Chemical structure of CAS 38176-02-2

(R)-Verapamil hydrochloride

In StockStarting at $559 for 5 mgPurity ≥ 99.48%
CAS No.38176-02-2
MDL No.N/A
MFC27H39ClN2O4
MW491.10
InChI KeyDOQPXTMNIUCOSY-HZPIKELBSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 mg99.48%$559In Stock
10 mg99.48%$999In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Dexverapamil hydrochloride is a hydrochloride salt formed from equimolar amounts of dexverapamil and hydrogen chloride. It competitively inhibits the multidrug resistance efflux pump P-glycoprotein (MDR-1, EC 3.6.3.44), enhancing the efficacy of antineoplastic drugs inactivated by MDR-1 mechanisms. It exhibits lower calcium antagonistic activity and toxicity compared to racemic verapamil hydrochloride. It functions as an EC 3.6.3.44 (xenobiotic-transporting ATPase) inhibitor and contains a dexverapamil(1+) ion. It is the enantiomer of (S)-verapamil hydrochloride.

CAS No.38176-02-2
Product Name(R)-Verapamil hydrochloride
Heavy Atom Count0Rotatable Bond Count0
Atom Stereo Count0Bond Stereo Count0
HBA0HBD0
TPSAN/ACharge0
Exact MassN/AComplexityN/A
pKaN/AXLogPN/A