Tri-heterocyclic derivatives, preparation process and uses thereof

作者: Yajun Yu , Heping Yang , Daxin Gao

DOI:

关键词: ChemistryOrganic chemistryHeterocyclic derivatives

摘要: The present invention relates to a tri-heterocyclic derivatives, preparation process and uses thereof, specifically derivatives of the formula (I) or pharmaceutically acceptable salt process, further composition comprising compounds (I), their pharmaceutical use as inhibitors kinase.

参考文章(6)
Qi Chao, Shripad Bhagwat, Kelly G. Sprankle, Robert M. Grotzfeld, Hitesh K Patel, Imidazolothiazole compounds for the treatment of disease ,(2007)
Joyce K. James, Darren E. Inski, Julius L. Apuy, Imidazolothiazole compounds as modulators of protein kinase ,(2009)
Timothy Bruno Lowinger, Uday Khire, Jeffrey Johnson, Jill E. Wood, Aniko Redman, William J. Scott, Roger A. Smith, Holger Paulsen, Bernd Riedl, Jacques Dumas, Wendy Lee, Holia Hatoum-Mokdad, Inhibition of p38 kinase activity using substituted heterocyclic ureas ,(1998)
Qi Chao, Kelly G. Sprankle, Robert M. Grotzfeld, Andiliy G. Lai, Todd A. Carter, Anne Marie Velasco, Ruwanthi N. Gunawardane, Merryl D. Cramer, Michael F. Gardner, Joyce James, Patrick P. Zarrinkar, Hitesh K. Patel, Shripad S. Bhagwat, Identification of N-(5-tert-butyl-isoxazol-3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea dihydrochloride (AC220), a uniquely potent, selective, and efficacious FMS-like tyrosine kinase-3 (FLT3) inhibitor. Journal of Medicinal Chemistry. ,vol. 52, pp. 7808- 7816 ,(2009) , 10.1021/JM9007533