-N
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