4-Fluoro-3′,4′,5′-trimethoxychalcone as a new anti-invasive agent. From discovery to initial validation in an in vivo metastasis model

被引:12
|
作者
Roman, Bart I. [1 ]
De Ryck, Tine [2 ]
Patronov, Atanas [3 ]
Slavov, Svetoslav H. [3 ]
Vanhoecke, Barbara W. A. [2 ]
Katritzky, Alan R. [3 ,4 ]
Bracke, Marc E. [2 ]
Stevens, Christian V. [1 ]
机构
[1] Univ Ghent, Dept Sustainable Organ Chem & Technol, Res Grp SynBioC, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Radiat Oncol & Expt Canc Res, Lab Expt Canc Res, B-9000 Ghent, Belgium
[3] Univ Florida, Ctr Heterocycl Cpds, Dept Chem, Gainesville, FL 32611 USA
[4] King Abdulaziz Univ, Dept Chem, Jeddah 21589, Saudi Arabia
关键词
Invasion; Metastasis; Chalcone; QSAR; Cancer; In vivo; BIOLOGICAL EVALUATION; CHEMICAL-STRUCTURE; ENDOTHELIAL-CELLS; DRUG DEVELOPMENT; BONE-MARROW; MOUSE MODEL; CHALCONES; QSAR; INHIBITOR; VITRO;
D O I
10.1016/j.ejmech.2015.06.029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Invasion and metastasis are responsible for 90% of cancer-related mortality. Herein, we report on our quest for novel, clinically relevant inhibitors of local invasion, based on a broad screen of natural products in a phenotypic assay. Starting from micromolar chalcone hits, a predictive QSAR model for diaryl propenones was developed, and synthetic analogues with a 100-fold increase in potency were obtained. Two nanomolar hits underwent efficacy validation and eADMET profiling; one compound was shown to increase the survival time in an artificial metastasis model in nude mice. Although the molecular mechanism(s) by which these substances mediate efficacy remain(s) unrevealed, we were able to eliminate the major targets commonly associated with antineoplastic chalcones. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:627 / 639
页数:13
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