Nakano Hiroaki | Departmetnt Of Pharmacy Hyogo University Of Health Sciences

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概要

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著作論文

Development of Quasi-Monoenergetic Neutron Source Using the 1H(13C,n) Reaction
NMR Studies on Structure and Action Mechanism of Sulfated Dodecyl Laminaripentaoside with High Anti-Human Immunodeficiency Virus Activity
Synthesis of Azidothymidine-Bound Sulfated Alkyl Oligosaccharides and Their Inhibitory Effects on AIDS Virus Infection In Vitro
Synthesis of Azidothymidine-Bound Curdlan Sulfate with Anti-Human Immunodeficiency Virus Activity in Vitro
アセタミド基含有硫酸化多糖の合成と抗HIV活性
1P011 コラーゲン分解酵素Pz-Aの立体構造と機能(蛋白質-構造,第48回日本生物物理学会年会)
Development of the Chemokine Receptor CXCR4 Antagonists as Multi-Pharmaceutical Agents Involving a New Class of Low Molecular Weight Antagonists
P-423 Structure-Activity Relationship Studies on Cyclic Peptide-Based CXCR4 Antagonists
Synthesis and Biological Evaluation of Peptidomimetic Analogs of the CXCR4 Antagonist FC131
The Chemokine Receptor CXCR4 as a Therapeutic Target for Several Diseases Including AIDS, Cancer and Rheumatoid Arthritis
New Leads of Low Molecular Weight CXCR4 Antagonists Based on Enhancement of the T140-based Pharmacophores
A New Strategy for Molecular-size Reduction of Bioactive Peptide, Using Two Orthogonal Libraries of Cyclic peptides
CXCR4 Antagonists Identified as Anti-Cancer-Metastatic Agents
Synthesis of Novel Anti-HIV Peptides Based on a CXCR4 Antagonist, T140, and Their SAR Study
Development of Specific CXCR4 Inhibitors Based on an Anti-HIV Peptide, T140, and Their Structure-Activity Relationships Study
Increase of R5 HIV-1 infection and CCR5 expression in T cells treated with high concentrations of CXCR4 antagonists and SDF-1
Sulfated Fibroin, a Novel Sulfated Peptide Derived from Silk, Inhibits Human Immunodeficiency Virus Replication in Vitro
HIV-cell Fusion Inhibitors Targeted to the HIV Second Receptor : T22 and Its Downsized Analogs with High Activity
Helix Inducible Motifs Affect Helicity and Bioactivity of Anti-HIV Peptides
Synthesis of Sulfated Deoxy-Ribofuranans Having Selective Anti-AIDS Virus Activity by Ring-Opening Copolymerization of 1,4-Anhydro Ribose Derivatives
Molecular Size of an Anti-HIV Peptide, T22, Can Be Reduced without Loss of the Activity
In Vitro Anti-Human Immunodeficiency Virus Activity of Polysaccharide from Rhizophora mucronata Poir.
Mangrove Halophytes: A source of antiviral substances
X-ray Crystallographic Study of the HIV-1 Fusion Inhibitor against the Drug-Resistant N43D Variant

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