Rapid inhibition of the K+-sensitive phosphoenzyme of Na+/K+-ATPase by (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference23 articles.
1. Structural basis for E1–E2 conformational transitions in Na, K-pump and Ca-pump proteins
2. OCCLUDED CATIONS IN ACTIVE TRANSPORT
3. A novel hydrophobic amine, (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine, as a probe of the K+ occlusion center of Na+/K+-ATPase
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The lipophilic weak base (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine (AU-1421) is a potent protonophore type cationic uncoupler of oxidative phosphorylation in mitochondria;Biochimica et Biophysica Acta (BBA) - Bioenergetics;1993-03
2. K+-site-directed pyridine derivative, AU-1421, activates hydrolysis of the K+-sensitive phosphoenzyme of sarcoplasmic reticulum Ca2+-ATPase and inactivates that of K+-transporting ATPases;Biochimica et Biophysica Acta (BBA) - Biomembranes;1992-04
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