Synthesis and biological evaluation of ursolic acid derivatives bearing triazole moieties as potential anti-Toxoplasma gondii agents

被引:25
|
作者
Luan, Tian [1 ]
Jin, Chunmei [1 ]
Jin, Chun-Mei [1 ]
Gong, Guo-Hua [2 ,3 ]
Quan, Zhe-Shan [1 ]
机构
[1] Yanbian Univ, Coll Pharm, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Yanji 133002, Jilin, Peoples R China
[2] Inner Mongolia Univ Nationalities, Clin Med Coll 1, Tongliao, Peoples R China
[3] Inner Mongolia Univ Nationalities, Inner Mongolia Key Lab Mongolian Med Pharmacol Ca, Tongliao, Peoples R China
基金
中国国家自然科学基金;
关键词
Toxoplasma gondii; ursolic acid; molecular docking; TgCDPK1; in vivo; in vitro; IN-VITRO; VIVO;
D O I
10.1080/14756366.2019.1584622
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ursolic acid (UA), a plant-derived compound, has many properties beneficial to health. In the present study, we synthesised three series of novel UA derivatives and evaluated their anti-Toxoplasma gondii activity both in vitro and in vivo. Most derivatives exhibited an improved anti-T. gondii activity in vitro when compared with UA (parent compound), whereas compound 3d exhibited the most potent anti-T. gondii activity in vivo. Spiramycin served as the positive control. Additionally, determination of biochemical parameters, including the liver and spleen indexes, indicated compound 3d to effectively reduce hepatotoxicity and significantly enhance anti-oxidative effects, as compared with UA. Furthermore, our molecular docking study indicated compound 3d to possess a strong binding affinity for T. gondii calcium-dependent protein kinase 1 (TgCDPK1). Based on these findings, we conclude that compound 3d, a derivative of UA, could act as a potential inhibitor of TgCDPK1.
引用
收藏
页码:761 / 772
页数:12
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