Synthesis and biological evaluation of bifendate–chalcone hybrids as a new class of potential P-glycoprotein inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of bifendate–chalcone hybrids as a new class of potential P-glycoprotein inhibitors

Published:2012-04 Issue:8 Volume:20 Page:2540-2548
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Gu Xiaoke,Ren Zhiguang,Tang Xiaobo,Peng Hui,Ma Yuanfang,Lai Yisheng,Peng Sixun,Zhang Yihua

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference24 articles.

1. Structure of P-Glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding

2. Identification of Compounds Selectively Killing Multidrug-Resistant Cancer Cells

3. N,N-bis(Cyclohexanol)amine Aryl Esters: A New Class of Highly Potent Transporter-Dependent Multidrug Resistance Inhibitors

4. ABC transporters in cancer: more than just drug efflux pumps

5. Efflux Pump Inhibitors: A Strategy to Combat P-Glycoprotein and the NorA Multidrug Resistance Pump

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5. Reversal of multidrug resistance by Fissistigma latifolium–derived chalconoid 2-hydroxy-4,5,6-trimethoxydihydrochalcone in cancer cell lines overexpressing human P-glycoprotein;Biomedicine & Pharmacotherapy;2022-12

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