...
首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >CCLab - A multi-objective genetic algorithm based combinatorial library design software and an application for histone deacetylase inhibitor design
【24h】

CCLab - A multi-objective genetic algorithm based combinatorial library design software and an application for histone deacetylase inhibitor design

机译:CCLab-基于多目标遗传算法的组合库设计软件及其在组蛋白脱乙酰基酶抑制剂设计中的应用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The introduction of the multi-objective optimization has dramatically changed the virtual combinatorial library design, which can consider many objectives simultaneously, such as synthesis cost and drug-likeness, thus may increase positive rates of biological active compounds. Here we described a software called CCLab (Combinatorial Chemistry Laboratory) for combinatorial library design based on the multi-objective genetic algorithm. Tests of the convergence ability and the ratio to re-take the building blocks in the reference library were conducted to assess the software in silico, and then it was applied to a real case of designing a 5 × 6 HDAC inhibitor library. Sixteen compounds in the resulted library were synthesized, and the histone deactetylase (HDAC) enzymatic assays proved that 14 compounds showed inhibitory ratios more than 50% against tested 3 HDAC enzymes at concentration of 20 μg/mL, with IC 50 values of 3 compounds comparable to SAHA. These results demonstrated that the CCLab software could enhance the hit rates of the designed library and would be beneficial for medicinal chemists to design focused library in drug development (the software can be downloaded at: http://202.127.30.184:8080/drugdesign.html).
机译:多目标优化的引入极大地改变了虚拟组合库的设计,可以同时考虑许多目标,例如合成成本和药物相似性,从而可以提高生物活性化合物的阳性率。在这里,我们描述了一种基于多目标遗传算法的,用于组合库设计的名为CCLab(组合化学实验室)的软件。在参考库中进行了收敛能力和重获构建基的比率测试,以评估计算机软件,然后将其应用于设计5×6 HDAC抑制剂库的实际案例中。合成了结果文库中的16种化合物,组蛋白去乙酰基转移酶(HDAC)酶法测定表明,在浓度为20μg/ mL的情况下,对测试的3种HDAC酶,有14种化合物的抑制率超过50%,3种化合物的IC 50值相当前往SAHA。这些结果表明,CCLab软件可以提高设计库的命中率,并且对药用化学家在药物开发中设计专注的库将是有益的(该软件可以从以下网址下载:http://202.127.30.184:8080/drugdesign。 html)。

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