Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

LI Xiuzheng, ZHAO Qingjie, DONG Jiaxiao, JIANG Yunyun, YE Guangming. Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 417-421. doi: 10.3969/j.issn.1006-0111.2018.05.007
Citation: LI Xiuzheng, ZHAO Qingjie, DONG Jiaxiao, JIANG Yunyun, YE Guangming. Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 417-421. doi: 10.3969/j.issn.1006-0111.2018.05.007

Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives

doi: 10.3969/j.issn.1006-0111.2018.05.007
  • Received Date: 2018-01-26
  • Rev Recd Date: 2018-05-03
  • Objective To synthesize position 1 substituted sinomenine derivatives and study their anti-inflammatory activity in vitro. Methods A series of substituted sinomenine derivatives were prepared by bromination of sinomenine and Suzuki coupling reaction on the A ring 1. All compounds were confirmed by 1H-NMR,13C-NMR and MS. The reporter gene method was used to study the effect of sinomenine derivatives on NF-κB transcriptional activity. Results All the compounds obtained with Suzuki coupling reaction exhibited better anti-inflammatory activity than the parent compound,sinomenine. Conclusion Two top performers, 4f and 4g ,can be used as drug candidates. A further study on those compounds will have significant implication for the development of rheumatoid arthritis drugs.
  • [1] ZHAO ZJ,ZHAO C,XIAO J,et al. Transdermal permeation and anti-inflammation activities of novel sinomenine derivatives[J]. Molecules,2016,21(11):1520.
    [2] 高晨鑫,张湛明,陈继红,等. 青藤碱对类风湿关节炎细胞因子影响的研究进展[J]. 风湿病与关节炎,2017,6(2):72-75.
    [3] ZHAO XX,PENG C,ZHANG H,et al.Sinomenium acutum:A review of chemistry,pharmacology,pharmacokinetics,and clinical use[J]. Pharm Biol,2012,50(8),1053-1061.
    [4] 吴娟,李燕红. 正清风痛宁药物治疗的副作用及防治[J].中国医药导刊,2012,14(2):250-252.
    [5] 游素芬,戈萌.青藤碱的医药新用途:CN1679574[P]. 2005-10-12.
    [6] CHEN C,XU HQ,ZHONG J.New use of sinomenine:1149456[P].1997-05-14.
    [7] 秦峰,蔡辉. 青藤碱药理作用研究进展[J]. 现代中药研究与实践,2016(4):81-86.
    [8] HE L,DUAN H,LI X,et al. Sinomenine down-regulates TLR4/TRAF6 expression and attenuates lipopolysaccharide-induced osteoclastogenesis and osteolysis[J]. Eur J Pharmacol,2016,779:66-79.
    [9] HUANG L,LI T,ZHOU H,et al. Sinomenine potentiates degranulation of RBL-2H3 basophils via up-regulation of phospholipase A2 phosphorylation by Annexin A1 cleavage and ERK phosphorylation without influencing on calcium mobilization[J]. Int Immunopharmacol,2015,28(2):945-951.
    [10] LOU YT,ZHOU HB,ZOU J,et al.Modification of poorly bioactive sinomenine into morepotent immunosuppressive agents by embedding of drug-like fragments[J].Tetrahedron Lett,2010,51(3):485-488.
    [11] 姚祝军,周海滨. C环连接有吡嗪环的青藤碱衍生物、合成方法及其用途:1687065 A[P]. 2005-10-26.
    [12] 姚祝军,周海滨. C环连接有五元杂环的青藤碱衍生物和合成方法:1687070 A[P]. 2007-10-26.
    [13] TANG J,ZHANG R,XU XQ,et al. Synthesis,characterization,and NF-kappa B pathway inhibition of;1-halogenated sinomenine derivatives[J]. Chem Nat Comp,2013,48(6):1031-1034.
  • 加载中
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(2657) PDF downloads(578) Cited by()

Related
Proportional views

Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives

doi: 10.3969/j.issn.1006-0111.2018.05.007

Abstract: Objective To synthesize position 1 substituted sinomenine derivatives and study their anti-inflammatory activity in vitro. Methods A series of substituted sinomenine derivatives were prepared by bromination of sinomenine and Suzuki coupling reaction on the A ring 1. All compounds were confirmed by 1H-NMR,13C-NMR and MS. The reporter gene method was used to study the effect of sinomenine derivatives on NF-κB transcriptional activity. Results All the compounds obtained with Suzuki coupling reaction exhibited better anti-inflammatory activity than the parent compound,sinomenine. Conclusion Two top performers, 4f and 4g ,can be used as drug candidates. A further study on those compounds will have significant implication for the development of rheumatoid arthritis drugs.

LI Xiuzheng, ZHAO Qingjie, DONG Jiaxiao, JIANG Yunyun, YE Guangming. Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 417-421. doi: 10.3969/j.issn.1006-0111.2018.05.007
Citation: LI Xiuzheng, ZHAO Qingjie, DONG Jiaxiao, JIANG Yunyun, YE Guangming. Synthesis and anti-inflammatory activity of position 1 substituted sinomenine derivatives[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 417-421. doi: 10.3969/j.issn.1006-0111.2018.05.007
Reference (13)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return