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Home >> Signaling Pathways >> Membrane Transporter/Ion Channel >> ATPase

ATPase

ATPase is a class of enzymes that catalyze the decomposition of ATP into ADP and a free phosphate ion, including some co-transporters and pumps.

Products for  ATPase

  1. Cat.No. Product Name Information
  2. GC40434 (±)16-HETE Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. (±)16-HETE Chemical Structure
  3. GC13430 (-)-Blebbistatin (-)-Blebbistatin Chemical Structure
  4. GC41719 (R)-nitro-Blebbistatin (R)-nitro-Blebbistatin is a more stable form of (+)-blebbistatin, which is the inactive form of (-)-blebbistatin. (R)-nitro-Blebbistatin Chemical Structure
  5. GC41557 (S)-3'-amino Blebbistatin (S)-3'-amino Blebbistatin is a more stable and less phototoxic form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-3'-amino Blebbistatin Chemical Structure
  6. GC41484 (S)-3'-hydroxy Blebbistatin (S)-3'-hydroxy Blebbistatin is a more stable and less phototoxic form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-3'-hydroxy Blebbistatin Chemical Structure
  7. GC41091 (S)-Lansoprazole (S)-Lansoprazole is a proton pump inhibitor that irreversibly inhibits H+/K+-stimulated ATPase pumps in parietal cells (IC50 = 5.2 μM), inhibiting gastric acid secretion and increasing intragastric pH. (S)-Lansoprazole Chemical Structure
  8. GC41739 (S)-nitro-Blebbistatin (S)-nitro-Blebbistatin is a more stable form of (-)-blebbistatin, which is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (S)-nitro-Blebbistatin Chemical Structure
  9. GC46047 14-Anhydrodigitoxigenin A cardenolide 14-Anhydrodigitoxigenin Chemical Structure
  10. GC40453 16(R)-HETE

    Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.

     16(R)-HETE Chemical Structure
  11. GC40454 16(S)-HETE Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 16(S)-HETE Chemical Structure
  12. GC40455 17(R)-HETE Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 17(R)-HETE Chemical Structure
  13. GC40456 17(S)-HETE Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 17(S)-HETE Chemical Structure
  14. GC12469 2,3-Butanedione-2-monoxime 2,3-Butanedione-2-monoxime (Diacetyl monoxime), a myosin ATPase inhibitor, is a skeletal and cardiac muscle contraction inhibitor. 2,3-Butanedione-2-monoxime Chemical Structure
  15. GC49575 4-hydroxy Omeprazole sulfide A metabolite of omeprazole 4-hydroxy Omeprazole sulfide Chemical Structure
  16. GC18474 Acetyldigitoxin Acetyldigitoxin is cardiac glycoside and an inhibitor of the Na+/K+ ATPase with an IC50 value of 5 nM in isolated rat pinealocytes. Acetyldigitoxin Chemical Structure
  17. GC42827 Apoptolidin Apoptolidin is an apoptosis inducer originally isolated from Nocardiopsis bacteria. Apoptolidin Chemical Structure
  18. GC17225 ARL 67156 trisodium salt ARL67156 (FPL 67156) trisodium is a selective ecto-ATPase inhibitor. ARL 67156 trisodium salt Chemical Structure
  19. GC35421 ATP synthase inhibitor 1 ATP synthase inhibitor 1 is a potent inhibitor of c subunit of the F1/FO-ATP synthase complex, inhibits mitochondrial permeability transition pore (mPTP) opening, does not affect ATP levels. ATP synthase inhibitor 1 Chemical Structure
  20. GC10934 Bafilomycin C1 vacuolar H+-ATPases (V-ATPases) inhibitor Bafilomycin C1 Chemical Structure
  21. GC12302 Bafilomycin D vacuolar H+ ATPases (V-ATPases) inhibitor Bafilomycin D Chemical Structure
  22. GC14664 BHQ BHQ (DTBHQ), the indirect food additive, regulates the activity of 5-lipoxygenase as well as the activity of COX-2 (IC50=1.8 and 14.1 μM for 5-LO and COX-2, respectively) . BHQ Chemical Structure
  23. GC42965 Bongkrekic Acid

    An inhibitor of mitochondrial adenine nucleotide translocase

     Bongkrekic Acid Chemical Structure
  24. GC17683 Brefeldin A

    Brefeldin A (BFA) is a fungal macrocyclic lactone and a potent, reversible inhibitor of intracellular vesicle formation and protein trafficking between the endoplasmic reticulum (ER) and the Golgi apparatus.

     Brefeldin A Chemical Structure
  25. GC16833 BTB06584 F1F0 ATP synthases BTB06584 Chemical Structure
  26. GC49706 Cerberin A cardiac glycoside with cytotoxic and cardiac modulatory activities Cerberin Chemical Structure
  27. GC11120 Ciclopirox ethanolamine Ciclopirox ethanolamine (Ciclopirox ethanolamine) is a synthetic antifungal agent that can be used for superficial mycoses reseaech. Ciclopirox ethanolamine Chemical Structure
  28. GC10268 Cyclopiazonic acid

    sarcoplasmic reticulum Ca2+-ATPase inhibitor

     Cyclopiazonic acid Chemical Structure
  29. GC18583 D-α-Hydroxyglutaric Acid Over-produced in the human neurometabolic disease D-2-HGA D-α-Hydroxyglutaric Acid Chemical Structure
  30. GC43412 Desacetyl Bisacodyl Desacetyl bisacodyl (DAB) is an active metabolite of two stimulant laxatives, bisacodyl and sodium picosulfate. Desacetyl Bisacodyl Chemical Structure
  31. GC13108 Digoxin Na+/K+ ATPase pump inhibitor Digoxin Chemical Structure
  32. GC10395 Dynasore Dynasore, as a GTPase inhibitor, can rapidly and reversibly inhibit dynamin activity, which prevents endocytosis. Dynasore Chemical Structure
  33. GC18105 Enterostatin Enterostatin, human, mouse, rat is a pentapeptide that reduces fat intake. Enterostatin Chemical Structure
  34. GC48984 Esomeprazole An H+/K+-ATPase inhibitor Esomeprazole Chemical Structure
  35. GC33234 Gboxin An inhibitor of oxidative phosphorylation in cancer cells Gboxin Chemical Structure
  36. GC16585 Golgicide A

    GBF1 inhibitor, potent, reversible and highly specific

     Golgicide A Chemical Structure
  37. GC11448 Istaroxime Istaroxime Chemical Structure
  38. GC17786 Istaroxime hydrochloride Istaroxime hydrochloride Chemical Structure
  39. GC16167 K 858 K858 Racemic is an ATP-uncompetitive inhibitor of kinesin Eg5 with an IC50 of 1.3 μM. K 858 Chemical Structure
  40. GC47532 KUS121 A VCP modulator KUS121 Chemical Structure
  41. GC49640 Lansoprazole N-oxide A potential impurity found in bulk preparations of lansoprazole Lansoprazole N-oxide Chemical Structure
  42. GC11254 Lithium carbonate Na+/K+ ATPase pump inhibitor Lithium carbonate Chemical Structure
  43. GC14059 ML 240 ATP-competitive inhibitor of p97 ATPase ML 240 Chemical Structure
  44. GC11411 ML-7 hydrochloride A smooth muscle myosin light chain kinase inhibitor ML-7 hydrochloride Chemical Structure
  45. GC15858 MYK-461 MYK-461 (MYK461) is an orally active modulator of cardiac myosin, with IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively. MYK-461 Chemical Structure
  46. GC11587 Ochratoxin A

    endoplasmic reticulum ATP-dependent calcium pump activator

     Ochratoxin A Chemical Structure
  47. GC16859 Oligomycin A Oligomycin A is an inhibitor of ATP synthase, which inhibits the process taking place on mitochondria coupling membrane that depended on ATP and oxidative phosphorylation. Oligomycin A Chemical Structure
  48. GC16409 Oligomycin B mitochondrial F1FO ATP synthase inhibitor Oligomycin B Chemical Structure
  49. GC16221 Oligomycin C mitochondrial F1FO-ATP synthase inhibitor Oligomycin C Chemical Structure
  50. GC16533 Oligomycin Complex Oligomycin Complex, an antifungal antibiotic, is an inhibitor of H+-ATP-synthase. Oligomycin Complex Chemical Structure
  51. GC12832 Omecamtiv mecarbil Cardiac myosin activator Omecamtiv mecarbil Chemical Structure
  52. GC49663 Pantoprazole sulfone N-oxide A potential impurity found in bulk preparations of pantoprazole Pantoprazole sulfone N-oxide Chemical Structure
  53. GC45539 Pantoprazole-d6   Pantoprazole-d6 Chemical Structure
  54. GC12788 Paprotrain

    mitotic kinesin-like protein 2 (MKLP-2) inhibitor

     Paprotrain Chemical Structure
  55. GC45944 para-amino-Blebbistatin A more stable and less phototoxic form of (–)-blebbistatin with enhanced water solubility para-amino-Blebbistatin Chemical Structure
  56. GC11082 Paxilline Paxilline, a tremorogenic fungal alkaloid, potently inhibits large conductance Ca2+ and voltage-activated K+(BK)-type channels, IC50 is approximately 10nM, Ki=1.9nM.. Paxilline Chemical Structure
  57. GC17027 POM 1 POM 1 (Sodium polyoxotungstate) is a potent ecto-nucleoside triphosphate diphosphohydrolase (ENTPDase) inhibitor, with Ki values of 2.58 μM, 3.26 μM, and 28.8 μM for NTPDase 1 (CD39), NTPDase 3 and NTPDase 2 respectively. POM 1 Chemical Structure
  58. GC10371 PSB 06126 NTPDase 3 inhibitor PSB 06126 Chemical Structure
  59. GC13186 PSB 069 NTPDase inhibitor PSB 069 Chemical Structure
  60. GC49627 Rabeprazole sulfone A metabolite of rabeprazole Rabeprazole sulfone Chemical Structure
  61. GC10906 RBC8 Ral GTPase inhibitor RBC8 Chemical Structure
  62. GC11151 SCH 28080 H+,K+-ATPase inhibitor SCH 28080 Chemical Structure
  63. GC14368 Sodium Orthovanadate PTP inhibitor Sodium Orthovanadate Chemical Structure
  64. GC15418 TAK-438 Blocker of potassium-competitive acid TAK-438 Chemical Structure
  65. GC18005 Tenatoprazole proton pump inhibitor Tenatoprazole Chemical Structure
  66. GC25991 tetrathiomolybdate Tetrathiomolybdate (TM) is used in the clinic for the treatment of Wilson's disease by inducing dimerization of the metal-binding domain of the cellular copper efflux protein ATP7B (WLN4) through a unique sulfur-bridged Mo2S6O2 cluster. tetrathiomolybdate Chemical Structure
  67. GC11482 Thapsigargin

    Thapsigargin?is an inhibitor of the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase pump.

     Thapsigargin Chemical Structure
  68. GC49503 Thujopsene A sesquiterpene with diverse biological activities Thujopsene Chemical Structure
  69. GC61374 Vonoprazan Fumarate A selective and reversible proton pump inhibitor Vonoprazan Fumarate Chemical Structure
  70. GC49430 Wee1 Inhibitor Wee1 Inhibitor is a potent checkpoint Wee1 kinase inhibitor with an IC50 of 0.011 μM. Wee1 Inhibitor Chemical Structure

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