Structure via PubChem · Public domain (PubChem)
antimycin A1b
Sign in to saveAlso known as (+)-antimycin A1b, antimycin A, Antimycin A
chemical compound
In the Vinony graph
Within Vinony's link graph, antimycin A1b is referenced by 15 other articles, and connects out to photosynthesis, Rodentia and vomiting.
Vinony files it under Antibiotics, Carboxylate esters and Chembox having GHS data.
Its subject is documented across 13 Wikipedia language editions.
Chemical data
- Formula
- C28H40N2O9
- Molecular weight
- 548.6 g/mol
- IUPAC name
- [(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
- SMILES
- CCCCCC[C@@H]1[C@H]([C@@H](OC(=O)[C@H]([C@H](OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
- InChIKey
- UIFFUZWRFRDZJC-SBOOETFBSA-N
- XLogP
- 5.3
- Polar surface area
- 157 Ų
- H-bond donors
- 3
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Research
3 papers- Organoboron-based allylation approach to the total synthesis of the medium-ring dilactone (+)-antimycin A(1b).The Journal of organic chemistry · 2014
- High-performance liquid chromatographic separation of subcomponents of antimycin A.Journal of chromatography · 1988
- Antimycins A(19) and A(20), two new antimycins produced by marine actinomycete Streptomyces antibioticus H74-18.The Journal of antibiotics · 2011
via PubMed
Wikidata facts
- Mass
- 548.273381
Show 6 more facts
- canonical SMILES
- CCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
- isomeric SMILES
- CCCCCC[C@@H]1[C@H]([C@@H](OC(=O)[C@H]([C@H](OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
- chemical formula
- C₂₈H₄₀N₂O₉
- found in taxon
- Streptomyces griseus
- subject has role
- antifungal
- Commons category
- Antimycin A
via Wikidata · CC0
Connections
photosynthesis
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Rodentia
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vomiting
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