Dexverapamil is the R-enantiomer of the calcium channel blocker verapamil. Dexverapamil competitively inhibits the multidrug resistance efflux pump P-glycoprotein (MDR-1), thereby potentially increasing the effectiveness of a wide range of antineoplastic drugs which are inactivated by MDR-1 mechanisms.
Molekulargewicht:
454.6
CAS Nummer:
[38321-02-7]
Formel:
C27H38N2O4
Target-Kategorie:
Others
T69317
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