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dc.contributor.authorLee, Byung-Hwan-
dc.contributor.authorChoi, Min Jung-
dc.contributor.authorJo, Mi Na-
dc.contributor.authorSeo, Hee Jeong-
dc.contributor.authorNah, Seung-Yeol-
dc.contributor.authorCho, Yong Seo-
dc.contributor.authorNam, Ghilsoo-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorRhim, Hyewhon-
dc.contributor.authorChoo, Hyunah-
dc.date.accessioned2024-01-20T21:03:47Z-
dc.date.available2024-01-20T21:03:47Z-
dc.date.created2021-09-03-
dc.date.issued2009-07-01-
dc.identifier.issn0968-0896-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/132323-
dc.description.abstract5-HT3A receptor antagonists have been used mainly for the treatment of nausea and vomiting. These days, the antagonists are of special interest due to their therapeutic potential to treat other diseases such as depression, psychotic disorder, drug abuse, and irritable bowel syndrome. To discover novel 5-HT3A receptor antagonists, we screened our in-house small molecule library, resulting in identifying the quinazolindione derivatives as potent 5-HT3A receptor antagonists. For the purpose of structure-activity relationship study, 24 quinazolindione analogues were biologically evaluated against 5-HT3A receptor. Among those, KKHT10612 shows the best antagonistic effect against 5-HT3A receptor with an IC50 value of 0.8 mu M which is comparable with that of the reference compound, MDL72222, and selectivity over T-type calcium channel as well. (C) 2009 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subject5HT3 RECEPTOR-
dc.subjectCHANNEL-
dc.subjectSELECTIVITY-
dc.subjectEXPRESSION-
dc.titleQuinazolindione derivatives as potent 5-HT3A receptor antagonists-
dc.typeArticle-
dc.identifier.doi10.1016/j.bmc.2009.04.029-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY, v.17, no.13, pp.4793 - 4796-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY-
dc.citation.volume17-
dc.citation.number13-
dc.citation.startPage4793-
dc.citation.endPage4796-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000266822900057-
dc.identifier.scopusid2-s2.0-66449125846-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlus5HT3 RECEPTOR-
dc.subject.keywordPlusCHANNEL-
dc.subject.keywordPlusSELECTIVITY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthor5-HT3A Receptor-
dc.subject.keywordAuthorAntagonist-
dc.subject.keywordAuthorQuinazolindione derivatives-
dc.subject.keywordAuthorMDL72222-
dc.subject.keywordAuthorCalcium channel-
dc.subject.keywordAuthorSerotonin-
dc.subject.keywordAuthorBemesetron-
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KIST Article > 2009
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