Compounds
ID | Spectrum Quality | Annotated Name |
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COMPOUND NPA031271
PROPERTIES
NPAID | NPA031271 |
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CLUSTER ID | 9104 |
NODE ID | 6119 |
NAME | (7S,8S,12E)-8,17-Epoxy-7-Hydroxylabda-12,14-diene |
FORMULA | C20H32O2 |
MOLECULAR WEIGHT (Da) | 304.4740 |
ACCURATE MASS (Da) | 304.2402 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | avermitilis SUKA22 (heterologous expression) |
InChIKey | VWQNLIAHGOKMCP-LZDKCEGCSA-N |
InChI | InChI=1S/C20H32O2/c1-6-14(2)8-9-15-19(5)11-7-10-18(3,4)16(19)12-17(21)20(15)13-22-20/h6,8,15-17,21H,1,7,9-13H2,2-5H3/b14-8+/t15-,16+,17+,19-,20-/m1/s1 |
SMILES | C=C/C(C)=C/C[C@@H]1[C@@]2(C)CCCC(C)(C)[C@@H]2C[C@H](O)[C@@]12CO2 |
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. | ||
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DOI | 10.1007/s10295-015-1694-6 | PMID | 26507838 |