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Volumn 4, Issue 9, 2013, Pages 835-840

Discovery, design, and optimization of isoxazole azepine BET inhibitors

Author keywords

BET inhibitors; bromodomain; fragments; isoxazoles; MYC

Indexed keywords

AZEPINE DERIVATIVE; ISOXAZOLE DERIVATIVE; MOLECULAR SCAFFOLD;

EID: 84884238437     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml4001485     Document Type: Article
Times cited : (100)

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    • Oncoprotein As a Therapeutic Target for Human Cancer
    • Vita, M.; Henricksson, M.; Myc, M. M. Oncoprotein As a Therapeutic Target for Human Cancer Semin. Cancer Biol. 2006, 16, 318-330
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  • 15
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    • Fragment-Based Discovery of Bromodomain Inhibitors Part 1: Inhibitor Binding Modes and Implications for Lead Discovery
    • Chung, C. W.; Dean, A. W.; Woolven, J. M.; Bamborough, P. Fragment-Based Discovery of Bromodomain Inhibitors Part 1: Inhibitor Binding Modes and Implications for Lead Discovery J. Med. Chem. 2012, 55, 576-586
    • (2012) J. Med. Chem. , vol.55 , pp. 576-586
    • Chung, C.W.1    Dean, A.W.2    Woolven, J.M.3    Bamborough, P.4
  • 21
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    • An Analysis of the Binding Efficiencies of Drugs and Their Leads in Successful Drug Discovery Programs
    • Perola, E. An Analysis of the Binding Efficiencies of Drugs and Their Leads in Successful Drug Discovery Programs J. Med. Chem. 2010, 53, 2986-2997
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    • Perola, E.1
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    • Ligand Efficiency Indices for Effective Drug Discovery
    • Abad-Zapatero, C. Ligand Efficiency Indices for Effective Drug Discovery Expert Opin. Drug Discovery 2007, 2, 469-488
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    • Abad-Zapatero, C.1
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    • N - Tert -Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines
    • Ellman, J. A.; Owens, T. D.; Tang, T. P. N-tert -Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines Acc. Chem. Res. 2002, 35, 984-995
    • (2002) Acc. Chem. Res. , vol.35 , pp. 984-995
    • Ellman, J.A.1    Owens, T.D.2    Tang, T.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.