Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 하정미 | - |
dc.date.accessioned | 2019-07-25T05:53:34Z | - |
dc.date.available | 2019-07-25T05:53:34Z | - |
dc.date.issued | 2006-05 | - |
dc.identifier.citation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v. 128, No. 18, Page. 5996-5997 | en_US |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | https://pubs.acs.org/doi/abs/10.1021/ja060136i | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/107873 | - |
dc.description.abstract | A “global” strategy for the acquisition of selective high affinity inhibitors for the Src kinase subfamily of tyrosine kinases is described. Members of the Src family exhibit a strong amino acid sequence homology. However, recent studies have revealed differences in the relative spatial relationships of the three distinct protein-binding domains present in these enzymes. We have constructed an inhibitor, using an amalgamation of combinatorial methods and directed design, which simultaneously associates with the active site and an ancillary protein-binding region (SH2 domain). The inhibitor exhibits high inhibitory potency and selectivity for the Group A versus Group B subset of Src kinases. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | AMER CHEMICAL SOC | en_US |
dc.title | Acquisition of a Group A-selective Src Kinase Inhibitor via a Global Targeting Strategy | en_US |
dc.type | Article | en_US |
dc.relation.volume | 128 | - |
dc.identifier.doi | 10.1021/ja060136i | - |
dc.relation.page | 5996-5997 | - |
dc.relation.journal | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.contributor.googleauthor | Hah, Jung-Mi | - |
dc.contributor.googleauthor | Sharma, Vyas | - |
dc.contributor.googleauthor | Li, Haishan | - |
dc.contributor.googleauthor | Lawrence, David S. | - |
dc.relation.code | 2009205895 | - |
dc.sector.campus | E | - |
dc.sector.daehak | COLLEGE OF PHARMACY[E] | - |
dc.sector.department | DEPARTMENT OF PHARMACY | - |
dc.identifier.pid | jhah | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.