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2duv
From Proteopedia
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[[Image:2duv.jpg|left|200px]] | [[Image:2duv.jpg|left|200px]] | ||
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'''Structure of CDK2 with a 3-hydroxychromones''' | '''Structure of CDK2 with a 3-hydroxychromones''' | ||
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[[Category: Lee, J.]] | [[Category: Lee, J.]] | ||
[[Category: Park, T.]] | [[Category: Park, T.]] | ||
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| - | [[Category: | + | [[Category: Protein kinase]] |
| - | [[Category: | + | [[Category: Serine/threonine-protein kinase]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 01:25:22 2008'' | |
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Revision as of 22:25, 3 May 2008
Structure of CDK2 with a 3-hydroxychromones
Overview
A novel series of 3-hydroxychromones were prepared and found to be CDK inhibitors. Isothiazolidine 1,1-dioxide analogues showed potent CDK1 and CDK2 inhibitory activities and inhibited proliferation of EJ, HCT116, SW620, and MDAMB468 cancer cells.
About this Structure
2DUV is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
3-Hydroxychromones as cyclin-dependent kinase inhibitors: synthesis and biological evaluation., Lee J, Park T, Jeong S, Kim KH, Hong C, Bioorg Med Chem Lett. 2007 Mar 1;17(5):1284-7. Epub 2006 Dec 15. PMID:17178224 Page seeded by OCA on Sun May 4 01:25:22 2008
