Recent Advances in Semisynthesis, Biosynthesis, Biological Activities, Mode of Action, and Structure-Activity Relationship of Podophyllotoxins: An Update (2008-2010)

被引:64
|
作者
Lv, M. [1 ]
Xu, H. [1 ]
机构
[1] NW A&F Univ, Lab Pharmaceut Design & Synth, Coll Plant Protect, Yangling 712100, Peoples R China
基金
中国国家自然科学基金;
关键词
Podophyllotoxin; anticancer activity; antiviral activity; insecticidal activity; semisynthesis; biosynthesis; mode of action; WALKER IN-VIVO; SPIN-LABELED DERIVATIVES; WATER-SOLUBLE PRODRUG; INSECTICIDAL AGENTS; ETOPOSIDE PHOSPHATE; DESIGN; DEOXYPODOPHYLLOTOXIN; ANALOGS; (-)-PODOPHYLLOTOXIN; ESTERS;
D O I
10.2174/138955711796575461
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Podophyllotoxin, one of the well-known naturally occurring aryltetralin lignans, has been used as the lead-compound for the preparation of potent anticancer agents, such as etoposide, teniposide, and etopophos. In our previous review, we described the advances of podophyllotoxin derivatives from 2003 and 2007. In recent years, an increased number of interesting research work has been carried out on the podophyllotoxins. As a continuation, the present review summarizes and highlights the update advances of podophyllotoxin derivatives from 2008 and 2010 in regard to semisynthesis, biosynthesis, biological activities, mode of action and structure-biological activity relationship.
引用
收藏
页码:901 / 909
页数:9
相关论文
共 50 条
  • [32] Recent advances in the synthesis of extensive libraries of heparan sulfate oligosaccharides for structure-activity relationship studies
    Ramadan, Sherif
    Mayieka, Morgan
    Pohl, Nicola L. B.
    Liu, Jian
    Hsieh-Wilson, Linda C.
    Huang, Xuefei
    CURRENT OPINION IN CHEMICAL BIOLOGY, 2024, 80
  • [33] Bicyclic polyprenylated acylphloroglucinols and their derivatives: structural modification, structure-activity relationship, biological activity and mechanism of action
    Phang, Yeelin
    Wang, Xueying
    Lu, Yue
    Fu, Wenwei
    Zheng, Changwu
    Xu, Hongxi
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 205
  • [34] Thiochromenes and thiochromanes: a comprehensive review of their diverse biological activities and structure-activity relationship (SAR) insights
    Jatin, Solai
    Murugappan, Solai
    Kirad, Shivani
    Ala, Chandu
    Kuthe, Pranali Vijaykumar
    Kondapalli, Chandra Sekhar Venkata Gowri
    Sankaranarayanan, Murugesan
    RSC MEDICINAL CHEMISTRY, 2025,
  • [35] Synthesis, Biological Activities, and Quantitative Structure-Activity Relationship (QSAR) Study of Novel Camptothecin Analogues
    Wu, Dan
    Zhang, Shao-Yong
    Liu, Ying-Qian
    Wu, Xiao-Bing
    Zhu, Gao-Xiang
    Zhang, Yan
    Wei, Wei
    Liu, Huan-Xiang
    Chen, An-Liang
    MOLECULES, 2015, 20 (05): : 8634 - 8653
  • [36] Molecular and absorption properties of 12 soy isoflavones and their structure-activity relationship with selected biological activities
    Chun, HS
    Chang, HJ
    Choi, EH
    Kim, HJ
    Ku, KH
    BIOTECHNOLOGY LETTERS, 2005, 27 (15) : 1105 - 1111
  • [37] New dihydrostilbenes from Macaranga heynei IM Johnson, biological activities and structure-activity relationship
    Kamarozaman, Aisyah Salihah
    Ahmat, Norizan
    Isa, Siti Nursyahirah Mohd
    Hafiz, Zetty Zulikha
    Adenan, Mohd Ilham
    Yusof, Mohd Izwan Mohamad
    Azmin, Nik Fatini Nik
    Latip, Jalifah
    PHYTOCHEMISTRY LETTERS, 2019, 30 : 174 - 180
  • [38] Synthesis and biological activities of 2-aminophenol-based Schiff bases and their structure-activity relationship
    Aslam, Muhammad
    Anis, Itrat
    Mehmood, Rashad
    Iqbal, Lubna
    Iqbal, Samina
    Khan, Inamullah
    Chishti, Muhammad Salman
    Perveen, Shagufta
    MEDICINAL CHEMISTRY RESEARCH, 2016, 25 (01) : 109 - 115
  • [39] Sodium channel modifiers from scorpion venom: Structure-activity relationship, mode of action and application
    Gurevitz, M
    Froy, O
    Zilberberg, N
    Turkov, M
    Strugatsky, D
    Gershburg, E
    Lee, D
    Adams, ME
    TOXICON, 1998, 36 (11) : 1671 - 1682
  • [40] Synthesis, Structure-Activity Relationship, and Mode-of-Action Studies of Antimalarial Reversed Chloroquine Compounds
    Burgess, Steven J.
    Kelly, Jane X.
    Shomloo, Shawheen
    Wittlin, Sergio
    Brun, Reto
    Liebmann, Katherine
    Peyton, David H.
    JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (17) : 6477 - 6489