磯田純郎 | Exploratory Research Laboratories Iii Daiichi Pharmaceutical Co. Ltd.

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Synthesis and Antiallergy Activity of [1,3,4]Thiadiazolo[3,2-α]-1,2,3-triazolo[4,5-d]pyrimidin-9(3H)-one Derivatives. II. 6-Alkyl- and 6-Cycloalkylalkyl Derivatives
Synthesis and Antiallergy Activity of [1,3,4]Thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d]pyrimidin-9(3H)-one Derivatives. I
A Reagent, Ethyl 2-(2-tert-Butyl-2H-tetrazol-5-yl)-3-(dimethylamino)acrylate (DMTE), for Facile Synthesis of 2,3-(Ring Fused)-5-(5-tetratzolyl)-4H-pyrimidin-4-one Derivatives
Studies on α_2-Plasmin Inhibitor Fragment T-11. III. Structure-Activity Relationships among the Fragments of T-11, the Plasminogen Binding Site(s) of Human α_2-Plasmin Inhibitor(Medicinal Chemistry,Chemical)
Studies on α_2-Plasmin Inhibitor Fragment T-11. II. Synthesis of the Entire Amino Acid Sequence of α_2-Plasmin Inhibitor Fragment T-11(Medicinal Chemistry,Chemical)
Studies on α_2-Piasmin Inhibitor Fragment T-11. I. Synthesis of the Protected Hexadecapeptide Ester Corresponding to Positions 11 through 26 of α_2-Plasmin Inhibitor Fragment T-11(Medicinal Chemistry,Chemical)
Spasmolytic Agents. I. Aminoalcohol Esters having a Phenethylamine-Like Moiety
Medicinal Chemical Studies on Antiplasmin Drugs. VIII. 4-Aminomethylcyclohexanecarboxylic Acid Derivatives having a Carboxyl or Carboxymethyl Group at C_2
Medicinal Chemical Studies on Antiplasmin Drugs. V. 4-Aminomethylcyclohexanecarboxylic Acid Derivatives having a Methyl Group at C_2 or C_3

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