Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Yoo, H. | - |
dc.contributor.author | Lee, J.Y. | - |
dc.contributor.author | Park, J.H. | - |
dc.contributor.author | Chung, B.Y. | - |
dc.contributor.author | Lee, Y.S. | - |
dc.date.accessioned | 2024-01-21T08:02:20Z | - |
dc.date.available | 2024-01-21T08:02:20Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 2003-12 | - |
dc.identifier.issn | 0014-827X | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/138068 | - |
dc.description.abstract | A series of styrylbenzofuran derivatives (8a-i) as styrylquinoline isosters were efficiently prepared by Wittig reaction and evaluated for inhibitory activity against HIV-1 integrase. In this series, compounds 8g, 8h and 8i containing a free catechol ring showed moderate inhibitory activities (IC50=∼40 μM) against HIV-1 integrase, while less than the corresponding styrylquinoline compound (I). ? 2003 ?ditions scientifiques et m?dicales Elsevier SAS. All rights reserved. | - |
dc.language | English | - |
dc.publisher | Elsevier Masson SAS | - |
dc.subject | 7 hydroxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylic acid | - |
dc.subject | 7 hydroxy 2 [2 (4 hydroxyphenyl)ethynyl] 6 benzofuran carboxylic acid | - |
dc.subject | 7 methoxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylic acid | - |
dc.subject | benzofuran derivative | - |
dc.subject | integrase inhibitor | - |
dc.subject | methyl 7 hydroxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | methyl 7 hydroxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | methyl 7 methoxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | methyl 7 methoxy 2 [2 (3,4 dimethoxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | methyl 7 methoxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | methyl 7 methoxy 2 [2 (4 methoxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject | quinoline derivative | - |
dc.subject | unclassified drug | - |
dc.subject | article | - |
dc.subject | drug activity | - |
dc.subject | drug screening | - |
dc.subject | drug structure | - |
dc.subject | drug synthesis | - |
dc.subject | enzyme inhibition | - |
dc.subject | Human immunodeficiency virus 1 | - |
dc.subject | IC 50 | - |
dc.subject | nonhuman | - |
dc.subject | Wittig reaction | - |
dc.title | Synthesis of styrylbenzofuran derivatives as styrylquinoline analogues for HIV-1 integrase inhibitor | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.farmac.2003.08.001 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | Farmaco, v.58, no.12, pp.1243 - 1250 | - |
dc.citation.title | Farmaco | - |
dc.citation.volume | 58 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 1243 | - |
dc.citation.endPage | 1250 | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.scopusid | 2-s2.0-0242468157 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | 7 hydroxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylic acid | - |
dc.subject.keywordPlus | 7 hydroxy 2 [2 (4 hydroxyphenyl)ethynyl] 6 benzofuran carboxylic acid | - |
dc.subject.keywordPlus | 7 methoxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylic acid | - |
dc.subject.keywordPlus | benzofuran derivative | - |
dc.subject.keywordPlus | integrase inhibitor | - |
dc.subject.keywordPlus | methyl 7 hydroxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | methyl 7 hydroxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | methyl 7 methoxy 2 [2 (3,4 dihydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | methyl 7 methoxy 2 [2 (3,4 dimethoxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | methyl 7 methoxy 2 [2 (4 hydroxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | methyl 7 methoxy 2 [2 (4 methoxyphenyl)ethenyl] 6 benzofuran carboxylate | - |
dc.subject.keywordPlus | quinoline derivative | - |
dc.subject.keywordPlus | unclassified drug | - |
dc.subject.keywordPlus | article | - |
dc.subject.keywordPlus | drug activity | - |
dc.subject.keywordPlus | drug screening | - |
dc.subject.keywordPlus | drug structure | - |
dc.subject.keywordPlus | drug synthesis | - |
dc.subject.keywordPlus | enzyme inhibition | - |
dc.subject.keywordPlus | Human immunodeficiency virus 1 | - |
dc.subject.keywordPlus | IC 50 | - |
dc.subject.keywordPlus | nonhuman | - |
dc.subject.keywordPlus | Wittig reaction | - |
dc.subject.keywordAuthor | AIDS | - |
dc.subject.keywordAuthor | HIV | - |
dc.subject.keywordAuthor | Integrase inhibitor | - |
dc.subject.keywordAuthor | Styrylbenzofuran | - |
dc.subject.keywordAuthor | Wittig reaction | - |
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