Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Chong, Youhoon | - |
dc.contributor.author | Choo, Hyunah | - |
dc.date.accessioned | 2024-01-20T18:04:52Z | - |
dc.date.available | 2024-01-20T18:04:52Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2010-11 | - |
dc.identifier.issn | 1354-3784 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/130937 | - |
dc.description.abstract | Importance 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.language | English | - |
dc.publisher | TAYLOR & FRANCIS LTD | - |
dc.subject | THERAPY-INDUCED EMESIS | - |
dc.subject | QUALITY-OF-LIFE | - |
dc.subject | RECEPTOR ANTAGONIST | - |
dc.subject | 5-HYDROXYTRYPTAMINE(3) RECEPTORS | - |
dc.subject | PHARMACOLOGICAL CHARACTERIZATION | - |
dc.subject | ANTIEMETIC ACTIVITY | - |
dc.subject | HIGHLY POTENT | - |
dc.subject | SEROTONIN | - |
dc.subject | RATS | - |
dc.subject | ONDANSETRON | - |
dc.title | 5-HT3 antagonists under development | - |
dc.type | Article | - |
dc.identifier.doi | 10.1517/13543784.2010.528388 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | EXPERT OPINION ON INVESTIGATIONAL DRUGS, v.19, no.11, pp.1309 - 1319 | - |
dc.citation.title | EXPERT OPINION ON INVESTIGATIONAL DRUGS | - |
dc.citation.volume | 19 | - |
dc.citation.number | 11 | - |
dc.citation.startPage | 1309 | - |
dc.citation.endPage | 1319 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000283319900001 | - |
dc.identifier.scopusid | 2-s2.0-77958504144 | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.type.docType | Review | - |
dc.subject.keywordPlus | THERAPY-INDUCED EMESIS | - |
dc.subject.keywordPlus | QUALITY-OF-LIFE | - |
dc.subject.keywordPlus | RECEPTOR ANTAGONIST | - |
dc.subject.keywordPlus | 5-HYDROXYTRYPTAMINE(3) RECEPTORS | - |
dc.subject.keywordPlus | PHARMACOLOGICAL CHARACTERIZATION | - |
dc.subject.keywordPlus | ANTIEMETIC ACTIVITY | - |
dc.subject.keywordPlus | HIGHLY POTENT | - |
dc.subject.keywordPlus | SEROTONIN | - |
dc.subject.keywordPlus | RATS | - |
dc.subject.keywordPlus | ONDANSETRON | - |
dc.subject.keywordAuthor | 5-HT3 antagonist | - |
dc.subject.keywordAuthor | anti-emesis | - |
dc.subject.keywordAuthor | chemotherapy | - |
dc.subject.keywordAuthor | IBS | - |
dc.subject.keywordAuthor | irritable bowel syndrome | - |
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