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p38 MAPK P38 mitogen-activated protein kinases

Cat.No.  Name Information
M1781 Adezmapimod (SB203580) Adezmapimod (SB203580) is a P38 MAPK inhibitor with an IC50 of 0.3-0.5 μM, which is 10 times less selective than SAPK3(106T) and SAPK4(106T), and inhibits PKB phosphorylation with an IC50 of 3-5 μM.
M2062 SB 202190 SB 202190 is a highly selective, potent and cell permeable inhibitor of p38 MAP kinase with IC50 values of 50 and 100 nM inhibiting p38α and p38β, respectively.
M1675 BIRB796 BIRB 796 (Doramapimod) is a protein kinase inhibitor of p38 MAPK with Kd of 100pM.
M20327 GI-505946 GI-505946 is a inhibitor of p38.
M20302 WAY-299819 WAY-299819 altering the lifespan of a eukaryotic organism
M20293 WAY-628644 WAY-628644 is a p38α inhibitor.
M20276 WAY-656283 WAY-656283 is a p38 kinase inhibitor.
M20233 WAY-632613 WAY-632613 is a p38 MAP Kinase inhibitor.
M20228 WAY-630998 WAY-630998 is a inhibitor of p38a kinase.
M20191 WAY-603359 WAY-603359 altering the lifespan of a eukaryotic organism
M20082 WAY-313013 WAY-313013 is a p38a Mitogen-Activated Protein Kinase inhibitor
M20042 WAY-270968 WAY-270968 is a p38 MAP Kinase inhibitor.
M20041 WAY-270966 WAY-270966 is a p38 MAP Kinase inhibitor.
M18154 Kaempferol 3-glucorhamnoside Kaempferol 3-glucorhamnoside
M18049 Methyl 4-hydroxy-3-methoxycinnamate Methyl 4-hydroxy-3-methoxycinnamate
M14174 BMS-582949 hydrochloride BMS-582949 hydrochloride is an orally active and highly selective p38α MAPK inhibitor, with an IC50 of 13 nM. BMS-582949 hydrochloride displays a significantly improved pharmacokinetic profile and is effective in inflammatory disease.
M14162 Cot inhibitor-1 Cot inhibitor-1 (compound 28) is a selective tumor progression loci-2 (Tpl2) kinase inhibitor with an IC50 of 28 nM. Cot inhibitor-1 shows an inhibition of TNF-alpha production in human whole blood with an IC50 of 5.7 nM.
M7249 SB 203580 hydrochloride SB 203580 hydrochloride is a selective inhibitor of p38 MAPK; water-soluble.




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