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Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., | 論文
- 2-(3-Pyridyl)thiazolidine-4-carboxamide Derivatives. II. Structure-Activity Relationships and Active Configuration of 2-(3-Pyridyl)thiazolidine-4-carboxamides as Platelet-Activating Factor Receptor Antagonists
- 2-(3-Pyridyl)thiazolidine-4-carboxamides. 1. Novel Orally Active Antagonists of Platelet-Activating Factor (PAF)
- Peptide Based Interleukin-1β Converting Enzyme (ICE) Inhibitors : Synthesis, Structure Activity Relationships and Crystallographic Study of the ICE-inhibitor Complex
- Synthesis and Structure-Activity Studies of a Series of 1-Oxa-2,8-diazaspiro[4.5]decan-3-ones and Related Compounds as M_1 Muscarinic Agonists
- In-situ X-ray Diffraction of Corrosion Products Formed on Iron Surfaces
- Studies on Prostaglandins. I. The Resolution of dl-(2β-Benzyloxymethyl-3α-hydroxy-4-cyclopenten-1α-yl) acetic Acid using L-Arginine
- Novel Potassium Channel Activators : Synthesis and Structure-Activity Relationship Studies of 3,4-Dihydro-2H-1,4-benzoxazine Derivatives
- A Novel Class of Inhibitors for Human Steroid 5α-Reductase : Synthesis and Biological Evaluation of Indole Derivatives. II
- A Novel Class of Inhibitors for Human Steroid 5α-Reductase : Phenoxybenzoic Acid Derivatives. I
- Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (±)-N-[2-(3,4-Dichlorophenyl)-4-(spiro-substituted piperidin-1'-yl)butyl]-N-methylbenzamides and Evaluation of NK_1-NK_2 Dual Antagonistic Activities
- Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (±)-N-[2-(3,4-Dichlorophenyl)-4-(spiro[isobenzofuran-1(3H), 4'-piperidin]-1'-yl)butyl]-N-methylbenzamide, YM-35375,as a New Lead Compound for Novel Neurokinin Rec
- Synthetic Studies on Selective Type 4 Phosphodiesterase (PDE 4) Inhibitors. 1. Structure-Activity Relationships and Pharmacological Evaluation of 1,8-Naphthyridin-2(1H)-one Derivatives
- Cycloaddition Reactions of a 3-(1,3-Butadienyl)cephalosporin and Antibacterial Activity of New Cephem Derivatives
- Studies on Nonpeptide Angiotensin II Receptor Antagonists. IV. Synthesis and Biological Evaluation of 4-Acrylamide-1H-imidazole Derivatives
- Studies on Nonpeptide Angiotensin II Receptor Antagonists. III. Synthesis and Biological Evaluation of 5-Alkylidene-3,5-dihydro-4H-imidazol-4-one-Derivatives
- Studies on Nonpeptide Angiotensin II Receptor Antagonists. II. Synthesis and Biological Evaluation of 5H-Pyrazolo[1,5-b][1,2,4]triazole Derivatives with a C-Linked Oxygen Functional Group at the 6-Position
- Studies no Nonpeptide Angiotensin II Receptor Antagonists. I. Synthesis and Biological Evaluation of Pyrazolo[1,5-b][1,2,4]triazole Derivatives with Alkyl Substituents
- Studies on Prostaglandins. VI. Synthesis of 16 (S)-Methyl-20-methoxy-PGE_2 (YPG-209) having Oral Bronchodilator Activity and Its Analogs
- Studies on Prostaglandins. II. Synthesis of 4-Alkoxymethyl-2-norbornen-5-one and Its Oxidation Reaction with m-Chloroperbenzoic Acid
- Studies on Prostaglandins. III. Synthesis of Bicyclo [4. 3. 0] nonane Derivatives
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