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Norverapamil hydrochloride

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Catalog No. T16339Cas No. 67812-42-4
Alias D591 hydrochloride, (±)-Norverapamil hydrochloride

Norverapamil hydrochloride (D591 hydrochloride) ((±)-Norverapamil hydrochloride) is an N-demethylated metabolite of Verapamil and it is an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor.

Norverapamil hydrochloride

Norverapamil hydrochloride

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Purity: 99.47%
Catalog No. T16339Alias D591 hydrochloride, (±)-Norverapamil hydrochlorideCas No. 67812-42-4
Norverapamil hydrochloride (D591 hydrochloride) ((±)-Norverapamil hydrochloride) is an N-demethylated metabolite of Verapamil and it is an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor.
Pack SizePriceAvailabilityQuantity
1 mg29 €In Stock
5 mg107 €In Stock
10 mg187 €In Stock
25 mg315 €In Stock
50 mg471 €In Stock
100 mg658 €In Stock
500 mg1.377 €In Stock
1 mL x 10 mM (in DMSO)112 €In Stock
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Purity:99.47%
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Product Introduction

Bioactivity
Description
Norverapamil hydrochloride (D591 hydrochloride) ((±)-Norverapamil hydrochloride) is an N-demethylated metabolite of Verapamil and it is an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor.
In vitro
Norverapamil inhibits macrophage-induced tolerance and attains serum levels comparable to verapamil. Both verapamil and its primary metabolite, Norverapamil, are identified as mechanism-based inhibitors and substrates of CYP3A, exhibiting non-linear pharmacokinetics clinically. Furthermore, ((±)-Norverapamil hydrochloride) proves as effective as verapamil in inhibiting tolerance and killing intracellular M. tuberculosis in monotherapy, matching its efficacy against isoniazid and rifampicin tolerance [1][3].
In vivo
Norverapamil hydrochloride (9 mg/kg; p.o.) exhibits a terminal half-life of 9.4 hours, an AUC of 260 ng ml−1 h, and a Cmax of 41.6 ng/mL[4].
AliasD591 hydrochloride, (±)-Norverapamil hydrochloride
Chemical Properties
Molecular Weight477.04
FormulaC26H37ClN2O4
Cas No.67812-42-4
SmilesCl.COc1ccc(CCNCCCC(C#N)(C(C)C)c2ccc(OC)c(OC)c2)cc1OC
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 50 mg/mL (104.81 mM)
DMSO: 31 mg/mL (64.98 mM)
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.0963 mL10.4813 mL20.9626 mL104.8130 mL
5 mM0.4193 mL2.0963 mL4.1925 mL20.9626 mL
10 mM0.2096 mL1.0481 mL2.0963 mL10.4813 mL
20 mM0.1048 mL0.5241 mL1.0481 mL5.2407 mL
50 mM0.0419 mL0.2096 mL0.4193 mL2.0963 mL
H2O
1mg5mg10mg50mg
100 mM0.0210 mL0.1048 mL0.2096 mL1.0481 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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