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Journal of Medicinal Chemistry|August 30, 2019
Triazole Bridged Flavonoid Dimers as Potent, Nontoxic, and Highly Selective Breast Cancer Resistance Protein (BCRP/ABCG2) InhibitorsXuezhen Zhu, Iris L K Wong, Kin-Fai Chan, et al.
Antimicrobial Agents and Chemotherapy|March 9, 2021
Amine-Linked Flavonoids as Agents Against Cutaneous LeishmaniasisChin-Fung Chan, Zhen Liu, Iris L K Wong, et al.
Frontiers in Bioscience : a Journal and Virtual Library|September 11, 2004
Green tea and tea polyphenols in cancer preventionDi Chen, Kenyon G Daniel, Deborah J Kuhn, et al.
Biochemical Pharmacology|December 17, 2016
Flavonoid dimers are highly potent killers of multidrug resistant cancer cells overexpressing MRP1Lauriane Dury, Rachad Nasr, Doriane Lorendeau, et al.
Anti-Cancer Agents in Medicinal Chemistry|December 17, 2014
Lessons from Nature: Sources and Strategies for Developing AMPK Activators for Cancer ChemotherapeuticsRichard T Arkwright, Rahul Deshmukh, Nikhil Adapa, et al.
Molecular Cancer Therapeutics|December 3, 2020
Disruption of SND1-MTDH Interaction by a High Affinity Peptide Results in SND1 Degradation and Cytotoxicity to Breast Cancer Cells <i>In Vitro</i> and <i>In Vivo</i>Peng Li, Yunjiao He, Teng Chen, et al.
European Journal of Medicinal Chemistry|October 23, 2018
Design, synthesis and antibacterial evaluation of 2,4-disubstituted-6-thiophenyl-pyrimidinesZhiyuan Fang, Sichao Zheng, Kin-Fai Chan, et al.
Chemmedchem|March 17, 2009
Flavonoid dimers as bivalent modulators for p-glycoprotein-based multidrug resistance: structure-activity relationshipsKin-Fai Chan, Yunzhe Zhao, Toby W S Chow, et al.
International Journal of Molecular Sciences|November 11, 2022
Characterization of a Potent, Selective, and Safe Inhibitor, Ac15(Az8)<sub>2</sub>, in Reversing Multidrug Resistance Mediated by Breast Cancer Resistance Protein (BCRP/ABCG2)Tsz Cheung Chong, Iris L K Wong, Jiahua Cui, et al.
Bioorganic Chemistry|May 4, 2020
Bioisosteric investigation of ebselen: Synthesis and in vitro characterization of 1,2-benzisothiazol-3(2H)-one derivatives as potent New Delhi metallo-β-lactamase inhibitorsWen Bin Jin, Chen Xu, Qipeng Cheung, et al.
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