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CAS No: 60559-98-0 Catalog No: AG00EB3I MDL No:
Title | Journal |
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Different potassium channels are involved in relaxation of rat renal artery induced by P1075. | Basic & clinical pharmacology & toxicology 20120701 |
ATP-sensitive potassium (KATP) channel activation decreases intraocular pressure in the anterior chamber of the eye. | Investigative ophthalmology & visual science 20110801 |
The effects of potassium channel opener P1075 on the human saphenous vein and human internal mammary artery. | Journal of cardiovascular pharmacology 20110601 |
Substitution of the Walker A lysine by arginine in the nucleotide-binding domains of sulphonylurea receptor SUR2B: effects on ligand binding and channel activity. | Naunyn-Schmiedeberg's archives of pharmacology 20100601 |
Discovery and structure-activity relationships of a novel series of benzopyran-based K(ATP) openers for urge urinary incontinence. | Bioorganic & medicinal chemistry 20090115 |
Syntaxin-1A inhibition of P-1075, cromakalim, and diazoxide actions on mouse cardiac ATP-sensitive potassium channel. | Cardiovascular research 20081201 |
Potassium fluxes, energy metabolism, and oxygenation in intact diabetic rat hearts under normal and stress conditions. | Canadian journal of physiology and pharmacology 20081001 |
Three C-terminal residues from the sulphonylurea receptor contribute to the functional coupling between the K(ATP) channel subunits SUR2A and Kir6.2. | The Journal of physiology 20080701 |
K(ATP) channel expression and pharmacological in vivo and in vitro studies of the K(ATP) channel blocker PNU-37883A in rat middle meningeal arteries. | British journal of pharmacology 20080501 |
GSK3beta inhibition and K(ATP) channel opening mediate acute opioid-induced cardioprotection at reperfusion. | Basic research in cardiology 20070701 |
Effects of substitution on 9-(3-bromo-4-fluorophenyl)-5,9-dihydro-3H,4H-2,6-dioxa-4- azacyclopenta[b]naphthalene-1,8-dione, a dihydropyridine ATP-sensitive potassium channel opener. | Journal of medicinal chemistry 20061116 |
Pharmacological characterization of urinary bladder smooth muscle contractility following partial bladder outlet obstruction in pigs. | European journal of pharmacology 20060217 |
P-1075 exerts diverse modulatory effects on mitochondrial ATP-sensitive K+ channels in rabbit ventricular myocytes. | Journal of cardiovascular pharmacology 20060201 |
Characterization of K(ATP)-channels in rat basilar and middle cerebral arteries: studies of vasomotor responses and mRNA expression. | European journal of pharmacology 20051031 |
Reduced effectiveness of HMR 1098 in blocking cardiac sarcolemmal K(ATP) channels during metabolic stress. | Journal of molecular and cellular cardiology 20051001 |
Lipids modulate ligand binding to sulphonylurea receptors. | British journal of pharmacology 20050801 |
Effect of thimerosal on arrhythmia induced by coronary ligation: the involvement of ATP-dependent potassium channels. | International heart journal 20050701 |
Identification and pharmacological characterization of sarcolemmal ATP-sensitive potassium channels in the murine atrial HL-1 cell line. | Journal of cardiovascular pharmacology 20050101 |
Alteration of binding sites for [3H]P1075 and [3H]glibenclamide in renovascular hypertensive rat aorta. | Acta pharmacologica Sinica 20050101 |
In vitro and in vivo characterization of a novel naphthylamide ATP-sensitive K+ channel opener, A-151892. | British journal of pharmacology 20040901 |
Synthesis and structure-activity relationships of a novel series of 2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide K(ATP) channel openers: discovery of (-)-(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 potent K(ATP) opener that selectively inhibits spontaneous bladder contractions. | Journal of medicinal chemistry 20040603 |
Interaction of a novel dihydropyridine K+ channel opener, A-312110, with recombinant sulphonylurea receptors and KATP channels: comparison with the cyanoguanidine P1075. | British journal of pharmacology 20040401 |
Small molecule mitochondrial F1F0 ATPase hydrolase inhibitors as cardioprotective agents. Identification of 4-(N-arylimidazole)-substituted benzopyran derivatives as selective hydrolase inhibitors. | Journal of medicinal chemistry 20040226 |
Sarcolemmal and mitochondrial effects of a KATP opener, P-1075, in 'polarized' and 'depolarized' Langendorff-perfused rat hearts. | Biochimica et biophysica acta 20031203 |
Selective ATP-sensitive potassium channel openers: fact or fiction. | Journal of molecular and cellular cardiology 20030901 |
P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts. | Journal of molecular and cellular cardiology 20030901 |
Cardioselective sulfonylthiourea HMR 1098 blocks mitochondrial uncoupling induced by a KATP channel opener, P-1075, in beating rat hearts. | Biochimica et biophysica acta 20030714 |
[125I]A-312110, a novel high-affinity 1,4-dihydropyridine ATP-sensitive K+ channel opener: characterization and pharmacology of binding. | Molecular pharmacology 20030701 |
Binding and effect of K ATP channel openers in the absence of Mg2+. | British journal of pharmacology 20030501 |
PNU-83757: a new agent for the treatment of erectile dysfunction. | Current urology reports 20021201 |
Development of a sensitive bioanalytical method for determination of PNU-83757 in rat, monkey and human plasma: from LC-UV to LC-MS/MS. | Journal of pharmaceutical and biomedical analysis 20021015 |
Structure-Activity studies for a novel series of tricyclic dihydropyrimidines as K(ATP) channel openers (KCOs). | Bioorganic & medicinal chemistry letters 20020603 |
The efficacy, safety and tolerability of intracavernous PNU-83757 for the treatment of erectile dysfunction. | The Journal of urology 20020601 |
Effects of K(ATP) channel openers, P-1075, pinacidil, and diazoxide, on energetics and contractile function in isolated rat hearts. | Journal of molecular and cellular cardiology 20020401 |
KCO912: a potent and selective opener of ATP-dependent potassium (K(ATP)) channels which suppresses airways hyperreactivity at doses devoid of cardiovascular effects. | Naunyn-Schmiedeberg's archives of pharmacology 20020301 |
Interaction of K(ATP) channel modulators with sulfonylurea receptor SUR2B: implication for tetramer formation and allosteric coupling of subunits. | Molecular pharmacology 20020201 |
Phenylcyanoguanidines as inhibitors of glucose-induced insulin secretion from beta cells. | Bioorganic & medicinal chemistry letters 20010709 |
Characterization of a mutant sulfonylurea receptor SUR2B with high affinity for sulfonylureas and openers: differences in the coupling to Kir6.x subtypes. | Molecular pharmacology 20010701 |
Functional implication of spare ATP-sensitive K(+) channels in bladder smooth muscle cells. | The Journal of pharmacology and experimental therapeutics 20010301 |
Pharmacological comparison of native mitochondrial K(ATP) channels with molecularly defined surface K(ATP) channels. | Molecular pharmacology 20010201 |
Fluorescence-based functional assay for sarcolemmal ATP-sensitive potassium channel activation in cultured neonatal rat ventricular myocytes. | Journal of pharmacological and toxicological methods 20010101 |
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