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发现 N-(2,4-二叔丁基-5-羟基苯基)-4-氧代-1,4-二氢喹啉-3-甲酰胺(VX-770,伊伐卡托),一种有效且口服生物利用度的 CFTR 增效剂。

Discovery of N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, ivacaftor), a potent and orally bioavailable CFTR potentiator.

机构信息

Vertex Pharmaceuticals Incorporated , 11010 Torreyana Road, San Diego, California 92121, United States.

出版信息

J Med Chem. 2014 Dec 11;57(23):9776-95. doi: 10.1021/jm5012808. Epub 2014 Dec 2.

Abstract

Quinolinone-3-carboxamide 1, a novel CFTR potentiator, was discovered using high-throughput screening in NIH-3T3 cells expressing the F508del-CFTR mutation. Extensive medicinal chemistry and iterative structure-activity relationship (SAR) studies to evaluate potency, selectivity, and pharmacokinetic properties resulted in the identification of N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, 48, ivacaftor), an investigational drug candidate approved by the FDA for the treatment of CF patients 6 years of age and older carrying the G551D mutation.

摘要

喹啉酮-3-甲酰胺 1 是一种新型 CFTR 增效剂,是通过在表达 F508del-CFTR 突变的 NIH-3T3 细胞中进行高通量筛选发现的。为了评估其效力、选择性和药代动力学特性,进行了广泛的药物化学和反复的结构-活性关系 (SAR) 研究,最终确定了 N-(2,4-二-叔丁基-5-羟基苯基)-4-氧代-1,4-二氢喹啉-3-甲酰胺(VX-770,48,ivacaftor),这是一种已被 FDA 批准用于治疗携带 G551D 突变的 6 岁及以上 CF 患者的研究性候选药物。

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