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Zeneca ZD 6169
Known as:
ZD6169
, ZD 6169
, Zeneca ZD6169
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Amides
Benzophenones
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Evaluation of von Willebrand Factor and von Willebrand Factor Propeptide in Models of Vascular Endothelial Cell Activation, Perturbation, and/or Injury
D. Brott
,
A. Katein
,
+4 authors
C. Louden
Toxicologic pathology (Print)
2014
Corpus ID: 19139528
Pharmacologically, vasoactive agents targeting endothelial and/or smooth muscle cells (SMC) are known to cause acute drug-induced…
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2013
2013
Coronary and Systemic Arterial Physiology and Immunohistochemical Markers Related to Early Coronary Arterial Lesions in Beagle Dogs Given the Potassium Channel Opener, ZD6169, or the Endothelin…
H. Jones
,
J. Björkman
,
J. Schofield
Toxicologic pathology (Print)
2013
Corpus ID: 27819465
We evaluated immunohistochemistry (von Willebrand Factor [vWF] or fibrinogen) and systemic and coronary arterial physiological…
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2004
2004
Effects of ZD6169, a KATP channel opener, on neurally-mediated plasma extravasation in the rat urinary bladder induced by chemical or electrical stimulation of nerves
Yongbei Yu
,
M. O. Fraser
,
W. C. Groat
Brain Research
2004
Corpus ID: 25302381
2004
2004
(−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), a Novel ATP-Sensitive Potassium Channel Opener: Hemodynamic Comparison to ZD-6169, WAY…
R. Fryer
,
L. Preusser
,
+7 authors
G. Reinhart
Journal of Cardiovascular Pharmacology
2004
Corpus ID: 8955810
The therapeutic utility of KATP channel opening agents (KCOs) in the treatment of overactive bladder may be limited by…
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2002
2002
(−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide (A-278637): A Novel ATP-Sensitive Potassium Channel Opener Efficacious in Suppressing Urinary…
M. Gopalakrishnan
,
S. Buckner
,
+16 authors
M. Coghlan
Journal of Pharmacology and Experimental…
2002
Corpus ID: 34209211
Alterations in the myogenic activity of the bladder smooth muscle are thought to serve as a basis for the involuntary detrusor…
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2002
2002
N-Arylated pyrrolidin-2-ones and morpholin-3-ones as potassium channel openers.
Pi-Hui Liang
,
L. Hsin
,
C. Cheng
Bioorganic & Medicinal Chemistry
2002
Corpus ID: 459939
2002
2002
(−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide (A-278637): A Novel ATP-Sensitive Potassium Channel Opener Efficacious in Suppressing Urinary…
M. Brune
,
T. Fey
,
+5 authors
M. Gopalakrishnan
Journal of Pharmacology and Experimental…
2002
Corpus ID: 19716370
ATP-sensitive potassium (KATP) channel openers (KCOs) have been shown to inhibit spontaneous myogenic contractile activity of the…
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2001
2001
The involvement of L‐type Ca2+ channels in the relaxant effects of the ATP‐sensitive K+ channel opener ZD6169 on pig urethral smooth muscle
N. Teramoto
,
T. Yunoki
,
+5 authors
Y. Ito
British Journal of Pharmacology
2001
Corpus ID: 1800109
The effects of ZD6169, a novel ATP‐sensitive K+ channel (KATP channel) opener, were investigated on membrane currents in isolated…
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2001
2001
Fluorescence-based functional assay for sarcolemmal ATP-sensitive potassium channel activation in cultured neonatal rat ventricular myocytes.
K. Whiteaker
,
R. Davis-Taber
,
Victoria E. Scott
,
Murali Gopalakrishnan
Journal of pharmacological and toxicological…
2001
Corpus ID: 33148790
1996
1996
N-aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: KATP potassium channel openers. Modifications on the western region.
C. Ohnmacht
,
K. Russell
,
+28 authors
K. Neilson
Journal of Medicinal Chemistry
1996
Corpus ID: 25816020
A subset of antiandrogen compounds, the N-aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides 1, were found to activate ATP…
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