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ATPase

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 (R)-N-(2-Hydroxyethyl)-N,2-dimethyl-8-((5-methylchroman-4-yl)amino)imidazo[1,2-a]pyridine-6-carboxamide 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 (S)-6-Methoxy-2-(((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)sulfinyl)-1H-benzo[d]imidazole 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 Diacetyl 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 4-Isopropoxy-N-(2-methylquinolin-8-yl)benzamide 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.
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