Search Results1-20 of  54

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  • SHUTO SATOSHI ID: 9000005134556

    Research Laboratories, Toyo Jozo Co., Ltd. (1987 from CiNii)

    Articles in CiNii:5

    • Synthesis of 6,5'-Cyclo-5'-deoxyuridines by Radical Cyclization : Nucleosides and Nucleotides. L (1984)
    • SYNTHESIS OF BREDININ FROM 5-AMINOIMIDAZOLE-4-CARBOXAMIDE-RIBOFURANOSIDE (AICA-RIBOSIDE) (1984)
    • Synthesis of 6,2'-Methano-cyclouridine, a Uridine Fixed in High-Anti Conformation (Nucleosides and Nucleotides. LX) (1985)
  • SHUTO SATOSHI ID: 9000254222724

    Articles in CiNii:1

    • Synthesis of 6,5'-cyclo-5'-deoxyuridines by radical cyclization (nucleosides and nucleotides. L). (1984)
  • SHUTO SATOSHI ID: 9000254225507

    Articles in CiNii:1

    • Nucleosides and nucleotides. LX. Synthesis of 6,2'-methano-cyclouridine, a uridine fixed in high-anti conformation. (1985)
  • SHUTO SATOSHI ID: 9000254694852

    Articles in CiNii:1

    • Synthesis of bredinin from 1-.BETA.-D-ribofuranosyl-5-aminoimidazole-4-carboxamide by a photo-reaction. (1986)
  • SHUTO SATOSHI ID: 9000254697630

    Articles in CiNii:1

    • A facile enzymatic synthesis of 5'-(3-sn-phosphatidyl) nucleosides and their antileukemic activities. (1988)
  • SHUTO Satoshi ID: 9000000586650

    Graduate School of Pharmaceutical Sciences, Hokkaido University (2001 from CiNii)

    Articles in CiNii:1

    • (1S,2R)-1-Phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PRDC), a New Class of NMDA-Receptor Antagonist: Molecular Design by a Novel Conformational Restriction Strategy (2001)
  • SHUTO Satoshi ID: 9000002085181

    Graduate School of Pharmaceutical Sciences, Hokkaido University (2007 from CiNii)

    Articles in CiNii:1

    • Total Synthesis and the Three-Dimensional Structure-Activity Relationship Study of Tripeptide Antibiotic Belactosin A, a Potent Proteasome Inhibitor (2007)
  • SHUTO Satoshi ID: 9000005152989

    Faculty of Pharmaceutical Sciences, Hokkaido University (2008 from CiNii)

    Articles in CiNii:6

    • Antineovascular therapy with angiogenic vessel-targeted polyethyleneglycol-shielded liposomal DPP-CNDAC (2008)
    • Conformationai Analysis of the NMDA Receptor Antagonist (1S,2R)-1-Phenyl-2-[(S)]-1-aminopropyl]-N,N-diethylcyclopropanecarboxmide(PPDC) Designed by a Novel Conformational Restriction Method Basedon the Structural Feature of Cyclopropane Ring (2002)
    • New Neplanocin Analogues. IX. A Practical Preparation of (6'R)-6'-C-Methylneplanocin A (RMNPA), a Potent Antiviral Agent, and the Determination of Its 6'-Configuration. Diastereoselective Deamination by Adenosine Deaminase (1997)
  • SHUTO Satoshi ID: 9000014186949

    Graduate School of Pharmaceutical Sciences, Hokkaido University (2008 from CiNii)

    Articles in CiNii:1

    • Preparation of Tethered Palladium Catalysis Supported on Gold(111) and Its Surface Characterization by X-ray Photoelectron Spectroscopy (XPS) (2008)
  • SHUTO Satoshi ID: 9000020354173

    Articles in CiNii:1

    • Therapeutic Effect of Reticuloendothelial System(RES)-Avoiding Liposomes Containing a Phospholipid Analogue of 5-Fluorouracil, Dipalmitoylphosphatidylfluorouridine, in Meth A Sarcoma-Bearing Mice. (1994)
  • SHUTO Satoshi ID: 9000254242465

    Articles in CiNii:1

    • Synthesis of Conformationally Restricted Analogs of Baclofen, a Potent GABAB Receptor Agonist, by the Introduction of a Cyclopropane Ring. (1999)
  • SHUTO Satoshi ID: 9000254709339

    Articles in CiNii:1

    • New Neplanocin Analogues. IV. 2-Fluoroneplanocin A: An Adenosine Deaminase-Resistant Equivalent of Neplanocin A. (1994)
  • SHUTO Satoshi ID: 9000254712194

    Articles in CiNii:1

    • New Neplanocin Analogues. IX. A Practical Preparation of (6'R)-6'-C-Methylneplanocin A (RMNPA), a Potent Antiviral Agent, and the Determination of Its 6'-Configuration. Diastereoselective Deamination by Adenosine Deaminase. (1997)
  • SHUTO Satoshi ID: 9000254713013

    Articles in CiNii:1

    • Nucleosides and Nucleotides. Part 154. New Neplanocin Analogues. VIII. Synthesis and Biological Activity of 6'-C-Ethyl, -Ethenyl, and -Ethynyl Derivatives of Neplanocin A. (1997)
  • SHUTO Satoshi ID: 9000254715894

    Articles in CiNii:1

    • Nucleosides and Nucleotides. 186. Synthesis and Biological Activities of Pyrimidine Carbocyclic Nucleosides with a Hydroxyamino Group Instead of a Hydroxymethyl Group at the 4'-Position of the Sugar Moiety. (1999)
  • SHUTO Satoshi ID: 9000258733858

    Faculty of Pharmaceutical Sciences, Hokkaido University (2013 from CiNii)

    Articles in CiNii:1

    • Design, Synthesis, and Validation of Peptidomimetics with Three-Dimensional Structural Diversity (2013)
  • SHUTO Satoshi ID: 9000272642062

    Faculty of Pharmaceutical Sciences, Hokkaido University (2012 from CiNii)

    Articles in CiNii:5

    • Palladium Material Supported on GaAs (001) or Gold for Drug Development (2010)
    • Development of Sulfur-Modified Au-Supported Pd ; Recyclable and Small Amount of Pd-Releasing Catalyst (2012)
    • Ca〔2+〕動員を介する細胞内情報伝達系を標的とする機能性分子の創製 (特集 メディカルケミストリーの最前線) (2002)
  • SHUTO Satoshi ID: 9000309571775

    北海道大学 (2014 from CiNii)

    Articles in CiNii:1

    • 非酵素的に高効率シグナル増幅を可能とする新規RNA検出法を開発 (2014)
  • SHUTO Satoshi ID: 9000391968844

    Hokkaido University, Faculty of Pharceutical Sciences (2010 from CiNii)

    Articles in CiNii:1

    • Development of Sulfur-modified Au-supported Pd "SAPd" and its Application to Constract a Drug Library of Three-dimentional Diversity (2010)
  • SHUTO Satoshi ID: 9000402240749

    北海道大学大学院薬学研究院 (2019 from CiNii)

    Articles in CiNii:1

    • 理想は「そうしな教授」 (2019)
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