Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596678 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
Abstract
Aldosterone, the final component of the renin-angiotensin-aldosterone system, plays an important role in the pathophysiology of hypertension and congestive heart failure. Aldosterone synthase (CYP11B2) catalyzes the last three steps of aldosterone biosynthesis, and as such appears to be a target for the treatment of these disorders. A sulfonamide-imidazole scaffold has proven to be a potent inhibitor of CYP11B2. Furthermore, this scaffold can achieve high levels of selectivity for CYP11B2 over CYP11B1, a key enzyme in the biosynthesis of cortisol.
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Authors
Christopher M. Adams, Chii-Whei Hu, Arco Y. Jeng, Rajeshri Karki, Gary Ksander, Dan LaSala, Jennifer Leung-Chu, Guiqing Liang, Qian Liu, Erik Meredith, Chang Rao, Dean F. Rigel, Jie Shi, Sherri Smith, Clayton Springer, Chun Zhang,