Iris K. Wong
State Key Laboratory Of Chemical Biology And Drug Discovery
Sar, China
Sar, China
Last Updated: 09/26/2026
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Found 29 publications
Fexinidazole optimization: enhancing anti-leishmanial profile, metabolic stability and hERG safety.
Journal: RSC medicinal chemistry
Published: June 12, 2024
Identification of Binding Sites in the Nucleotide-Binding Domain of P-Glycoprotein for a Potent and Nontoxic Modulator, the Amine-Containing Monomeric Flavonoid FM04.
Journal: Journal of medicinal chemistry
Published: April 25, 2023
In Vivo Reversal of P-Glycoprotein-Mediated Drug Resistance in a Breast Cancer Xenograft and in Leukemia Models Using a Novel, Potent, and Nontoxic Epicatechin EC31.
Journal: International journal of molecular sciences
Published: January 09, 2023
Discovery of a Flavonoid FM04 as a Potent Inhibitor to Reverse P-Glycoprotein-Mediated Drug Resistance in Xenografts and Improve Oral Bioavailability of Paclitaxel.
Journal: International journal of molecular sciences
Published: October 14, 2022
Characterization of a Potent, Selective, and Safe Inhibitor, Ac15(Az8)2, in Reversing Multidrug Resistance Mediated by Breast Cancer Resistance Protein (BCRP/ABCG2).
Journal: International journal of molecular sciences
Published: September 20, 2022
Localization of Epigenetic Markers in Leishmania Chromatin.
Journal: Pathogens (Basel, Switzerland)
Published: August 02, 2022
Flavonoid Monomers as Potent, Nontoxic, and Selective Modulators of the Breast Cancer Resistance Protein (ABCG2).
Journal: Journal of medicinal chemistry
Published: October 04, 2021
Synthesis and evaluation of stereoisomers of methylated catechin and epigallocatechin derivatives on modulating P-glycoprotein-mediated multidrug resistance in cancers.
Journal: European journal of medicinal chemistry
Published: April 23, 2021
Amine-Linked Flavonoids as Agents Against Cutaneous Leishmaniasis.
Journal: Antimicrobial agents and chemotherapy
Published: March 09, 2021
SALL4 promotes tumor progression in breast cancer by targeting EMT.
Journal: Molecular carcinogenesis
Published: April 15, 2020
Disruption of SND1-MTDH Interaction by a High Affinity Peptide Results in SND1 Degradation and Cytotoxicity to Breast Cancer Cells In Vitro and In Vivo.
Journal: Molecular cancer therapeutics
Published: February 24, 2020
Triazole Bridged Flavonoid Dimers as Potent, Nontoxic, and Highly Selective Breast Cancer Resistance Protein (BCRP/ABCG2) Inhibitors.
Journal: Journal of medicinal chemistry
Published: August 30, 2019
Last Updated: 09/26/2026