奥村和央 | New Drug Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.,

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著作論文

Agents for Treatment of Overactive Detrusor. II. Synthesis and Inhibitory Activity on Detrusor Contraction of 1,1'-Biphenyl-2,6-dicarboxylic Acid Diesters with an Aminoalkyl Group in the Ester Function
Agents for the Treatment of Overactive Detrusor. I. Synthesis and Structure-Activity Relationships of 1,1'-Biphenyl Derivatives
Agents for the Treatment of Overactive Detrusor. VIII. Synthesis and Pharmacological Properties of 4,4-Diphenyl-2-cycloalkenylamines Including FK584 and 3,3-or 4,4-Diphenylcycloalkylamines
Agents for the Treatment of Overactive Detrusor. VII. Synthesis and Pharmacological Properties of 2,3- and 3,4-Diphenylcyclopentylamines, 2,3-Diphenyl-2-cyclopentenylamines, and Related Compounds
Agents for the Treatment of Overactive Detrusor. VI. Synthesis and Pharmacological Properties of Acetamide Derivatives Bearing Cyclic Amines in N-Substituents
Agents for the Treatment of Overactive Detrusor. IV. Synthesis and Structure-Activity Relationships of Cyclic Analogues of Terodiline
Agents for the Treatment of Overactive Detrusor. III. Synthesis and Structure-Activity Relationships of N-(4-Amino-2-butynyl)acetamide Derivatives
Studies on Nilvadipine. IV. Synthesis of Deuteriated and Optically Active Isopropyl 2-Cyano-3-methoxycarbonyl-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine-5-carboxylate (Nilvadipine)
Studies on Nilvadipine. III. Syntheses of Metabolites of Nilvadipine and Their Related Compounds
Studies on Nilvadipine. II. Synthesis and Structure-Activity Relationships of 2-Hydroxymethyl- and 2-Cyano-1,4-dihydropyridines Containing Heteroatom-Substituted Ester at the 5-Position
Studies on Nilvadipine. I. Synthesis and Structure-Activity Relationships of 1,4-Dihydropyridines Containing Novel Substituents at the 2-Position

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