Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA009375
PROPERTIES
NPAID | NPA009375 |
---|---|
CLUSTER ID | 427 |
NODE ID | 385 |
NAME | 5,6-dihydrocineromycin B |
FORMULA | C17H28O4 |
MOLECULAR WEIGHT (Da) | 296.4070 |
ACCURATE MASS (Da) | 296.1988 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | sp. (strain Go 40/10) |
InChIKey | IDGNDQYOCKRQMV-WMZCOYIESA-N |
InChI | InChI=1S/C17H28O4/c1-12-6-5-7-13(2)15(18)8-10-17(4,20)11-9-16(19)21-14(12)3/h7,9,11-12,14-15,18,20H,5-6,8,10H2,1-4H3/b11-9+,13-7+/t12-,14+,15-,17+/m0/s1 |
SMILES | C[C@H]1CC/C=C(/[C@H](CC[C@@](/C=C/C(=O)O[C@@H]1C)(C)O)O)\C |
ORIGINAL ISOLATION REFERENCE
CITATION | Schiewe, Hans-Joerg; Zeeck, Axel Cineromycins, γ-butyrolactones and ansamycins by analysis of the secondary metabolite pattern created by a single strain of Streptomyces Journal of Antibiotics 1999 52 (7) 635-642. | ||
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DOI | 10.7164/antibiotics.52.635 | PMID | 10513843 |
SYNTHESES
CITATION 1 | Li G; Yang X; Zhai H Total synthesis of (-)-5,6-dihydrocineromycin B. Journal of Organic Chemistry 2009 74 (3) 1356-1359. DOI: 10.1021/jo802503x PMID: 19115810 | ||
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CITATION 2 | Tietze LF; Völkel L Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B. Angewandte Chemie International Edition 2001 40 (5) 901-902. DOI: 10.1002/1521-3773(20010302)40:5<901::AID-ANIE901>3.0.CO;2-F PMID: 29712170 | ||
CITATION 3 | Tietze LF; Völkel L Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B. Angewandte Chemie International Edition 2001 40 (5) 901-902. DOI: 10.1002/1521-3773(20010302)40:5<901::AID-ANIE901>3.0.CO;2-F PMID: 29712170 |