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Departmetnt Of Pharmacy Hyogo University Of Health Sciences | 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
- Design, Synthesis and Activity of Shortened Analogs of an Anti-HIV Peptide, T22
- Helix Inducible Motifs Affect Helicity and Bioactivity of Anti-HIV Peptides
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