| Weight | 548.633 g/mol |
|---|---|
| Formula | C28H40N2O9 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 12 |
antimycin A1 (1397-94-0, 642-15-9)
Antimycin A
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- Structure of Antimycin A1, a Specific Electron Transfer Inhibitor of UbiquinolCytochrome c Oxidoreductase (Journal of the American Chemical Society, 1999)
- Inhibition of Glucose and Tolbutamide-Induced Insulin Release by Iodoacetate and Antimycin A1 (Endocrinology, 1971)
- Inhibition of angiogenesis and HIF-1 activity by antimycin A1 (Biological & Pharmaceutical Bulletin, 2006)
- The Total Synthesis of Dehexyl-deisovaleryloxy-antimycin A1 (Bulletin of the Chemical Society of Japan, 1969)
- Simple Isolation of Antimycin A1 and Some of Its Toxicological Properties (Applied and Environmental Microbiology, 1969)
- 1H and 13C resonance designation of antimycin A1 by two-dimensional NMR spectroscopy (Magnetic Resonance in Chemistry, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Antimycin A
-
SMILESCCCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)OC(=O)CC(C)C
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InChIKeyUIFFUZWRFRDZJC-UHFFFAOYSA-N
- Pubchem - antimycin A1
- Wikipedia - Antimycin A
Antimycins are a group of secondary metabolites produced by Streptomyces bacteria. It is classified as an extremely hazardous substance in the United States, as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C.
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