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2000
Volume 16, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A series of new phenanthrene-based tylophorine derivatives (PBTs) were synthesized in good yield and their structures were characterized by 1H-NMR spectroscopy and ESI MS. In vitro antitumor activity of these compounds against five human carcinoma cell lines, including HCT116 (colorectal), BGC-823 (gastric), HepG-2 (hepatic), Hela (cervical) and H460 (lung) cells, was evaluated by MTT assay. Among these PBTs, compound 6b showed the highest antitumor activities against HCT116 and HepG-2 cell lines with IC50 values of 6.1 and 6.4 μM, respectively, which were comparable to that of adriamycin hydrochloride. The structure-activity relationship of these compounds was also discussed based on the results of their antitumor activity.

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/content/journals/loc/10.2174/1570178615666181025115513
2019-06-01
2025-09-16
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  • Article Type:
    Research Article
Keyword(s): antitumor; cytotoxicity; derivative; phenanthrene; Synthesis; tylophorine
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