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 92 productos para "ATPasa".
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Trichlormethiazide
CAS:Trichlormethiazide (Naqua) is a short-acting, 3-dichloromethyl derivative of hydrochlorothiazide, belonging to the class of thiazide diuretics.Fórmula:C8H8Cl3N3O4S2Pureza:98.8% - 99.54%Forma y color:White SolidPeso molecular:380.66Gboxin
CAS:Gboxin is an inhibitor of oxidative phosphorylation that targets glioblastoma,inhibits the activity of F0F1 ATP synthase, with antitumour activity.Fórmula:C22H33ClN2O2Pureza:99.96% - >99.99%Forma y color:SolidPeso molecular:392.96Ref: TM-T15373
1mg42,00€2mg55,00€1mL*10mM (DMSO)87,00€5mg88,00€10mg126,00€25mg245,00€50mg385,00€100mg612,00€200mg850,00€Diazoxide
CAS:Diazoxide (Proglycem) is a benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies.Fórmula:C8H7ClN2O2SPureza:99% - 99.83%Forma y color:SolidPeso molecular:230.67ATP synthase inhibitor 1
CAS:ATP synthase inhibitor 1 is an inhibitor of the c subunit of the F1/FO-ATP synthase complex.Fórmula:C17H18ClN3O3S2Pureza:99.83%Forma y color:SolidPeso molecular:411.93Suloctidil
CAS:Suloctidil is a peripheral vasodilator that was formerly used in the management of peripheral and cerebral vascular disorders.Fórmula:C20H35NOSPureza:99.75% - >99.99%Forma y color:White SolidPeso molecular:337.56Tolbutamide
CAS:Tolbutamide (HLS 831) is a sulphonylurea hypoglycemic agent with actions and uses similar to those of CHLORPROPAMIDE.Fórmula:C12H18N2O3SPureza:99.80% - 99.93%Forma y color:White Crystalline PowderPeso molecular:270.35Prilocaine hydrochloride
CAS:Prilocaine HCl: local amino amide anesthetic, blocks voltage-gated sodium channels in neurons, inhibits Na+ permeability.Fórmula:C13H21ClN2OPureza:99.97%Forma y color:SolidPeso molecular:256.77Ciliobrevin D
CAS:Ciliobrevin D is a AAA+ ATPase motor cytoplasmic dynein inhibitor.Fórmula:C17H8Cl3N3O2Pureza:98.09%Forma y color:Orange SolidPeso molecular:392.62Ref: TM-T14965
1mg60,00€2mg87,00€5mg133,00€1mL*10mM (DMSO)148,00€10mg203,00€25mg401,00€50mg592,00€100mg827,00€Fenbufen
CAS:Fenbufen (Lederfen) is a non-steroidal anti-inflammatory drug used primarily to treat inflammation in osteoarthritis, ankylosing spondylitis, and tendinitis.Fórmula:C16H14O3Pureza:98.35% - 98.74%Forma y color:White SolidPeso molecular:254.28Transdermal Peptide Disulfide
CAS:TD 1 peptide, an 11-amino acid, binds ATP1B1's C-terminus, enhancing transdermal drug delivery.Fórmula:C40H64N14O16S2Pureza:98%Forma y color:SolidPeso molecular:1061.1517(S)-HETE
CAS:17(S)-HETE is an arachidonic acid metabolite generated via the CYP450 pathway. 17(S)-HETE acts as an allosteric activator of CYP450 1B1 and an ATPase inhibitor.Fórmula:C20H32O3Forma y color:Transparent LiquidPeso molecular:320.47Prilocaine acetate
Prilocaine acetate, an amino amide compound, functions as a Na/K-ATPase inhibitor, exhibiting neurotoxic effects [1] [2].Fórmula:C15H24N2O3Forma y color:SolidPeso molecular:280.36(±)16-HETE
CAS:Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.473LC-MF-4
LC-MF-4 is a selective FGFR3 PROTAC degrader with a DC50 of 30.89 nM in KMS-11 cells. It inhibits the metabolic functions of FGFR3-TACC3 fusion-positive cancers by reducing ATP synthesis and suppressing mitochondrial biogenesis genes. LC-MF-4 demonstrates potent anti-tumor activity in the Ba/F3-FGFR3-TACC3 xenograft mouse model and is applicable for research on FGFR3 gene mutation cancers such as bladder cancer and urothelial carcinoma (UC).Forma y color:Odour SolidNSC799462
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.Fórmula:C30H32F2N6O3SForma y color:SolidPeso molecular:594.68P259
P259 is a Drp1-Mff inhibitor that selectively impedes the interaction between Drp1 and Mff, thereby differentiating physiological fission from pathological fission. It leads to mitochondrial elongation and impairs mitochondrial function and motility. P259 reduces ATP levels in the brain, alters mitochondrial structure, induces behavioral defects in wild-type mice, and shortens the lifespan of Huntington's disease (HD) model mice.Forma y color:Odour SolidBMS 199264
CAS:BMS 199264 hydrochlorid a inhibitor of mitochondrial F1F0 ATP hydrolase, thus preventing ATP reduction to ameliorate cardiac necrosis during ischemia.Fórmula:C26H31ClN4O4SPureza:99.83%Forma y color:SolidPeso molecular:531.07SC 4453
CAS:SC 4453 is a digoxin analog and a cardiac glycoside derivative.Fórmula:C41H64N2O12Forma y color:SolidPeso molecular:776.965ATP Synthesis-IN-1
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.Forma y color:Odour SolidCyclocreatine
CAS:Cyclocreatine, a creatine analogue and substrate for creatine kinase, inhibits creatine metabolism and prostate cancer cell proliferation.Fórmula:C5H9N3O2Pureza:99.86%Forma y color:White SolidPeso molecular:143.14
