Recent progress in the structural modification and pharmacological activities of ligustrazine derivatives

被引:70
|
作者
Zou, Jinmi [1 ]
Gao, Ping [1 ]
Hao, Xia [1 ]
Xu, Haoran [1 ]
Zhan, Peng [1 ]
Liu, Xinyong [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Minist Educ, Dept Med Chem,Key Lab Chem Biol, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China
关键词
Ligustrazine derivatives; Pharmacological activities; Drug design; Antioxidation; Anticardiovascular disease; Anticancer; Neuroprotective; Antibacterial; Anti-inflammatory; RESISTANT BREAST-CANCER; BIOLOGICAL EVALUATION; OXIDATIVE STRESS; NATURAL-PRODUCTS; IN-VITRO; INDUCED NEUROTOXICITY; MULTIDRUG-RESISTANCE; ACID-DERIVATIVES; OLEANOLIC ACID; FREE-RADICALS;
D O I
10.1016/j.ejmech.2018.01.097
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ligustrazine is a main active fraction of the traditional medicine known as Ligusticum chuanxiong hort, which has been used as clinical medication for cerebral thrombosis, coronary heart disease and stenocardia recently. The rapid metabolism and short half-life of ligustrazine seriously limits its application in clinical practice. Therefore, derivatives of ligustrazine are designed and synthesized in our and other labs, including piperazine, cinnamic acid, styrene, acylguanidine, amides, curcumin and triterpenes derivatives of ligustrazine. Most of these compounds present better pharmacodynamics activities and more favorable pharmacokinetic properties compared to the parent compound. Besides, some new biological activities of these compounds are discovered. Hence, this review continues the previous review of our group as well as aims to highlight recent prominent advances in this field in the past ten years. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:150 / 162
页数:13
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