Search Results - "HANSEN, J. Bondo"
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NNC 55-0396 [(1S,2S)-2-(2-(N-[(3-benzimidazol-2-yl)propyl]-N-methylamino)ethyl)-6-fluoro-1,2,3,4-tetrahydro-1-isopropyl-2-naphtyl cyclopropanecarboxylate dihydrochloride]: a new selective inhibitor of T-type calcium channels
Published in The Journal of pharmacology and experimental therapeutics (01-04-2004)“…Mibefradil is a Ca2+ channel antagonist that inhibits both T-type and high-voltage-activated Ca2+ channels. We previously showed that block of…”
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Inhibition of insulin secretion as a new drug target in the treatment of metabolic disorders
Published in Current medicinal chemistry (01-06-2004)“…The pattern of insulin release is crucial for regulation of glucose and lipid haemostasis. Deficient insulin release causes hyperglycemia and diabetes, whereas…”
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New 3-Alkylamino-4H-thieno-1,2,4-thiadiazine 1,1-Dioxide Derivatives Activate ATP-Sensitive Potassium Channels of Pancreatic Beta Cells
Published in Journal of medicinal chemistry (13-07-2006)“…Compound 1a (NN414) is a potent opener of Kir6.2/SUR1 K ATP channels. Compound 1a inhibits insulin release in vitro and in vivo and preserves beta cell…”
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Openers of ATP-dependent K+-channels protect against a signal-transduction-linked and not freely reversible defect of insulin secretion in a rat islet transplantation model of Type 2 diabetes
Published in Diabetologia (01-05-2004)“…We tested whether chronic overstimulation by levels of hyperglycaemia commonly found in Type 2 diabetes can irreversibly desensitise beta cells and, if so,…”
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A potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin release
Published in Diabetologia (01-06-2000)“…To characterise the effects of BPDZ 73 (7-chloro-3-isopropylamino-4H-1,2,4-benzothiadiazine 1,1-dioxide), a newly synthesised diazoxide analogue, on insulin…”
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Selective blockade of T-type Ca2+ channels suppresses human breast cancer cell proliferation
Published in Cancer letters (18-08-2008)“…Abstract We have measured the expression of T-type Ca2+ channel mRNA in breast cancer cell lines (MCF-7 (ERα+) using Western blot and quantitative real-time…”
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6-Chloro-3-alkylamino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-Dioxide Derivatives Potently and Selectively Activate ATP Sensitive Potassium Channels of Pancreatic β-Cells
Published in Journal of medicinal chemistry (12-09-2002)“…6-Chloro-3-alkylamino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide derivatives were synthesized and characterized as activators of adenosine 5‘-triphosphate…”
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Towards selective antagonists of T-type calcium channels: design, characterization and potential applications of NNC 55-0396
Published in Cardiovascular drug reviews (01-06-2005)“…NNC 55-0396 is a structural analog of mibefradil (Ro 40-5967) that inhibits both T-type and high-voltage-activated (HVA) Ca2+ channels with a higher…”
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Potent and selective activation of the pancreatic beta-cell type KATP channel by two novel diazoxide analogues
Published in Diabetologia (01-10-2003)“…We investigated the pharmacological properties of two novel ATP sensitive potassium (K(ATP)) channel openers, 6-Chloro-3-isopropylamino-4 H-thieno[3,2-…”
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Alkoxyfurocoumarin derivatives as potential mesolimbic selective antipsychotics
Published in European journal of medicinal chemistry (1997)“…A series of potential antipsychotic compounds have been synthesized by combining a furocoumarin heterocycle through a linker of different sizes with an…”
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Potent and selective activation of the pancreatic beta-cell type K ATP channel by two novel diazoxide analogues
Published in Diabetologia (01-10-2003)Get full text
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Selective blockade of T-type Ca 2+ channels suppresses human breast cancer cell proliferation
Published in Cancer letters (2008)“…We have measured the expression of T-type Ca 2+ channel mRNA in breast cancer cell lines (MCF-7 (ERα+) using Western blot and quantitative real-time PCR…”
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Potent and selective activation of the pancreatic beta-cell type K(ATP) channel by two novel diazoxide analogues
Published in Diabetologia (01-10-2003)“…We investigated the pharmacological properties of two novel ATP sensitive potassium (K(ATP)) channel openers, 6-Chloro-3-isopropylamino-4 H-thieno[3,2-…”
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Protection of rat pancreatic islets by potassium channel openers against alloxan, sodium nitroprusside and interleukin-1beta mediated suppression--possible involvement of the mitochondrial membrane potential
Published in Diabetologia (01-01-2003)“…We aimed to study the effects of two K(ATP) channel openers (KCO), diazoxide and the more potent compound NNC 55-0118, on beta-cell suppression and/or toxicity…”
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Protection of rat pancreatic islets by potassium channel openers against alloxan, sodium nitroprusside and interleukin-1[beta] mediated suppression--possible involvement of the mitochondrial membrane potential
Published in Diabetologia (01-01-2003)“…Aims/hypothesis. We aimed to study the effects of two KATP channel openers (KCO), diazoxide and the more potent compound NNC 55-0118, on beta-cell suppression…”
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Phenylcyanoguanidines as inhibitors of glucose-induced insulin secretion from beta cells
Published in Bioorganic & medicinal chemistry letters (09-07-2001)“…3,5-Disubstituted-phenylcyanoguanidines have been identified as activators of SUR1/Kir6.2 potassium channels and as potent inhibitors of insulin release from…”
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Two polymorphs - which one is stable at ambient conditions?
Published in Acta crystallographica. Section A, Foundations of crystallography (23-08-2005)“…Abstract only…”
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