國家衛生研究院 NHRI:Item 3990099045/9133
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    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/9133


    题名: Cover Picture: Facile identification of dual FLT3–aurora a inhibitors: A computer-guided drug design approach (ChemMedChem 5/2014)
    作者: Chang Hsu, Y;Ke, YY;Shiao, HY;Lee, CC;Lin, WH;Chen, CH;Yen, KJ;Hsu, JTA;Chang, C;Hsieh, HP
    贡献者: Institute of Biotechnology and Pharmaceutical Research
    摘要: The front cover picture shows the in silico design of dual FMS-like receptor tyrosine kinase-3 (FLT3) and Aurora kinase A (AURKA) inhibitors—a potential new class of acute myeloid leukemia (AML) therapeutic agents. Computer-aided drug design (CADD) has various advantages over traditional approaches, such as mitigating laborious optimization work, as well as saving time and being more cost effective. In this work, two consecutive CADD approaches were employed to modify the core structure and side chain of an initial hit compound with AURKA inhibitory activity. A set of virtual compounds derived from the hit structure were designed in silico, and subsequently screened against an FLT3 homology model. The best ranked compounds were then synthesized and evaluated in vitro. Through this approach, a potent, dual FLT3–AURKA inhibitor was generated in a time-efficient manner. For further details, see the Full Paper by Hui-Yi Shiao, Hsing-Pang Hsieh et al. on p. 953 ff.
    日期: 2014-05
    關聯: ChemMedChem. 2014 May;9(5):861.
    Link to: http://dx.doi.org/10.1002/cmdc.201490015
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1860-7179&DestApp=IC2JCR
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