2no3: Difference between revisions

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==About this Structure==
==About this Structure==
2NO3 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NO3 OCA].  
2NO3 is a 4 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NO3 OCA].  


==Reference==
==Reference==
Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies., Liu M, Wang S, Clampit JE, Gum RJ, Haasch DL, Rondinone CM, Trevillyan JM, Abad-Zapatero C, Fry EH, Sham HL, Liu G, Bioorg Med Chem Lett. 2007 Feb 1;17(3):668-72. Epub 2006 Nov 2. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17107797 17107797]
<ref group="xtra">PMID:17107797</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Mitogen-activated protein kinase]]
[[Category: Single protein]]
[[Category: Abad-Zapatero, C.]]
[[Category: Abad-Zapatero, C.]]
[[Category: Anilinopyrimidines jnk1 inhibitor]]
[[Category: Anilinopyrimidines jnk1 inhibitor]]
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[[Category: Jnk1 inhibitor]]
[[Category: Jnk1 inhibitor]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 15:58:24 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 11:47:43 2009''

Revision as of 09:47, 17 February 2009

File:2no3.png

Template:STRUCTURE 2no3

Novel 4-anilinopyrimidines as potent JNK1 Inhibitors

Template:ABSTRACT PUBMED 17107797

About this Structure

2NO3 is a 4 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Liu M, Wang S, Clampit JE, Gum RJ, Haasch DL, Rondinone CM, Trevillyan JM, Abad-Zapatero C, Fry EH, Sham HL, Liu G. Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies. Bioorg Med Chem Lett. 2007 Feb 1;17(3):668-72. Epub 2006 Nov 2. PMID:17107797 doi:https://dx.doi.org/10.1016/j.bmcl.2006.10.093

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