Department of Medicinal Chemistry and Institute for Therapeutics Discovery and Development, College of Pharmacy, University of Minnesota, 717 Delaware Street Southeast, Minneapolis, Minnesota 55414, United States.
ACS Comb Sci. 2020 Mar 9;22(3):150-155. doi: 10.1021/acscombsci.9b00186. Epub 2020 Feb 17.
The readily available natural product stevioside provides a unique diterpene core structure that can be explored for small molecule library development by diversity-oriented synthesis and functional group transformations. Validation arrays were prepared from steviol, isosteviol, and related analogues, derived from stevioside, to produce over 90 compounds. These compounds were submitted to the NIH Molecular Libraries Small Molecule Repository for screening in the Molecular Libraries Screening Center Network. Micromolar hits were identified in multiple high-throughput assays for several library members. A cheminformatics analysis of the compounds was performed that verified the expected diversity and complexity of this set of compounds. The screening results indicate that scaffolds-derived natural products can provide screening hits against multiple target proteins.
甜菊苷是一种易于获得的天然产物,它提供了独特的二萜核心结构,可以通过多样性导向合成和官能团转化来探索小分子文库的发展。从甜菊醇、异甜菊醇和相关类似物中衍生出的甜菊苷验证数组,制备了超过 90 种化合物。这些化合物被提交给美国国立卫生研究院小分子文库,供分子文库筛选中心网络进行筛选。在多个高通量测定中,多种文库成员都鉴定出了有希望的化合物。对化合物进行了化学信息学分析,证实了这组化合物具有预期的多样性和复杂性。筛选结果表明,来源于天然产物的支架可以提供针对多种靶蛋白的筛选命中。