2duv

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==Overview==
==Overview==
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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.
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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==
==About this Structure==
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==Reference==
==Reference==
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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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17178224 17178224]
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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:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17178224 17178224]
[[Category: Cyclin-dependent kinase]]
[[Category: Cyclin-dependent kinase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Hong, C.]]
[[Category: Hong, C.]]
[[Category: Jeong, S.]]
[[Category: Jeong, S.]]
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[[Category: Kim, K.H.]]
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[[Category: Kim, K H.]]
[[Category: Lee, J.]]
[[Category: Lee, J.]]
[[Category: Park, T.]]
[[Category: Park, T.]]
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[[Category: serine/threonine-protein kinase]]
[[Category: serine/threonine-protein kinase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:22:36 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:02:56 2008''

Revision as of 15:02, 21 February 2008


2duv, resolution 2.2Å

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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 with as ligand. Active as Cyclin-dependent kinase, with EC number 2.7.11.22 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 Thu Feb 21 17:02:56 2008

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