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首页> 外文期刊>Journal of combinatorial chemistry >Design, Synthesis, and In Vitro Evaluation of Potential West Nile Virus Protease Inhibitors Based on the 1-Oxo-1,2,3,4-tetrahydroisoquinoline and 1-Oxo-1,2-dihydroisoquinoline Scaffolds
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Design, Synthesis, and In Vitro Evaluation of Potential West Nile Virus Protease Inhibitors Based on the 1-Oxo-1,2,3,4-tetrahydroisoquinoline and 1-Oxo-1,2-dihydroisoquinoline Scaffolds

机译:基于1-Oxo-1,2,3,4-四氢异喹啉和1-Oxo-1,2-二氢异喹啉支架的潜在西尼罗河病毒蛋白酶抑制剂的设计,合成和体外评估

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摘要

The 1-oxo-1, 2, 3, 4-tetrahydroisoquinoline and 1-Oxo-1, 2-dihydroisoquinoline scaffolds were utilized in the design and solution phase synthesis of focused libraries of compounds for screening against West Nile Virus (WNV) protease. Exploratory studies have led to the identification of a WNV protease inhibitor (a 1-oxo-1, 2-dihydroisoquinoline-based derivative, 12j) which could potentially serve as a launching pad for a hit-to-lead optimization campaign. The identified hit was devoid of any inhibitory activity toward a panel of mammalian serine proteases.
机译:1-oxo-1、2、3、4-四氢异喹啉和1-Oxo-1、2-二氢异喹啉支架用于设计和溶液相合成重点化合物库,以筛选西尼罗河病毒(WNV)蛋白酶。探索性研究已导致鉴定出WNV蛋白酶抑制剂(一种基于1-oxo-1、2-二氢异喹啉的衍生物12j),该抑制剂有可能充当铅到铅优化运动的发射台。所确定的命中没有对一组哺乳动物丝氨酸蛋白酶的任何抑制活性。

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