Levemopamil

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{{Drugbox | Verifiedfields = changed | verifiedrevid = 477242123 | IUPAC_name = (2S)-3-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]-2-phenylpropyl 3,4,5-trimethoxybenzoate | image = Levemopamil.svg | width = 250 | CAS_number = 88864-40-0 | ATC_prefix = none | PubChem = 65870 | ChemSpiderID = 59287 | UNII = 0F5N573A2Y | KEGG = D08112 | ChEMBL = 2104050 | C=29 | H=37 | N=1 | O=7 | smiles = COc1cc(cc(c1OC)OC)CCN(C)C[C@@H](COC(=O)c2cc(c(c(c2)OC)OC)OC)c3ccccc3 | StdInChI = 1S/C29H37NO7/c1-30(18-17-20-11-9-8-10-12-20)19-21(28-22-13-15-23(31-2)16-14-22)29(36)37-27-25(34-4)24(33-3)21-26(35-5)27/h8-16,21H,17-19H2,1-7H3/t21-/m0/s1 | StdInChIKey = ZQXQXKZQJQZKJH-NRFANRHFSA-N }}

Levemopamil is a pharmaceutical compound that belongs to the class of calcium channel blockers. It is a stereoisomer of emopamil, which is known for its vasodilatory effects. Levemopamil is primarily investigated for its potential use in treating cardiovascular conditions such as hypertension and angina pectoris.

Pharmacology[edit | edit source]

Levemopamil functions by inhibiting the influx of calcium ions through L-type calcium channels in the smooth muscle cells of the cardiovascular system. This action results in the relaxation of vascular smooth muscle, leading to vasodilation and a subsequent decrease in blood pressure. The reduction in peripheral vascular resistance also decreases the workload on the heart, which can be beneficial in conditions like angina.

Clinical Applications[edit | edit source]

While levemopamil has shown promise in preclinical studies, its clinical applications are still under investigation. It is not yet approved for widespread clinical use, and further studies are needed to fully understand its efficacy and safety profile in humans.

Side Effects[edit | edit source]

As with other calcium channel blockers, potential side effects of levemopamil may include:

Research and Development[edit | edit source]

Research on levemopamil is ongoing, with studies focusing on its pharmacokinetics, pharmacodynamics, and potential therapeutic applications. The compound's stereochemistry is of particular interest, as the different isomers may exhibit varying degrees of biological activity.

Also see[edit | edit source]


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