Research Topics
| Noriyuki YamaotsuSummaryAffiliation: Kitasato University Country: Japan Publications
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Detail Information
Publications
Determination of ligand-binding sites on proteins using long-range hydrophobic potentialNoriyuki Yamaotsu
Laboratory of Physical Chemistry for Drug Design, School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan
Biol Pharm Bull 31:1552-8. 2008..Surprisingly, the binding sites on sugar binding proteins were the most hydrophobic sites. It implies that the hydrophobic interaction plays an important role in the formation of protein-ligand complexes...
Identification of the three-dimensional pharmacophore of kappa-opioid receptor agonistsNoriyuki Yamaotsu
School of Pharmacy, Kitasato University, Minato ku, Tokyo 108 8641, Japan
Bioorg Med Chem 18:4446-52. 2010....
3D-pharmacophore identification for kappa-opioid agonists using ligand-based drug-design techniquesNoriyuki Yamaotsu
School of Pharmacy, Kitasato University, 5 9 1 Shirokane, Minato ku, Tokyo 108 8641, Japan
Top Curr Chem 299:277-307. 2011..This utilizes conformational sampling of agonists by high-temperature molecular dynamics and pharmacophore extraction through a series of molecular superpositions...
Essential structure of opioid κ receptor agonist nalfurafine for binding to κ receptor 1: synthesis of decahydroisoquinoline derivatives and their pharmacologiesHiroshi Nagase
School of Pharmacy, Kitasato University, 5 9 1 Shirokane, Tokyo 108 8641, Japan
Chem Pharm Bull (Tokyo) 60:945-8. 2012..These findings that the simple decahydroisoquinoline derivatives showed the affinities for the opioid receptors, especially some of the compounds showed κ selectivity, are the first example in the opioid field...
Drug design and synthesis of a novel kappa opioid receptor agonist with an oxabicyclo[2.2.2]octane skeleton and its pharmacologyHiroshi Nagase
School of Pharmacy, Kitasato University, 5 9 1 Shirokane, Minato ku, Tokyo 108 8641, Japan
Bioorg Med Chem Lett 20:121-4. 2010..2.2]octane skeleton. KNT-63 showed profound antinociceptive effects via the kappa receptor which were as potent as that of TRK-820...
In silico multi-filter screening approaches for developing novel beta-secretase inhibitorsTaku Fujimoto
School of Pharmaceutical Sciences, Kitasato University, 5 9 1, Shirokane, Minato ku, Tokyo, Japan
Bioorg Med Chem Lett 18:2771-5. 2008....
NMR spectroscopy and computational analysis of interaction between Serratia marcescens chitinase B and a dipeptide derived from natural-product cyclopentapeptide chitinase inhibitor argifinHiroaki Gouda
School of Pharmacy, Kitasato University, Minato ku, Tokyo, Japan
Bioorg Med Chem 18:5835-44. 2010..The improved total electrostatic component was derived from more favorable electrostatic interactions. Therefore, we conclude that dipeptide 2 was also better optimized against SmChiB than 1 in an electrostatic point of view...
