ATPasi
Le ATPasi sono enzimi che catalizzano la decomposizione dell'ATP in ADP e un ione fosfato libero, una reazione che rilascia energia utilizzata per guidare molti processi all'interno della cellula, incluso il trasporto attivo attraverso le membrane. Le ATPasi svolgono un ruolo cruciale nel mantenimento dell'omeostasi cellulare, dell'equilibrio del pH e dei gradienti ionici. Le disfunzioni dell'attività delle ATPasi sono associate a malattie come l'insufficienza cardiaca, l'ipertensione e la neurodegenerazione. Presso CymitQuimica, forniamo inibitori e modulatori di ATPasi di alta qualità per supportare la tua ricerca in energetica cellulare, trasporto di membrana e patologia delle malattie.
Trovati 100 prodotti di "ATPasi"
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Dicirenone
CAS:Dicirenone (SC26304) inhibits the Mineralocorticoid receptor (MR), aldosterone regulation of the urinary K+:Na+ ratio, and aldosterone binding to renalFormula:C26H36O5Purezza:99.1%Colore e forma:SolidPeso molecolare:428.56ATPase-IN-2
CAS:ATPase-IN-2: ATPase inhibitor (IC50 = 0.9μM), also blocks C. difficile toxin B (AC50 = 30.91μM). Used in ATP research.Formula:C22H20N2O4Colore e forma:SolidPeso molecolare:376.41Istaroxime hydrochloride
CAS:Istaroxime hydrochloride (PST2744 hydrochloride) is a Na+/K+-ATPase inhibitor and SERCA 2 activator, and is a novel positive inotropic compound.Formula:C21H33ClN2O3Colore e forma:SolidPeso molecolare:396.95FSBA hydrochloride
CAS:FSBA hydrochloride(5'-p-Fluorosulfonylbenzoyladenosine) is an ATP analogue serving as an affinity probe for the ATP site of Na/K-ATPase.Formula:C17H17ClFN5O7SPurezza:97.96%Colore e forma:SolidPeso molecolare:489.86Istaroxime
CAS:Istaroxime is an effective inhibitor of Na+, K+-ATPase (IC50: 0.11 μM).Formula:C21H32N2O3Purezza:98%Colore e forma:SolidPeso molecolare:360.49Leminoprazole
CAS:<p>Leminoprazole is an orally available H+,K(+)-ATPase inhibitor that protects gastric mucosal cells from various cellular damages.</p>Formula:C19H23N3OSPurezza:99.08% - 99.56%Colore e forma:SolidPeso molecolare:341.47Tiludronate disodium
CAS:Tiludronate disodium: osteoclast inhibitor for metabolic bone disorder research.Formula:C7H7ClNa2O6P2SPurezza:>99.99% - >99.99%Colore e forma:Fine White To Off-White Crystalline PowderPeso molecolare:362.57SCH28080
CAS: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 potentFormula:C17H15N3OPurezza:99.24%Colore e forma:SolidPeso molecolare:277.32FR-167356
CAS:<p>FR-167356 inhibits a3 isoform H⁺-ATPase (IC50: 170-370 nM), targeting osteoclasts, kidneys, macrophages; reduces B16-F10 bone metastasis.</p>Formula:C19H17Cl2NO3Purezza:98.44% - 99.74%Colore e forma:SolidPeso molecolare:378.25AGN-201904
CAS: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.Formula:C25H25N3O8S2Purezza:97.32%Colore e forma:SolidPeso molecolare:559.61SKF96067
CAS:SKF96067 is a reversible gastric H+/K+-ATPase inhibitor that can induce relaxation of human airway smooth muscle in vitro.Formula:C21H22N2O2Purezza:99.89%Colore e forma:SolidPeso molecolare:334.41NC-1300-B
CAS:NC-1300-B inhibits H(+)-K(+)-ATPase and is used in the study of gastric ulcers.Formula:C17H19N3OSPurezza:99.50%Colore e forma:SolidPeso molecolare:313.42BMS-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>Formula:C26H32Cl2N4O4SPurezza:99.86%Colore e forma:SolidPeso molecolare:567.53Ro 18-5364
CAS:Ro 18-5364 is a potent inhibitor of the gastric (H+ + K+)-ATPase with an apparent Ki of 0.1 μM at pH 6.Formula:C22H25N3O3SPurezza:98%Colore e forma:SolidPeso molecolare:411.523′-Acetate-ATP
CAS:3’-Acetate-ATP, an analogue of ATP and its acetylation product, exhibits maximum ultraviolet absorption at 259 nm in neutral aqueous solutions.Formula:C12H18N5O14P3Colore e forma:SolidPeso molecolare:549.22ATP 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>Formula:C21H22N2O3SColore e forma:SolidPeso molecolare:382.48Hsp90-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>Formula:C28H35N3O5Colore e forma:SolidPeso molecolare:493.595Suloctidil HCl
CAS:Suloctidil HCl is a peripheral vascular dilator.Formula:C20H36ClNOSColore e forma:SolidPeso molecolare:374.02Antimalarial agent 7
Antimalarial agent 7 is a potent and effective inhibitor of PfATP4. Antimalarial agent 7 has potential for the study of the human plasmodium falciparum.Formula:C23H22F2N4O3Colore e forma:SolidPeso molecolare:440.44Vonoprazan fumarate
CAS:<p>Vonoprazan fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase.</p>Formula:C17H16FN3O2S·C4H4O4Purezza:99.16% - 99.98%Colore e forma:SolidPeso molecolare:461.46
