Search Results - "Maclntyre, D. Euan"
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1-Amino-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid as a Tic mimetic: Application in the synthesis of potent human melanocortin-4 receptor selective agonists
Published in Bioorganic & medicinal chemistry letters (15-07-2005)“…The discovery of 1-amino-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid analogs as potent human melanocortin-4 selective agonists is described. The discovery…”
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1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia
Published in Bioorganic & medicinal chemistry letters (01-02-2011)“…1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) attenuated the enhanced glucose excursion following an intraperitoneal glucose tolerance test and…”
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Chronic MCH-1 receptor modulation alters appetite, body weight and adiposity in rats
Published in European journal of pharmacology (15-08-2003)“…Central administration of the neuropeptide melanin-concentrating hormone (MCH) stimulates feeding in rodents. We studied the effects of intracerebroventricular…”
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Characterization of a novel and selective cannabinoid CB1 receptor inverse agonist, Imidazole 24b, in rodents
Published in European journal of pharmacology (28-01-2008)“…We document in vitro and in vivo effects of a novel, selective cannabinoid CB(1) receptor inverse agonist, Imidazole 24b…”
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Cyclopentane-based human NK1 antagonists. Part 2: Development of potent, orally active, water-soluble derivatives
Published in Bioorganic & medicinal chemistry letters (01-09-2006)“…The optimization of a cyclopentane-based hNK1 antagonist scaffold will be discussed in the context of enhanced water-solubility, sub-nanomolar hNK1 binding…”
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Bicyclic amidine inhibitors of nitric oxide synthase: discovery of perhydro-iminopyrindine and perhydro-iminoquinoline as potent, orally active inhibitors of inducible nitric oxide synthase
Published in Bioorganic & medicinal chemistry letters (15-04-2005)“…The synthesis and nitric oxide synthase inhibitory activity of bicyclic amidines are described. The 6,6 and 5,6 fused amidines 8a and 10a are potent,…”
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