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ATPase
| 货号 | 产品名 | CAS号 | 信息 |
|---|---|---|---|
| CSN21089 | Thapsigargin | 67526-95-8 | Thapsigargin is a naturally occurring tumor promoter derived from the plant Thapsia garganica. Potent inhibitor of sarco-endoplasmic reticulum Ca2+-ATPases. Causes ER stress; can be used to induce autophagy in mammalian cells. |
| CSN22045 | Soraprazan | 261944-46-1 | Soraprazan is a reversible and fast-acting inhibitor of gastric H+/K+ ATPase. |
| CSN11956 | Sodium orthovanadate | 13721-39-6 | Sodium orthovanadate is an alkaline phosphatase and (Na,K)-ATPase inhibitor with IC50 of 10 μM. |
| CSN22053 | SKF96067 | 115607-61-9 | SKF96067 is a reversible inhibitor of the gastric H+/K+-ATPase. |
| CSN24637 | SCH28080 | 76081-98-6 | SCH 28080 is an inhibitor of H+, K+-ATPase with IC50 of 20 nM. |
| CSN21796 | Picoprazole | 78090-11-6 | Picoprazole is a selective inhibitor of H+/K+-ATPase with IC50 of 3.1 ± 0.4 μM. |
| CSN17177 | PF-3716556 | 928774-43-0 | PF 03716556 is a selective H+,K+ ATPase inhibitor with pIC50 value of 6.009. |
| CSN40150 | Paxilline | 57186-25-1 | Paxilline is a toxic, tremorgenic diterpene indole polycyclic alkaloid molecule produced by Penicillium paxilli. It works as BK channels inhibitor and SERCA inhibitor. |
| CSN27252 | KM91104 | 304481-60-5 | KM91104 is a specific v-ATPase inhibitor. It specifically targets the interaction between v-ATPase subunit a3 and subunit B2. |
| CSN22553 | Ilaprazole | 172152-36-2 | Ilaprazole inhibited TOPK activities with high affinity and selectivity. |
| CSN10985 | FCCP | 370-86-5 | FCCP is a potent uncoupler of oxidative phosphorylation in mitochondria that disrupts ATP synthesis by transporting protons across cell membranes. |
| CSN12672 | Esomeprazole | 119141-88-7 | Esomeprazole is a proton-pump inhibitor which reduces stomach acid. |
| CSN21631 | Enterostatin(human,mouse,rat) | 117830-79-2 | Enterostatin is a pentapeptide that reduces fat intake and can bind to the β-subunit of F1-ATPase. |
| CSN24507 | EN6 | 1808714-73-9 | EN6 covalently targets cysteine 277 in the ATP6V1A subunit of the lysosomal the vacuolar H+ ATPase (v-ATPase). It is a small-molecule in vivo activator of autophagy. |
| CSN20881 | Diphyllin | 22055-22-7 | Diphyllin, a natural arylnaphthalene, is potent inhibitor of vacuolar H(+)-ATPase (V-ATPase) that inhibits lysosomal acidification in osteoclasts. |
| CSN23546 | Biacetyl monoxime | 57-71-6 | Diacetyl Monoxime is an inhibitor of skeletal muscle myosin-II. |
| CSN26260 | Concanamycin A | 80890-47-7 | Concanamycin A is a macrolide antibiotic and a specific vacuolar type H+-ATPase (V-ATPase) inhibitor. |
| CSN20382 | Citreoviridin | 25425-12-1 | Citreoviridin is a mycotoxin isolated from several Penicillium species that has been shown to inhibit the mitochondrial ATP synthetase system. |
| CSN16740 | Ciclopirox olamine | 41621-49-2 | Ciclopirox Olamine is a synthetic antifungal agent for topical dermatologic treatment of superficial mycoses. |
| CSN18949 | Chebulinic acid | 18942-26-2 | Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation and H+ K+-ATPase activity. |
| CSN25372 | CDN1163 | 892711-75-0 | CDN1163 is an allosteric sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) activator that improves Ca2+ homeostasis. CDN1163 attenuates diabetes and metabolic disorders. |
| CSN18115 | BTB06584 | 219793-45-0 | BTB06584 is an IF1-dependent selective inhibitor of the mitochondrial F1Fo-ATPase. |
| CSN10482 | Brefeldin A | 20350-15-6 | Brefeldin A inhibits protein translocation from the endoplasmic reticulum (ER) to the Golgi apparatus reversibly, can be used to induce autophagy in mammalian cells. |
| CSN23530 | 2,5-Di-tert-butylhydroquinone | 88-58-4 | BHQ is a selective inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase (SERCA). |
| CSN18154 | Linaprazan | 248919-64-4 | AZD0865 inhibits gastric H+,K+-ATPase by K+-competitive binding. |
| CSN19865 | Blebbistatin | 674289-55-5 | (-)-Blebbistatin is a cell-permeable inhibitor for non muscle myosin II ATPase with IC50 of ~2 μM in cell-free assays, does not inhibit myosin light chain kinase, inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. |
