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Compounds

COMPOUND NPA008000

STRUCTURE
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PROPERTIES
NPAID NPA008000
CLUSTER ID 1818
NODE ID 1472
NAME Feigrisolide C
FORMULA C22H38O6
MOLECULAR WEIGHT (Da) 398.5400
ACCURATE MASS (Da) 398.2668
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES griseus
InChIKey NRPVEMPAQOVIJK-LAVUOVMJSA-N
InChI InChI=1S/C22H38O6/c1-5-16(23)12-18-7-8-20(28-18)14(3)19(24)11-13(2)10-17-6-9-21(27-17)15(4)22(25)26/h13-18,20-21,23H,5-12H2,1-4H3,(H,25,26)/t13-,14+,15+,16+,17-,18+,20-,21+/m0/s1
SMILES CC[C@@H](O)C[C@H]1CC[C@@H]([C@H](C)C(=O)C[C@@H](C)C[C@@H]2CC[C@H]([C@@H](C)C(=O)O)O2)O1
ORIGINAL ISOLATION REFERENCE
CITATION Tang; Sattler; Thiericke; Grabley; Feng Feigrisolides A, B, C and D, new lactones with antibacterial activities from Streptomyces griseus Journal of Antibiotics 2000 53 (9) 934-943.
DOI 10.7164/antibiotics.53.934 PMID 11099227
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 Kim WH; Jung JH; Lee E Feigrisolide C: structural revision and synthesis. Journal of Organic Chemistry 2005 70 (20) 8190-8192. DOI: 10.1021/jo051107d PMID: 16277346
REVISIONS
VERSION SMILES CITATION
Original Isolation CC[C@H](C[C@@H]1CC[C@H]([C@H](C(=O)O[C@H](C[C@H]2CC[C@H](O2)[C@@H](C(=O)O1)C)C)C)O)O Tang; Sattler; Thiericke; Grabley; Feng Feigrisolides A, B, C and D, new lactones with antibacterial activities from Streptomyces griseus Journal of Antibiotics 2000 53 (9) 934-943. DOI: 10.7164/antibiotics.53.934 PMID: 11099227
2 CC[C@@H](O)C[C@H]1CC[C@@H]([C@H](C)C(=O)C[C@@H](C)C[C@@H]2CC[C@H]([C@@H](C)C(=O)O)O2)O1 Kim WH; Jung JH; Lee E Feigrisolide C: structural revision and synthesis. Journal of Organic Chemistry 2005 70 (20) 8190-8192. DOI: 10.1021/jo051107d PMID: 16277346
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