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Verapamil-d3 hydrochloride
Biological Activity：Verapamil-d3 ((±)-Verapamil-d3) hydrochloride is the deuterium labeled Verapamil hydrochloride. Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil hydrochloride also inhibits CYP3A4. Verapamil hydrochloride has the potential for high blood pressure, heart arrhythmias and angina research[2][3].
Research Area：Cardiovascular Disease
Targets：Calcium Channel|P-glycoprotein|Cytochrome P450
Related Small Molecules:Benidipine hydrochloride;SR9186;AMG-208;CaV1.3 antagonist-1;14-Deoxyandrographolide;(Rac)-MEM 1003;CYP1B1-IN-1;CYP2C9/CYP2C19-IN-1;Glaucine;Efonidipine hydrochloride monoethanolate;Biricodar;L-Ascorbic acid sodium salt;Brompheniramine-d6 maleate;Hypericin;MRS 1523;Nilvadipine;P-gp inhibitor 4;Lercanidipine;CP-060;Galeterone;Sinapine thiocyanate;Anipamil-d25 hydrochloride;Ranitidine
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