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Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr.

Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Research Abstract Details 

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  • Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Abstract Text:

    celia dominguezCelia Dominguez,leon smithLeon Smith,qi huangQi Huang,chester yuanChester Yuan,xiaohu ouyangXiaohu Ouyang,lynn caiLynn Cai,paul chenPaul Chen,joseph kimJoseph Kim,timothy harveyTimothy Harvey,rashid syedRashid Syed,tae-seong kimTae-Seong Kim,andrew taskerAndrew Tasker,ling wangLing Wang,michael zhangMichael Zhang,angela coxonAngela Coxon,james breadyJames Bready,charles starnesCharles Starnes,danlin chenDanlin Chen,yongmei ganYongmei Gan,sesha neervannanSesha Neervannan,gondi kumarGondi Kumar,anthony polverinoAnthony Polverino,richard kendallRichard Kendall,celia dominguezCelia Dominguez,leon smithLeon Smith,qi huangQi Huang,chester yuanChester Yuan,xiaohu ouyangXiaohu Ouyang,lynn caiLynn Cai,paul chenPaul Chen,joseph kimJoseph Kim,timothy harveyTimothy Harvey,rashid syedRashid Syed,tae-seong kimTae-Seong Kim,andrew taskerAndrew Tasker,ling wangLing Wang,michael zhangMichael Zhang,angela coxonAngela Coxon,james breadyJames Bready,charles starnesCharles Starnes,danlin chenDanlin Chen,yongmei ganYongmei Gan,sesha neervannanSesha Neervannan,gondi kumarGondi Kumar,anthony polverinoAnthony Polverino,richard kendallRichard Kendall,

    Inhibition of tumor-induced angiogenesis is a promising strategy in anticancer research. Neovascularization is a process required for both tumor growth and metastasis. Enhanced understanding of the underlying molecular mechanisms has led to the discovery of a variety of pharmaceutically attractive targets. Decades of investigation suggest that vascular endothelial growth factor (VEGF) and its receptors, in particular VEGFR2 or kinase insert-domain-containing receptor (Kdr), play a critical role in the growth and survival of endothelial cells in newly forming vasculature. The clinical utility of inhibitors of this receptor tyrosine kinase is currently under intense investigation. Herein we report our efforts in this arena.

    Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Publishing Authors By Initials

    c dominguezC Dominguez,l smithL Smith,q huangQ Huang,c yuanC Yuan,x ouyangX Ouyang,l caiL Cai,p chenP Chen,j kimJ Kim,t harveyT Harvey,r syedR Syed,ts kimTS Kim,a taskerA Tasker,l wangL Wang,m zhangM Zhang,a coxonA Coxon,j breadyJ Bready,c starnesC Starnes,d chenD Chen,y ganY Gan,s neervannanS Neervannan,g kumarG Kumar,a polverinoA Polverino,r kendallR Kendall,c dominguezC Dominguez,l smithL Smith,q huangQ Huang,c yuanC Yuan,x ouyangX Ouyang,l caiL Cai,p chenP Chen,j kimJ Kim,t harveyT Harvey,r syedR Syed,ts kimTS Kim,a taskerA Tasker,l wangL Wang,m zhangM Zhang,a coxonA Coxon,j breadyJ Bready,c starnesC Starnes,d chenD Chen,y ganY Gan,s neervannanS Neervannan,g kumarG Kumar,a polverinoA Polverino,r kendallR Kendall,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Bioorganic & medicinal chemistry letters

    VOLUME: 17

    Page Numbers: 6003-8

    Journal Abbreviation: Bioorg. Med. Chem. Lett.

    ISSN: 0960-894X

    DAY: 22

    MONTH: 08

    YEAR: 2007

    Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9107377

    Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr. Information

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    Grant and Affiliation Information for Discovery of N-phenyl nicotinamides as potent inhibitors of Kdr.

    AFFILIATION: Chemistry Research and Discovery, One Amgen Center Drive Thousand Oaks, CA 91320, USA. celia.dominguez@chdi-inc.org

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Bioorg Med Chem Lett

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