dc.citation.endPage |
1690 |
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dc.citation.number |
12 |
- |
dc.citation.startPage |
1687 |
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dc.citation.title |
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS |
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dc.citation.volume |
9 |
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dc.contributor.author |
Wender, PA |
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dc.contributor.author |
Lippa, B |
- |
dc.contributor.author |
Park, Cheol-Min |
- |
dc.contributor.author |
Irie, K |
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dc.contributor.author |
Nakahara, A |
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dc.contributor.author |
Ohigashi, H |
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dc.date.accessioned |
2023-12-22T12:11:14Z |
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dc.date.available |
2023-12-22T12:11:14Z |
- |
dc.date.created |
2014-11-10 |
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dc.date.issued |
1999-06 |
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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. |
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dc.identifier.bibliographicCitation |
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.9, no.12, pp.1687 - 1690 |
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dc.identifier.doi |
10.1016/S0960-894X(99)00263-2 |
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dc.identifier.issn |
0960-894X |
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dc.identifier.scopusid |
2-s2.0-0033591714 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/8571 |
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dc.identifier.url |
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0033591714 |
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dc.identifier.wosid |
000080896500013 |
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dc.language |
영어 |
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dc.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
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dc.title |
Selective binding of bryostatin analogues to the cysteine rich domains of protein kinase C isozymes |
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dc.type |
Article |
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dc.description.journalRegisteredClass |
scopus |
- |