Please wait a minute...

本期目录

    2020年, 第15卷, 第5期 刊出日期:2020-10-20 上一期    下一期
    Regular Article
    Isolation, structure elucidation and antioxidant activity of natural products from the root bark of Ailanthus altissima (Mill.) Swingle
    Ye Chang, Yuxi Wang, Xiaoxiao Huang, Shaojiang Song
    2020 (5):  217-227. 
    摘要 ( 435 )   PDF(1129KB) ( 386 )  
    Eight compounds (1-8) were isolated from Ailanthus altissima (Mill.) Swingle, including four lignans, three phenylpropanoids and a simple aromatic compound, their structures were identified by nuclear magnetic resonance spectra and mass spectrometry data. Among them, compounds 1, 3, 5 and 8 were first obtained from this genus. In addition, free radical scavenging ability of compounds 1-8 were evaluated using DPPH, ABTS, and FRAP assays and the results showed that compound 2 exhibited potent antioxidant activity in DPPH and ABTS radical scavenging assays and compound 7 showed the highest value of FRAP radical scavenging.
    相关文章 | 计量指标
    Bioactive Constituents of the Seed Kernels from Vernicia fordii
    Jiayi Li, Jing Ding, Zisong Bai, Gang Chen, Di Zhou, Ning Li
    2020 (5):  228-238. 
    摘要 ( 413 )   PDF(1105KB) ( 313 )  
    A new compound, (2′R)-(5-oxo-2,5-dihydrofuran-2-yl)methyl octanoate (1), together with 9 known ones (2-10) were isolated from the bioactive extract of the seed kernels from Vernicia fordii. Their structures were determined by spectroscopic analyses, including Nuclear Magnetic Resonance (NMR) and High Resolution Electrospray Ionization Mass Spectroscopy (HRESI-MS). Their cytotoxicities against three human cancer cell lines (A549, HepG2 and Caco2 cells) and anti-neuroinflammatory effects were evaluated. Cytotoxicity assay revealed that compound 9 could inhibit the growth of HepG2 cells, while compound 6 had a moderate inhibitory effect against A549 cells. Further anti-neuroinflammatory activity assay showed that compound 10 exhibited moderate inhibitory effect on the release of NO in LPS-stimulated BV2 microglia cells.
    相关文章 | 计量指标
    Main alkaloids of Rhizoma Coptidis improved palmitic acidinduced insulin resistance in HepG2 cells via AMPK and MAPK signaling pathway
    Ming Qu, Ying Wang, Shijie Cao, Yalu Liu, Da Liu, Feng Qiu, Ning Kang
    2020 (5):  239-254. 
    摘要 ( 442 )   PDF(1405KB) ( 310 )  
    Rhizoma Coptidis, a traditional Chinese herbal medicine, has been used for treating diabetes for thousands of years. However, the molecular basis for this action has not been elucidated. In the present study, the effects of seven main alkaloids of Rhizoma Coptidis on glycometabolism were investigated and the related molecular mechanism of five active compounds on insulin resistant (IR) cell model was explored for the first time. Results showed that berberine, palmatine, epiberberine, columbamine and groenlandicine enhanced glucose consumption in the palmitic acid (PA)-induced IR-HepG2 cells, indicating that these compounds could improve IR. In addition, we found that among these active alkaloids, berberine, columbamine, epiberberine and groenlandicine could inhibit the activation of ERK and p38 pathway, while berberine, columbamine, palmatine and epiberberine could activate AMPK pathway. Moreover, palmatine and columbamine regulated the mRNA expression of GLUT2 to ameliorate IR via activating AMPK and inactivating p38 MAPK signal pathway. To sum up, berberine, columbamine, palmatine, epiberberine and groenlandicine might be the active reagents, which contribute to the glucose lowering effects of Rhizoma Coptidis.
    相关文章 | 计量指标
    Study of the mechanism underlying inhibitory effect of terpenoids from Daphne plants on liver cancer cells using a network pharmacology-based approach
    Jingxian Ren, Zhuoyang Cheng, Peng Zhao, Xiaoxiao Huang, Shaojiang Song
    2020 (5):  255-262. 
    摘要 ( 297 )   PDF(1182KB) ( 328 )  
    Daphne plants, belonging to Thymelaeaceae, have been used as traditional Chinese medicine for thousands of years. Previous studies suggested that they exerted anti-tumor activities and reported a number of compounds with anti-tumor activities, isolated from the genus Daphne. However, the targets of these compounds have not been determined yet. In this study, network pharmacology was used to analyze 128 terpenoid compounds from the genus Daphne and 49 target proteins of liver cancer. The results suggested that the target with the most number of directed edges was 5yz0. The compound which docked with 5yz0 best is AR.DT.25 (acutilobin D), and the compounds with total docking score greater than 10 were almost all Daphnane diterpenoids. The network pharmacology results predicted that the 5yz0 protein was one of the potential targets of the terpenoids from the genus Daphne and then suggested several new targets and compounds for further liver cancer research.
    相关文章 | 计量指标
    Review
    A review on chemical constituents and bioactivities of Viburnum odoratissimum
    Xiaobian Xue, Guodong Yao
    2020 (5):  263-287. 
    摘要 ( 416 )   PDF(4010KB) ( 486 )  
    Viburnum odoratissimum belongs to viburnum genus of the Caprifoliaceae family. Previous studies reported many chemical constituents in this plant, including monoterpenoids, sesquiterpenoids, vibsane-type diterpenes, triterpenes, coumarins, and lignans, and various pharmacological bioactivities the extracts of V. odoratissimum such as anti-tumor, neuroprotective, antiinflammatory, ichthyism and anti-oxidant activity. Besides, the total synthesis of vibsane-type diterpenes and their derivatives have attracted considerable attention because of their wide-ranging anti-tumor activity. This present study not only systematically summarizes the compounds isolated from V. odoratissimum, and the structure-activity relationship of these compounds.
    相关文章 | 计量指标
    A review of phytochemistry and pharmacology perspectives of Viburnum suspensum Lindley
    Shiqi Hao, Zhuoyang Cheng, Dingding Zhang, Lili Lou
    2020 (5):  288-292. 
    摘要 ( 328 )   PDF(1017KB) ( 296 )  
    Viburnum suspensum Lindley, belonging to genus Viburnum of Caprifoliaceae family, is distributed in subtropical area of Japan. Phytochemical reports showed that the main chemical constituents of V. suspensum are irldold glycosldes, labdane-type diglucosides, vibsane-type diterpenoids and oleanane triterpenoids. These compounds were found to possess several biological activities and have attracted great attention of researchers worldwide. This study reviews the chemical constituents and biological activities of V. suspensum, aiming to provide insight for further research on this plant.
    相关文章 | 计量指标