2ofv: Difference between revisions

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[[Image:2ofv.jpg|left|200px]]
{{Seed}}
[[Image:2ofv.png|left|200px]]


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{{STRUCTURE_2ofv|  PDB=2ofv  |  SCENE=  }}  
{{STRUCTURE_2ofv|  PDB=2ofv  |  SCENE=  }}  


'''crystal structure of aminoquinazoline 1 bound to Lck'''
===crystal structure of aminoquinazoline 1 bound to Lck===




==Overview==
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The lymphocyte-specific kinase (Lck) is a cytoplasmic tyrosine kinase of the Src family expressed in T cells and natural killer (NK) cells. Genetic evidence in both mice and humans demonstrates that Lck kinase activity is critical for signaling mediated by the T cell receptor (TCR), which leads to normal T cell development and activation. Selective inhibition of Lck is expected to offer a new therapy for the treatment of T-cell-mediated autoimmune and inflammatory disease. Screening of our kinase-preferred collection identified aminoquinazoline 1 as a potent, nonselective inhibitor of Lck and T cell proliferation. In this report, we describe the synthesis and structure-activity relationships of a series of novel aminoquinazolines possessing in vitro mechanism-based potency. Optimized, orally bioavailable compounds 32 and 47 exhibit anti-inflammatory activity (ED(50) of 22 and 11 mg/kg, respectively) in the anti-CD3-induced production of interleukin-2 (IL-2) in mice.
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{{ABSTRACT_PUBMED_16970394}}


==Disease==
==Disease==
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[[Category: Kinase domain]]
[[Category: Kinase domain]]
[[Category: Lck]]
[[Category: Lck]]
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