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11β-羟基类固醇脱氢酶1型抑制剂:近期专利综述

11beta-hydroxysteroid dehydrogenase type 1 inhibitors: a review of recent patents.

作者信息

Boyle Craig D, Kowalski Timothy J

机构信息

CNS and CV/Metabolic Chemical Research, Schering-Plough Research Institute, 2015 Galloping Hill Road, K-15-2-2545, Kenilworth, NJ 07033-1300, USA.

出版信息

Expert Opin Ther Pat. 2009 Jun;19(6):801-25. doi: 10.1517/13543770902967658.

Abstract

BACKGROUND

The main components of metabolic syndrome (obesity, insulin resistance, hypertension and dyslipidemia) have become prevalent worldwide, and excess glucocorticoid levels have been implicated in patients with these symptoms. 11beta-Hydroxysteroid dehydrogenase type 1 (11beta-HSD1) is an enzyme involved in glucocorticoid regulation through catalysis of the conversion of inactive cortisone to its active form cortisol. Numerous rodent studies have demonstrated the potential use of 11beta-HSD1 inhibitors as treatment for the components of metabolic syndrome and limited clinical data in humans have shown 11beta-HSD1 inhibition to improve glucose levels, insulin sensitivity and lipid profiles. Many organizations have been active in the 11beta-HSD1 academic and patent literature, and two previous articles from this journal have reviewed disclosures through August 2007.

OBJECTIVE

To summarize the recent patent literature and progress in defining the utility of small molecule 11beta-HSD1 inhibitors.

METHODS

This review covers the recent 11beta-HSD1 patent literature and clinical activity ranging from late 2007 through the end of 2008.

RESULTS/CONCLUSION: The exploration of 11beta-HSD1 inhibitors continues, as a number of structural classes have been reported by several pharmaceutical companies over the past 16 months. Current clinical trials will ultimately shed light on the feasibility of 11beta-HSD1 inhibitors as pharmaceutical agents for the various components of metabolic syndrome.

摘要

背景

代谢综合征的主要组成部分(肥胖、胰岛素抵抗、高血压和血脂异常)在全球范围内已变得普遍,且糖皮质激素水平过高与出现这些症状的患者有关。11β-羟基类固醇脱氢酶1型(11β-HSD1)是一种通过催化无活性的可的松转化为其活性形式皮质醇来参与糖皮质激素调节的酶。众多啮齿动物研究已证明11β-HSD1抑制剂有可能用于治疗代谢综合征的各个组成部分,而在人类中的有限临床数据显示抑制11β-HSD1可改善血糖水平、胰岛素敏感性和血脂状况。许多机构活跃于11β-HSD1的学术和专利文献领域,本期刊之前的两篇文章已对截至2007年8月的相关披露进行了综述。

目的

总结近期关于小分子11β-HSD1抑制剂效用的专利文献及进展。

方法

本综述涵盖了2007年末至2008年底的近期11β-HSD1专利文献及临床研究情况。

结果/结论:对11β-HSD1抑制剂的探索仍在继续,在过去16个月里多家制药公司已报道了多个结构类别。当前的临床试验最终将阐明11β-HSD1抑制剂作为治疗代谢综合征各个组成部分药物的可行性。

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