期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 21, 期 7, 页码 2048-2054出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2011.02.006
关键词
Synthesis and SAR; Structure-activity relationships; Benzoxaborole; HCV NS3 protease; Acyclic inhibitors
We have synthesized and evaluated a new series of acyclic P4-benzoxaborole-based HCV NS3 protease inhibitors. Structure-activity relationships were investigated, leading to the identification of compounds 5g and 17 with low nanomolar potency in the enzymatic and cell-based replicon assay. The linker-truncated compound 5j was found to exhibit improved absorption and oral bioavailability in rats, suggesting that further reduction of molecular weight and polar surface area could result in improved drug-like properties of this novel series. (C) 2011 Elsevier Ltd. All rights reserved.
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