Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA031269
PROPERTIES
| NPAID | NPA031269 |
|---|---|
| CLUSTER ID | 1675 |
| NODE ID | 1369 |
| NAME | 2-Hydroxycyslabdan A |
| FORMULA | C25H41NO6S |
| MOLECULAR WEIGHT (Da) | 483.6710 |
| ACCURATE MASS (Da) | 483.2655 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Streptomyces |
| ORIGIN SPECIES | avermitilis SUKA22 (heterologous expression) |
| InChIKey | PTRRHQHGAOYEKT-KYXZTKSHSA-N |
| InChI | InChI=1S/C25H41NO6S/c1-7-15(2)8-9-19-24(6)12-17(28)11-23(4,5)20(24)10-21(29)25(19,32)14-33-13-18(22(30)31)26-16(3)27/h7-8,17-21,28-29,32H,1,9-14H2,2-6H3,(H,26,27)(H,30,31)/b15-8+/t17-,18-,19+,20-,21-,24+,25+/m0/s1 |
| SMILES | C=C/C(C)=C/C[C@@H]1[C@@]2(C)C[C@@H](O)CC(C)(C)[C@@H]2C[C@H](O)[C@@]1(O)CSC[C@H](NC(C)=O)C(=O)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Haruo Ikeda, Kazuo Shin-ya, Tohru Nagamitsu, Hiroshi Tomoda Biosynthesis of mercapturic acid derivative of the labdane-type diterpene, cyslabdan that potentiates imipenem activity against methicillin-resistant Staphylococcus aureus: cyslabdan is generated by mycothiol-mediated xenobiotic detoxification. Journal of Industrial Microbiology and Biotechnology 2016 43 (2-3) 325-342. | ||
|---|---|---|---|
| DOI | 10.1007/s10295-015-1694-6 | PMID | 26507838 |
