2of4

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[[Image:2of4.gif|left|200px]]
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{{STRUCTURE_2of4| PDB=2of4 | SCENE= }}
{{STRUCTURE_2of4| PDB=2of4 | SCENE= }}
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'''crystal structure of furanopyrimidine 1 bound to lck'''
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===crystal structure of furanopyrimidine 1 bound to lck===
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==Overview==
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2,3-Diarylfuro[2,3-b]pyridine-4-amines are a novel class of potent and selective inhibitors of Lck. The discovery, synthesis, and structure activity relationships of this series of inhibitors are reported. The most promising compounds were also profiled to deduce their pharmacokinetic properties.
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(as it appears on PubMed at http://www.pubmed.gov), where 17276681 is the PubMed ID number.
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{{ABSTRACT_PUBMED_17276681}}
==Disease==
==Disease==
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[[Category: Kinase domain]]
[[Category: Kinase domain]]
[[Category: Lck]]
[[Category: Lck]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 10:46:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 12:08:11 2008''

Revision as of 09:08, 29 July 2008

Template:STRUCTURE 2of4

Contents

crystal structure of furanopyrimidine 1 bound to lck

Template:ABSTRACT PUBMED 17276681

Disease

Known disease associated with this structure: SCID due to LCK deficiency OMIM:[153390]

About this Structure

2OF4 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Discovery of novel 2,3-diarylfuro[2,3-b]pyridin-4-amines as potent and selective inhibitors of Lck: synthesis, SAR, and pharmacokinetic properties., Martin MW, Newcomb J, Nunes JJ, Bemis JE, McGowan DC, White RD, Buchanan JL, DiMauro EF, Boucher C, Faust T, Hsieh F, Huang X, Lee JH, Schneider S, Turci SM, Zhu X, Bioorg Med Chem Lett. 2007 Apr 15;17(8):2299-304. Epub 2007 Jan 24. PMID:17276681

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