期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 22, 期 7, 页码 2522-2526出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2012.01.133
关键词
HIV; Inhibitor; 3,4-Dihydropyrimidin-2(1H)-one; Biginelli reaction; Bioisostere
资金
- National Research foundation of Korea (NRF)
- Korea government (MEST) [2011-00244]
- Gyeonggi-do
- KISTI
Following the previous SAR of a novel dihydropyrimidinone scaffold as HIV-1 replication inhibitors a detailed study directed towards optimizing the metabolic stability of the ester functional group in the dihydropyrimidinone (DHPM) scaffold is described. Replacement of the ester moiety by thiazole ring significantly improved the metabolic stability while retaining antiviral activity against HIV-1 replication. These novel and potent DHPMs with bioisosteres could serve as advanced leads for further optimization. (C) 2012 Elsevier Ltd. All rights reserved.
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