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PPAR의 리간드로서 새로운 요소 유도체의 분자설계 및 합성
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 김윤정 | - |
| dc.contributor.author | 전라옥 | - |
| dc.date.available | 2021-02-22T15:31:26Z | - |
| dc.date.issued | 2006-02 | - |
| dc.identifier.issn | 1225-3723 | - |
| dc.identifier.uri | https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15197 | - |
| dc.description.abstract | PPAR is one of the significant drug targets and activation of PPAR □ by several thiazolidinedione derivatives is well established. Herein bioisosteric replacement of thiazolidinedione to urea was carried out. Non-thiazolidinedione derivatives, [4-(2-carbazol-9-ylethoxy)phenyl]ureas (5, 6) were designed and synthesized to obtain novel PPAR activators. | - |
| dc.language | 한국어 | - |
| dc.language.iso | KOR | - |
| dc.publisher | 숙명여자대학교 약학연구소 | - |
| dc.title | PPAR의 리간드로서 새로운 요소 유도체의 분자설계 및 합성 | - |
| dc.title.alternative | Design and Synthesis of Novel Urea Analog as a PPAR ligand | - |
| dc.type | Article | - |
| dc.publisher.location | 대한민국 | - |
| dc.identifier.bibliographicCitation | 약학논문집-숙명여자대학교, v.23, pp 50 - 54 | - |
| dc.citation.title | 약학논문집-숙명여자대학교 | - |
| dc.citation.volume | 23 | - |
| dc.citation.startPage | 50 | - |
| dc.citation.endPage | 54 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | domestic | - |
| dc.identifier.url | https://dl.nanet.go.kr/SearchDetailView.do?sysid=openap&cn=KINX2006067653 | - |
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