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基于生物活性和分子对接的滇鸡血藤水煎液质量控制研究
引用本文:朱泓宇,乔子璇,徐裕彬,任广喜,李萌,姜丹,刘春生.基于生物活性和分子对接的滇鸡血藤水煎液质量控制研究[J].中国药事,2023(11):1319-1325.
作者姓名:朱泓宇  乔子璇  徐裕彬  任广喜  李萌  姜丹  刘春生
作者单位:北京中医药大学中药学院,北京 102488;河北橘井药业有限公司,安国 071200
基金项目:中央高校横向课题项目(编号 2020110031001469)
摘    要:目的:初步探究滇鸡血藤水煎液活血功效的生物评价方法并挖掘参与凝血酶抑制的核心成分。方法:采用体外凝血酶活性抑制试验,评价滇鸡血藤水煎液体外凝血酶抑制活性。然后利用超高效液相色谱-质谱(UPLC-MS)挖掘滇鸡血藤水煎液中的化学成分,并通过分子对接技术对这些化学成分的生物活性进行评估,筛选核心抗凝成分。结果:凝血酶抑制试验表明滇鸡血藤的标准煎剂(0.2 g·m L-1)具有高达78.40%的凝血酶抑制率,并从滇鸡血藤水煎液中推测鉴定了14个化合物,将其与凝血酶进行分子对接评价:戈米辛C(-7.9 kcal·mol-1)、戈米辛G(-7.6 kcal·mol-1)、内南五味子素C(-8.1kcal·mol-1)、内南五味子素D(-9.4 kcal·mol-1)、阿里山五味子灵C(-9.4 kcal·mol-1)、五味子素C(-7.9 kcal·mol-1)、五味子素A(-7.3 kcal·mol-1)、异型南五味子素...

关 键 词:滇鸡血藤  抗凝血酶活性  分子对接  质量评价
收稿时间:2023/5/6 0:00:00

Study on Quality Control of Kadsurae Caulis Decoction Based on Biological Activity and Molecular Docking
Zhu Hongyu,Qiao Zixuan,Xu Yubin,Ren Guangxi,Li Meng,Jiang Dan,Liu Chunsheng.Study on Quality Control of Kadsurae Caulis Decoction Based on Biological Activity and Molecular Docking[J].Chinese Pharmaceutical Affairs,2023(11):1319-1325.
Authors:Zhu Hongyu  Qiao Zixuan  Xu Yubin  Ren Guangxi  Li Meng  Jiang Dan  Liu Chunsheng
Institution:Schoolof Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488 , China;Hebei JujingPharmaceutical Industry Co.Ltd., Anguo 071200 , China
Abstract:Objective: To preliminary explore the biological evaluation method for the blood activating effect of kadsurae caulis decoction, and to explore the core components involved in thrombin inhibition. Methods: In vitro thrombin inhibition test was used to evaluate the thrombin inhibition activity of kadsurae caulis decoction. The chemical constituents in kadsurae caulis decoction were illuminated by UPLC-MS. The pharmacological activities of these compounds were evaluated by molecular docking, and potential thrombin activity inhibitors were screened from them. Results: The thrombin inhibition test showed that the thrombin inhibition rate of kadsurae caulis decoction is up to 78.40%, and 14 compounds were speculated and identified from the decoction by UPLC-MS, and their molecular docking with thrombin was evaluated: Gomisin C(-7.9 kcal·mol-1), Gomisin G(-7.6 kcal·mol-1), Interiorin C(-8.1 kcal·mol-1), Interiorin D(-9.4 kcal·mol-1), Schiarisanrin C(-9.4 kcal·mol-1), Schisandrin C(-7.9 kcal·mol-1), Schizandrin A(-7.3 kcal·mol-1), Heteroclitin E(-8.2 kcal·mol-1), Schisantherin D (-8.6 kcal·mol-1), Rubschisandrin(-7.4 kcal·mol-1), Interiotherin B(-7.6 kcal·mol-1), Interiotherin A(-8.1 kcal·mol-1), Acetoxyl Oxokadsurane(-8.5 kcal·mol-1), Interiotherin D(-9.2 kcal·mol-1). The docking results of these compounds indicated that Interiorin D and Schiarisanrin C had a highly compact spatial configuration and binding energy with thrombin protein. Conclusion: The thrombin inhibitory activity of kadsurae caulis decoction is excellent, and 2 core components with thrombin inhibitory activity have been screened out, that can be used as candidate components for the quality markers. This provides a reference basis for the establishment of a biological activity evaluation method and quality control research of kadsurae caulis decoction.
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