Synthesis of 1,2,3-triazole analogs of CFTR potentiator VX-770

被引：0

作者：

Ody, Britton ^{[1
]}

机构：

[1] Berry Coll, Chem & Biochem, Mt Berry, GA USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2019年 / 257卷

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中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

324

引用

页数：1

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[37] Identifying the molecular target sites for CFTR potentiators GLPG1837 and VX-770 [J].

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[39] Synthesis of 1,2,3-triazole glycoconjugates as inhibitors of α-glucosidases [J].

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[40] VX-770 IN SUBJECTS WITH CF AND HOMOZYGOUS FOR THE F508DEL-CFTR MUTATION [J].

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