Dou Dengfeng, Viwanathan Prasanth, Li Yi, He Guijia, Alliston Kevin R, Lushington Gerald H, Brown-Clay Joshua D, Padmanabhan R, Groutas William C
Department of Chemistry, Wichita State University, Wichita, Kansas 67260, USA.
J Comb Chem. 2010 Nov 8;12(6):836-43. doi: 10.1021/cc100091h. Epub 2010 Sep 30.
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.
1-氧代-1,2,3,4-四氢异喹啉和1-氧代-1,2-二氢异喹啉支架被用于设计和溶液相合成针对西尼罗河病毒(WNV)蛋白酶的聚焦化合物库。探索性研究已鉴定出一种WNV蛋白酶抑制剂(一种基于1-氧代-1,2-二氢异喹啉的衍生物,12j),它有可能作为从命中到先导优化活动的起点。所鉴定出的命中物对一组哺乳动物丝氨酸蛋白酶没有任何抑制活性。