|M10261||Gboxin||Gboxin is an inhibitor of oxidative phosphorylation that targets glioblastoma, inhibits the activity of F0F1 ATP synthase, with antitumour activity.|
|M9719||ML367||ML367 is an inhibitor of ATAD5 stabilization.|
|M9587||NDI-091143||NDI-091143 is a novel potent inhibitor of human ATP-citrate lyase with an IC50 of 2.1 nM (ADP-Glo assay).|
|M9134||Citreoviridin||Citreoviridin is a mycotoxin and potent inhibitor of mitochondrial ATPase.|
|M5161||Sodium orthovanadate||Sodium orthovanadate is an alkaline phosphatase and (Na,K)-ATPase inhibitor with IC50 of 10 μM.|
|M3696||Rostafuroxin||Rostafuroxin is a novel antihypertensive agent developed as a selective inhibitor of Src-SH2 interaction with mutant adducin- and ouabain-activated Na,K-ATPase.|
|M3593||Ciclopirox ethanolamine||Ciclopirox ethanolamine (Ciclopirox olamine, HOE 296) is a broad-spectrum antifungal agent working as an iron chelator.|
|M3448||Esomeprazole Sodium||Esomeprazole Sodium is a sodium salt of esomeprazole that is a potent proton pump inhibitor with an IC50 of 0.076 mg/kg.|
|M2725||Golgicide A||Golgicide A is a potent and rapidly reversible GBF1 inhibitor.|
|M2474||BTB06584||BTB06584 is an IF1-dependent, selective inhibitor of the mitochondrial F1 Fo-ATPase.|
|M2459||Blebbistatin||Blebbistatin is a cell-permeable inhibitor for non muscle myosin II ATPase with IC50 of ~2 μM, does not inhibit myosin light chain kinase, inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly.|
|M2294||Brefeldin A||Brefeldin A is a lactone antibiotic and ATPase inhibitor for protein transport with IC50 of 0.2 μM in HCT 116 cells.|
|M2004||Omecamtiv mecarbil||Omecamtiv mecarbil (formerly CK-1827452) is a sarcomere-directed cardiac myosin activator for acute and chronic heart disease.|
|M1997||Oligomycin A||Oligomycin A is an inhibitor of mitochondrial ATP synthase and uncoupler of oxidative phosphorylation.|
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