MATSUOKA Masao | Institute for Virus Research, Kyoto University

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概要

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著作論文

New Leads of Low Molecular Weight CXCR4 Antagonists Based on Enhancement of the T140-based Pharmacophores
CXCR4 Antagonists Identified as Anti-Cancer-Metastatic Agents
Synthesis of Novel Anti-HIV Peptides Based on a CXCR4 Antagonist, T140, and Their SAR Study
Helix Inducible Motifs Affect Helicity and Bioactivity of Anti-HIV Peptides
Development of Fusion-inhibiting Anti-HIV-1 Peptides Based on the Structure of Molecular Complex Involved in HIV-1-cell Fusion
Synthesis and Application of Novel Fluorescence-Labeled CXCR4 Antagonists
Design and Synthesis of Highly Active Anti-HIV Peptide Based on Gp41-C34 Peptide
Synthesis of Alkene Type Dipeptide Isosteres and Their Use to Probe the Structural Requirements of Peptide Transporter (PEPT1)
Stereoselective Synthesis of Diketopiperazine Mimetics as Promising Scaffolds for Drug Discovery Utilizing Organocopper-Mediated anti-S_N2' Reaction
P-39 2'-DEXY-4'-C-ETHYNYL-2-FLUOROADENOSINE, A NRTI THAT COULD BE AN IDEAL DRUG FOR BOTH HIV-AND HBV-INFECTIONS
Leukemogenesis of Adult T-Cell Leukemia
Oligoarginine-mediated Delivery of Bioactive Peptides into Living cells
Identification of Novel HIV-1 Fusion Inhibitors by Template-Assisted Peptide Aldehyde Ligation
Structure Activity Relationship Study of the Helix-inducible Motifs in HIV Fusion Inhibitors
X-ray Crystallographic Study of the HIV-1 Fusion Inhibitor against the Drug-Resistant N43D Variant
Bioorganic Synthesis of End-capped HIV-1 Fusion Inhibitor SC35EK
SOMATIC ALTERATIONS IN ADULT T-CELL LEUKEMIA CELLS

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