Indole-3-carboxylic acid
Cat. No.：YN372620
| 产品名称: | Indole-3-carboxylic acid |
| CAS No.: | 771-50-6 |
| Chemical Name: | 1H-indole-3-carboxylic acid |
| Synonyms: | 3-Indoleformic acid, 3-Carboxyindole, β-Indolylcarboxylic acid, 3-indolecarboxylate, 3-indoleformate |
| 分子量: | 161.16 |
| 分子式: | C₉H₇NO₂ |
| SMILES: | O=C(O)C1=CNC2=CC=CC=C12 |
| 存储: | Please store the product under the recommended conditions in theCertificate of Analysis. |
| 运输: | Room temperature in continental US; may vary elsewhere. |
| 产品描述: | Indole-3-carboxylic acid 是一种正常的尿吲哚色氨酸代谢物，在肝病患者中浓度会升高。 |
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Iven, T., König, S., Singh, S., et al.Transcriptional activation and production of tryptophan-derived secondary metabolites in Arabidopsis roots contributes to the defense against the fungal vascular pathogen Verticillium longisporumMol. Plant5(6),1389-1402(2012)
Gamir, J., Pastor, V., Sánchez-Bel, P., et al.Starch degradation, abscisic acid and vesicular trafficking are important elements in callose priming by indole-3-carboxylic acid in response to Plectosphaerella cucumerina infectionPlant J.96(3),518-531(2018)
Wu, P.-L., Lin, F.-W., Wu, T.-S., et al.Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensisChem. Pharm. Bull. (Tokyo)52(3),345-349(2004)
Kumar, D., Kumar, N.M., Chang, K.-A., et al.Synthesis and anticancer activity of 5-(3-indolyl)-1,3,4-thiadiazolesEur. J. Med. Chem.45(10),4664-4668(2010)
