Oligomycin 100mg 100mg | Purity Not Available
Adooq Bioscience
Oligomycin is a macrolide that acts as a specific inhibitor of the mitochondrial ATP-synthase and blocks oxidative phosphorylation.
More Information Supplier PageOligomycin is a macrolide that acts as a specific inhibitor of the mitochondrial ATP-synthase and blocks oxidative phosphorylation.
More Information Supplier PageTriacsin C, originally isolated from Streptomyces sp., is an inhibitor of long fatty acid acyl-CoA synthetase (IC50 = 6.3 ??M in Raji cells).
More Information Supplier PageTriacsin C, originally isolated from Streptomyces sp., is an inhibitor of long fatty acid acyl-CoA synthetase (IC50 = 6.3 ??M in Raji cells).
More Information Supplier PageTriacsin C, originally isolated from Streptomyces sp., is an inhibitor of long fatty acid acyl-CoA synthetase (IC50 = 6.3 ??M in Raji cells).
More Information Supplier PageDMOG is a cell permeable, competitive inhibitor of HIF-PH. It acts to stabilize HIF-1?? expression at normal oxygen tensions in cultured cells, at concentrations between 0.1 and 1 mM.
More Information Supplier PageDMOG is a cell permeable, competitive inhibitor of HIF-PH. It acts to stabilize HIF-1?? expression at normal oxygen tensions in cultured cells, at concentrations between 0.1 and 1 mM.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageATB-346 exhibits anti-inflammatory properties similar to naproxen, but with substantially reduced gastrointestinal toxicity.
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