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Synthesis and anti-tumor activity of EF24 analogues as IKKβ inhibitors.

Authors :
Jin R
Chen Q
Yao S
Bai E
Fu W
Wang L
Wang J
Du X
Wei T
Xu H
Jiang C
Qiu P
Wu J
Li W
Liang G
Source :
European journal of medicinal chemistry [Eur J Med Chem] 2018 Jan 20; Vol. 144, pp. 218-228. Date of Electronic Publication: 2017 Dec 07.
Publication Year :
2018

Abstract

EF24 is an IKKβ inhibitor (IC <subscript>50</subscript> : 72 μM) containing various anti-tumor activities. In this study, a series of EF24 analogs targeting IKKβ were designed and synthesized. Several IKKβ inhibitors with better activities than EF24 were screened out and B3 showed best IKKβ inhibitory (IC <subscript>50</subscript> : 6.6 μM). Molecular docking and dynamic simulation experiments further confirmed this inhibitory effect. B3 obviously suppressed the viability of Hela229, A549, SGC-7901 and MGC-803 cells. Then, in SGC-7901 and MGC-803 cells, B3 blocked the NF-κB signal pathway by inhibiting IKKβ phosphorylation, and followed arrested the cell cycle at G2/M phase by suppressing the Cyclin B1 and Cdc2 p34 expression, induced the cell apoptosis by down-regulating Bcl-2 protein and up-regulating cleaved-caspase3. Moreover, B3 significantly reduced tumor growth and suppressed the IKKβ-NF-κB signal pathway in SGC-7901 xenograft model. In total, this study present a potential IKKβ inhibitor as anti-tumor precursor.<br /> (Copyright © 2017. Published by Elsevier Masson SAS.)

Details

Language :
English
ISSN :
1768-3254
Volume :
144
Database :
MEDLINE
Journal :
European journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
29351887
Full Text :
https://doi.org/10.1016/j.ejmech.2017.11.077