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6-取代1-氮杂苯并蒽酮衍生物的合成及抗肿瘤活性研究

唐煌 王志宇 钟书明 覃江克

广西师范大学学报(自然科学版)2012,Vol.30Issue(2):78-82,5.
广西师范大学学报(自然科学版)2012,Vol.30Issue(2):78-82,5.

6-取代1-氮杂苯并蒽酮衍生物的合成及抗肿瘤活性研究

Synthesis and Antitumor Activity of 6-Substituted 1-Azabenzanthrone

唐煌 1王志宇 1钟书明 1覃江克1

作者信息

  • 1. 广西师范大学药用资源化学与药物分子工程教育部重点实验室,广西桂林541004
  • 折叠

摘要

Abstract

A series of novel 6-Substituted 1-Azabenzanthrone derivatives 3a~3e had been synthesized based on double helix DNA. All the target compounds were characterized by ESI-MS,'H NMR and element analysis. The interaction of derivatives with calf thymus DNA was performed by UV spectra. The in vitro cytotoxicity of derivatives for five cell lines (HepG2,SGC-7901,SW480,786-O and NCI-H460) was evaluated using MTT method. The experimental results indicated that the derivatives could intercalate calf thymus DNA and showed moderate cytotoxicity against different tumor cell lines.

关键词

氧化异阿朴菲衍生物/DNA/抗肿瘤/合成

Key words

oxoisoaporphine derivatives /DNA/ antitumor/ synthesis

分类

化学化工

引用本文复制引用

唐煌,王志宇,钟书明,覃江克..6-取代1-氮杂苯并蒽酮衍生物的合成及抗肿瘤活性研究[J].广西师范大学学报(自然科学版),2012,30(2):78-82,5.

基金项目

国家自然科学基金资助项目(21002015) (21002015)

广西师范大学博士启动基金资助项目 ()

广西师范大学学报(自然科学版)

OA北大核心CSTPCD

1001-6600

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