Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA031864
PROPERTIES
| NPAID | NPA031864 |
|---|---|
| CLUSTER ID | 9283 |
| NODE ID | 6226 |
| NAME | 4-hydroxy-3-(4-methoxy-1H-indol-3-yl)-2-thioxothiazolidine-4-carboxylic acid |
| FORMULA | C13H12N2O4S2 |
| MOLECULAR WEIGHT (Da) | 324.3830 |
| ACCURATE MASS (Da) | 324.0238 |
| ORIGIN ORGANISM TYPE | Fungus |
| ORIGIN GENUS | Colletotrichum |
| ORIGIN SPECIES | dematium and Colletotrichum higginsianum |
| InChIKey | NFDILGISCWCPPR-UHFFFAOYSA-N |
| InChI | InChI=1S/C13H12N2O4S2/c1-19-9-4-2-3-7-10(9)8(5-14-7)15-12(20)21-6-13(15,18)11(16)17/h2-5,14,18H,6H2,1H3,(H,16,17) |
| SMILES | COC1=CC=CC2=C1C(N1C(=S)SCC1(O)C(=O)O)=CN2 |
ORIGINAL ISOLATION REFERENCE
| CITATION | Pedras, M Soledade C; Thapa, Chintamani Unveiling fungal detoxification pathways of the cruciferous phytoalexin rapalexin A: Sequential L-cysteine conjugation, acetylation and oxidative cyclization mediated by Colletotrichum spp. Phytochemistry 2020 169 112188. | ||
|---|---|---|---|
| DOI | 10.1016/j.phytochem.2019.112188 | PMID | 31683228 |
