DC Field | Value | Language |
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dc.contributor.author | Venkatesan, N | - |
dc.contributor.author | Kim, BH | - |
dc.date.accessioned | 2016-03-31T12:58:20Z | - |
dc.date.available | 2016-03-31T12:58:20Z | - |
dc.date.created | 2009-03-19 | - |
dc.date.issued | 2002-12 | - |
dc.identifier.issn | 0929-8673 | - |
dc.identifier.other | 2002-OAK-0000003021 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/18818 | - |
dc.description.abstract | Design and synthesis of metabolically stable peptide analogs that can either mimic or block the bioactivity of natural peptides or enzymes is an important constituent of bioorganic and medicinal chemistry research. Isosteric replacement of a scissile peptide bond represents a viable and popular approach in the rational design of peptidomimetics. Peptidomimetics find applications as drugs, in protein engineering and so on. This is evident from the wealth of therapeutically useful peptidomimetic leads incorporating any of the peptide isosteres that are currently available. In this review, we have given a brief account of the types of peptide isosteres widely known till date. With this background, we have described some of the recent developments in synthetic approaches. This includes methods involving a common intermediate to synthesize different possible isosteres and their peptide analogs, solid phase synthesis and combinatorial approach. One such method involving stereoselective nitrile oxide cycloaddition as the key step has been studied extensively in our research laboratory. Finally, we have also discussed about some of the recent reports on the design and inhibitory activities of peptidic or non-peptidic analogs against aspartic proteases (HIV-1, renin, ACE and pepsin) and peptide analogs of an immunomodulating hexapeptide. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | BENTHAM SCIENCE PUBL LTD | - |
dc.relation.isPartOf | CURRENT MEDICINAL CHEMISTRY | - |
dc.subject | peptide isosteres | - |
dc.subject | peptidomimetics | - |
dc.subject | enzyme inhibitors | - |
dc.subject | pseudopeptides | - |
dc.subject | HIV PROTEASE INHIBITORS | - |
dc.subject | HUMAN-IMMUNODEFICIENCY-VIRUS | - |
dc.subject | SOLID-PHASE SYNTHESIS | - |
dc.subject | HYDROXYETHYLENE DIPEPTIDE ISOSTERES | - |
dc.subject | TRANSITION-STATE ANALOG | - |
dc.subject | STRUCTURE-BASED DESIGN | - |
dc.subject | ANGIOTENSIN-CONVERTING ENZYME | - |
dc.subject | SECONDARY STRUCTURE MIMETICS | - |
dc.subject | NONPEPTIDE RENIN INHIBITORS | - |
dc.subject | GRB2-SH2 DOMAIN INHIBITORS | - |
dc.title | Synthesis and enzyme inhibitory activities of novel peptide isosteres | - |
dc.type | Article | - |
dc.contributor.college | 화학과 | - |
dc.identifier.doi | 10.2174/0929867023368692 | - |
dc.author.google | Venkatesan, N | - |
dc.author.google | Kim, BH | - |
dc.relation.volume | 9 | - |
dc.relation.issue | 24 | - |
dc.relation.startpage | 2243 | - |
dc.relation.lastpage | 2270 | - |
dc.contributor.id | 10142056 | - |
dc.relation.journal | CURRENT MEDICINAL CHEMISTRY | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | CURRENT MEDICINAL CHEMISTRY, v.9, no.24, pp.2243 - 2270 | - |
dc.identifier.wosid | 000179347400005 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 2270 | - |
dc.citation.number | 24 | - |
dc.citation.startPage | 2243 | - |
dc.citation.title | CURRENT MEDICINAL CHEMISTRY | - |
dc.citation.volume | 9 | - |
dc.contributor.affiliatedAuthor | Kim, BH | - |
dc.identifier.scopusid | 2-s2.0-0036433385 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 44 | - |
dc.type.docType | Review | - |
dc.subject.keywordPlus | HIV PROTEASE INHIBITORS | - |
dc.subject.keywordPlus | SOLID-PHASE SYNTHESIS | - |
dc.subject.keywordPlus | HYDROXYETHYLENE DIPEPTIDE ISOSTERES | - |
dc.subject.keywordPlus | IMMUNODEFICIENCY-VIRUS PROTEASE | - |
dc.subject.keywordPlus | STRUCTURE-BASED DESIGN | - |
dc.subject.keywordPlus | ANGIOTENSIN-CONVERTING ENZYME | - |
dc.subject.keywordPlus | NITRILE OXIDE CYCLOADDITIONS | - |
dc.subject.keywordPlus | GRB2-SH2 DOMAIN INHIBITORS | - |
dc.subject.keywordPlus | STATE ANALOG INHIBITORS | - |
dc.subject.keywordPlus | RETRO-INVERSO PEPTIDES | - |
dc.subject.keywordAuthor | peptide isosteres | - |
dc.subject.keywordAuthor | peptidomimetics | - |
dc.subject.keywordAuthor | enzyme inhibitors | - |
dc.subject.keywordAuthor | pseudopeptides | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
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