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Structure-activity relationship (SAR) studies of 3-(2-amino-ethyl)-5-(4-ethoxy-benzylidene)-thiazolidine-2,4-dione: Development of potential substrate-specific ERK1/2 inhibitors

  作者 Li, QB; Al-Ayoubi, A; Guo, TL; Zheng, H; Sarkar, A; Nguyen, T; Eblen, ST; Grant, S; Kellogg, GE; Zhang, SJ  
  选自 期刊  Bioorganic & Medicinal Chemistry Letters;  卷期  2009年19-21;  页码  6042-6046  
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[摘要]A series of analogs of 3-(2-amino-ethyl)-5-(4-ethoxy-benzylidene)-thiazolidine-2,4-dione, a putative substrate-specific ERK1/2 inhibitor, were synthesized and biologically characterized in human leukemia U937 cells to de. ne its pharmacophore. It was discovered that shift of ethoxy substitution from the 4-to the 2-position on the phenyl ring significantly improved functional activities of inhibiting cell proliferation and inducing apoptosis. This may provide access to a new lead for developing ERK1/2 substrate-specific inhibitors. Published by Elsevier Ltd.

 
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