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Overview
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Venturicidin B (Aabomycin A2) is a 20-member macrolide glycoside compound that was originally isolated from a Streptomyces sp.by Glaxo Labs in 1961. Venturicidin B is a potent antifungal and toxic antibiotic compound, that has also shown cytotoxicity to trypanosomes.
Venturicidin B is a potent inhibitor of bacterial and mitochondrial ATP-synthase complexes acting on the F0 membrane sector, with experiments suggesting that the compound strongly inhibits ATP-driven proton transport and ATP hydrolysis. Venturicidin B demonstrates the ability to drastically decrease the open probability of voltage sensitive K+ channels. Venturicidin B is an inhibitor of ATP5 as well as a potential inhibitor of E. coli H+-ATPase.
Venturicidin B is soluble in ethanol, methanol, DMF and DMSO.Please contact us at for specific academic pricing.
Background
Venturicidin B binds to the subunit-c of the coupling factor o, or Fo of mitochondrial and bacterial ATP synthase complex. Once bound to the ATP synthase, Venturicidin B blocks proton translocation and inhibits ATP synthesis in both fungi and bacteria.
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- Properties
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Overview