Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aneesa Amar"'
Autor:
Alan J. Kraker, Charles W. Moore, Barvian Mark Robert, Brian G. Hartl, H. D. Hollis Showalter, Aneesa Amar
Publikováno v:
Biochemical Pharmacology. 60:885-898
Increased expression or activity of c-Src tyrosine kinase has been associated with the transformed phenotype in tumor cells and with progression of neoplastic disease. A number of pyrido[2, 3-d]pyrimidines have been characterized biochemically and in
Autor:
Aneesa Amar, Gina H. Lu, Alan J. Kraker, H. D. Hollis Showalter, James Marino Hamby, Barvian Mark Robert, Brian G. Hartl, Robert L. Panek
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2903-2908
Fibroblast growth factor receptor (FGFr) mediated signal transduction is implicated in vascular proliferative diseases and some cancers. We have identified methyl 1-oxo-3-phenyl-1H-indene-2-carboxylic ester as a small molecule inhibitor of the tyrosi
Autor:
Wayne D. Klohs, James Marino Hamby, Alan J. Kraker, David W. Fry, Cindy Shen, Aneesa Amar, Robert L. Panek, Gina H. Lu, Barvian Mark Robert, Connolly Cleo, Mel C. Schroeder, Annette Marian Doherty
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2415-2420
The inhibition of tyrosine kinase-mediated signal transduction pathways represents a therapeutic approach to the intervention of proliferative diseases such as cancer, atherosclerosis, and restenosis. A novel series of pyrido[2,3-d]pyrimidine inhibit
Autor:
Alan J. Kraker, Brian G. Hartl, Gina H. Lu, James Marino Hamby, H. D. Hollis Showalter, Aneesa Amar, Robert L. Panek, Barvian Mark Robert
Publikováno v:
ChemInform. 29
Fibroblast growth factor receptor (FGFr) mediated signal transduction is implicated in vascular proliferative diseases and some cancers. We have identified methyl 1-oxo-3-phenyl-1H-indene-2-carboxylic ester as a small molecule inhibitor of the tyrosi
Autor:
Joan A. Keiser, Tawny K. Dahring, Mel C. Schroeder, and Hussein Hallak, David W. Fry, H. D. Hollis Showalter, James Marino Hamby, Aneesa Amar, Alan J. Kraker, Gina H. Lu, R. Thomas Winters, C. J. C. Connolly, Cindy Shen, James M. Nelson, Annette Marian Doherty, Michael J. Ryan, T C Major, Laura A. Bradford, Veronika Slintak, Bronislawa Olsewski, Robert L. Panek
Publikováno v:
Journal of medicinal chemistry. 40(15)
Screening of a compound library for inhibitors of the fibroblast growth factor (FGFr) and platelet-derived growth factor (PDGFr) receptor tyrosine kinases led to the development of a novel series of ATP competitive pyrido[2,3-d]pyrimidine tyrosine ki