An iridium(iii)-based irreversible protein–protein interaction inhibitor of BRD4 as a potent anticancer agent† †Electronic supplementary information (ESI) available: Synthetic methods, characterization and biological assays details. See DOI: 10.1039/c5sc02321a Click here for additional data file.
نویسندگان
چکیده
State Key Laboratory of Quality Research i Medical Sciences, University of Macau, Ma mo Department of Chemistry, Hong Kong Bapti China. E-mail: [email protected] National Center for Protein Science Shangh Institute of Biochemistry and Cell Biolo Sciences, Chinese Academy of Sciences, Sha Department of Applied Biology and Chemica University, Hung Hom, Kowloon, Hong Kon Partner State Key Laboratory of Environmen Chemistry, Hong Kong Baptist University, 2 Kong SAR, P. R. China. E-mail: zwcai@hkbu Department of Fragrance and Cosmetic Kaohsiung 807, Taiwan, Republic of China. Graduate Institute of Natural Products, K 807, Taiwan, Republic of China † Electronic supplementary information characterization and biological assays det ‡ These authors contributed equally to th Cite this: Chem. Sci., 2015, 6, 5400
منابع مشابه
Formation of a C–C double bond from two aliphatic carbons. Multiple C–H activations in an iridium pincer complex† †Electronic supplementary information (ESI) available: Experimental details, characterization data, Cartesian coordinates, additional graphs and computational details. CCDC 1024127–1024129. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4sc03839h Click here for additional data file. Click here for additional data file.
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Oligobenzamide proteomimetic inhibitors of the p53–hDM2 protein–protein interaction† †Electronic supplementary information (ESI) available: Synthetic procedures, protein expression and FP assays. See DOI: 10.1039/b908207g Click here for additional data file.
Oligobenzamide inhibitors of the p53-hDM2 protein-protein interaction are described.
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عنوان ژورنال:
دوره 6 شماره
صفحات -
تاریخ انتشار 2015