The present disclosure provides pharmaceutical compositions, pharmaceutical preparations and methods for increasing activity of a mutant cystic fibrosis transmembrane conductance regulator protein (mutant-CFTR). The pharmaceutical compositions, pharmaceutical preparations and methods are useful for the study and treatment of disorders associated with mutant-CFTR, such as cystic fibrosis. The pharmaceutical compositions and pharmaceutical preparations may include one or more cyanoquinoline-containing compounds of the embodiments, or an analog or derivative thereof.
本公开提供了药物组成物、药物制剂和方法,用于增加突变型囊性纤维化跨膜传导调节因子蛋白(突变-CFTR)的活性。这些药物组成物、药物制剂和方法对于研究和治疗与突变-CFTR相关的疾病,如囊性纤维化,具有用处。药物组成物和药物制剂可以包括本实施例中的一种或多种含有
氰基
喹啉的化合物,或其类似物或衍
生物。