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12-N-Methylated 5,6-dihydrobenzo[c]acridine derivatives: A new class of highly selective ligands for c-myc G-quadruplex DNA

Authors :
Liao, Sheng-Rong
Zhou, Chen-Xi
Wu, Wei-Bin
Ou, Tian-Miao
Tan, Jia-Heng
Li, Ding
Gu, Lian-Quan
Huang, Zhi-Shu
Source :
European Journal of Medicinal Chemistry. Jul2012, Vol. 53, p52-63. 12p.
Publication Year :
2012

Abstract

Abstract: 12-N-Methylated and non-methylated 5,6-dihydrobenzo[c]acridine derivatives were designed and synthesized as new series of c-myc G-quadruplex binding ligands. Their interactions with c-myc G-quadruplex were evaluated using fluorescence resonance energy transfer (FRET) melting assay, circular dichroism (CD) spectroscopy, surface plasmon resonance (SPR), polymerase chain reaction (PCR) stop assay, and molecular modeling. Compared with the non-methylated derivatives, 12-N-methylated derivatives had stronger binding affinity and stabilizing ability to c-myc G-quadruplex structure, and could more effectively stack on the G-quartet surface. All these derivatives had high selectivity for c-myc G-quadruplex DNA over duplex DNA. The reverse transcription (RT) PCR assay showed that compound 21c could down-regulate transcription of c-myc gene in Ramos cell line containing NHE III1 element, but had no effect in CA46 cell line with NHE III1 element removed. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
02235234
Volume :
53
Database :
Academic Search Index
Journal :
European Journal of Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
76181262
Full Text :
https://doi.org/10.1016/j.ejmech.2012.03.034