2c68: Difference between revisions

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[[Image:2c68.gif|left|200px]]
{{Seed}}
[[Image:2c68.png|left|200px]]


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{{STRUCTURE_2c68|  PDB=2c68  |  SCENE=  }}  
{{STRUCTURE_2c68|  PDB=2c68  |  SCENE=  }}  


'''CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR'''
===CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR===




==Overview==
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Crystallographic and modelling data, in conjunction with a medicinal chemistry template-hopping approach, led to the identification of a series of novel and potent inhibitors of human cyclin-dependent kinase 2 (CDK2), with selectivity over glycogen synthase kinase-3beta (GSK-3beta). One example had a CDK2 IC(50) of 120 nM and showed selectivity over GSK-3beta of 167-fold.
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{{ABSTRACT_PUBMED_16325401}}


==About this Structure==
==About this Structure==
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[[Category: Transferase]]
[[Category: Transferase]]
[[Category: Triazolopyrimidine inhibitor]]
[[Category: Triazolopyrimidine inhibitor]]
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