Indexed by:
期刊论文
First Author:
Zhang Zhi-chao
Correspondence Author:
Zhang, ZC (reprint author), Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China.
Co-author:
Zhang Jing,Yuan Chun-li,Wu Gui-ye,Qian Xu-hong
Date of Publication:
2008-07-01
Journal:
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
Included Journals:
SCIE、ISTIC、CSCD
Document Type:
J
Volume:
24
Issue:
4
Page Number:
449-453
ISSN No.:
1005-9040
Key Words:
intercalation; cytotoxicity;
8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carboxylic acid esters
Abstract:
To explore new platform for DNA intercalation and potent antitumor agent, a series of 8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carboxylic acid esters chromophores has been studied. Their intercalation geometries with DNA were revealed through absorption titration, SYBR Green-DNA melt curve, circular dichroism(CD), and docking studies. It was identified that some of the compounds could intercalate into DNA along their long axis parallel to the base-pair long axis, making right-handed B form DNA transform to A-like conformation. Their binding potency varied with the different steric hindrance. Their cytotoxicity(IC(50)) against MCF-7 cells was found to range between 1.3 to 40.9 mu mol/L by MTT assay. Interestingly, the IC(50) values did not show any obvious correlation to their binding constants with DNA. The chromophore with a carboxyl group exhibited the most potency of intercalating DNA and could be the promising precursor for the future intercalator for DNA, while the bromide demonstrated the highest cytotoxic activity in this series of compounds.
Translation or Not:
no
