Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.bmc.2007.10.006
Title: Functionalized chalcones as selective inhibitors of P-glycoprotein and breast cancer resistance protein
Authors: Liu, X.-L.
Tee, H.-W.
Go, M.-L. 
Keywords: Breast cancer resistance protein
Chalcones with basic functionalities
Inhibition of ABC transport proteins
P-glycoprotein
Structure-activity analysis
Issue Date: 1-Jan-2008
Citation: Liu, X.-L., Tee, H.-W., Go, M.-L. (2008-01-01). Functionalized chalcones as selective inhibitors of P-glycoprotein and breast cancer resistance protein. Bioorganic and Medicinal Chemistry 16 (1) : 171-180. ScholarBank@NUS Repository. https://doi.org/10.1016/j.bmc.2007.10.006
Abstract: A library of chalcones with basic functionalities were screened for inhibition of P-glycoprotein (Pgp, ABCB1) by the calcein-AM accumulation assay on MDCKII/MDR1 cells. Three members that had ring A substituted with 5-(1-ethylpiperidin-4-yl) and 2,4-dimethoxy groups were found to increase calcein-AM accumulation to a greater extent than verapamil, a Pgp inhibitor. These compounds were subsequently shown to enhance the uptake of doxorubicin by MCF-7 cells that over-expressed Pgp. However, when tested for inhibition of the breast cancer resistance protein (BCRP, ABCG2) by the mitoxantrone uptake assay, the same compounds fared poorly. In comparison, a non-basic chalcone (5-14, 3-(4-chlorophenyl)-1-(2,4-dimethoxyphenyl)prop-2-en-1-one) increased mitoxantrone uptake by BCRP over-expressing MCF-7 cells (MCF-7/MX) by more than 300% at 5 μM. Thus, introducing a basic group on the chalcone template enhanced Pgp inhibition at the expense of BCRP inhibition. The basic chalcones were also better Pgp inhibitors than their non-basic counterparts which may in turn be better BCRP inhibitors. Structure activity analysis showed that lipophilicity of the chalcones was not the overriding factor for Pgp inhibitory activity. Rather, good activity was associated with appropriately placed electron donor atoms, of which the meta-disubstituted dimethoxy motif on either ring A or B was of particular relevance. In spite of differing structural requirements for inhibition of Pgp and BCRP, chalcone 3-100 [3-(2,4-dimethoxyphenyl)-1-(4-(piperazin-1-yl)phenyl)prop-2-en-1-one] inhibited both Pgp and BCRP to a reasonable extent and may be a useful starting point for the design of dual inhibitors. © 2007 Elsevier Ltd. All rights reserved.
Source Title: Bioorganic and Medicinal Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/105975
ISSN: 09680896
DOI: 10.1016/j.bmc.2007.10.006
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