
ATPase
ATPases are enzymes that catalyze the decomposition of ATP into ADP and a free phosphate ion, a reaction that releases energy used to drive many processes within the cell, including active transport across membranes. ATPases play crucial roles in maintaining cellular homeostasis, pH balance, and ion gradients. Dysfunctions in ATPase activity are associated with diseases such as heart failure, hypertension, and neurodegeneration. At CymitQuimica, we provide high-quality ATPase inhibitors and modulators to support your research in cellular energetics, membrane transport, and disease pathology.
Found 93 products of "ATPase"
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Tiludronate disodium
CAS:<p>Tiludronate disodium: osteoclast inhibitor for metabolic bone disorder research.</p>Formula:C7H7ClNa2O6P2SPurity:>99.99% - >99.99%Color and Shape:Fine White To Off-White Crystalline PowderMolecular weight: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>Formula:C17H15N3OPurity:99.24%Color and Shape:SolidMolecular weight:277.32Leminoprazole
CAS:<p>Leminoprazole is an orally available H+,K(+)-ATPase inhibitor that protects gastric mucosal cells from various cellular damages.</p>Formula:C19H23N3OSPurity:99.08% - 99.56%Color and Shape:SolidMolecular weight:341.47NC-1300-B
CAS:<p>NC-1300-B inhibits H(+)-K(+)-ATPase and is used in the study of gastric ulcers.</p>Formula:C17H19N3OSPurity:99.50%Color and Shape:SolidMolecular weight: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>Formula:C21H22N2O2Purity:99.89%Color and Shape:SolidMolecular weight: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>Formula:C25H25N3O8S2Purity:97.32%Color and Shape:SolidMolecular weight: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>Formula:C19H17Cl2NO3Purity:98.44% - 99.74%Color and Shape:SolidMolecular weight: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>Formula:C12H18N5O14P3Color and Shape:SolidMolecular weight: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>Formula:C26H32Cl2N4O4SPurity:99.86%Color and Shape:SolidMolecular weight: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>Formula:C21H22N2O3SColor and Shape:SolidMolecular weight:382.48Suloctidil HCl
CAS:<p>Suloctidil HCl is a peripheral vascular dilator.</p>Formula:C20H36ClNOSColor and Shape:SolidMolecular weight: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>Formula:C28H35N3O5Color and Shape:SolidMolecular weight: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>Formula:C23H22F2N4O3Color and Shape:SolidMolecular weight:440.44

