Oligomycin A 060 Bepotastine besilate is a selective

Bepotastine besilate is a selective antagonist of histamine 1 (H1) receptor with pIC50 of 5

about 3-fold selectivity over DDR2

which potently and selectively kills cells containing an MLL translocation

is a specific inverse agonist of estrogen-related receptor γ (ERRγ) that inhibits pro-inflammatory cytokine-induced catabolic factors

Chemical Name: 3-Amino-2-(4-chlorophenyl)propane-1-sulfonic acid

Oligomycin A 060 Bepotastine besilate is a selectiveOligomycin A, also known as MCH 32, is an inhibitor of ATP synthase. Oligomycin A inhibits ATP synthase by blocking its proton channel (Fo subunit), which is necessary for oxidative phosphorylation of ADP to ATP (energy production). The inhibition of ATP synthesis by oligomycin A will significantly reduce electron flow through the electron transport chain; however, electron flow is not stopped completely due to a process known as proton leak or