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Synthesis and evaluation of bi-functional 7-hydroxycoumarin platinum(IV) complexes as antitumor agents.

Authors :
Wang, Qingpeng
Chen, Yan
Li, Guoshuai
Liu, Zhifang
Ma, Jing
Liu, Min
Li, Dacheng
Han, Jun
Wang, Bingquan
Source :
Bioorganic & Medicinal Chemistry. May2019, Vol. 27 Issue 10, p2112-2121. 10p.
Publication Year :
2019

Abstract

Graphical abstract Highlights • Bifunctional 7-hydroxycoumarin platinum(IV) complexes as antitumor agents. • Have much potential in overcoming cisplatin drug-resistance. • Antitumor mechanism was investigated. • Enhanced accumulation in whole cells and DNA. • Combination with HSA by noncovalent forces. Abstract A series of bi-functional 7-hydroxycoumarin platinum(IV) complexes were synthesized, characterized, and evaluated for antitumor activities. The 7-hydroxycoumarin platinum(IV) complexes display moderate to effective antitumor activities toward the tested cell lines and show much potential in overcoming drug resistance of platinum(II) drugs. In reducing microenvironment, the title compounds could be reduced to platinum(II) complex accompanied with two equivalents of coumarin units. By a unique mechanism, the 7-hydroxycoumarin platinum(IV) complex attacks DNA via the released platinum(II) compound, meanwhile it also inhibits the activities of cyclooxygenase by coumarin fragment. This action mechanism might be of much benefit for reducing tumor-related inflammation in the progress of inhibiting tumor proliferation and overcoming cisplatin resistance. The incorporation of 7-hydroxycoumarin leads to significantly enhanced platinum accumulation in both whole tumor cells and DNA. The HSA interaction investigation reveals that the tested coumarin platinum(IV) compound could effectively combine with HSA via van der Waals force and hydrogen bond. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09680896
Volume :
27
Issue :
10
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
135959550
Full Text :
https://doi.org/10.1016/j.bmc.2019.04.009