Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA002918
PROPERTIES
NPAID | NPA002918 |
---|---|
CLUSTER ID | 1675 |
NODE ID | 1369 |
NAME | Cyslabdan |
FORMULA | C25H41NO5S |
MOLECULAR WEIGHT (Da) | 467.6720 |
ACCURATE MASS (Da) | 467.2705 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | sp. K04-0144 |
InChIKey | PSUMRJNLBIVEFF-SOJAJMJSSA-N |
InChI | InChI=1S/C25H41NO5S/c1-7-16(2)9-10-19-24(6)12-8-11-23(4,5)20(24)13-21(28)25(19,31)15-32-14-18(22(29)30)26-17(3)27/h7,9,18-21,28,31H,1,8,10-15H2,2-6H3,(H,26,27)(H,29,30)/b16-9+/t18-,19+,20-,21-,24+,25+/m0/s1 |
SMILES | C=C/C(C)=C/C[C@@H]1[C@@]2(C)CCCC(C)(C)[C@@H]2C[C@H](O)[C@@]1(O)CSC[C@H](NC(C)=O)C(=O)O |
ORIGINAL ISOLATION REFERENCE
CITATION | Fukumoto, Atsushi; Kim, Yong-Pil; Hanaki, Hideaki; Shiomi, Kazuro; Tomoda, Hiroshi; Ōmura, Satoshi Cyslabdan, a New Potentiator of Imipenem Activity against Methicillin-resistant Staphylococcus aureus, Produced by Streptomyces sp. K04-0144 Journal of Antibiotics 2008 61 (1) 7-10. | ||
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DOI | 10.1038/ja.2008.102 | PMID | 18305353 |
REVISIONS
VERSION | SMILES | CITATION | ||
---|---|---|---|---|
Original Isolation | C/C(=C\C[C@@H]1[C@]2(CCCC([C@@H]2C[C@@H]([C@@]1(CSC[C@@H](C(=O)O)NC(=O)C)O)O)(C)C)C)/C=C | Fukumoto, Atsushi; Kim, Yong-Pil; Hanaki, Hideaki; Shiomi, Kazuro; Tomoda, Hiroshi; Ōmura, Satoshi Cyslabdan, a New Potentiator of Imipenem Activity against Methicillin-resistant Staphylococcus aureus, Produced by Streptomyces sp. K04-0144 Journal of Antibiotics 2008 61 (1) 7-10. DOI: 10.1038/ja.2008.102 PMID: 18305353 | ||
2 | C=C/C(C)=C/C[C@@H]1[C@@]2(C)CCCC(C)(C)[C@@H]2C[C@H](O)[C@@]1(O)CSC[C@H](NC(C)=O)C(=O)O | Ohtawa, Masaki; Hishinuma, Yusuke; Takagi, Eiji; Yamada, Takafumi; Ito, Fumihiro; Arima, Shiho; Uchida, Ryuji; Kim, Yong-Pil; Ōmura, Satoshi; Tomoda, Hiroshi; Nagamitsu, Tohru Synthesis and Structural Revision of Cyslabdan. Chemical and Pharmaceutical Bulletin 2016 64 (9) 1370-7. DOI: 10.1248/cpb.c16-00382 PMID: 27581641 |