Optimization of sulfonamide derivatives as highly selective EP1 receptor antagonists

…, H Yamamoto, H Okada, T Maruyama, H Nakai…

Index: Naganawa, Atsushi; Matsui, Toshiaki; Ima, Masaki; Yoshida, Koji; Tsuruta, Hiroshi; Yamamoto, Shingo; Yamamoto, Hiroshi; Okada, Hiroki; Maruyama, Takayuki; Nakai, Hisao; Kondo, Kigen; Toda, Masaaki Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 23 p. 7774 - 7789

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Citation Number: 11

Abstract

A series of 4-[(2-{isobutyl [(5-methyl-2-furyl) sulfonyl] amino} phenoxy) methyl] benzoic acids and 4-({2-[isobutyl (1, 3-thiazol-2-ylsulfonyl) amino] phenoxy} methyl) benzoic acids were synthesized and evaluated for their EP receptor affinities and EP1 receptor antagonist activities. Further structural optimization was carried out to reduce inhibitory activity against hepatic cytochrome P450 isozymes, which could represent a harmful potential drug ...

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Optimization of sulfonamide derivatives as highly selective EP1 receptor antagonists

[Bioorganic and Medicinal Chemistry, , vol. 14, # 23 p. 7774 - 7789]

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