抽象的

Using nanobiotechnology to find new drugs discovery

Peter Lucas


Although the "rule-of-five" (also known as "Lipinski's rule of drug-likeness") is a very helpful guideline for designing orally accessible small-molecule drugs, it has in some ways been overemphasised. First off, only 51% of all small-molecule medications that have received FDA approval are taken orally and adhere to the "rule-of-five." This doesn't even take into account the growing number of biologicals, some of which have become "blockbuster" hits. Secondly, it does not encompass natural product and semisynthetic natural product medications, which constitute roughly one-third of all marketed small-molecule pharmaceuticals. Instead of relying too heavily on 'rule-of-five' compliance, a more balanced and systematic approach to drug discovery ought to be more fruitful. These are especially important when attempting to combat "best-in-class" and/or extremely difficult targets, such proteases and those involving protein-protein interactions. Additionally, greater work should go into studying natural products. Synthetic biology, which involves genetically altering living things to make small-molecule medicines, may be able to address some of the difficult problems associated with natural product-based drug development, such as synthetic feasibility and ligand efficiency.


索引于

  • 中国社会科学院
  • 谷歌学术
  • 打开 J 门
  • 中国知网(CNKI)
  • 引用因子
  • 宇宙IF
  • 电子期刊图书馆
  • 研究期刊索引目录 (DRJI)
  • 秘密搜索引擎实验室
  • ICMJE

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