ATPasa
Las ATPasas son enzimas que catalizan la descomposición del ATP en ADP y un ion fosfato libre, una reacción que libera energía utilizada para impulsar muchos procesos dentro de la célula, incluido el transporte activo a través de las membranas. Las ATPasas juegan un papel crucial en el mantenimiento de la homeostasis celular, el equilibrio del pH y los gradientes de iones. Las disfunciones en la actividad de las ATPasas están asociadas con enfermedades como insuficiencia cardíaca, hipertensión y neurodegeneración. En CymitQuimica, ofrecemos inhibidores y moduladores de ATPasa de alta calidad para apoyar su investigación en energética celular, transporte de membranas y patología de enfermedades.
Se han encontrado 93 productos de "ATPasa"
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Prilocaine hydrochloride
CAS:<p>Prilocaine HCl: local amino amide anesthetic, blocks voltage-gated sodium channels in neurons, inhibits Na+ permeability.</p>Fórmula:C13H21ClN2OPureza:99.97%Forma y color:Needles White Or Off White Crystalline PowderPeso molecular:256.77Tolbutamide
CAS:<p>Tolbutamide (HLS 831) is a sulphonylurea hypoglycemic agent with actions and uses similar to those of CHLORPROPAMIDE.</p>Fórmula:C12H18N2O3SPureza:99.80% - 99.93%Forma y color:White Crystalline PowderPeso molecular:270.35Clorsulon
CAS:<p>Clorsulon (L631529) is utilized for the treatment of Fasciola hepatica infections in calves and sheep.</p>Fórmula:C8H8Cl3N3O4S2Pureza:99.66% - 99.87%Forma y color:White To Off-White Crystalline PowderPeso molecular:380.66Fenbufen
CAS:<p>Fenbufen (Lederfen) is a non-steroidal anti-inflammatory drug used primarily to treat inflammation in osteoarthritis, ankylosing spondylitis, and tendinitis.</p>Fórmula:C16H14O3Pureza:98.35% - 98.46%Forma y color:White SolidPeso molecular:254.28Ciclopirox olamine
CAS:<p>Ciclopirox olamine is a broad-spectrum antifungal agent with additional antibacterial and anti-inflammatory activities.</p>Fórmula:C14H24N2O3Pureza:99.16% - >99.99%Forma y color:White To Yellow Solid Solid Particulate/PowderPeso molecular:268.35Chlorpropamide
CAS:<p>Chlorpropamide (Diabinese) is a sulfonylurea hypoglycemic agent used in the treatment of non-insulin-dependent diabetes mellitus not responding to dietary</p>Fórmula:C10H13ClN2O3SPureza:98.90%Forma y color:Crystals From Dil Ethanol Physical Description White Crystalline Powder With A Slight Odor (Ntp 1992)Peso molecular:276.74Trichlormethiazide
CAS:<p>Trichlormethiazide (Naqua) is a short-acting, 3-dichloromethyl derivative of hydrochlorothiazide, belonging to the class of thiazide diuretics.</p>Fórmula:C8H8Cl3N3O4S2Pureza:98.8% - 99.54%Forma y color:SolidPeso molecular:380.66Suloctidil
CAS:<p>Suloctidil is a peripheral vasodilator that was formerly used in the management of peripheral and cerebral vascular disorders.</p>Fórmula:C20H35NOSPureza:99.75% - >99.99%Forma y color:SolidPeso molecular:337.56Diazoxide
CAS:<p>Diazoxide (Proglycem) is a benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies.</p>Fórmula:C8H7ClN2O2SPureza:99% - 99.83%Forma y color:SolidPeso molecular:230.67ATP synthase inhibitor 1
CAS:<p>ATP synthase inhibitor 1 is an inhibitor of the c subunit of the F1/FO-ATP synthase complex.</p>Fórmula:C17H18ClN3O3S2Pureza:99.83%Forma y color:SolidPeso molecular:411.93Permethrin
CAS:<p>Permethrin (NRDC-143) is a pyrethroid insecticide commonly used in the treatment of LICE INFESTATIONS and SCABIES.</p>Fórmula:C21H20Cl2O3Pureza:99.37% - 99.54%Forma y color:Colorless Crystals To A Viscous Liquid; Color White To Pale Yellow Permethrin Is A Pale Brown Liquid Relatively Water Insoluble Used As An InsecticidePeso molecular:391.29Ciliobrevin D
CAS:<p>Ciliobrevin D is a AAA+ ATPase motor cytoplasmic dynein inhibitor.</p>Fórmula:C17H8Cl3N3O2Pureza:98.09%Forma y color:SolidPeso molecular:392.62Gboxin
CAS:<p>Gboxin is an inhibitor of oxidative phosphorylation that targets glioblastoma,inhibits the activity of F0F1 ATP synthase, with antitumour activity.</p>Fórmula:C22H33ClN2O2Pureza:99.96% - >99.99%Forma y color:SolidPeso molecular:392.96Prilocaine acetate
<p>Prilocaine acetate, an amino amide compound, functions as a Na/K-ATPase inhibitor, exhibiting neurotoxic effects [1] [2].</p>Fórmula:C15H24N2O3Forma y color:SolidPeso molecular:280.3614-Anhydrodigitoxigenin
CAS:<p>14-Anhydrodigitoxigenin, a digitoxin derivative, inhibits guinea pig heart Na+/K+-ATPase by 15% at 10 μM concentration.</p>Fórmula:C23H32O3Forma y color:SolidPeso molecular:356.506S-WJM992
<p>S-WJM992 (compound 10ahb) serves as an antiparasitic agent, effectively inhibiting ATPase activity in high [Na+] environments. It also significantly counteracts parasites resistant to PfATP4 inhibitors. Additionally, S-WJM992 acts as a potential transmission blocker by impeding gamete development and halting the transmission of parasites to mosquitoes during blood feeding.</p>Fórmula:C22H18ClFN6O3Forma y color:SolidPeso molecular:468.87BMS 199264
CAS:<p>BMS 199264 hydrochlorid a inhibitor of mitochondrial F1F0 ATP hydrolase, thus preventing ATP reduction to ameliorate cardiac necrosis during ischemia.</p>Fórmula:C26H31ClN4O4SPureza:99.83%Forma y color:SoildPeso molecular:531.07Transdermal Peptide Disulfide
CAS:<p>TD 1 peptide, an 11-amino acid, binds ATP1B1's C-terminus, enhancing transdermal drug delivery.</p>Fórmula:C40H64N14O16S2Pureza:98%Forma y color:SolidPeso molecular:1061.15NSC799462
<p>NSC799462, a triazole inhibitor, specifically targets p97 ATPase, exerting its effect by binding to a designated site on the p97 enzyme. This interaction induces localized structural alterations in p97, effectively inhibiting its ATPase activity with an IC 50 value of 15 nM.</p>Fórmula:C30H32F2N6O3SForma y color:SolidPeso molecular:594.68Ouabagenin
CAS:<p>Ouabagenin, a naturally occurring LXR ligand with selective agonist activity, functions as an EC 3.6.3.9 (Na(+)/K(+)-transport ATPase) inhibitor [1] [2].</p>Fórmula:C23H34O8Forma y color:SolidPeso molecular:438.51(±)17-HETE
CAS:<p>Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.473PK095
CAS:<p>PK095 is a proprietary compound in the guanidine - based F1F0-ATPase inhibitor family.</p>Fórmula:C20H18N4O2SPureza:96.84%Forma y color:SoildPeso molecular:378.45Cyclocreatine
CAS:<p>Cyclocreatine, a creatine analogue and substrate for creatine kinase, inhibits creatine metabolism and prostate cancer cell proliferation.</p>Fórmula:C5H9N3O2Pureza:99.864%Forma y color:SolidPeso molecular:143.14SC 4453
CAS:<p>SC 4453 is a digoxin analog and a cardiac glycoside derivative.</p>Fórmula:C41H64N2O12Forma y color:SolidPeso molecular:776.965Chlorpropylate
CAS:<p>Chlorpropylate is an insecticide.</p>Fórmula:C17H16Cl2O3Pureza:98%Forma y color:SolidPeso molecular:339.21ATP Synthesis-IN-1
<p>ATP Synthesis-IN-1 (Compound 4), a quinoline derivative, potently inhibits PA ATP synthesis with an IC50 of 11.1μg/mL and exhibits antibacterial properties.</p>Forma y color:Odour Solid(S)-PF-03716556
CAS:<p>(S)-PF-03716556 can be used as an acid pump inhibitor for the treatment of disease conditions mediated by acid pump inhibitory activity.</p>Fórmula:C22H26N4O3Pureza:99.8% - 99.91%Forma y color:SoildPeso molecular:394.47Digoxigenin Monodigitoxoside
CAS:<p>Digoxigenin monodigitoxoside is a cardiac glycoside metabolite of digoxin and a Na+/K+ ATPase inhibitor.</p>Fórmula:C29H44O8Forma y color:SolidPeso molecular:520.663(±)16-HETE
CAS:<p>Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.47317(S)-HETE
CAS:<p>Arachidonic acid and its CYP450 metabolite, 17(S)-HETE, regulate kidney electrolytes; 17(S)-HETE reduces proximal tubule ATPase activity by 70% at 2 μM.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.473A 80915A
CAS:<p>A80915A: Semi-naphthoquinone antibiotic, blocks gastric (H(+)-K+)-ATPase; potency varies with enzyme conformation; K+ reduces binding rate.</p>Fórmula:C26H31Cl3O5Forma y color:SolidPeso molecular:529.885-Hydroxydecanoic acid
CAS:<p>5-Hydroxydecanoic acid is a selective ATP-sensitive K+ (KATP) channel blocker (IC50 of ~30 μM). 5-Hydroxydecanoic acid is a substrate for mitochondrial outer membrane acyl-CoA synthetase and has antioxidant activity.</p>Fórmula:C10H20O3Pureza:99.24%Forma y color:SolidPeso molecular:188.26L-Palmitoylcarnitine
CAS:<p>L-Palmitoylcarnitine (L-PC) inhibits Na/K ATPase activity and potentiates fibrinolytic enzymes and tPA to inhibit thrombosis.</p>Fórmula:C23H45NO4Pureza:97% - 99.81%Forma y color:SolidPeso molecular:399.61Anti-ATP7B Antibody (4W208)
<p>Anti-ATP7B Antibody (4W208) is an antibody targeting ATP7B. Anti-ATP7B Antibody (4W208) can be used in ELISA, IHC, IF, FCM.</p>Forma y color:Odour LiquidAnti-ATP7B Antibody (7M703)
<p>Anti-ATP7B Antibody (7M703) is an antibody targeting ATP7B. Anti-ATP7B Antibody (7M703) can be used in ELISA, IF, FCM.</p>Forma y color:Odour Liquid(+)-SJ733
CAS:<p>(+)-SJ733 (SJ000557733) is a potent Na+-ATPase PfATP4 inhibitor with antimalarial activity for the study of malaria.</p>Fórmula:C24H16F4N4O2Pureza:99.21%Forma y color:SolidPeso molecular:468.4Luciferase, firefly
CAS:<p>Luciferase, firefly is a reporter gene in cellular imaging studies to quantify target gene expression levels and measure intracellular ATP content,</p>Pureza:98%Forma y color:SolidPeso molecular:N/ATenatoprazole
CAS:<p>Tenatoprazole (TU-199), a prodrug of the proton pump inhibitor (PPI) class, can inhibit proton transport (IC50: 3.2 μM).</p>Fórmula:C16H18N4O3SPureza:99.57%Forma y color:White Crystalline PowderPeso molecular:346.4BRITE-338733
CAS:<p>BRITE-338733 is a novel inhibitor of ATPase. BRITE 338733 inhibits the expression of RecA in bacteria (IC50=4.7 μM) for the bacterial infections treatment.</p>Fórmula:C27H35N3O2Pureza:99.85%Forma y color:SolidPeso molecular:433.59Tirofiban hydrochloride monohydrate
CAS:<p>Tirofiban（MK383） hydrochloride monohydrate is a non-peptide glycoprotein IIb/IIIa antagonist. Cost-effective and quality-assured.</p>Fórmula:C22H39ClN2O6SPureza:98.81% - >99.99%Forma y color:White SolidPeso molecular:495.07Tegoprazan
CAS:<p>Tegoprazan is an orally active, highly selective gastric H+/K+-ATPase inhibitor.Cost-effective and quality-assured.</p>Fórmula:C20H19F2N3O3Pureza:98.22%Forma y color:SolidPeso molecular:387.38Apoptozole
CAS:<p>Apoptozole (Apoptosis Activator VII) is an inhibitor of the ATPase domain of Hsc70 and Hsp70, and can induce apoptosis.</p>Fórmula:C33H25F6N3O3Pureza:99.75%Forma y color:SolidPeso molecular:625.56Eniporide
CAS:<p>Eniporide is a Na(+)/H(+) exchange inhibitor.</p>Fórmula:C14H16N4O3SPureza:96.78% - 99.26%Forma y color:SolidPeso molecular:320.37Mitiglinide Calcium
CAS:<p>Mitiglinide Calcium (KAD-1229) is a blood glucose-lowering drugs, stimulating insulin secretion by closing the ATP-sensitive K+ channels in pancreatic beta-</p>Fórmula:(C19H24NO3)2·CaPureza:99.83%Forma y color:White Crystal PosderPeso molecular:668.88Esomeprazole Magnesium
CAS:<p>Esomeprazole Magnesium (NEXIUM) is the S-isomer of omeprazole, can reduce gastric acid secretion with selective and irreversible proton pump inhibitor activity.</p>Fórmula:C34H36MgN6O6S2Pureza:98.76% - 99.73%Forma y color:SolidPeso molecular:713.12Rabeprazole sodium
CAS:<p>Rabeprazole sodium treats stomach ulcers and Zollinger-Ellison syndrome, blocking ATPase in gastric cells.</p>Fórmula:C18H20N3NaO3SPureza:98% - 99.912%Forma y color:White Or Off White Crystalline PowderPeso molecular:381.42DHQ
CAS:<p>DHQ (2,3-dihydroxy-quinoxalin) is an inducer of ATPase activity that of Herpes Simplex Virus thymidine kinase.</p>Fórmula:C8H6N2O2Pureza:99.89%Forma y color:SolidPeso molecular:162.15CB-5083
CAS:<p>CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor ( IC50=11 nM).</p>Fórmula:C24H23N5O2Pureza:95.95% - 99.92%Forma y color:SolidPeso molecular:413.47FCCP
CAS:<p>FCCP (Trifluoromethoxy carbonylcyanide phenylhydrazone) is an oxidative phosphorylation (OXPHOS) inhibitor and mitochondrial proton carrier uncoupler.</p>Fórmula:C10H5F3N4OPureza:98% - 99.65%Forma y color:White SolidPeso molecular:254.17Chloroprocaine
CAS:<p>Chloroprocaine: Na,K-ATPase inhibitor, IC50=13 mM, local anesthetic.</p>Fórmula:C13H19ClN2O2Forma y color:SolidPeso molecular:270.76Blebbistatin
CAS:<p>Blebbistatin ((±)-Blebbistatin) is a non-muscle myosin II (NMII)-selective and non-muscle myosin heavy chain 9 (MYH9)-specific inhibitor.Cost-effective and quality-assured.</p>Fórmula:C18H16N2O2Pureza:99.88% - 99.97%Forma y color:Bright Yellow SolidPeso molecular:292.33Rabeprazole Sulfide
CAS:<p>Rabeprazole Sulfide (Rabeprazole Related Compound E) is an antiulcer drug in the class of proton pump inhibitors.</p>Fórmula:C18H21N3O2SPureza:99.34% - 99.78%Forma y color:Off-White Crystalline PowderPeso molecular:343.44Rbin-1
CAS:<p>Rbin-1 (Ribozinoindole-1) is a potent,specific inhibitor of eukaryotic ribosome biogenesis.</p>Fórmula:C13H12N4SPureza:99.83%Forma y color:SolidPeso molecular:256.33Omecamtiv mecarbil
CAS:<p>Omecamtiv mecarbil (CK-1827452) has been used in trials studying the treatment and basic science of Heart Failure, Echocardiogram, Pharmacokinetics, Chronic</p>Fórmula:C20H24FN5O3Pureza:98% - 99.23%Forma y color:SolidPeso molecular:401.43Chloroprocaine hydrochloride
CAS:<p>Chloroprocaine hydrochloride (Chloroprocaine HCl) is a local anesthetic during surgical procedures.</p>Fórmula:C13H20Cl2N2O2Pureza:99.65%Forma y color:White Crystalline PowderPeso molecular:307.22NPD8733
CAS:<p>NPD8733 is an inhibitor of cancer cell-enhanced fibroblast migration. It specifically binds to valosin-containing protein (VCP)/p97.</p>Fórmula:C18H15NO4Pureza:98.48%Forma y color:SolidPeso molecular:309.32D-α-Hydroxyglutaric acid disodium
CAS:<p>D-α-Hydroxyglutaric acid disodium (Disodium (R)-2-Hydroxyglutarate) is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases with Ki of 0.628 mM.</p>Fórmula:C5H6Na2O5Pureza:97.16%Forma y color:SolidPeso molecular:192.08Parimifasor
CAS:<p>Parimifasor (LYC30937) is an immunomodulator, with anti-inflammatory activity.</p>Fórmula:C18H11Cl2F4N5OPureza:96.77% - 98.97%Forma y color:SolidPeso molecular:460.21Revaprazan hydrochloride
CAS:<p>Revaprazan hydrochloride (YH1885) is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.</p>Fórmula:C22H24ClFN4Pureza:99.62% - 99.91%Forma y color:SolidPeso molecular:398.9Transdermal Peptide Disulfide Acetate
<p>Transdermal Peptide acetate(888486-23-5 free base) (TD 1 (peptide) acetate) is a 11-amino acid peptide, binds toNa+/K+-ATPase beta-subunit (ATP1B1), and mainly</p>Fórmula:C42H68N14O18S2Pureza:99.97%Forma y color:SolidPeso molecular:1121.2(-)-Blebbistatin
CAS:<p>(-)-Blebbistatin ((S)-(-)-Blebbistatin) is an S enantiomer of blebbistatin. It is a potent and selective myosin II inhibitor with IC50 ranging from 0.5 to 5 μM.</p>Fórmula:C18H16N2O2Pureza:99.38% - 99.61%Forma y color:SolidPeso molecular:292.33Vonoprazan fumarate
CAS:<p>Vonoprazan fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase.</p>Fórmula:C17H16FN3O2S·C4H4O4Pureza:99.16% - 99.98%Forma y color:SolidPeso molecular:461.46BTS
CAS:<p>BTS (N-Tosylbenzylamine) is a potent inhibitor of Ca2+-stimulated myosin S1 ATPase (IC50 : 5 μM) .</p>Fórmula:C14H15NO2SPureza:99.45%Forma y color:White Crystalline SolidPeso molecular:261.34Prilocaine
CAS:<p>Prilocaine (NSC-40027) is a local anesthetic of the amino amide type, which acts on the sodium channel on the neuronal membrane and limits the spread of</p>Fórmula:C13H20N2OPureza:98.49%Forma y color:Needles SolidPeso molecular:220.31NSC 617145
CAS:<p>NSC 617145 (NSC617145) is an inhibitor of WRN helicase that inhibits the ATPase, but not exonuclease, activity of WRN helicase in a concentration-dependent</p>Fórmula:C13H10Cl4N2O4Pureza:99.72%Forma y color:SolidPeso molecular:400.04Rostafuroxin
CAS:<p>Rostafuroxin (PST 2238) has been used in trials studying the treatment of Essential Hypertension.</p>Fórmula:C23H34O4Pureza:99.08% - >99.99%Forma y color:SolidPeso molecular:374.51KM 91104
CAS:<p>KM 91104 is a cell permeable inhibitor of V-ATPase. KM91104 specifically targets the interaction between V-ATPase subunit A3 and subunit B2.</p>Fórmula:C14H12N2O4Pureza:99.04%Forma y color:SolidPeso molecular:272.26PF 03716556
CAS:<p>PF 03716556 (PF-3716556) , an effective and specific P-CAB (potassium-competitive acid blocker), is utilized for the treatment of gastroesophageal reflux</p>Fórmula:C22H26N4O3Pureza:99.79% - 99.85%Forma y color:SolidPeso molecular:394.47Tetradifon
CAS:<p>Tetradifon is a broad-spectrum organochlorine acaricide that inhibits mitochondrial OSCP, blocking energy production (IC50=4.5-27nmoL/mg) with oligomycin-like effects.</p>Fórmula:C12H6Cl4O2SPureza:99.84%Forma y color:Yellowish Odorless OilPeso molecular:356.05Ro18-5362
CAS:<p>Ro18-5362 is the less active prodrug of Ro 18-5364.</p>Fórmula:C22H25N3O2SPureza:98%Forma y color:SolidPeso molecular:395.52FSBA hydrochloride
CAS:<p>FSBA hydrochloride(5'-p-Fluorosulfonylbenzoyladenosine) is an ATP analogue serving as an affinity probe for the ATP site of Na/K-ATPase.</p>Fórmula:C17H17ClFN5O7SPureza:97.96%Forma y color:SolidPeso molecular:489.86Dicirenone
CAS:<p>Dicirenone (SC26304) inhibits the Mineralocorticoid receptor (MR), aldosterone regulation of the urinary K+:Na+ ratio, and aldosterone binding to renal</p>Fórmula:C26H36O5Pureza:99.1%Forma y color:SolidPeso molecular:428.56Bifenazate
CAS:<p>Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.</p>Fórmula:C17H20N2O3Pureza:99.62%Forma y color:Solid CrystallinePeso molecular:300.35Istaroxime hydrochloride
CAS:<p>Istaroxime hydrochloride (PST2744 hydrochloride) is a Na+/K+-ATPase inhibitor and SERCA 2 activator, and is a novel positive inotropic compound.</p>Fórmula:C21H33ClN2O3Forma y color:SolidPeso molecular:396.95Azeloprazole
CAS:<p>Azeloprazole, a proton pump inhibitor, is used potentially for the treatment of gastroesophageal reflux disease (GERD).</p>Fórmula:C22H27N3O4SPureza:98%Forma y color:SolidPeso molecular:429.53RS 029
CAS:<p>RS 029 is a nitroimidazole that has been exhibited to significantly inhibit (Na+K+) ATP-ase activity.</p>Fórmula:C13H16N6O6Pureza:98%Forma y color:SolidPeso molecular:352.3FCPT
CAS:<p>FCPT is an ATP competitive kinesin-5 inhibitor.</p>Fórmula:C17H13FN2SPureza:98%Forma y color:SolidPeso molecular:296.36Laurinterol
CAS:<p>Laurinterol is an antimicrobial from the marine alga Laurencia okamurai.</p>Fórmula:C15H19BrOForma y color:SolidPeso molecular:295.21Istaroxime oxalate
CAS:<p>Istaroxime (PST-2744) is a positive inotrope that inhibits Na+/K+ ATPase, raising intracellular sodium and calcium levels.</p>Fórmula:C23H34N2O7Forma y color:SolidPeso molecular:450.53Istaroxime
CAS:<p>Istaroxime is an effective inhibitor of Na+, K+-ATPase (IC50: 0.11 μM).</p>Fórmula:C21H32N2O3Pureza:98%Forma y color:SolidPeso molecular:360.49Tiludronate disodium
CAS:<p>Tiludronate disodium: osteoclast inhibitor for metabolic bone disorder research.</p>Fórmula:C7H7ClNa2O6P2SPureza:>99.99% - >99.99%Forma y color:Fine White To Off-White Crystalline PowderPeso molecular:362.57SCH28080
CAS:<p>SCH28080 is a reversible and K+-competitive inhibitor of gastric H+/K+-ATPase with an IC50 value of 20 nM (rabbit microsomal membrane).SCH28080 is a potent</p>Fórmula:C17H15N3OPureza:99.24%Forma y color:SolidPeso molecular:277.32Leminoprazole
CAS:<p>Leminoprazole is an orally available H+,K(+)-ATPase inhibitor that protects gastric mucosal cells from various cellular damages.</p>Fórmula:C19H23N3OSPureza:99.08% - 99.56%Forma y color:SolidPeso molecular:341.47NC-1300-B
CAS:<p>NC-1300-B inhibits H(+)-K(+)-ATPase and is used in the study of gastric ulcers.</p>Fórmula:C17H19N3OSPureza:99.50%Forma y color:SolidPeso molecular:313.42SKF96067
CAS:<p>SKF96067 is a reversible gastric H+/K+-ATPase inhibitor that can induce relaxation of human airway smooth muscle in vitro.</p>Fórmula:C21H22N2O2Pureza:99.89%Forma y color:SolidPeso molecular:334.41AGN-201904
CAS:<p>AGN-201904 is a proton pump inhibitor, an omeprazole prodrug, which delays aging and may be used for the prevention and treatment of peptic ulcers.</p>Fórmula:C25H25N3O8S2Pureza:97.32%Forma y color:SolidPeso molecular:559.61FR-167356
CAS:<p>FR-167356 inhibits a3 isoform H⁺-ATPase (IC50: 170-370 nM), targeting osteoclasts, kidneys, macrophages; reduces B16-F10 bone metastasis.</p>Fórmula:C19H17Cl2NO3Pureza:98.44% - 99.74%Forma y color:SolidPeso molecular:378.253′-Acetate-ATP
CAS:<p>3’-Acetate-ATP, an analogue of ATP and its acetylation product, exhibits maximum ultraviolet absorption at 259 nm in neutral aqueous solutions.</p>Fórmula:C12H18N5O14P3Forma y color:SolidPeso molecular:549.22BMS-199264 hydrochloride
CAS:<p>BMS-199264 hydrochloride is selective inhibitor of mitochondrial F1F0 ATP hydrolase,inhibit decline of ATP and myocardial necrosis during myocardial ischemia.</p>Fórmula:C26H32Cl2N4O4SPureza:99.86%Forma y color:SolidPeso molecular:567.53ATP synthase inhibitor 2
CAS:<p>ATP synthase inhibitor 2 blocks P. aeruginosa ATP synthase; IC50=10 μg/mL, fully inhibits at 128 μg/mL.</p>Fórmula:C21H22N2O3SForma y color:SolidPeso molecular:382.48Suloctidil HCl
CAS:<p>Suloctidil HCl is a peripheral vascular dilator.</p>Fórmula:C20H36ClNOSForma y color:SolidPeso molecular:374.02Hsp90-IN-38
CAS:<p>Hsp90-IN-38 (compound 20m) is an inhibitor of HSP90 (heat shock protein). It demonstrates a strong binding affinity to HSP90 with a Kd of 87 nM. The compound inhibits ATPase activity with an IC50 of 0.13 μM. Hsp90-IN-38 also shows inhibitory effects on HCT116, MCF-7, SKBr3, K562, and A549 cells with IC50 values of 0.187, 0.072, 0.105, 0.403, and 0.031 μM, respectively.</p>Fórmula:C28H35N3O5Forma y color:SolidPeso molecular:493.595Antimalarial agent 7
<p>Antimalarial agent 7 is a potent and effective inhibitor of PfATP4. Antimalarial agent 7 has potential for the study of the human plasmodium falciparum.</p>Fórmula:C23H22F2N4O3Forma y color:SolidPeso molecular:440.44
