2-Methyl-thiazolidine-4-carboxylic acid 2-甲基噻唑烷-4-羧酸
CAS 4165-32-6 MFCD00278415
化学结构图
SMILES: CC1NC(C(=O)O)CS1
化学属性
| Mol. Formula | C5H9NO2S |
|---|---|
| Mol. Weight | 147.20 |
| Boiling Point | 333° |
| Melting Point | 174-175° |
别名和识别编码
| Chemical Name | 2-Methyl-thiazolidine-4-carboxylic acid |
|---|---|
| CAS Number | 4165-32-6 |
| Alfabeta Name | METHYLTHIAZOLIDINECARBOXYLICACID 24---- |
| MDL Number | MFCD00278415 |
| Synonym | 2-Methylthiazolidine-4-carboxylic acid {LY} 2-Methylthiazolidine-4-carboxylic acid {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-Methylthiazolidine-4-carboxylic acid {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} 2-M |
| Chemical Name Translation | 2-甲基噻唑烷-4-羧酸 |
| LabNetwork Molecule ID | LN00120452 |
| PubChem Substance ID | 160736 |
| InChI | InChI=1S/C5H9NO2S/c1-3-6-4(2-9-3)5(7)8/h3-4,6H,2H2,1H3,(H,7,8) |
| Canonical SMILES | O=C(C1NC(C)SC1)O |
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分类
- Heterocycles
- Pharmaceuticals
- Intermediates & Fine Chemicals
- Sulfur & Selenium Compounds
产品应用
- An Cysteine prodrug, protective aginst the fungal T-2 toxin. It is also a precursor to pharmaceuticals used in the treatment of cataracts.
相关文献及参考
- Shirota, F., et al.: Biochem. Pharmacol., 43, 916 (1992),
- Wlodek, L., et al.: Int. J. Biochem., 25, 107 (1993),
- Rathbun, W., et al.: Biochem. Pharmacol., 51, 1111 (1996),
