Name | SB 706504 |
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Synonyms | {2-[N-(2-{[8-(2,6-Difluorophenyl)-4-(4-fluoro-2-methylphenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl]amino}ethyl)carbamimidoyl]hydraziniumylidyne}methanide |
Description | SB 706504 is a potent p38 MAPK inhibitor that inhibits Lipopolysaccharides (HY-D1056)-stimulated inflammatory gene expression in macrophages in chronic obstructive pulmonary disease (COPD)[1]. |
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Related Catalog | |
In Vitro | SB 706504 (3 μM, 6 h)可显着降低 IL-1β、IL-6、GM-CSF、TNFα 和 IL-8 mRNA 水平,在 LPS 刺激的 单核细胞来源的巨噬细胞 (MDM)中[1]。 SB 706504(3 μM, 6 h)可显着降低 COPD 患者肺泡巨噬细胞(AM)中 LPS 诱导的 TNFα 水平,抑制率为 67.4%[1]。 |
References |
Molecular Formula | C24H19F3N8O |
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Molecular Weight | 492.456 |
Exact Mass | 492.163391 |