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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

Novel hybrids of natural β-elemene bearing isopropanolamine moieties: synthesis, enhanced anticancer profile, and improved aqueous solubility Thumbnail


Authors

Jichao Chen

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

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