PMID- 18057750 OWN - NLM STAT- MEDLINE DCOM- 20080128 LR - 20190706 IS - 0009-2363 (Print) IS - 0009-2363 (Linking) VI - 55 IP - 12 DP - 2007 Dec TI - Synthesis and HIV-1 integrase inhibition of novel bis- or tetra-coumarin analogues. PG - 1740-3 AB - Present studies were undertaken on the preparation of synthetic analogues of bis- or tetra-coumarins and their activity against HIV-1 integrase (HIV-1 IN). Among these coumarin analogues, compounds 14, 16 and 18 were found to be potent molecules against HIV-1 IN at IC50 values of 0.96, 0.58, and 0.49 microM, respectively. The results provided a tool for guiding the further design of more potent antiviral agents and for predicting the affinity of related compounds. FAU - Chiang, Chih-Chia AU - Chiang CC AD - Department of Applied Chemistry and Materials Science, Institute of Technology, National Defense University, Ta-shi, Tao-yuan, Taiwan, ROC.. FAU - Mouscadet, Jean-Francois AU - Mouscadet JF FAU - Tsai, Hou-Jen AU - Tsai HJ FAU - Liu, Chi-Tsan AU - Liu CT FAU - Hsu, Ling-Yih AU - Hsu LY LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Japan TA - Chem Pharm Bull (Tokyo) JT - Chemical & pharmaceutical bulletin JID - 0377775 RN - 0 (Coumarins) RN - 0 (HIV Integrase Inhibitors) RN - 0 (Oligonucleotides) RN - EC 2.7.7.- (HIV Integrase) SB - IM MH - Chemical Phenomena MH - Chemistry, Physical MH - Coumarins/*chemical synthesis/*pharmacology MH - HIV Integrase/metabolism MH - HIV Integrase Inhibitors/*chemical synthesis/*pharmacology MH - HIV-1/*drug effects/*enzymology MH - Magnetic Resonance Spectroscopy MH - Mass Spectrometry MH - Oligonucleotides/chemical synthesis/pharmacology MH - Spectrophotometry, Infrared EDAT- 2007/12/07 09:00 MHDA- 2008/01/29 09:00 CRDT- 2007/12/07 09:00 PHST- 2007/12/07 09:00 [pubmed] PHST- 2008/01/29 09:00 [medline] PHST- 2007/12/07 09:00 [entrez] AID - JST.JSTAGE/cpb/55.1740 [pii] AID - 10.1248/cpb.55.1740 [doi] PST - ppublish SO - Chem Pharm Bull (Tokyo). 2007 Dec;55(12):1740-3. doi: 10.1248/cpb.55.1740.