• DocumentCode
    2481304
  • Title

    Synthesis of novel antofine and Cryptopleurine analogues

  • Author

    Song, Yanling ; Meng, Yanqiu

  • Author_Institution
    Dept. of Pharm. Eng., Shenyang Univ. of Chem. Technol., Shenyang, China
  • fYear
    2011
  • fDate
    24-26 June 2011
  • Firstpage
    7928
  • Lastpage
    7931
  • Abstract
    Antofine and Cryptopleurine, natural products belong to the phenanthroindolizidine and phenanthroquinolizidine group of alkaloids, have attracted much attention because of their extremely potent inhibition of cancer cell growth. In this paper, seven analogues with different substituents on phenanthrene ring were designed and synthesized, the chemical structures of these derivatives were characterized by MS and 1H-NMR.
  • Keywords
    biological NMR; cancer; mass spectra; molecular biophysics; molecular configurations; organic compounds; 1H-NMR technique; Antofine analogues; Cryptopleurine analogues; MS technique; alkaloids; cancer cell growth; chemical structure; phenanthrene ring; phenanthroindolizidine group; phenanthroquinolizidine group; Cryptography; Heating; Nitrogen; Silicon compounds; Solvents; Suspensions; Antofine; Cryptopleurine; analogues; design; synthesis;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Remote Sensing, Environment and Transportation Engineering (RSETE), 2011 International Conference on
  • Conference_Location
    Nanjing
  • Print_ISBN
    978-1-4244-9172-8
  • Type

    conf

  • DOI
    10.1109/RSETE.2011.5966287
  • Filename
    5966287