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ATPase

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ATPase

Chemical Structure Cat. No. Product Name CAS No.
Suloctidil Chemical Structure
 BCP24317 Suloctidil 54767-75-8
Suloctidil is a new drug that is currently being evaluated in many clinical trials for use in dementia and thrombotic disorders Target： Effect of suloctidil on Na+/K+ ATPase activity and on membrane fluidity in rat brain synaptosomes.
(+)-SJ733 Chemical Structure
 BCP45645 (+)-SJ733 1424799-20-1
(+)-SJ733 is an inhibitor of plasmodium ATP4, leading to rapid clearance in vivo by inducing physical changes in infected, treated red cells.
MitMAB Chemical Structure
 BCP45369 MitMAB 1119-97-7
MitMAB, an organic building block and cationic surfactant, is a dynamin inhibitor that inhibits the GTPase activity of dynamin I (Ki = 940 nM; IC50 = 3.1 μM).
NSC 617145 Chemical Structure
 BCP41809 NSC 617145 203115-63-3
NSC 617145 is a werner syndrome helicase inhibitor with IC50 value of 250 nM. It is used as an antineoplastic.
ATP synthase inhibitor 1 Chemical Structure
 BCP37578 ATP synthase inhibitor 1 1023043-30-2
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.
BRITE 338733 Chemical Structure
 BCP21036 BRITE 338733 503105-88-2
BRITE 338733 is a novel ATPase inhibitor.
PST2774 oxalate Chemical Structure
 BCP11905 PST2774 oxalate 203737-94-4
PST2774 oxalate, also known as Istaroxime oxalate, is a Na-K ATPase inhibitor.
PST2286 Chemical Structure
 BCP08064 PST2286 26629-41-4
PST2286, also known as 17-Hydroxydigitoxigenin, is a rostafuroxin metabolite.
AHAS inhibitor Chemical Structure
 BCP10634 AHAS inhibitor 219793-45-0
AHAS inhibitor is a novel acetohydroxyacid synthase(AHAS) inhibitor, a promising drug target against Mycobacterium tuberculosis (MTB).
Chlorpropamide Chemical Structure
 BCP09162 Chlorpropamide 94-20-2
Chlorpropamide is a sulfonylurea class drug for type 2 diabetes mellitus.
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