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Results for "

CP-16533-1

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

3

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-14275
    Verapamil
    40+ Cited Publications

    (±)-Verapamil; CP-16533-1

    		 Calcium Channel P-glycoprotein Cytochrome P450 Metabolic Disease Cancer
    Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research .
    Verapamil
  • HY-A0064
    Verapamil hydrochloride
    40+ Cited Publications

    (±)-Verapamil hydrochloride; CP-16533-1 hydrochloride

    		 Calcium Channel P-glycoprotein Cytochrome P450 Cardiovascular Disease
    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 .
    Verapamil hydrochloride
  • HY-A0064S1
    Verapamil-d6 hydrochloride

    (±)-Verapamil-d6 hydrochloride; CP-16533-1-d6 hydrochloride

    		 Isotope-Labeled Compounds Cardiovascular Disease
    Verapamil-d6 (CP-16533-1-d6) hydrochloride is the deuterium labled Verapamil (hydrochloride) (HY-A0064). 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 .
    Verapamil-d6 hydrochloride
  • HY-A0064S
    Verapamil-d3 hydrochloride

    (±)-Verapamil-d3 hydrochloride; CP-16533-1-d3 hydrochloride

    		 Isotope-Labeled Compounds Calcium Channel P-glycoprotein Cytochrome P450 Cardiovascular Disease
    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[1][2][3].
    Verapamil-d3 hydrochloride
  • HY-A0064R
    Verapamil hydrochloride (Standard)

    (±)-Verapamil hydrochloride (Standard); CP-16533-1 hydrochloride (Standard)

    		 Calcium Channel P-glycoprotein Cytochrome P450 Cardiovascular Disease Cancer
    Verapamil (hydrochloride) (Standard) is the analytical standard of Verapamil (hydrochloride). This product is intended for research and analytical applications. 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 .
    Verapamil hydrochloride (Standard)
  • HY-14275S1
    Verapamil-d7

    (±)-Verapamil-d7; CP-16533-1-d7

    		 Isotope-Labeled Compounds Calcium Channel P-glycoprotein Cytochrome P450 Metabolic Disease Cancer
    Verapamil-d7 is the deuterium labeled Verapamil (HY-14275). Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research .
    Verapamil-d7

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