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dc.contributor.authorChong, Youhoon-
dc.contributor.authorChoo, Hyunah-
dc.date.accessioned2024-01-20T18:04:52Z-
dc.date.available2024-01-20T18:04:52Z-
dc.date.created2021-09-05-
dc.date.issued2010-11-
dc.identifier.issn1354-3784-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130937-
dc.description.abstractImportance of the field: The main therapeutic area of 5-HT3 receptor antagonists is the treatment of chemotherapy-induced nausea and vomiting (CINV), which is the most common and distressing side effects of anticancer treatment. The second major clinical application of 5-HT3 receptor antagonists is in the treatment of irritable bowel syndrome (IBS). 5-HT3 antagonists have been widely used and found to decrease gut transit, increase fluid absorption and reduce pain. The uses of 5-HT3 antagonists are expending to treatment of CNS diseases such as anxiety and sleep disorders as antipsychotics and so on. Areas covered in this review: The structures, in vitro activities, in vivo effects and some clinical data on 5-HT3 receptor antagonists under development. What the reader will gain: Future research directions in 5-HT3 antagonists based on the clinical trial data of the pipeline molecules. Take home message: Most drug candidates in clinical trials were discovered in the early 1990s and their patent expiry is imminent. Acquiring intellectual properties of novel 5-HT3 receptor antagonists with improved efficacies would provide a bright future. Particularly, as the current 5-HT3 receptor antagonists are classified into only three representative structural families (one third are zacopride-like benzamides and the others are ondansteron-like tricyclic compounds and dolansetron-like bicyclic compounds), structurally diverse compound libraries need to be extensively investigated for identification of novel 5-HT3 receptor antagonists.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectTHERAPY-INDUCED EMESIS-
dc.subjectQUALITY-OF-LIFE-
dc.subjectRECEPTOR ANTAGONIST-
dc.subject5-HYDROXYTRYPTAMINE(3) RECEPTORS-
dc.subjectPHARMACOLOGICAL CHARACTERIZATION-
dc.subjectANTIEMETIC ACTIVITY-
dc.subjectHIGHLY POTENT-
dc.subjectSEROTONIN-
dc.subjectRATS-
dc.subjectONDANSETRON-
dc.title5-HT3 antagonists under development-
dc.typeArticle-
dc.identifier.doi10.1517/13543784.2010.528388-
dc.description.journalClass1-
dc.identifier.bibliographicCitationEXPERT OPINION ON INVESTIGATIONAL DRUGS, v.19, no.11, pp.1309 - 1319-
dc.citation.titleEXPERT OPINION ON INVESTIGATIONAL DRUGS-
dc.citation.volume19-
dc.citation.number11-
dc.citation.startPage1309-
dc.citation.endPage1319-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000283319900001-
dc.identifier.scopusid2-s2.0-77958504144-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeReview-
dc.subject.keywordPlusTHERAPY-INDUCED EMESIS-
dc.subject.keywordPlusQUALITY-OF-LIFE-
dc.subject.keywordPlusRECEPTOR ANTAGONIST-
dc.subject.keywordPlus5-HYDROXYTRYPTAMINE(3) RECEPTORS-
dc.subject.keywordPlusPHARMACOLOGICAL CHARACTERIZATION-
dc.subject.keywordPlusANTIEMETIC ACTIVITY-
dc.subject.keywordPlusHIGHLY POTENT-
dc.subject.keywordPlusSEROTONIN-
dc.subject.keywordPlusRATS-
dc.subject.keywordPlusONDANSETRON-
dc.subject.keywordAuthor5-HT3 antagonist-
dc.subject.keywordAuthoranti-emesis-
dc.subject.keywordAuthorchemotherapy-
dc.subject.keywordAuthorIBS-
dc.subject.keywordAuthorirritable bowel syndrome-
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