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合成黄芩素衍生物以提高生物活性和水溶性。

Synthesis of scutellarein derivatives to increase biological activity and water solubility.

作者信息

Shi Zhi-Hao, Li Nian-Guang, Shi Qian-Ping, Zhang Wei, Dong Ze-Xi, Tang Yu-Ping, Zhang Peng-Xuan, Gu Ting, Wu Wen-Yu, Fang Fang, Li He-Min, Yang Jian-Ping, Duan Jin-Ao

机构信息

Jiangsu Collaborative Innovation Center of Chinese Medicine Resources Industrialization, Jiangsu Key Laboratory for High Technology Research of TCM Formulae, and National and Local Collaborative Engineering Center of Chinese Medicine Resources, Nanjing University of Chinese Medicine, Nanjing 210023, China; Department of Organic Chemistry, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.

Jiangsu Collaborative Innovation Center of Chinese Medicine Resources Industrialization, Jiangsu Key Laboratory for High Technology Research of TCM Formulae, and National and Local Collaborative Engineering Center of Chinese Medicine Resources, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Bioorg Med Chem. 2015 Nov 1;23(21):6875-84. doi: 10.1016/j.bmc.2015.09.047. Epub 2015 Oct 1.

Abstract

In order to improve the biological activity and water solubility of scutellarin (1), some derivatives of its main metabolite (scutellarein) were designed and synthesized. All the compounds were tested for their thrombin inhibition activity through the analyzation of thrombin time (TT), activated partial thromboplastin time (APTT), prothrombin time (PT) and fibrinogen (FIB). Their antioxidant activities were assessed by measuring their scavenging capacities toward 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) and the ability to protect PC12 cells against H2O2-induced cytotoxicity, their water solubility were also assessed by ultraviolet (UV) spectrophotometer. The results showed that compound 8b demonstrated stronger anticoagulant and antioxidant activity, better water solubility compared with scutellarein (2), which warrants it as a promising agent for the treatment of ischemic cerebrovascular disease.

摘要

为了提高灯盏花素(1)的生物活性和水溶性,设计并合成了其主要代谢产物(灯盏花乙素)的一些衍生物。通过分析凝血酶时间(TT)、活化部分凝血活酶时间(APTT)、凝血酶原时间(PT)和纤维蛋白原(FIB),对所有化合物的凝血酶抑制活性进行了测试。通过测量它们对1,1-二苯基-2-苦基肼自由基(DPPH)的清除能力以及保护PC12细胞免受H2O2诱导的细胞毒性的能力来评估它们的抗氧化活性,还用紫外(UV)分光光度计评估了它们的水溶性。结果表明,与灯盏花乙素(2)相比,化合物8b表现出更强的抗凝和抗氧化活性以及更好的水溶性,这使其成为治疗缺血性脑血管疾病的有前景的药物。

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