Target Validation Information
Target ID T55729
Target Name Mitogen-activated protein kinase 11
Target Type
Clinical Trial
Drug Potency against Target ML-3403 Drug Info IC50 = 990 nM [526668]
RWJ-68354 Drug Info IC50 = 7 nM [526530]
ML-3163 Drug Info IC50 = 880 nM [526355]
ML-3375 Drug Info IC50 = 1200 nM [526668]
BMS-582949 Drug Info IC50 = 1.5 nM [529348]
References
Ref 526668J Med Chem. 2003 Jul 17;46(15):3230-44.Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes.
Ref 526530Bioorg Med Chem Lett. 2003 Feb 10;13(3):347-50.Imidazopyrimidines, potent inhibitors of p38 MAP kinase.
Ref 526355J Med Chem. 2002 Jun 20;45(13):2733-40.From imidazoles to pyrimidines: new inhibitors of cytokine release.
Ref 526668J Med Chem. 2003 Jul 17;46(15):3230-44.Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes.
Ref 529348Bioorg Med Chem Lett. 2008 Mar 15;18(6):1762-7. Epub 2008 Feb 16.The discovery of (R)-2-(sec-butylamino)-N-(2-methyl-5-(methylcarbamoyl)phenyl) thiazole-5-carboxamide (BMS-640994)-A potent and efficacious p38alpha MAP kinase inhibitor.

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