(±)-Methoxy<wbr/>verapamil (hydrochloride)

(±)-Methoxyverapamil (hydrochloride)

CAT N°: 24270
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From 48.00 40.80

(±)-Methoxyverapamil is a phenylalkylamine L-type calcium channel blocker and methoxy derivative of verapamil (Item No. 14288).{38991} (±)-Methoxyverapamil blocks recombinant rat L-type calcium channels expressed in tsA201 cells with IC50 values of 782 and 8,000 nM at holding potentials of 10 and -60 mV, respectively. It blocks maitotoxin-induced calcium influx in NIH3T3 fibroblasts (IC50 = 16 ?M) and inhibits histamine-induced acid secretion by primary enriched guinea pig parietal cells (IC50 = 10.9 ?M).{38992,38993} (±)-Methoxyverapamil binds to rat myocardial membranes (IC50 = 16 nM) and inhibits electrically-stimulated contractions in rat right myocardial ventricular strips (EC50 = 1.95 ?M).{38994} In conscious, ovariectomized, post-partum rats, it decreases blood pressure by 30 mm Hg and induces 60% inhibition of uterine contractions when administered at doses of 204 and 324 ?g/kg, respectively.{38995}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • ?-[3-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]propyl]-3,4,5-trimethoxy-?-(1-methylethyl)-benzeneacetonitrile, monohydrochloride
  • Correlated keywords
    • 16662-47-8 56949-75-8 NSC274966 Procorum D600 D-600 Algocor Methoxy-verapamil ts-A201 NIH-3T3
  • Product Overview:
    (±)-Methoxyverapamil is a phenylalkylamine L-type calcium channel blocker and methoxy derivative of verapamil (Item No. 14288).{38991} (±)-Methoxyverapamil blocks recombinant rat L-type calcium channels expressed in tsA201 cells with IC50 values of 782 and 8,000 nM at holding potentials of 10 and -60 mV, respectively. It blocks maitotoxin-induced calcium influx in NIH3T3 fibroblasts (IC50 = 16 ?M) and inhibits histamine-induced acid secretion by primary enriched guinea pig parietal cells (IC50 = 10.9 ?M).{38992,38993} (±)-Methoxyverapamil binds to rat myocardial membranes (IC50 = 16 nM) and inhibits electrically-stimulated contractions in rat right myocardial ventricular strips (EC50 = 1.95 ?M).{38994} In conscious, ovariectomized, post-partum rats, it decreases blood pressure by 30 mm Hg and induces 60% inhibition of uterine contractions when administered at doses of 204 and 324 ?g/kg, respectively.{38995}

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