Literature DB >> 16714120

Isoquino[4,5-bc]acridines: design, synthesis and evaluation of DNA binding, anti-tumor and DNA photo-damaging ability.

Peng Yang1, Qing Yang, Xuhong Qian, Lianpeng Tong, Xiaolian Li.   

Abstract

Several novel isoquino[4,5-bc]acridine derivatives have been designed and synthesized. Their DNA-binding, anti-tumor and DNA-photo-damaging properties were investigated. A4 exhibited the highest anti-tumor activities against both A 549 (human lung cancer cell) and P388 (murine leukemia cells). All these compounds were found to be more cytotoxic against P388 than against A549. Under 365-nm light irradiation, A3 damaged plasmid DNA pBR322 at <2 microM and cleaved DNA from form I to 100% form II by 50 microM. The mechanism studies revealed that A3 damaged DNA by electron transfer mechanism and singlet oxygen species.

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Year:  2006        PMID: 16714120     DOI: 10.1016/j.jphotobiol.2006.03.005

Source DB:  PubMed          Journal:  J Photochem Photobiol B        ISSN: 1011-1344            Impact factor:   6.252


  2 in total

1.  9-(3-Bromo-5-chloro-2-hy-droxy-phen-yl)-10-(2-hy-droxy-eth-yl)-3,6-diphenyl-3,4,9,10-tetra-hydro-acridine-1,8(2H,5H)-dione.

Authors:  Mehmet Akkurt; Shaaban K Mohamed; Antar A Abdelhamid; Abdel-Aal M Gaber; Mustafa R Albayati
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-05-17

2.  Negatively Charged Red-Emitting Acridine Dyes for Facile Reductive Amination, Separation, and Fluorescent Detection of Glycans.

Authors:  Maksim A Fomin; Jan Seikowski; Vladimir N Belov; Stefan W Hell
Journal:  Anal Chem       Date:  2020-03-19       Impact factor: 6.986

  2 in total

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