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Gastric H,K-ATPase as therapeutic target.

作者信息

Sachs G, Carlsson E, Lindberg P, Wallmark B

机构信息

CURE, Wadsworth Veterans Administration Hospital, Los Angeles, California.

出版信息

Annu Rev Pharmacol Toxicol. 1988;28:269-84. doi: 10.1146/annurev.pa.28.040188.001413.

DOI:10.1146/annurev.pa.28.040188.001413
PMID:2898235
Abstract
摘要

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Gastric H,K-ATPase as therapeutic target.胃H,K-ATP酶作为治疗靶点。
Annu Rev Pharmacol Toxicol. 1988;28:269-84. doi: 10.1146/annurev.pa.28.040188.001413.
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Inhibition of gastric H+, K+ adenosine triphosphatase (ATPase) by substituted naphthylalkylimidazoles.
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SCH 28080 is a more selective inhibitor than SCH 32651 at the K+ site of gastric K+/H+-ATPase.
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Inhibition of the gastric (H+ + K+)-ATPase by fenoctimine.
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Effect of salvianolic acid A, a depside from roots of Salvia miltiorrhiza, on gastric H+,K(+)-ATPase.丹参中分离出的一种缩酚酸——丹酚酸A对胃H⁺,K⁺-ATP酶的作用
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Inhibition of gastric H+,K(+)-ATPase by the anti-ulcer agent, sofalcone.
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Oleic acid as an inhibitor of gastric H+, K(+)-ATPase.油酸作为胃H⁺,K⁺-ATP酶的抑制剂。
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Inhibition of H+K+ATPase by SCH 28080 and SCH 32651.SCH 28080和SCH 32651对H⁺K⁺ATP酶的抑制作用。
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[Inhibition of H+/K+-ATPase in the parietal cell with omeprazole: a new principle of gastric acid inhibition].[奥美拉唑对壁细胞H⁺/K⁺-ATP酶的抑制作用:胃酸抑制的新原理]
Ned Tijdschr Geneeskd. 1985 Apr 13;129(15):679-82.

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