| Literature DB >> 20053559 |
Ikyon Kim1, Jong Hwan Song, Chang Min Park, Joon Won Jeong, Hyung Rae Kim, Jin Ryul Ha, Zaesung No, Young-Lan Hyun, Young Sik Cho, Nam Sook Kang, Dong Ju Jeon.
Abstract
Described herein is design, synthesis, and biological evaluation of novel series of 2-aryl-7-(3',4'-dialkoxyphenyl)-pyrazolo[1,5-a]pyrimidines acting as inhibitors of type 4 phosphodiesterase (PDE4) which is known as a good target for the treatment of asthma and COPD. For this purpose, structure optimization was conducted with the aid of structure-based drug design using the known X-ray crystallography. Also, biological effects of these compounds on the target enzyme were evaluated by using in vitro assays, leading to the potent and selective PDE-4 inhibitor (IC(50)<10nM). Copyright (c) 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 20053559 DOI: 10.1016/j.bmcl.2009.12.070
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823