Novel nannocystin A analogues as anticancer therapeutics: Synthesis, biological evaluations and structure–activity relationship studies

European Journal of Medicinal Chemistry
2019.0

Abstract

Nannocystin A is a novel 21-membered macrocyclic lactam that targets eukaryotic translation elongation factor 1α (eEF1A) and displays potent antiproliferative activities. Herein, a series of nannocystin A analogues were synthesized and their structure-activity relationship (SAR) were established based on the MTT assay and western blotting analysis. The SAR enabled us to identify a structurally simplified nannocystin A analogue LQ18, which exhibited potent antiproliferative activities with IC50 values ranging from 4.3 to 48 nM against the tested cell lines, and inhibited eEF1A1 expression in A549 cell line. LQ18 arrested cell cycle at G2 phase and induced A549 cell apoptosis via up-regulation of caspase-3, caspase-9 and bax protein expressions in a dose-dependent manner, while it significantly decreased the bcl-2 expression. Collectively, these data demonstrated that LQ18 could be a promising lead for the development of structurally novel eEF1A1 inhibitor for cancer treatment.

Knowledge Graph

Similar Paper

Novel nannocystin A analogues as anticancer therapeutics: Synthesis, biological evaluations and structure–activity relationship studies
European Journal of Medicinal Chemistry 2019.0
Synthesis and biological evaluation of nannocystin analogues toward understanding the binding role of the (2R,3S)-Epoxide in nannocystin A
European Journal of Medicinal Chemistry 2018.0
Discovery, Structure Elucidation, and Biological Characterization of Nannocystin A, a Macrocyclic Myxobacterial Metabolite with Potent Antiproliferative Properties
Angewandte Chemie International Edition 2015.0
Site-directed late-stage diversification of macrocyclic nannocystins facilitating anticancer SAR and mode of action studies
RSC Medicinal Chemistry 2022.0
Discovery of Autophagy Inhibitors with Antiproliferative Activity in Lung and Pancreatic Cancer Cells
ACS Medicinal Chemistry Letters 2015.0
Synthesis and Cytotoxic Evaluation of Some Cribrostatin–Ecteinascidin Analogues
Journal of Natural Products 2008.0
Design, synthesis and anticancer activity of Michael-type thiol adducts of α-santonin analogue with exocyclic methylene
European Journal of Medicinal Chemistry 2015.0
The pterocarpanquinone LQB-118 inhibits tumor cell proliferation by downregulation of c-Myc and cyclins D1 and B1 mRNA and upregulation of p21 cell cycle inhibitor expression
Bioorganic & Medicinal Chemistry 2014.0
Synthesis and biological evaluation of l-cysteine derivatives as mitotic kinesin Eg5 inhibitors
Bioorganic & Medicinal Chemistry Letters 2007.0
Design, synthesis and biological evaluation of 1,4-dihydroxyanthraquinone derivatives as anticancer agents
Bioorganic & Medicinal Chemistry Letters 2019.0