Search Results - "Asproni, B"
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The novel cannabinoid antagonist SM-11 reduces hedonic aspect of food intake through a dopamine-dependent mechanism
Published in Pharmacological research (01-11-2016)“…[Display omitted] Cannabinoids, endogenous and exogenously administered, are known to positively regulate food intake and energy balance. Since CB1 receptor…”
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Synthesis of biologically active bridged diazabicycloheptanes
Published in Current medicinal chemistry (01-11-2012)“…The chemistry underlying how diazabicycloheptanes are assembled is described, subdivided according to chemical structure of two types, the 3,6…”
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3
Sensitization to methyl methacrylate in the plastic catheter of an insulin pump infusion set
Published in Contact dermatitis (01-07-2001)Get full text
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4
Synthesis and aldose reductase inhibitory activities of novel thienocinnolinone derivatives
Published in European journal of pharmaceutical sciences (01-03-2004)“…A novel series of tetrahydrothieno[2,3- h]cinnolinone derivatives were synthesized and evaluated in vitro for their ability to inhibit aldose reductase (ALR2),…”
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Thienocinnolinone alkanoic acid derivatives as aldose reductase inhibitors
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-01-2006)“…A new series of 8-halogen-4,4a,5,6-tetrahydrothieno[2,3-h]cinnolinone-N2-alkanoic acids was prepared and tested for aldose reductase (ALR2) inhibitory…”
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Synthesis of substituted N-(4-piperidyl)-N-(3-pyridyl)amides with antiarrhythmic activity. Note 1
Published in Pharmazie (01-12-2000)“…The synthesis of analogues of N,2-diphenyl-N-(4-piperidyl)acetamide endowed with antiarrhythmic activity is reported. Benzoyl, cinnamoyl, acetyl and propionyl…”
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Isolation, characterization and pharmacological activity of Magydaris pastinacea (Lam) Paol. glucosides
Published in Farmaco (Società chimica italiana : 1989) (01-12-1995)“…The glycoside fraction of fresh rhizomes from Magydaris pastinacea (Lam.) Paol. was separated from the alcoholic extract using the method of Kobayashi et al…”
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Determination of amphetamine-derived designer drugs in human urine by SPE extraction and capillary electrophoresis with mass spectrometry detection
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (05-01-2005)“…In recent years, a number of newer designer drugs have entered the illicit drug market. The methylenedioxy-derivates of amphetamine represent the largest group…”
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Fungicidal activity of some o-nitrophenyl-hydrazones
Published in Farmaco (Società chimica italiana : 1989) (01-01-1996)“…The antimycotic activity of 16 o-nitrophenylhydrazones against strains of Hansenula anomala, Saccharomyces cerevisiae, Candida parapsylosis, and Cryptococcus…”
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Synthesis, structure-activity relationships at the GABA(A) receptor in rat brain, and differential electrophysiological profile at the recombinant human GABA(A) receptor of a series of substituted 1,2-diphenylimidazoles
Published in Journal of medicinal chemistry (07-04-2005)“…A series of new 1,2-diphenylimidazole derivatives (1a-x) were synthesized and evaluated for their ability to potentiate gamma-aminobutyric acid (GABA)-evoked…”
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11
Determination of amphetamines in human whole blood by capillary electrophoresis with photodiode array detection
Published in Journal of pharmaceutical and biomedical analysis (01-08-2002)“…A capillary electrophoresis (CE) with photodiode array detection (DAD) method for the analysis of amphetamines in human whole blood samples is described…”
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Journal Article Conference Proceeding -
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Synthesis, Structure-Activity Relationships at the GABA sub(A) Receptor in Rat Brain, and Differential Electrophysiological Profile at the Recombinant Human GABA sub(A) Receptor of a Series of Substituted 1,2-Diphenylimidazoles
Published in Journal of medicinal chemistry (07-04-2005)“…A series of new 1,2-diphenylimidazole derivatives (1a-x) were synthesized and evaluated for their ability to potentiate gamma -aminobutyric acid (GABA)-evoked…”
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Anti-inflammatory and Analgesic Amides: New Developments
Published in Archiv der Pharmazie (Weinheim) (01-01-2000)“…A series of substituted N‐cycloalkyl benzamides, cinnamamides, and indole‐3‐carboxamides were synthesized and evaluated for their analgesic, antiinflammatory…”
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Synthesis of N-[4-(propyl)cyclohexyl]-amides with anti-inflammatory and analgesic activities
Published in Farmaco (Società chimica italiana : 1989) (01-06-2000)“…Seventeen (un)substituted N-[4-(propyl)cyclohexyl]-amides ( 6a– h, 7a– h and 8) were synthesized and tested as anti-inflammatory and analgesic agents. The…”
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Synthesis of N-[4-(alkyl)cyclohexyl]-substituted benzamides with anti-inflammatory and analgesic activities
Published in Farmaco (Società chimica italiana : 1989) (30-08-1999)“…Two series of N-[4-(alkyl)cyclohexyl]-substituted benzamides, i.e. a series of N-[4-( tert-butyl)cyclohexyl]-substituted benzamides and a series of…”
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