Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T55729 | ||||
Target Name | Stress-activated protein kinase 2b (p38 beta) | ||||
Type of Target |
Clinical trial |
||||
Drug Potency against Target | BMS-582949 | Drug Info | IC50 = 1.5 nM | [4] | |
ML-3163 | Drug Info | IC50 = 880 nM | [1] | ||
ML-3375 | Drug Info | IC50 = 1200 nM | [3] | ||
ML-3403 | Drug Info | IC50 = 990 nM | [3] | ||
RWJ-68354 | Drug Info | IC50 = 7 nM | [2] | ||
References | |||||
REF 1 | From imidazoles to pyrimidines: new inhibitors of cytokine release. J Med Chem. 2002 Jun 20;45(13):2733-40. | ||||
REF 2 | Imidazopyrimidines, potent inhibitors of p38 MAP kinase. Bioorg Med Chem Lett. 2003 Feb 10;13(3):347-50. | ||||
REF 3 | Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes. J Med Chem. 2003 Jul 17;46(15):3230-44. | ||||
REF 4 | The discovery of (R)-2-(sec-butylamino)-N-(2-methyl-5-(methylcarbamoyl)phenyl) thiazole-5-carboxamide (BMS-640994)-A potent and efficacious p38alph... Bioorg Med Chem Lett. 2008 Mar 15;18(6):1762-7. | ||||
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