AU 1421

Known as: AU-1421, Pyridine, 5-methyl-2-(2-(1-naphthalenyl)ethenyl)-4-(1-piperidinyl)-, monohydrochloride, (Z)- 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1990-1992
02419901992

Papers overview

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1993
1993
The lipophilic weak base AU-1421 acts as a simple protonophoric uncoupler of oxidative phosphorylation in rat liver mitochondria… (More)
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1992
1992
(Z)-5-Methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine, AU-1421, interacted at 0 degree C with the K(+)-sensitive… (More)
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1991
1991
We investigated the environmental differences of a pyridine derivative-access sites between hog gastric (H+,K+)-ATPase and dog… (More)
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1991
1991
Membrane-bound Na+,K(+)-ATPase (0.1 mg/ml) was incubated with the K(+)-site-directed probe (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl… (More)
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1990
1990
A novel pyridine derivative, (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidonopyridine hydrochloride, AU-1421, was found to… (More)
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1990
1990
Recently, we have shown that a hydrophobic amine (AU-1421) produces an irreversible inactivation of Na+/K(+)-ATPase activity… (More)
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1990
1990
A newly synthesized pyridine derivative, (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine hydrochloride (AU-1421), was… (More)
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1990
1990
A hydrophobic amine, (Z)-5-methyl-2-[2-(1-naphthyl)ethenyl]-4-piperidinopyridine (AU-1421), was examined as a probe of the K… (More)
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