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他拉罗唑,一种细胞色素P450介导的全反式维甲酸的选择性抑制剂,用于治疗银屑病和痤疮。

Talarozole, a selective inhibitor of P450-mediated all-trans retinoic acid for the treatment of psoriasis and acne.

作者信息

Geria Aanand N, Scheinfeld Noah S

机构信息

University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark, NJ 07101, USA.

出版信息

Curr Opin Investig Drugs. 2008 Nov;9(11):1228-37.

Abstract

Talarozole, being developed by Barrier Therapeutics Inc under license from Johnson & Johnson, is a potent and selective inhibitor of cytochrome P450 26-mediated breakdown of endogenous all-trans retinoic acid for the treatment of psoriasis and acne. Phase II clinical trials of an oral formulation of talarozole in patients with psoriasis and with acne, and a phase I clinical trial of a topical formulation have been completed. At the time of publication, Barrier Therapeutics had suspended the development of talarozole as part of a series of cost-cutting initiatives; the company had also been acquired by Stiefel Laboratories Inc. No formal announcement had been made regarding the further development of talarozole.

摘要

塔拉唑勒由巴rier治疗公司根据强生公司的许可进行研发,是一种强效且选择性的细胞色素P450 26介导的内源性全反式维甲酸分解抑制剂,用于治疗银屑病和痤疮。塔拉唑勒口服制剂在银屑病和痤疮患者中的II期临床试验以及局部用制剂的I期临床试验均已完成。在发表本文时,作为一系列成本削减举措的一部分,巴rier治疗公司已暂停塔拉唑勒的研发;该公司也已被施泰福实验室公司收购。关于塔拉唑勒的进一步研发尚未发布正式公告。

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