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Dihydroxylated 2,4,6-triphenyl pyridines: Synthesis, topoisomerase i and II inhibitory activity, cytotoxicity, and structure-activity relationship study
- Title
- Dihydroxylated 2,4,6-triphenyl pyridines: Synthesis, topoisomerase i and II inhibitory activity, cytotoxicity, and structure-activity relationship study
- Authors
- Karki R.; Thapa P.; Yoo H.Y.; Kadayat T.M.; Park P.-H.; Na Y.; Lee E.; Jeon K.-H.; Cho W.-J.; Choi H.; Kwon Y.; Lee E.-S.
- Ewha Authors
- 권영주
- SCOPUS Author ID
- 권영주
- Issue Date
- 2012
- Journal Title
- European Journal of Medicinal Chemistry
- ISSN
- 0223-5234
- Citation
- European Journal of Medicinal Chemistry vol. 49, pp. 219 - 228
- Indexed
- SCI; SCIE; SCOPUS
- Document Type
- Article
- Abstract
- Twelve dihydroxylated 2,4,6-triphenyl pyridines were designed and synthesized which contain hydroxyl groups at ortho, meta or para position of 2- and 6-phenyl, or 2- and 4-phenyl rings attached to the central pyridine. They were evaluated for topoisomerase I and II inhibitory activity, and cytotoxicity against several human cancer cell lines for the development of novel anticancer agents. Generally, dihydroxylated 2,4,6-triphenyl pyridines exhibited stronger topoisomerase II inhibitory activity, and cytotoxicity compared to those of monohydroxylated 2,4,6-triphenyl pyridines. The concrete structure-activity relationship was observed that dihydroxylated 2,4,6-triphenyl pyridines with hydroxyl group at meta or para position of 2-phenyl ring displayed significant topoisomerase II inhibitory activity as well as cytotoxicity. Positive correlation between topoisomerase II inhibitory activity and cytotoxicity was observed for compounds 10, 12, 13, 17-20 and 22. © 2012 Elsevier Masson SAS. All rights reserved.
- DOI
- 10.1016/j.ejmech.2012.01.015
- Appears in Collections:
- 약학대학 > 약학과 > Journal papers
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