NPS Allelix Corp.

A review with 196 referencesIn the last four years discovery of pharmacotherapeutic treatments for migraine headaches has received much attention.Since the patent literature was last reviewed in 1997 [1], advances have been made in the understanding of mechanism and pathophysiol. of migraine.Introduction of sumatriptan to the market has led to acceleration in research efforts towards finding safe and effective treatments for migraine.The importance of this field is evidenced by the number of compounds in clin. trials and by the number of patents filed in recent years.For example, besides sumatriptan, a second generation of three new drugs (naratriptan [2], zolmitriptan [3] and rizatriptan [4]) has entered the marketplace and few others are presently in clin. evaluation.In addition, classical drug design has yielded highly potent and selective ligands to target relevant receptor subtypes in migraine treatment.This article highlights and reviews the research advances published in patent literature between Jan. 1997 through Nov. 2000.The article is supplemented with selected references on design and development of novel agents with which to treat migraine and to study its mechanism and pathophysiol.Emphasis is made on serotonergic agents, namely serotonin (5-hydroxytryptamine, 5-HT) receptor subtype (5-HT_1D, 5-HT_1F and 5-HT₅) agonists, drug combinations (e.g., 5-HT_1D agonists with COX-2 inhibitors or NSAIDs), tachykinin receptor (NK1) antagonists and GABAergic agents.Also included are patents describing chem. entities that may be effective in migraine therapy based on their pharmacol. actions as anticonvulsants, LTD₄ receptor blocker agents and thromboxane inhibitors.By no means has any attempt been made to exhaustively review the literature; but rather, primary references along with citations to latest literature reviews have been included in each section.

A series of 5-alkyltryptamines (6) and the corresponding conformationally constrained analogues (8) have been synthesized. The structure activity relationships (SAR) at the 5-position of the indole skeleton and the ethylamine side chain have been studied. Functional activities were assessed using isolated rabbit saphenous vein. Potent, selective ligands were found (6e, Ki 2.5 nM, 5-HT1B/5-HT1D 125-fold) that have potential for treating acute migraine.