BABA Masanori | Division of Antiviral Chemotherapy, Center for Chronic Viral Diseases, Faculty of Medicine, Kagoshim

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著作論文

抗エイズウイルス活性を有する親水性フルオロシランカップリングオリゴマ-の合成
Orally Active CCR5 Antagonists as Anti-HIV-1 Agents : Synthesis and Biological Activity of 1-Benzothiepine 1, 1-Dioxide and 1-Benzazepine Derivatives Containing a Tertiary Amine Moiety
Orally Active CCR5 Antagonists as Anti-HIV-1 Agents 2 : Synthesis and Biological Activities of Anilide Derivatives Containing a Pyridine N-Oxide Moiety
CCR5 Antagonists as Anti-HIV-1 Agents.1. Synthesis and Biological Evaluation of 5-Oxopyrrolidine-3-carboxamide Derivatives
EM2487, a Novel Anti - HIV - 1 Antibiotic, Produced by Streptomyces sp. Mer - 2487: Taxonomy, Fermentation, Biological Properties, Isolation and Structure Elucidation
Different Properties of Wild Type and Drug-Resistant Mutants of Human Immunodeficiency Virus Type 1 Reverse Transcriptase In Vitro
Anti-rheumatic compound aurothioglucose inhibits tumor necrosis factor-α-induced HIV-1 replication in latently infected OM10.1 and Ach2 cells
Synthesis and Properties of Gelling Fluoroalkylated End-Capped Oligomers Containing Hydroxy Segments
Syntheses and Properties of Fluoroalkylated Oligomers Containing Oligo(oxyethylene) Units
Sho-Saiko-To, a Traditional Kampo Medicine, Enhances the Anti-HIV-1 Activity of Lamivudine(3TC)In Vitro
Stereoselective Synthesis of 4'-α-Alkylcarbovir Derivatives Based on an Asymmetric Synthesis or Chemoenzymatic Procedure
Synthesis and Anti-human Immunodeficiency Virus Activity of the Skeleton Isomers of 3′,4′-Di-(O)-(−)-camphanoyl-(+)-khellactone
Organosilicon Compounds as Adult T-Cell Leukemia Cell Proliferation Inhibitors

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