Studies on the mechanism of action of A80915A, a semi-naphthoquinone natural product, as an inhibitor of gastric (H+-K+)-ATPase (Q68326157)

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23 September 2019

title

Studies on the mechanism of action of A80915A, a semi-naphthoquinone natural product, as an inhibitor of gastric (H(+)-K+)-ATPase (English)

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23 September 2019

Studies on the mechanism of action of A80915A, a semi-naphthoquinone natural product, as an inhibitor of gastric (H+-K+)-ATPase (English)

1 reference

https://api.crossref.org/works/10.1016/0006-2952(91)90603-3

28 October 2022

1 reference

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28 October 2022

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28 October 2022

author name string

A. H. Dantzig

1

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28 October 2022

P. L. Minor

2

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28 October 2022

J. L. Garrigus

3

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28 October 2022

D. S. Fukuda

4

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28 October 2022

J. S. Mynderse

5

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28 October 2022

language of work or name

English

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publication date

1 October 1991

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23 September 2019

24 October 1991

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1683772

full work available at URL

28 October 2022

https://api.elsevier.com/content/article/PII:0006295291906033?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0006-2952(91)90603-3

https://api.elsevier.com/content/article/PII:0006295291906033?httpAccept=text/plain

28 October 2022

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28 October 2022

published in

Biochemical Pharmacology

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23 September 2019

volume

42

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23 September 2019

issue

10

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23 September 2019

page(s)

2019-2026

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The mechanism and structure of the gastric H,K-ATPase

23 September 2019

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Gastric H,K-ATPase as therapeutic target

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Functional domains of the gastric HK ATPase

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Ion transport studies with H+-K+-ATPase-rich vesicles: implications for HCl secretion and parietal cell physiology

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Treatment of acid-peptic diseases by inhibition of gastric H+,K+-ATPase

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Substituted benzimidazoles inhibit gastric acid secretion by blocking (H+ + K+) ATPase

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2-((2-Pyridylmethyl)sulfinyl)benzimidazoles: acid sensitive suicide inhibitors of the proton transport system in the parietal cell

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Studies on proton pump inhibitors. II. Synthesis and antiulcer activity of 8-[(2-benzimidazolyl)sulfinylmethyl]-1,2,3,4-tetrahydroquinolines and related compounds

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By 1023/SK&F 96022: biochemistry of a novel (H+ + K+)-ATPase inhibitor

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Evidence for acid-induced transformation of omeprazole into an active inhibitor of (H+ + K+)-ATPase within the parietal cell

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Inhibition of H+K+ATPase by SCH 28080 and SCH 32651.

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Antiulcer agents. 4-substituted 2-guanidinothiazoles: reversible, competitive, and selective inhibitors of gastric H+,K(+)-ATPase

28 October 2022

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Mechanisms of gastric proton pump inhibition by calcium channel antagonists

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Inhibition of (H+ + K+)-ATPase and H+ accumulation in hog gastric membranes by trifluoperazine, verapamil and 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate

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SCH 28080 is a lumenally acting, K+-site inhibitor of the gastric (H+ + K+)-ATPase

28 October 2022

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Inhibition of gastric H+/K+-ATPase by substituted imidazo[1,2-a]pyridines

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Melittin inhibition of the gastric (H+ + K+) ATPase and photoaffinity labeling with [125I]azidosalicylyl melittin

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[125I]azidosalicylyl melittin binding domains: evidence for a polypeptide receptor on the gastric (H+ + K+)ATPase

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A80915, a new antibiotic complex produced by Streptomyces aculeolatus. Discovery, taxonomy, fermentation, isolation, characterization, and antibacterial evaluation

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H+ transport by reconstituted gastric (H+ + K+)-ATPase

28 October 2022

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The colorimetric determination of phosphorus

28 October 2022

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Protein measurement with the Folin phenol reagent

28 October 2022

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28 October 2022

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Conformational states of (K+ + H+)-ATPase studied using tryptic digestion as a tool

28 October 2022

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Competitive binding of ATP and the fluorescent substrate analogue 2',3'-O-(2,4,6-trinitrophenylcyclohexadienylidine) adenosine 5'-triphosphate to the gastric H+,K+-ATPase: evidence for two classes of nucleotide sites

28 October 2022

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Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1683772%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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