| Literature DB >> 17533128 |
Yang Wang1, Shao-Xu Huang, Peng Xia, Yi Xia, Zheng-Yu Yang, Nicole Kilgore, Susan L Morris-Natschke, Kuo-Hsiung Lee.
Abstract
Three 9,10-di-O-(-)-camphanoyl-7,8,9,10-tetrahydro-benzo[h]chromen-2-one (7-carbon-DCK) analogs (3a-c) were synthesized and evaluated for inhibition of HIV-1 replication in H9 lymphocytes. All three new carbon bioisosteres of the anti-HIV lead DCK showed anti-HIV activity. Compound 3a had an EC(50) value of 0.068 microM, which was comparable to that of DCK in the same assay. The preliminary results indicated that 7-carbon-DCK analogs merit attention as potential HIV-1 inhibitors for further development into clinical trials candidates.Entities:
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Year: 2007 PMID: 17533128 PMCID: PMC2697499 DOI: 10.1016/j.bmcl.2007.05.026
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823