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SB-242235

A selective p38 MAPK inhibitor; inhibits IL-1 beta induction of p38 MAPK in primary human chondrocytes with IC50 of 1 uM; inhibits LPS-stimulated serum levels of TNFalpha in normal rats with mean ED50 of 3.99 mg/kg.Rheumatoid Arthritis Discontinued (In Vitro) :SB 242235 (0-10 μM) dose-dependently inhibits the activation of MAPKAP K2 with an IC50 of 1.0 μM in human chondrocytes stimulated with IL-1β.SB 242235 inhibits intracellular p38 activity, MAPKAP K2 was then isolated from these cells and assayed using HSP27 as a substrate. (In Vivo) :SB242235 (100 mg/kg; p.o.) abolishes MAP-KAPK-2 activity and HSP27 phosphorylation.SB242235 inhibits expression of the pro-inflammatory cytokines interleukin (IL) -6 and KC (murine IL-8) and COX-2.SB-242235 is demonstrated non-linear elimination kinetics that manifested as a decrease in clearance with increasing dose and apparent oral bioavailability > 100% at high oral doses in rat and monkey.

Product Specifications

CAS Number

193746-75-7

Product Name Alternative

SB 242235 | SB242235

Purity

>98% (HPLC)

Solubility

DMSO: ≥ 48 mg/mL

Smiles

O=C (C1=CC=CN=C1) NC2=NC3=C (C=CC (OC) =C3OC) C4=NCCN24

Molecular Formula

C19H20FN5O

Molecular Weight

353.3934

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

Pyrimidine, 4-[4- (4-fluorophenyl) -1- (4-piperidinyl) -1H-imidazol-5-yl]-2-methoxy-

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