Detalhe da pesquisa
1.
Synthesis, biological evaluation and molecular modelling of 2,4-disubstituted-5-(6-alkylpyridin-2-yl)-1H-imidazoles as ALK5 inhibitors.
J Enzyme Inhib Med Chem;
35(1): 702-712, 2020 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32164459
2.
Synthesis and biological evaluation of 2-pyridyl-substituted pyrazoles and imidazoles as transforming growth factor-beta type 1 receptor kinase inhibitors.
Bioorg Med Chem Lett;
20(14): 4228-32, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20621731
3.
Synthesis and biological evaluation of 4(5)-(6-methylpyridin-2-yl)imidazoles and -pyrazoles as transforming growth factor-beta type 1 receptor kinase inhibitors.
Bioorg Med Chem;
18(12): 4459-67, 2010 Jun 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20472445
4.
Synthesis and biological evaluation of trisubstituted imidazole derivatives as inhibitors of p38alpha mitogen-activated protein kinase.
Bioorg Med Chem Lett;
18(14): 4006-10, 2008 Jul 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18571921
5.
Protein tyrosine phosphatases and their inhibitors.
Curr Med Chem;
12(1): 1-22, 2005.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15638728
6.
Synthesis and biological evaluation of benzenesulfonamide-substituted 4-(6-alkylpyridin-2-yl)-5-(quinoxalin-6-yl)imidazoles as transforming growth factor-beta type 1 receptor kinase inhibitors.
Eur J Med Chem;
44(2): 568-76, 2009 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18467006
7.
Traceless solid-phase synthesis of carbolinones.
J Comb Chem;
6(6): 855-8, 2004.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15530109