1. Membrane Transporter/Ion Channel Neuronal Signaling
  2. Calcium Channel
  3. Manidipine

Manidipine is a calcium channel blocker that is used clinically as an antihypertensive.

At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Manidipine dihydrochloride) usually boasts enhanced water solubility and stability.

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Manidipine Chemical Structure

Manidipine Chemical Structure

CAS No. : 89226-50-6

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Description

Manidipine is a calcium channel blocker that is used clinically as an antihypertensive. Target: Calcium Channel Manidipine is a dihydropyridine calcium antagonist, which causes systemic vasodilation by inhibiting the voltage-dependent calcium inward currents in smooth muscle cells. Manidipine was well tolerated in clinical trials, with most adverse effects related to vasodilation [1]. Manidipine is a lipophilic, third-generation dihydropyridine calcium channel antagonist with a high degree of selectivity for the vasculature, thereby inducing marked peripheral vasodilation with negligible cardiodepression. manidipine represents a first-line treatment option for patients with essential mild-to-moderate hypertension [2]. Manidipine has neutral effects on glucose and lipid metabolism and is generally well tolerated. Manidipine thus represents a first-line option for lowering BP in patients with mild-to-moderate hypertension [3].

Clinical Trial
Molecular Weight

610.70

Formula

C35H38N4O6

CAS No.
SMILES

O=C(C1=C(C)NC(C)=C(C(OC)=O)C1C2=CC=CC([N+]([O-])=O)=C2)OCCN3CCN(C(C4=CC=CC=C4)C5=CC=CC=C5)CC3

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Please store the product under the recommended conditions in the Certificate of Analysis.

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Manidipine
Cat. No.:
HY-B0419
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