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Inhibitors
| Cat.No. | Name | Information |
|---|---|---|
| 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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