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Volumn 42, Issue 25, 1999, Pages 5120-5130

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 kinases

Author keywords

[No Author keywords available]

Indexed keywords

2 INDOLINONE DERIVATIVE; FIBROBLAST GROWTH FACTOR RECEPTOR; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PYRROLE DERIVATIVE; TYROSINE KINASE RECEPTOR; UNCLASSIFIED DRUG; VASCULOTROPIN RECEPTOR;

EID: 19244370071     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9904295     Document Type: Article
Times cited : (269)

References (15)
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    • Synthesis and biological evaluations of 3-substituted indolin-2-ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity towards particular receptor tyrosine kinases
    • Sun, L.; Tran, N.; Tang, T.; App, H.; Hirth, P.; McMahon, G.; Tang, C. Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity towards particular receptor tyrosine kinases. J. Med. Chem. 1998, 41 (14), 2588-2603.
    • (1998) J. Med. Chem. , vol.41 , Issue.14 , pp. 2588-2603
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  • 7
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    • Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors
    • Mohammadi, M.; McMahon, G., Sun, L.; Tang, P. C.; Hirth, P.; Yeh, B. K.; Hubbard, S. R.; Schlessinger, J. Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 1997, 276, 955-960.
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  • 8
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    • SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (Flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization, and growth of multiple tumor types
    • Fong, A. T. T.; Shawver, L. K.; Sun, L.; Tang, C.; App. H.; Powell, T. J.; Kim, Y. H.; Schreck, R.; Wang, X. Y.; Risau, W.; Ullrich, A.; Hirth, K. P.; McMahon, G. SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (Flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization, and growth of multiple tumor types. Cancer Res. 1999, 59, 99-106.
    • (1999) Cancer Res. , vol.59 , pp. 99-106
    • Fong, A.T.T.1    Shawver, L.K.2    Sun, L.3    Tang, C.4    App, H.5    Powell, T.J.6    Kim, Y.H.7    Schreck, R.8    Wang, X.Y.9    Risau, W.10    Ullrich, A.11    Hirth, K.P.12    McMahon, G.13
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.