ATPase | Membrane Transporter/Ion Channel| CSNpharm

ATPase

ATPase
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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.

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