2c4g: Difference between revisions

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[[Image:2c4g.gif|left|200px]]
{{Seed}}
[[Image:2c4g.png|left|200px]]


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{{STRUCTURE_2c4g|  PDB=2c4g  |  SCENE=  }}  
{{STRUCTURE_2c4g|  PDB=2c4g  |  SCENE=  }}  


'''STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514'''
===STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514===




==Overview==
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We have recently reported about a new class of Aurora-A inhibitors based on a bicyclic tetrahydropyrrolo[3,4-c]pyrazole scaffold. Here we describe the synthesis and early expansion of CDK2/cyclin A-E inhibitors belonging to the same chemical class. Synthesis of the compounds was accomplished using a solution-phase protocol amenable to rapid parallel expansion. Compounds with nanomolar activity in the biochemical assay and able to efficiently inhibit CDK2-mediated tumor cell proliferation have been obtained.
The line below this paragraph, {{ABSTRACT_PUBMED_16290148}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16290148 is the PubMed ID number.
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{{ABSTRACT_PUBMED_16290148}}


==About this Structure==
==About this Structure==
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[[Category: Serine/threonine-protein kinase]]
[[Category: Serine/threonine-protein kinase]]
[[Category: Transferase]]
[[Category: Transferase]]
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