2p33 | pdb_00002p33
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Synthesis and SAR of Aminopyrimidines as Novel c-Jun N-Terminal Kinase (JNK) Inhibitors
Overview
The development of a series of novel aminopyrimidines as inhibitors of, c-Jun N-terminal kinases is described. The synthesis, in vitro inhibitory, values for JNK1, JNK2 and CDK2, and the in vitro inhibitory value for a, c-Jun cellular assay are discussed.
About this Structure
2P33 is a Single protein structure of sequence from Homo sapiens with J07 as ligand. Active as Mitogen-activated protein kinase, with EC number 2.7.11.24 Full crystallographic information is available from OCA.
Reference
Synthesis and SAR of aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors., Alam M, Beevers RE, Ceska T, Davenport RJ, Dickson KM, Fortunato M, Gowers L, Haughan AF, James LA, Jones MW, Kinsella N, Lowe C, Meissner JW, Nicolas AL, Perry BG, Phillips DJ, Pitt WR, Platt A, Ratcliffe AJ, Sharpe A, Tait LJ, Bioorg Med Chem Lett. 2007 Jun 15;17(12):3463-7. Epub 2007 Mar 30. PMID:17459703
Page seeded by OCA on Wed Jan 23 14:50:15 2008
