Search Results - "Balwierczak, J L"
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Characterization of a potent and selective endothelin-B receptor antagonist, IRL 2500
Published in Journal of cardiovascular pharmacology (1995)“…IRL 2500 [N-(3,5-dimethylbenzoyl)-N-methyl-(D)-(4-phenylphenyl)-alany l-L- tryptophan] inhibited the binding of [125I]-endothelin-1 (ET-1) to human ETB (IC50…”
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The relationship of KCl‐ and prostaglandin F2α‐mediated increases in tension of the porcine coronary artery with changes in intracellular Ca2+measured with fura‐2
Published in British journal of pharmacology (01-10-1991)“…1 Changes in intracellular free Ca2+concentration ([Ca2+]i) were measured simultaneously with changes in muscle tension by use of the fluorescent…”
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Effects of metalloprotease inhibitors on smooth muscle endothelin-converting enzyme activity
Published in Biochemical pharmacology (31-01-1995)“…The enzyme responsible for the conversion of exogenous big endothelin-1 to endothelin-1 by porcine coronary arterial smooth muscle has been shown to be a…”
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Effects of adenosine A2 receptor agonists on nucleoside transport
Published in The Journal of pharmacology and experimental therapeutics (01-10-1989)“…A series of adenosine A2 receptor agonists were examined for their ability to activate adenosine A2 receptors and inhibit nucleoside transport. A2 receptor…”
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The relationship between the binding site of [3H]-d-cis-diltiazem and that of other non-dihydropyridine calcium entry blockers in cardiac sarcolemma
Published in Molecular pharmacology (01-02-1987)“…[3H]-d-cis-Diltiazem binds to canine cardiac sarcolemma in a specific, saturable, and reversible manner with a KD = 58.0 +/- 9.5 nM and a receptor site density…”
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Effects of bepridil and diltiazem on [3H]nitrendipine binding to canine cardiac sarcolemma. Potentiation of pharmacological effects of nitrendipine by bepridil
Published in The Journal of pharmacology and experimental therapeutics (01-04-1986)“…[3H]Nitrendipine binds to canine cardiac sarcolemma in a specific, saturable and rapid manner. Bepridil, a Ca++ channel inhibitor, stimulates this binding at…”
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Comparative effects of a selective adenosine A2 receptor agonist, CGS 21680, and nitroprusside in vascular smooth muscle
Published in European journal of pharmacology (17-04-1991)“…CGS 21680 (2-[p-(2-carboxyethyl)phenylethylamino]-5'-N-ethyolcarboxamidoa denosine) is an adenosine agonist that has been reported recently to bind selectively…”
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A simple assay for the measurement of conversion of big endothelin-1 to endothelin-1 by smooth muscle
Published in European journal of pharmacology (21-12-1993)“…The conversion of exogenous big endothelin-1 to endothelin-1 by the smooth muscle of denuded porcine coronary arterial strips was measured by radioimmunoassay…”
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Specific binding of [3H]d-cis-diltiazem to cardiac sarcolemma and its inhibition by calcium
Published in European journal of pharmacology (08-10-1985)Get more information
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Decrease in immunoreactivity and vasoactivity of endothelin-1 after exposure to oxygen
Published in Biochemistry international (01-09-1992)“…Endothelin-1 (ET-1) caused a dose-dependent contraction of porcine coronary arterial rings. Preincubation of ET-1 in oxygenated Krebs solution at 37 degrees C…”
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Two subtypes of the endothelin receptor (ETA and ETB) mediate vasoconstriction in the perfused rat heart
Published in Journal of cardiovascular pharmacology (1993)“…The effects of endothelin-1 (ET-1) are mediated by two subclasses of the endothelin receptor, ETA and ETB. The Langendorff perfused rat heart was used to…”
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Benzofused Macrocyclic Lactams as Triple Inhibitors of Endothelin-Converting Enzyme, Neutral Endopeptidase 24.11, and Angiotensin-Converting Enzyme
Published in Journal of cardiovascular pharmacology (1998)“…The purpose of this study was to identify endothelin-converting enzyme (ECE) inhibitors that also possess inhibitory activity for neutral endopeptidase 24.11…”
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Different affinities and selectivities of endothelin-1 and endothelin-3 binding to various rat tissues
Published in Biochemistry international (01-11-1990)“…Inhibition of [125I]endothelin-1 ([125I]ET-1) binding to membrane fractions from various rat tissues by ET-1 and endothelin-3 (ET-3) was investigated. Brain…”
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Evidence that BKCa channel activation contributes to K+ channel opener induced relaxation of the porcine coronary artery
Published in Naunyn-Schmiedeberg's archives of pharmacology (01-08-1995)“…The rank order of potency of a series of benzopyran and cyanoguanidine K+ channel openers (KCOs) for causing relaxation of the PGF2 alpha-precontracted porcine…”
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Purification and characterization of an endothelin degradation enzyme from rat kidney
Published in Journal of biochemistry (Tokyo) (01-01-1994)“…A soluble protease which effectively inactivated endothelin-1 was purified 2,700-fold from rat kidney using DE52 anion exchange, concanavalin A-Sepharose,…”
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Effects of metalloprotease inhibitors on the conversion of proendothelin-1 to endothelin-1
Published in Biochemistry and molecular biology international (01-12-1993)“…The IC50 values of phosphoramidon, CGS 25015, CGS 26129, thiorphan and benazeprilat for inhibition of endothelin converting enzyme partially purified from…”
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Dipeptide sulfonamides as endothelin ETA/ETB receptor antagonists
Published in Canadian journal of physiology and pharmacology (01-05-2002)“…Endothelin-1 (ET-1) is a potent mitogen and modulator of vascular tone. It is synthesized and released from endothelial cells and acts upon two receptor…”
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