Article ID Journal Published Year Pages File Type
1398055 European Journal of Medicinal Chemistry 2009 10 Pages PDF
Abstract

A series of bicyclic analogues having indan and tetrahydronaphthalene templates in the A-region were designed as conformationally constrained analogues of our previously reported potent TRPV1 antagonists (1, 3). The activities for rat TRPV1 of the conformationally restricted analogues were moderately or markedly diminished, particularly in the case of the tetrahydronaphthalene analogues. The analysis indicated that steric constraints at the benzylic position in the bicyclic analogues may be an important factor for their unfavorable interaction with the receptor.

Graphical abstractA series of bicyclic analogues having indan and tetrahydronaphthalene templates in the A-region have been investigated as conformationally constrained analogues of our previously reported potent TRPV1 antagonists (1, 3).Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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