首页> 外文期刊>Current opinion in chemical biology >Indolocarbazole antitumour compounds by combinatorial biosynthesis
【24h】

Indolocarbazole antitumour compounds by combinatorial biosynthesis

机译:组合生物合成吲哚咔唑抗肿瘤化合物

获取原文
获取原文并翻译 | 示例
       

摘要

The indolocarbazoles constitute a family of natural products with potential therapeutic applications in the treatment of cancer and neurodegenerative disorders. Members of this family are either potent stabilizers of topoisomerase I-DNA covalent complex or potent inhibitors of protein kinases. Rebeccamycin, staurosporine, AT2433 and K252a are members of this family, which are produced by different actinomycete strains, and whose biosynthesis gene clusters have been isolated and characterized. A number of indolocarbazole derivatives have been generated by applying combinatorial biosynthesis technologies to these clusters either in the producer strain or in the heterologous hosts after expression of part or the entire gene cluster. Combinatorial biosynthesis is therefore providing a new approach for increasing structural diversity in this family of natural products.
机译:吲哚并咔唑构成一类天然产物,在癌症和神经退行性疾病的治疗中具有潜在的治疗应用。该家族的成员是拓扑异构酶I-DNA共价复合物的有效稳定剂或蛋白激酶的有效抑制剂。瑞贝卡霉素,星形孢菌素,AT2433和K252a是该家族的成员,它们是由不同的放线菌菌株产生的,其生物合成基因簇已被分离和鉴定。在部分或全部基因簇表达后,通过在生产菌株或异源宿主中对这些簇应用组合生物合成技术,已经产生了许多吲哚并咔唑衍生物。因此,组合生物合成为增加该天然产物家族的结构多样性提供了一种新方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号