Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Hayat, Faisal | - |
dc.contributor.author | Cho, Sungjin | - |
dc.contributor.author | Rhim, Hyewhon | - |
dc.contributor.author | Viswanath, Ambily Nath Indu | - |
dc.contributor.author | Pae, Ae Nim | - |
dc.contributor.author | Lee, Jae Yeol | - |
dc.contributor.author | Choo, Dong Joon | - |
dc.contributor.author | Choo, Hea-Young Park | - |
dc.date.accessioned | 2024-01-20T11:32:56Z | - |
dc.date.available | 2024-01-20T11:32:56Z | - |
dc.date.created | 2021-09-04 | - |
dc.date.issued | 2013-09-01 | - |
dc.identifier.issn | 0968-0896 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/127679 | - |
dc.description.abstract | The exclusive distribution of 5-HT6 receptor in the brain regions and high affinity for antipsychotic and antidepressant drugs makes 5-HT6 receptor a promising target in treatment of CNS diseases. Based on a pharmacophore model reported in the literature, we designed and synthesized a novel series of 5-HT6 receptor ligands having indole as a central aromatic core and 1-amino-4-methyl piperazine as positive ionizable group. Out of 32 compounds we have successfully identified 10 new compounds as 5-HT6 receptor antagonists. The structure-activity relationship (SAR) studies have been carried out by mapping the compounds with the 3D QSAR model. (C) 2013 Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | MEMORY FORMATION | - |
dc.subject | ANTAGONISTS | - |
dc.subject | POTENT | - |
dc.title | Design and synthesis of novel series of 5-HT6 receptor ligands having indole, a central aromatic core and 1-amino-4 methyl piperazine as a positive ionizable group | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.bmc.2013.05.051 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | BIOORGANIC & MEDICINAL CHEMISTRY, v.21, no.17, pp.5573 - 5582 | - |
dc.citation.title | BIOORGANIC & MEDICINAL CHEMISTRY | - |
dc.citation.volume | 21 | - |
dc.citation.number | 17 | - |
dc.citation.startPage | 5573 | - |
dc.citation.endPage | 5582 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000323294600075 | - |
dc.identifier.scopusid | 2-s2.0-84881376737 | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | MEMORY FORMATION | - |
dc.subject.keywordPlus | ANTAGONISTS | - |
dc.subject.keywordPlus | POTENT | - |
dc.subject.keywordAuthor | 5-HT6 receptor antagonist | - |
dc.subject.keywordAuthor | 1-Amino-4-methylpiperazine | - |
dc.subject.keywordAuthor | Sulfonyl indole | - |
dc.subject.keywordAuthor | 3D QSAR | - |
dc.subject.keywordAuthor | Pharmacophore mapping | - |
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