Search Results - "HAMADA, Noritaka"
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Synthesis and Evaluation of Novel Phenylethanolamine Derivatives containing Acetanilides as Potent and Selective β3-Adrenergic Receptor Agonists
Published in Chemical & Pharmaceutical Bulletin (01-04-2010)“…In the search for potent and selective human β3-adrenergic receptor (AR) agonists as potential pharmacotherapies for the treatment of obesity and non-insulin…”
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Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure–activity relationships of pyrimidine-5-carboxamide derivatives
Published in Bioorganic & medicinal chemistry (15-08-2005)“…We discovered the 4-anilinopyrimidine-5-carboxamides as novel Syk inhibitors. These compounds showed high selectivity for Syk compared to other kinases, such…”
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Synthesis and evaluation of novel phenylethanolamine derivatives containing acetanilides as potent and selective beta3-adrenergic receptor agonists
Published in Chemical & pharmaceutical bulletin (2010)“…In the search for potent and selective human beta3-adrenergic receptor (AR) agonists as potential pharmacotherapies for the treatment of obesity and…”
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Quantitative Determination of Amorphous Nicardipine Hydrochloride in Long Acting Formula (NIC-LA®) Using Light Anhydrous Silicic Acid
Published in Chemical & pharmaceutical bulletin (01-12-2004)“…We investigated a method to quantitatively determine amorphous nicardipine hydrochloride (NIC) in the NIC-long acting formula (LA) model formulas prepared…”
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Synthesis and Biological Evaluation of 3-Biphenyl-4-yl-4-phenyl-4 H -1,2,4-triazoles as Novel Glycine Transporter 1 Inhibitors
Published in Journal of medicinal chemistry (13-01-2011)Get full text
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Chronic treatment with olanzapine via a novel infusion pump induces adiposity in male rats
Published in Life sciences (1973) (25-04-2011)“…Clinical use of olanzapine has been suggested to be associated with weight gain and adiposity in schizophrenic patients. While studies in experimental animals…”
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Synthesis and Biological Evaluation of 3-Biphenyl-4-yl-4-phenyl-4H-1,2,4-triazoles as Novel Glycine Transporter 1 Inhibitors
Published in Journal of medicinal chemistry (13-01-2011)“…We describe the preparation and evaluation of a novel series of glycine transporter 1 (GlyT1) inhibitors derived from a high-throughput screening hit. The SAR…”
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Practical and efficient synthesis of the (R)-atropisomer of a 4-phenyl 1,2,4-triazole derivative as a selective GlyT1 inhibitor
Published in Tetrahedron: asymmetry (15-12-2012)“…Herein we describe a novel and efficient method for synthesizing the (R)-atropisomer of…”
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Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors
Published in Bioorganic & medicinal chemistry (01-12-2008)“…As a result of the various N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives with a hydroxy moiety synthesized in an effort to discover novel glycogen…”
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Synthesis and Evaluation of Novel Phenylethanolamine Derivatives containing Acetanilides as Potent and Selective [beta]3-Adrenergic Receptor Agonists
Published in Chemical & pharmaceutical bulletin (01-04-2010)“…In the search for potent and selective human β3-adrenergic receptor (AR) agonists as potential pharmacotherapies for the treatment of obesity and non-insulin…”
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Synthesis and structure–activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists
Published in Bioorganic & medicinal chemistry (2008)“…The 6-fluoro-2-naphthylmethyl derivatives were prepared, and their inhibitory activities against CCR3 were evaluated. A novel class of potent CCR3 receptor…”
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(+)-(2R,5S)-4-[4-Cyano-3-(trifluoromethyl)phenyl]-2,5-dimethyl-N-[6-(trifluoromethyl)pyridin-3- yl]piperazine-1-carboxamide (YM580) as an Orally Potent and Peripherally Selective Nonsteroidal Androgen Receptor Antagonist
Published in Journal of medicinal chemistry (26-01-2006)“…A novel series of trans-N-aryl-2,5-dimethylpiperazine-1-carboxamide derivatives was synthesized and their androgen receptor (AR) antagonist activities and in…”
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Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1 H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors
Published in Bioorganic & medicinal chemistry (2008)“…5-Chloro- N-[(5 R)-1,3,6,6-tetrafluoro-5-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl]-1 H-indole-2-carboxamide are potent inhibitors of human liver glycogen…”
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Crystallization of Syndiotactic Polystyrene in β-Form. 3. Energetic Analysis of the Incorporation Mechanism of Stacking Faults into the Crystal
Published in Macromolecules (20-10-1997)“…Crystallization-temperature (T c) dependence of the probability of the presence of stacking faults, p, in the solution-grown β-form single crystal of…”
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Crystallization of Syndiotactic Polystyrene in β-Form. 1. Positional Identification of Stacking Faults in the Solution-Grown Single Crystals
Published in Macromolecules (14-07-1997)“…The locations of the stacking faults in β-form single crystals of syndiotactic polystyrene, which were grown isothermally from a dilute solution at…”
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Crystallization of Syndiotactic Polystyrene in β-Form. 2. Quantification of Stacking Faults in the Solution-Grown Single Crystals
Published in Macromolecules (03-11-1997)“…The probability of the presence of stacking faults in the β-form single crystals of syndiotactic polystyrene, which were grown isothermally from a dilute…”
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