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Manidipine dihydrochloride

SKU: orb1223733

Description

A dihydropyridine type calcium channel blocker that is used as an antihypertensive.Hypertension Approved.

Images & Validation

Key Properties

CAS Number89226-75-5
MW683.6213
Purity>98% (HPLC)
FormulaC35H40Cl2N4O6
SMILES[H+].[H+].[Cl-].[Cl-].COC(=O)C1=C(C)NC(C)=C(C1C1=CC(=CC=C1)[N+]([O-])=O)C(=O)OCCN1CCN(CC1)C(C1=CC=CC=C1)C1=CC=CC=C1
TargetCalcium Channel
Solubility10 mM in DMSO

Bioactivity

In Vivo
Animal model: IFNAR-/-mice. Dosage: 10 mg/kg. Administration: Intraperitoneal injection (i.p.), b. i. d. at day 4, day 5. Result: Exhibited a modest, but statistically significant increase in the survival rate of lethal Animal model with SFTSV infection, significantly reduced viral titers in the spleen and kidney. Animal model: Adult female BALB/c mice (age, 4 weeks). Dosage: 25 mg/kg. Administration: Intraperitoneal injection (i.p.), b. i. d. for 2 days, then daily for 19 days. Result: Reduced the mortality rate from 73% to 20%, significantly reduced the viral load in infected mice while remarkably alleviated brain damage phenomena. Had little effect on peripheral JEV infection, which indicated that manidipine protected the mice against JEV-induced lethality by decreasing the viral load in the brain. Animal model: 8-week-old male Wistar rats. Dosage: 3 mg/kg. Administration: Intragastric gavage (i. g.), once per day for 7 d. Result: Prevented isoproterenol-induced left ventricular hypertrophy (2.26±0.02 g/kg; p<0.01) as isoproterenol increased left ventricular weight (2.40±0.04 g/kg; p<0.01). Inhibited expression of mRNA of ANP (0.9-fold of the control value; p<0.01), collagen types I (1.1-fold; p<0.01) and type III (1.6-fold; p<0.01), and fibronectin (1.1-fold; p<0.01).

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

CV-4093

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    C35H40Cl2N4O6

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Manidipine dihydrochloride (orb1223733)

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500 mg
50 mg
$ 90.00
100 mg
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200 mg
$ 160.00