Synthesis and antiproliferative activities against Hep-G2 of salicylanide derivatives: potent inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase
摘要:
A series of salicylanilide derivatives (compounds 1--32) were synthesised by reacting substituted salicylic acids and anilines. The chemical structures of these compounds were determined by
Analogues of the active metabolite of leflunomide, and to the use thereof as immunosuppressive and/or antinflammatory agents.
Leflunomide的活性代谢物的类似物,以及将其用作免疫抑制和/或抗炎剂的用途。
US5905090A
申请人:——
公开号:US5905090A
公开(公告)日:1999-05-18
Synthesis and antiproliferative activities against Hep-G2 of salicylanide derivatives: potent inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase
A series of salicylanilide derivatives (compounds 1--32) were synthesised by reacting substituted salicylic acids and anilines. The chemical structures of these compounds were determined by