Synthesis and antitumor activity of 4-hydroxycoumarin derivatives
JC Jung, JH Lee, S Oh, JG Lee, OS Park
Index: Jung, Jae-Chul; Lee, Ji-Ho; Oh, Seikwan; Lee, Jae-Gon; Park, Oee-Sook Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 22 p. 5527 - 5531
Full Text: HTML
Citation Number: 63
Abstract
A series of 4-hydroxycoumarin derivatives was prepared and evaluated for antitumor activity. The key fragments were 2a–c, 5c, 12b, 13b, 17, and 18 which were prepared via dianion ring cyclization, Friedel–Crafts acylation, and Reformatsky reaction. Compound 20b showed the most potent antitumor activity among the total 12 derivatives and compounds 19a and 19b exhibited efficacy comparable to etoposide in vitro antitumor activity.
Related Articles:
[Van Heerden, Pieter S.; Bezuidenhoudt, Barend C. B.; Ferreira, Daneel Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 8 p. 1141 - 1146]