Synthesis and structure–activity relationships of thioflavone derivatives as specific inhibitors of the ERK-MAP kinase signaling pathway
T Kataoka, S Watanabe, E Mori, R Kadomoto…
Index: Bioorganic and Medicinal Chemistry, , vol. 12, # 9 p. 2397 - 2407
Full Text: HTML
Citation Number: 28
Abstract
... Bioorganic & Medicinal Chemistry. ... b Laboratory of Cell Regulation, Department of Pharmaceutical Sciences, Graduate School of Biomedical Sciences, Nagasaki University, 1-14, Bunkyo-machi, Nagasaki 852-8521, Japan. ...
Related Articles:
Design and synthesis of 6, 6-fused heterocyclic amides as raf kinase inhibitors
[Ramurthy, Savithri; Costales, Abran; Jansen, Johanna M.; Levine, Barry; Renhowe, Paul A.; Shafer, Cynthia M.; Subramanian, Sharadha Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 4 p. 1678 - 1681]
A novel and practical synthesis of 2-amino-5-hydroxypropiophenone
[Xiong, Xiao-Dong; Chen, Wen-Xue; Kuang, Yun-Yan; Chen, Fen-Er Organic Preparations and Procedures International, 2009 , vol. 41, # 5 p. 423 - 427]
Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction
[Gavara, Laurent; Boisse, Thomas; Henichart, Jean-Pierre; Daich, Adam; Rigo, Benoit; Gautret, Philippe Tetrahedron, 2010 , vol. 66, # 38 p. 7544 - 7561]
2-amino and 2'-aminocombretastatin derivatives as potent antimitotic agents
[Journal of Medicinal Chemistry, , vol. 49, # 21 p. 6412 - 6415]
[Liebigs Annalen der Chemie, , # 6 p. 537 - 538]