organic heterocyclic compound antimycin A 0 548.27338 548.633 beilstein:72665 (2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxybenzoyl)amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate C28H40N2O9 metacyc.compound:CPD-5744 antimycin A1b CHEBI:40908 [H]C(=O)Nc1cccc(C(=O)N[C@@H]2C(=O)O[C@@H](C)[C@H](OC(=O)CC(C)C)[C@@H](CCCCCC)C(=O)O[C@@H]2C)c1O InChI=1S/C28H40N2O9/c1-6-7-8-9-11-20-25(39-22(32)14-16(2)3)18(5)38-28(36)23(17(4)37-27(20)35)30-26(34)19-12-10-13-21(24(19)33)29-15-31/h10,12-13,15-18,20,23,25,33H,6-9,11,14H2,1-5H3,(H,29,31)(H,30,34)/t17-,18+,20-,23+,25+/m1/s1 CHEBI:2762 Antipiricullin pubmed:29790043 Fintrol kegg.compound:C11339 (2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxybenzoyl)amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate chebi_ontology pubmed:30914247 UIFFUZWRFRDZJC-SBOOETFBSA-N pubmed:31079230 CHEBI:22584 A nine-membered bis-lactone having methyl substituents at the 2- and 6-positions, an n-hexyl substituent at the 8-position, an acyloxy substituent at the 7-position and an aroylamido substituent at the 3-position. It is produced by <em>Streptomyces</em> bacteria and has found commercial use as a fish poison. cas:1397-94-0 pubmed:32662599 Virosin pubmed:16819166 cas:642-15-9 Antimycin A1 pdb-ccd:AY1 phenols carboxamide