2p33: Difference between revisions

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==Overview==
==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.
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.
 
==Disease==
Known diseases associated with this structure: Epileptic encephalopathy, Lennox-Gastaut type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602897 602897]]


==About this Structure==
==About this Structure==
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[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ceska, T.A.]]
[[Category: Ceska, T A.]]
[[Category: Dickson, K.M.]]
[[Category: Dickson, K M.]]
[[Category: Fortunato, M.]]
[[Category: Fortunato, M.]]
[[Category: Platt, A.]]
[[Category: Platt, A.]]
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[[Category: jnk3 kinase]]
[[Category: jnk3 kinase]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:25:27 2008''

Revision as of 16:25, 21 February 2008

File:2p33.jpg


2p33, resolution 2.40Å

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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.

Disease

Known diseases associated with this structure: Epileptic encephalopathy, Lennox-Gastaut type OMIM:[602897]

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

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