| Weight | 133.172 g/mol |
|---|---|
| Formula | C4H7NO2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Thiazolidine-2-carboxylic acid (16310-13-7)
Score:
#1977 in Biochemistry
,
#4174 in Biology
,
#5260 in Chemistry
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- The exchanger inhibitory peptide region-dependent inhibition of Na+/Ca2+ exchange by SN-6 [2-[4-(4-nitrobenzyloxy)benzyl]thiazolidine-4-carboxylic acid ethyl ester], a novel benzyloxyphenyl derivative. (Molecular Pharmacology, 2004)
- X-ray and NMR studies on thiazolidines: crystal structure and conformational equilibriums of N-acetyl-2-(p-tolyl)thiazolidine-4-carboxylic acid ad related thiazolidine derivatives (Journal of the American Chemical Society, 1976)
- Diversion of ethanol metabolism by sulfhydryl amino acids. D-penicillamine-directed excretion of 2,5,5-trimethyl-D-thiazolidine-4-carboxylic acid in the urine of rats after ethanol administration (Life Sciences, 1975)
- Thiazolidine-2-carboxylic acid, an adduct of cysteamine and glyoxylate, as a substrate for D-amino acid oxidase. (Journal of Biological Chemistry, 1982)
- Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors. (Biochimie, 2012)
- Captan Metabolism in Humans Yields two Biomarkers, Tetrahydrophthalimide (THPI) and Thiazolidine-2-Thione-4-Carboxylic Acid (TTCA) in Urine (Drug and Chemical Toxicology, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CSC(N1)C(=O)O
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InChIKeyULSZVNJBVJWEJE-UHFFFAOYSA-N
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