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

被引:63
|
作者
Boyle, Craig D. [1 ]
Kowalski, Timothy J. [2 ]
机构
[1] Schering Plough Res Inst, CNS & CV Metab Chem Res, Kenilworth, NJ 07033 USA
[2] Schering Plough Res Inst, CV Metab Dis Res, Kenilworth, NJ 07033 USA
关键词
11 beta-hydroxysteroid dehydrogenase type 1; glucocorticoids; inhibitor; metabolic syndrome; obesity; type; 2; diabetes; HEPATIC INSULIN SENSITIVITY; BODY-FAT DISTRIBUTION; ADIPOSE-TISSUE; METABOLIC SYNDROME; HEXOSE-6-PHOSPHATE DEHYDROGENASE; SELECTIVE INHIBITORS; 11-BETA-HSD1; INHIBITORS; CORTISOL METABOLISM; HUMAN OBESITY; 11BETA-HYDROXYSTEROID DEHYDROGENASE;
D O I
10.1517/13543770902967658
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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. 11 beta-Hydroxysteroid dehydrogenase type 1 (11 beta-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 11 beta-HSD1 inhibitors as treatment for the components of metabolic syndrome and limited clinical data in humans have shown 11 beta-HSD1 inhibition to improve glucose levels, insulin sensitivity and lipid profiles. Many organizations have been active in the 11 beta-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 11 beta-HSD1 inhibitors. Methods: This review covers the recent 11 beta-HSD1 patent literature and clinical activity ranging from late 2007 through the end of 2008. Results/conclusion: The exploration of 11 beta-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 11 beta-HSD1 inhibitors as pharmaceutical agents for the various components of metabolic syndrome.
引用
收藏
页码:801 / 825
页数:25
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