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P 1075
Known as:
P-1075
, P1075
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Characterization of K(ATP)-channels in rat basilar and middle cerebral arteries: studies of vasomotor responses and mRNA expression.
I. Jansen-Olesen
,
C. Mortensen
,
Najat El-Bariaki
,
K. B. Ploug
European Journal of Pharmacology
2005
Corpus ID: 35851148
Highly Cited
2003
Highly Cited
2003
P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts.
O. Oldenburg
,
Xi-ming Yang
,
+4 authors
J. Downey
Journal of Molecular and Cellular Cardiology
2003
Corpus ID: 22518596
2002
2002
Interaction of K(ATP) channel modulators with sulfonylurea receptor SUR2B: implication for tetramer formation and allosteric coupling of subunits.
C. Löffler-Walz
,
A. Hambrock
,
U. Quast
Molecular Pharmacology
2002
Corpus ID: 26502343
Sulfonylurea receptors (SURs) are subunits of ATP-sensitive K(+) channels (K(ATP) channels); they mediate the channel-closing…
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Highly Cited
2001
Highly Cited
2001
Functional Roles of Cardiac and Vascular ATP-Sensitive Potassium Channels Clarified by Kir6.2-Knockout Mice
Masashi Suzuki
,
Ronald A. Li
,
+8 authors
H. Nakaya
Circulation Research
2001
Corpus ID: 12369901
Abstract— ATP-sensitive potassium (KATP) channels were discovered in ventricular cells, but their roles in the heart remain…
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Highly Cited
2001
Highly Cited
2001
Characterization of a mutant sulfonylurea receptor SUR2B with high affinity for sulfonylureas and openers: differences in the coupling to Kir6.x subtypes.
A. Hambrock
,
C. Löffler-Walz
,
U. Russ
,
U. Lange
,
Ulrich Quast
Molecular Pharmacology
2001
Corpus ID: 18938608
ATP-dependent K(+) channels are composed of pore-forming subunits of the Kir6.x family and of sulfonylurea receptors (SURs). SUR1…
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Highly Cited
2000
Highly Cited
2000
Differential response of K(ATP) channels containing SUR2A or SUR2B subunits to nucleotides and pinacidil.
F. Reimann
,
F. Gribble
,
F. M. Ashcroft
Molecular Pharmacology
2000
Corpus ID: 6217459
ATP-sensitive K-channels (K(ATP) channels) are the target for K(ATP)-channel openers (KCOs), such as pinacidil and P1075. These…
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Highly Cited
1999
Highly Cited
1999
Characterization of the ATP-sensitive potassium channels (KATP) expressed in guinea pig bladder smooth muscle cells.
M. Gopalakrishnan
,
K. Whiteaker
,
+9 authors
J. Brioni
Journal of Pharmacology and Experimental…
1999
Corpus ID: 11909113
ATP-sensitive K+ (KATP) channels play an important role in the regulation of smooth muscle membrane potential. To investigate the…
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Highly Cited
1999
Highly Cited
1999
Coexpression with the inward rectifier K(+) channel Kir6.1 increases the affinity of the vascular sulfonylurea receptor SUR2B for glibenclamide.
U. Russ
,
A. Hambrock
,
+4 authors
U. Quast
Molecular Pharmacology
1999
Corpus ID: 5623347
ATP-sensitive K(+) channels are closed by the hypoglycemic sulfonylureas like glibenclamide (GBC) and activated by a class of…
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Highly Cited
1993
Highly Cited
1993
Binding of the K+ channel opener [3H]P1075 in rat isolated aorta: relationship to functional effects of openers and blockers.
U. Quast
,
K. Bray
,
H. Andres
,
P. Manley
,
Y. Baumlin
,
J. Dosogne
Molecular Pharmacology
1993
Corpus ID: 13116658
P1075 [N-cyano-N'-(1,1-dimethylpropyl)-N"-3-pyridylguanidine], an analogue of the K+ channel opener pinacidil, was shown to be a…
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Highly Cited
1992
Highly Cited
1992
Antiarrhythmic Effects of Potassium Channel Openers in Rhythm Abnormalities Related to Delayed Repolarization
L. Carlsson
,
C. Abrahamsson
,
L. Drews
,
G. Duker
Circulation
1992
Corpus ID: 1557701
Background Earlier observations have indicated that repolarization-delaying agents may, under certain circumstances, have the…
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