Synthesis of 13-β-elemene ester derivatives and evaluation of their antioxidant activity in human umbilical vein endothelial cells.
10.1016/S1875-5364(15)30058-3
- Author:
Ji-Chao CHEN
1
,
2
;
Wen-Li DUAN
1
,
3
;
Ren-Ren BAI
1
,
2
;
He-Quan YAO
1
,
2
;
Xiao-Ming WU
1
,
4
;
Jing SHANG
1
,
5
;
Jin-Yi XU
1
,
6
Author Information
1. State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China
2. Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China.
3. Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, China.
4. Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China. Electronic address: xmwu@cpu.edu.cn.
5. Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, China. Electronic address: shangjing21cn@163.com.
6. Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China. Electronic address: jinyixu@china.com.
- Publication Type:Journal Article
- Keywords:
Antioxidant;
HUVECs;
ROS;
Stability;
β-Elemene
- MeSH:
Antioxidants;
chemical synthesis;
metabolism;
pharmacology;
Cells, Cultured;
Curcuma;
chemistry;
Drug Stability;
Drugs, Chinese Herbal;
chemistry;
pharmacology;
Endothelium, Vascular;
cytology;
drug effects;
metabolism;
Human Umbilical Vein Endothelial Cells;
drug effects;
Humans;
Hydrogen Peroxide;
metabolism;
Malondialdehyde;
metabolism;
Nitric Oxide;
metabolism;
Oxidation-Reduction;
Oxidative Stress;
drug effects;
Phthalic Acids;
chemical synthesis;
pharmacology;
Sesquiterpenes;
chemical synthesis;
pharmacology;
Succinates;
chemical synthesis;
pharmacology;
Superoxide Dismutase;
metabolism
- From:
Chinese Journal of Natural Medicines (English Ed.)
2015;13(8):618-627
- CountryChina
- Language:English
-
Abstract:
In the present study, a series of 13-β-elemene ester derivatives were designed and prepared, and their antioxidant activity was investigated in the H2O2-treated human umbilical vein endothelial cells (HUVECs). Among the test compounds, the dimer compounds 5v and 5w exhibited the most potent antioxidant activity with significant ROS suppression being observed. Both compounds markedly inhibited the H2O2-induced changes in various biochemical substances, such as superoxide dismutase (SOD), malonyldialdehyde (MDA), nitric oxide (NO), and lactic dehydrogenase (LDH), which were superior to that of the positive control vitamin E. Further more, they did not produce any obvious cytotoxicity, but increased the viability of HUVECs injured by H2O2 in a dose-dependent manner. Additionally, compound 5w, designed as a prodrug-like compound, showed improved stability relative to compound 4 in vitro.
