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- Park, Cheol-Min
- Synthetic and Medicinal Chemistry Lab.
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 1690 | - |
| dc.citation.number | 12 | - |
| dc.citation.startPage | 1687 | - |
| dc.citation.title | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | - |
| dc.citation.volume | 9 | - |
| dc.contributor.author | Wender, PA | - |
| dc.contributor.author | Lippa, B | - |
| dc.contributor.author | Park, Cheol-Min | - |
| dc.contributor.author | Irie, K | - |
| dc.contributor.author | Nakahara, A | - |
| dc.contributor.author | Ohigashi, H | - |
| dc.date.accessioned | 2023-12-22T12:11:14Z | - |
| dc.date.available | 2023-12-22T12:11:14Z | - |
| dc.date.created | 2014-11-10 | - |
| dc.date.issued | 1999-06 | - |
| dc.description.abstract | Designed bryostatin analogues are assayed for binding affinity to individual cysteine rich domains of several protein kinase C (PKC) isozymes. These analogues exhibit significant selectivity for the PKCδ-C1B peptide in terms of absolute affinity and the PKCδ-C1A peptide in terms of relative affinity when compared to phorbol-12,13-dibutyrate. | - |
| dc.identifier.bibliographicCitation | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.9, no.12, pp.1687 - 1690 | - |
| dc.identifier.doi | 10.1016/S0960-894X(99)00263-2 | - |
| dc.identifier.issn | 0960-894X | - |
| dc.identifier.scopusid | 2-s2.0-0033591714 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/8571 | - |
| dc.identifier.url | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0033591714 | - |
| dc.identifier.wosid | 000080896500013 | - |
| dc.language | 영어 | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.title | Selective binding of bryostatin analogues to the cysteine rich domains of protein kinase C isozymes | - |
| dc.type | Article | - |
| dc.description.journalRegisteredClass | scopus | - |
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