Kurihara Ken-ichi | Pharmaceutical Research Center Meiji Seika Kaisha Ltd.

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著作論文

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
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics III. Efficient Synthesis of 4-0-Alkyl-L-cladinose Analogues: Improved Antibacterial Activities Compatible with Pharmacokinetics

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