Verapamil hydrochloride

  • CAT Number: A000837
  • CAS Number: 152-11-4
  • Molecular Formula: C27H38N2O4.HCl
  • Molecular Weight: 491.07
  • Purity: ≥95%
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<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Verapamil hydrochloride ( CAS&nbsp;152-11-4)&nbsp;<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">is the hydrochloride form of&nbsp;Verapamil, which is a phenylalkylamine calcium channel blocking agent.&nbsp;Verapamil&nbsp;inhibits the transmembrane influx of extracellular&nbsp;calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents.</span></span></span></span></p>

Catalog Number A000837
CAS Number 152-11-4
Molecular Formula

C27H38N2O4.HCl

Purity 95%
Target Calcium Channel
Solubility >14.5mg/mL in DMSO
Storage Store at -20C
IUPAC Name 2-(3,4-dimethoxyphenyl)-5-[2-(3,4-dimethoxyphenyl)ethyl-methylamino]-2-propan-2-ylpentanenitrile;hydrochloride
InChI InChI=1S/C27H38N2O4.ClH/c1-20(2)27(19-28,22-10-12-24(31-5)26(18-22)33-7)14-8-15-29(3)16-13-21-9-11-23(30-4)25(17-21)32-6;/h9-12,17-18,20H,8,13-16H2,1-7H3;1H
InChIKey DOQPXTMNIUCOSY-UHFFFAOYSA-N
SMILES CC(C)C(CCCN(C)CCC1=CC(=C(C=C1)OC)OC)(C#N)C2=CC(=C(C=C2)OC)OC.Cl
Reference

<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">McTavish, Donna, and Eugene M. Sorkin. &quot;Verapamil.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Drugs</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;38.1 (1989): 19-76.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Singh, Bramah N., Gray Ellrodt, and C. Thomas Peter. &quot;Verapamil: a review of its pharmacological properties and therapeutic use.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Drugs</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;15.3 (1978): 169-197.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Wang, Feihu, et al. &quot;Synergistic effect of folate-mediated targeting and verapamil-mediated P-gp inhibition with paclitaxel-polymer micelles to overcome multi-drug resistance.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Biomaterials</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;32.35 (2011): 9444-9456.<br />
4.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Futscher, Bernard W., et al. &quot;Verapamil suppresses the emergence of P‐glycoprotein‐mediated multi‐drug resistance.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">International journal of cancer</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;66.4 (1996): 520-525.</span></span></span></span></p>

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