Diversity-Oriented Library Synthesis from Steviol and Isosteviol-Derived Scaffolds

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2020-02-17 DOI:10.1021/acscombsci.9b00186
Trinh A. D. Holth, Michael A. Walters, Oliver E. Hutt, Gunda I. Georg*
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引用次数: 1

Abstract

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.

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甜菊醇和等甜菊醇衍生支架的多样性文库合成
天然产物甜菊糖苷提供了独特的二萜核心结构,可通过多样性合成和官能团转化开发小分子文库。从甜菊糖苷衍生的甜菊醇、异甜菊醇和相关类似物制备了验证阵列,共制备了90多种化合物。这些化合物被提交到NIH分子文库小分子库,在分子文库筛选中心网络中进行筛选。在多个高通量分析中确定了几个文库成员的微摩尔命中。对化合物进行了化学信息学分析,验证了这组化合物的预期多样性和复杂性。筛选结果表明,支架衍生的天然产物可提供针对多种靶蛋白的筛选靶点。
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CiteScore
7.20
自引率
4.30%
发文量
567
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