3TT0

Co-structure of Fibroblast Growth Factor Receptor 1 kinase domain with 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (BGJ398)

3TT0 の概要

• エントリーDOI: 10.2210/pdb3tt0/pdb
• 分子名称: Basic fibroblast growth factor receptor 1, 3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-(6-{[4-(4-ethylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)-1-methylurea, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: kinase domain, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cell membrane; Single-pass type I membrane protein: P11362
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 90377.77

構造登録者

Bussiere, D.E.,Murray, J.M.,Shu, W. (登録日: 2011-09-13, 公開日: 2012-06-13, 最終更新日: 2024-02-28)

主引用文献

Guagnano, V.,Furet, P.,Spanka, C.,Bordas, V.,Le Douget, M.,Stamm, C.,Brueggen, J.,Jensen, M.R.,Schnell, C.,Schmid, H.,Wartmann, M.,Berghausen, J.,Drueckes, P.,Zimmerlin, A.,Bussiere, D.,Murray, J.,Graus Porta, D.
Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase.
J.Med.Chem., 54:7066-7083, 2011

PubMed Abstract: A novel series of N-aryl-N'-pyrimidin-4-yl ureas has been optimized to afford potent and selective inhibitors of the fibroblast growth factor receptor tyrosine kinases 1, 2, and 3 by rationally designing the substitution pattern of the aryl ring. On the basis of its in vitro profile, compound 1h (NVP-BGJ398) was selected for in vivo evaluation and showed significant antitumor activity in RT112 bladder cancer xenografts models overexpressing wild-type FGFR3. These results support the potential therapeutic use of 1h as a new anticancer agent.

PubMed: 21936542
DOI: 10.1021/jm2006222

実験手法

X-RAY DIFFRACTION (2.8 Å)