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Compounds

COMPOUND NPA009375

STRUCTURE
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EXTERNAL LINKS
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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.
DOI 10.7164/antibiotics.52.635 PMID 10513843
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Streptomycetales LPSN 85011
Family Streptomycetaceae LPSN 2062
Genus Streptomyces LPSN 1883
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
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
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