| Weight | 133.172 g/mol |
|---|---|
| Formula | C4H7NO2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Thiazolidine-4-carboxylic acid
thioproline · thiaproline · gamma-thiaproline
45521-09-3, 444-27-9, 2756-91-4, 19291-02-2
Score:
#4209 in Biology
,
#5307 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)
- Dimerization of an intermediate during the sodium in liquid ammonia reduction of l-thiazolidine-4-carboxylic acid (Canadian Journal of Chemistry, 1967)
- Residue-specific bioincorporation of non-natural, biologically active amino acids into proteins as possible drug carriers: Structure and stability of the per-thiaproline mutant of annexin V (Proceedings of the National Academy of Sciences of the United States of America, 1998)
- Proline, thioproline and potassium mediated stimulation of somatic embryogenesis in alfalfa (Medicago sativa L.) (Plant Science, 1993)
- Thioproline inhibits development of esophageal adenocarcinoma induced by gastroduodenal reflux in rats (Carcinogenesis, 2003)
- 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)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thioproline
- thiaproline
- gamma-thiaproline
- thiazolidine-4-carboxylic acid, (R)-isomer
- Heparegen
- norgamem
- thiazolidine-4-carboxylic acid, sodium salt
-
SMILESC1C(NCS1)C(=O)O
-
InChIKeyDZLNHFMRPBPULJ-UHFFFAOYSA-N
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