Jichao Chen
Novel hybrids of natural β-elemene bearing isopropanolamine moieties: synthesis, enhanced anticancer profile, and improved aqueous solubility
Chen, Jichao; Wang, Tianyu; Xu, Shengtao; Aijun, Lin; Yao, Hequan; Xie, Weijia; Zhu, Zheying; Xu, Jinyi
Authors
Tianyu Wang
Shengtao Xu
Lin Aijun
Hequan Yao
Weijia Xie
ZHEYING ZHU Zheying.Zhu@nottingham.ac.uk
Associate Professor in International Pharmacy and Traditional Medicines
Jinyi Xu
Abstract
A series of novel β-elemene isopropanolamine derivatives were synthesized and evaluated for their antitumor activity. The results indicated that all of the compounds showed stronger antiproliferative activities than β-elemene as well as improved aqueous solubility. In particular dimer 6q showed the strongest cytotoxicity against four tumor cell lines (SGC-7901, HeLa, U87 and A549) with IC50 values ranging from 4.37 to 10.20 μM. Moreover, combination of 6q with cisplatin exhibited a synergistic effect on these cell lines with IC50 values ranging from 1.21 to 2.94 μM, and reversed the resistance of A549/DPP cells with an IC50 value of 2.52 μM. The mechanism study revealed that 6q caused cell cycle arrest at the G2 phase and induced apoptosis of SGC-7901 cells through a mitochondrial-dependent apoptotic pathway. Further in vivo study in H22 liver cancer xenograft mouse model validated the antitumor activity of 6q with a tumor inhibitory ratio (TIR) of 60.3%, which was higher than that of β-elemene (TIR, 49.1%) at a dose of 60 mg/kg. Altogether, the potent antitumor activity of 6qin vitro and in vivo warranted further preclinical investigation for potential anticancer chemotherapy.
Citation
Chen, J., Wang, T., Xu, S., Aijun, L., Yao, H., Xie, W., …Xu, J. (2017). Novel hybrids of natural β-elemene bearing isopropanolamine moieties: synthesis, enhanced anticancer profile, and improved aqueous solubility. Fitoterapia, 120, https://doi.org/10.1016/j.fitote.2017.05.002
Journal Article Type | Article |
---|---|
Acceptance Date | May 16, 2017 |
Online Publication Date | May 31, 2017 |
Publication Date | Jul 1, 2017 |
Deposit Date | Jul 4, 2017 |
Publicly Available Date | Jul 4, 2017 |
Journal | Fitoterapia |
Print ISSN | 0367-326X |
Electronic ISSN | 1873-6971 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 120 |
DOI | https://doi.org/10.1016/j.fitote.2017.05.002 |
Keywords | β-Elemene; Isopropanolamine; Dimer; Antitumor activity; Aqueous solubility |
Public URL | https://nottingham-repository.worktribe.com/output/967731 |
Publisher URL | http://www.sciencedirect.com/science/article/pii/S0367326X17301429 |
Contract Date | Jul 4, 2017 |
Files
Fitoterapia 052017.pdf
(1.2 Mb)
PDF
Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by-nc-nd/4.0
You might also like
The structural modification of natural products for novel drug discovery
(2016)
Journal Article
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search