MDL | - |
---|---|
Molecular Weight | 791.06 |
Molecular Formula | C45H74O11 |
SMILES | O=C(/C=C/[C@H](C)[C@@H](O)[C@H](C)C([C@H](C)[C@@H](O)[C@@H]1C)=O)O[C@@]([C@@H]2C)([H])[C@H](C)[C@@]3(CC[C@H](C)[C@H](C[C@H](O)C)O3)O[C@@]2([H])CC[C@@H](CC)/C=C/C=C/C[C@@H](C)[C@H](O)[C@@](C)(O)C1=O |
Oligomycin A (MCH 32), created by Streptomyces , acts as a mitochondrial F 0 F 1 -ATPase inhibitor, with a K i of 1 μM; Oligomycin A shows anti-fungal activity.
Ki: 1 μM (F 0 F 1 -ATPase) [1]
Oligomycin A is a mitochondrial F 0 F 1 -ATPase inhibitor with a K i of 1 μM. Oligomycin A shows cytotoxic to the NCI-60 cell lines, with GI 50 of 10 nM. Oligomycin A also inhibits the activity of Triton X-100-solubilized ATPase with a K i of 0.1 μM. Furthermore, Oligomycin A has anti-fungal activity [1] . Oligomycin A (2.4 µM) inhibits the ability of spermatozoa to achieve feasible in vitro capacitation (IVC), and also suppresses progesterone-induced in vitro acrosome exocytosis (IVAE) as well as the concomitant peaks of O 2 consumption and ATP levels [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Streptomyces diastatochromogenes
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 100 mg/mL ( 126.41 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 1.2641 mL | 6.3206 mL | 12.6413 mL |
5 mM | 0.2528 mL | 1.2641 mL | 2.5283 mL |
10 mM | 0.1264 mL | 0.6321 mL | 1.2641 mL |