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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. |
| CSN11956 | Sodium Orthovanadate | 13721-39-6 | Sodium orthovanadate is an alkaline phosphatase and (Na,K)-ATPase inhibitor with IC50 of 10 μM. |
| CSN17177 | PF-03716556 | 928774-43-0 | PF 03716556 is a selective H+,K+ ATPase inhibitor with pIC50 value of 6.009. |
| 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. |
| CSN23546 | Diacetyl Monoxime | 57-71-6 | Diacetyl Monoxime is an inhibitor of skeletal muscle myosin-II. |
| 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. |
| 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. |
| 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 | BHQ | 88-58-4 | BHQ is a selective inhibitor of sarco-endoplasmic reticulum Ca2+-ATPase (SERCA). |