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Research Institute, Daiichi Pharmaceutical Co., Ltd., | 論文
- Studies on Peptides. CXXXIII. : Synthesis and Biological Activity of Galanin, a Novel Porcine Intestinal Polypeptide
- Direct Transformation of O-Glycoside into Glyosyl Bromide with the Combination of Trimethylsilyl Bromide and Zinc Bromide
- Synthesis and Biological Activities of Analogs of a Lipid A Biosynthetic Precursor : 1-O-Phosphono-oxyethyl-4'-O-phosphono-disaccharides with (R)-3-Hydroxytetradecanoyl or Tetradecanoyl Groups at Positions 2,3,2' and 3'
- A Novel Glycoside Anomerization Catalyzed by Trimethylsilyl Bromide and Zinc Bromide in Combination
- Synthesis and Antitumor Activity of Lipid A Analogs Having a Phosphonooxyehyl Group with α- or β-Configuration at Position 1
- Novel Stereoselective Glycosidation by the Combined Use of Trityl Halide and Lewis Acid
- Aryloxyacetic Acid Diuretics with Uricosuric Activity. II. Substituted [(4-Oxo-4H-1-benzopyran-7-yl)oxy]acetic Acids and the Related Compounds
- Aryloxy Acetic Acid Diuretics with Uricosuric Activity. I. Polycyclic Aryloxy Acetic Acids
- Studies on Peptides. CLXVI. : Solid-Phase Syntheses and Immunological Properties of Fragment Peptides Related to Human Hepatitis B Virus Surface Antigen (HBsAg) and Its Pre-S2 Gene
- Studies on Peptides. CXXIV. Solution Synthesis of the Hentetracontapeptide Amide Corresponding to the Entire Amino Acid Sequence of Human Corticotropin Releasing Factor (hCRF)
- Studies on Peptides. CXXIII. Preparations of Nine Peptide Fragments for the Synthesis of Human Corticotropin Releasing Factor (hCRF)
- SYNTHESIS OF A HENTETRACONTAPEPTIDE AMIDE CORRESPONDING TO THE ENTIRE AMINO ACID SEQUENCE OF HUMAN CORTICOTROPIN RELEASING FACTOR (hCRF)
- Structure of Gardneramine and 18-Demethylgardneramine
- 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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