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Volumn 46, Issue 22, 2003, Pages 4676-4686

Structure-Activity Relationships of the p38α MAP Kinase Inhibitor 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy) naphthalen-1-yl]urea (BIRB 796)

Author keywords

[No Author keywords available]

Indexed keywords

1 [5 TERT BUTYL 2 (4 TOLYL 2H PYRAZOL 3 YL)] 3 [4 (2 MORPHOLIN 4 YLETHOXY)NAPHTHALEN 1 YL]UREA; ADENOSINE TRIPHOSPHATE; AROMATIC COMPOUND; DORAMAPIMOD; IMIDAZOLE; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MORPHOLINE; PHOSPHOTRANSFERASE; PYRAZOLE DERIVATIVE; PYRIDINE; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG;

EID: 0142028917     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm030121k     Document Type: Article
Times cited : (123)

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    • note
    • Human p38-α and murine p38-α differ by two amino acids: Leu47 to His47 and Thr262 to Ala262. We have shown that these differences have negligible effects on the binding affinity for this class of inhibitors (data not shown).


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