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Verapamil HCl(CP-16533-1)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Verapamil HCl(CP-16533-1)图片
CAS NO:152-11-4
规格:≥98%
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议
1g电议
2g电议
5g电议
10g电议
25g电议
50g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)491.06
FormulaC27H38N2O4.HCl
CAS No.152-11-4
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 98 mg/mL (199.6 mM)
Water: 50 mg/mL (101.8 mM)
Ethanol: 12 mg/mL (24.4 mM)
Other infoChemical Name: 2-(3,4-dimethoxyphenyl)-5-[2-(3,4-dimethoxyphenyl)ethyl-methylamino]-2-propan-2-ylpentanenitrile hydrochloride
InChi Key: DOQPXTMNIUCOSY-UHFFFAOYSA-N
InChi Code: 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
SMILES Code: N#CC(C(C)C)(C1=CC=C(OC)C(OC)=C1)CCCN(CCC2=CC=C(OC)C(OC)=C2)C.[H]Cl
SynonymsCP-16533-1; Lekoptin; Izoptin; CP16533-1; CP 16533-1; (±)-Verapamil hydrochloride; Isoptine, Isoptin, Verapamil HCl, Verapamil, Calan, Cordilox, Dexverapamil, Falicard, Finoptin, Hydrochloride, Iproveratril,
实验参考方法
In Vitro

In vitro activity: The enzyme hydrolase activity of recombinant CES2 is substantially inhibited by diltiazem and verapamil (Ki = 0.25 ± 0.02 and 3.84 ± 0.99μM, respectively).


Cell Assay: Cells (1×105) are treated with 10 nM Bortezomib and/or 70 μM Verapamil for 16 hours and incubated for another 4 hours with Alamar-Blue. Activity of the mitochondrial dehydrogenase results in conversion of the coloring, which is followed by measurement of the absorption using a spectrophotometer.

In VivoVerapamil confers an anti-arrhythmic effect via calcium influx inhibition, inhibition of oxygen consumption and accompanied by preservation of Cx43 protein in rat heart.
Animal modelRats
Formulation & DosageAdult male Sprague-Dawley (SD) rats (250–350 g) are used. Verapamil (1 mg/kg) is injected i.v. into a femoral vein 10 min prior to ischemia. A sham group undergoes the same surgical procedures, except the suture underneath the LAD is left untied. In another series of experiment, arrhythmia is induced by Bay K8644, an L-type calcium channel agonist, at a dose of 0.1 mg/kg given i.v. into the FV. Verapamil (1 mg/kg) is administered 10 min prior to Bay K8644. All injections are performed within 30 sec
ReferencesDrug Metab Pharmacokinet. 2013;28(6):468-74; PLoS One. 2013 Aug 12;8(8):e71567.