Name | 2-(3-methoxyphenyl)-2-[3-[2-(3-methoxyphenyl)ethyl-methylamino]propyl]tetradecanenitrile |
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Synonyms |
Anipamil
Anipamilum Anipamilum [Latin] 2-(3-((m-Methoxyphenethyl)methylamino)propyl)-2-(m-methoxyphenyl)tetradecanenitrile Anipamil [INN] EINECS 280-213-5 Anipamilo Anipamilo [Spanish] |
Description | Anipamil is a long-acting calcium channel blocker, used for the treatment of cardiovascular disease. |
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Related Catalog | |
In Vivo | Anipamil (40 mg, p.o.)-treated 2K-1C rabbits reveal absent or negligible intimal thickening and a decrease of postnatal-type SMC from the underlying media. Anipamil inhibits the growth of SMC accompanied by the expression of SM-MyHC in all SMC, ie, the appearance of a more differentiated cell phenotype compared to control cultures[1]. In the arrhythmic assay, anipamil (1.0 mg/kg + 0.10 mg/kg/min infusion, n=8 or 5.0 mg/kg + 0.50 mg/kg/min infusion, n=12) reduces VT but not VF[2]. In rats with subtotal (five-sixths) nephrectomy treated with anipamil (0.5 mg/kg/day, p.o.), the mortality is less, and the mean arterial blood pressure is also more well controlled, and the serum creatinine concentration is lower than control group. The anipamil (2 mg/kg/day)-treated group exhibits significantly greater protection of renal function than does the hydralazine-treated group for the same level of blood pressure control[3]. |
Animal Admin | Preliminary studies are performed to determine the anipamil dose response. Anipamil is mixed with food to give a dose of 0.5, 2 or 5 mg/kg/day. One week after five-sixths nephrectomy, rats are paired according to renal function, blood pressure and body weight. Rats are then pair-fed and receive either the long-acting calcium channel blocker anipamil (2 mg/kg/day in food, n=20) or placebo (n=20). |
References |
Density | 0.983g/cm3 |
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Boiling Point | 641.9ºC at 760 mmHg |
Molecular Formula | C34H52N2O2 |
Molecular Weight | 520.78900 |
Flash Point | 342ºC |
Exact Mass | 520.40300 |
PSA | 45.49000 |
LogP | 8.73088 |
Index of Refraction | 1.517 |