Nimodipine | Enzo Life Sciences ALX-550-277-G001 product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Enzo Life Sciences

other brands :

Stressgen, BioMol, Alexis Corporation, Assay Designs, Alexis

product type :

chemical

product name :

Nimodipine

catalog :

ALX-550-277-G001

quantity :

1 g

citations: 8

Reference
Kappelle A, Bravenboer B, Van Buren T, Traber J, Erkelens D, Gispen W. Amelioration by the Ca2+ antagonist, nimodipine of an existing neuropathy in the streptozotocin-induced, diabetic rat. Br J Pharmacol. 1993;108:780-5 pubmed
Formenti A, Arrigoni E, Mancia M. Low-voltage activated calcium channels are differently affected by nimodipine. Neuroreport. 1993;5:145-7 pubmed
Kappelle A, Biessels G, Bravenboer B, Van Buren T, Traber J, de Wildt D, et al. Beneficial effect of the Ca2+ antagonist, nimodipine, on existing diabetic neuropathy in the BB/Wor rat. Br J Pharmacol. 1994;111:887-93 pubmed
Fisher M, Grotta J. New uses for calcium channel blockers. Therapeutic implications. Drugs. 1993;46:961-75 pubmed
Triggle D, Rampe D. 1,4-Dihydropyridine activators and antagonists: structural and functional distinctions. Trends Pharmacol Sci. 1989;10:507-11 pubmed
Dolin S, Hunter A, Halsey M, Little H. Anticonvulsant profile of the dihydropyridine calcium channel antagonists, nitrendipine and nimodipine. Eur J Pharmacol. 1988;152:19-27 pubmed
Izquierdo I. Nimodipine and the recovery of memory. Trends Pharmacol Sci. 1990;11:309-10 pubmed
McCarthy R, TanPiengco P. Multiple types of high-threshold calcium channels in rabbit sensory neurons: high-affinity block of neuronal L-type by nimodipine. J Neurosci. 1992;12:2225-34 pubmed

product information

Product ID :

ALX-550-277

Catalog Number :

ALX-550-277-G001

Product Name :

Nimodipine

Product Type :

Biochemical

Size :

1 g

list of Pubmed id :

8467365, 8111001, 8019766, 7510613, 2694544, 2463174, 2203191, 1318957

Product Description :

Ca2+ channel antagonist. Highly potent at L-type channels. Block some low-voltage activated Ca2+ channels. Enhances memory in old or brain-damaged animals. Ameliorates experimental diabetic neuropathy in streptozotocin-induced diabetic rats. Vasodilator.

ALTnames :

1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-methoxyethyl-1-methylethyl ester

Purity :

≥99% (Assay)

Storage :

Ambient