Record number :
1306521
Title of article :
Novel acenaphtho[1,2-b]pyrrole-carboxylic acid family: Synthesis, cytotoxicity, DNA-binding and cell cycle evaluation Original Research Article
Author/Authors :
Lijuan Xie، نويسنده , , Yi Xiao، نويسنده , , Fang Wang، نويسنده , , Yufang Xu، نويسنده , , Xuhong Qian، نويسنده , , Rong Zhang، نويسنده , , Jingnan Cui، نويسنده , , Jianwen Liu، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
7
From page :
7615
To page :
7621
Abstract :
A family of 8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carboxylic acid derivatives were synthesized as a result of our efforts to modify a series of acenaphthopyrrole aromatic-heterocycle compounds that proved to be potent anticancer drugs. Among the derivatives, 3d (3-(dimethylamino-propylamino)-8-oxo-8H-acenaphtho-[1,2-b]pyrrole-9-carboxylic acid) and 3g (3-piperidine-8-oxo-8H-acenaphtho-[1,2-b]pyrrole-9-carboxylic acid) showed potential anticancer activity and different action mechanism from our previously reported compounds. UV–vis absorption, circular dichroism and viscosity measurement indicated that effect of both compounds on the advanced DNA conformation was different, although they could bind to DNA in the same way. Cell cycle analysis showed that 3d could induce S-phase arrest followed by apoptosis, while 3g induced apoptosis. The results seem to imply that different action mechanism could contribute to the dissimilitude of biological activities toward 3d and 3g.
Keywords :
2-b]pyrrole , cell cycle , apoptosis , DNA
Journal title :
Bioorganic and Medicinal Chemistry
Link To Document :