Ajito Keiichi | Pharmaceutical Research Center Meiji Seika Kaisha Ltd.

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著作論文

Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
Novel Azalides Derived from Sixteen-Membered Macrolides : I. Isolation of the Mobile Dialdehyde and Its One-Pot Macrocyclization with an Amine
Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position I. Epimerization and Methylation of the 3-Hydroxyl Group
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics VI. Synthesis of metabolically Programmed, Highly Potent Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics V. Preparation of Unsubstituted L-Cladinose Analogues: Effect of Methylation of a 3''-Hydroxyl Group on the Bioactivity
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics II. Preparation of Pharmacokinetically Improved Analogues via Biotransformation
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation
Model Study for Preparation of asymmetric N, N'-Disubstituted piperazine Library:Efficient Synthesis of Aryl Piperazine and Benzyl Piperazine Derivatives on the Solid Support
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics III. Efficient Synthesis of 4-0-Alkyl-L-cladinose Analogues: Improved Antibacterial Activities Compatible with Pharmacokinetics
Synthesis of Potent α_vβ_3/α_β_3 Dual Antagonists Tricyclic Pharmacophore-based Molecules and Their Selectivity Control
Synthesis of novel lincomycin derivatives and their in vitro antibacterial activities

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