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Journal of Medicinal Chemistry|July 14, 2000
Identification of substituted 3-[(4,5,6, 7-tetrahydro-1H-indol-2-yl)methylene]-1,3-dihydroindol-2-ones as growth factor receptor inhibitors for VEGF-R2 (Flk-1/KDR), FGF-R1, and PDGF-Rbeta tyrosine kinasesL Sun, N Tran, C Liang, et al.Journal of Medicinal Chemistry|December 22, 1999
Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinasesL Sun, N Tran, C Liang, et al.Journal of Medicinal Chemistry|July 3, 1998
Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinasesL Sun, N Tran, F Tang, et al.Cancer Research|August 17, 2001
A novel cdk2-selective inhibitor, SU9516, induces apoptosis in colon carcinoma cellsM E Lane, B Yu, A Rice, et al.Science (New York, N.Y.)|May 9, 1997
Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitorsM Mohammadi, G McMahon, L Sun, et al.Cancer Research|April 28, 2001
Indolinone tyrosine kinase inhibitors block Kit activation and growth of small cell lung cancer cellsG W Krystal, S Honsawek, D Kiewlich, et al.Circulation Research|April 3, 2001
Weekly dosing with the platelet-derived growth factor receptor tyrosine kinase inhibitor SU9518 significantly inhibits arterial stenosisY Yamasaki, K Miyoshi, N Oda, et al.Environmental Health Perspectives|December 1, 1994
The genetics of human cancer: implications for ecotoxicologyG McMahonJAMA|January 13, 1975
Efficacy of an antihypertensive agent. Comparison of methyldopa and hydrochlorothiazide in combination and singlyF G McMahonPageof 550