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Medicinal Chemistry Research Laboratories, Fujisawa Pharmaceutical Co., Ltd. | 論文
- FR225659-binding Proteins : Identification as Serine/Threonine Protein Phosphatase PP1 and PP2A Using High-performance Affinity Beads
- The Anti-inflammatory Effect of FR188582, a Highly Selective Inhibitor of Cyclooxygenase-2, With an Ulcerogenic Sparing Effect in Rats
- Studies on β-Lactam Antibiotics Synthesis and Antibacterial Activity of Novel C-3 Alkyne-substituted Cephalosporins
- Synthesis and Structure-Activity Relationships of a New Orally Active Caphalosporin, FK482 and the Related Compounds
- WA8242A_1, A_2 and B, Novel Secretary Phospholipase A_2 Inhibitors Produced by streptomyces violaceusinger III. Structure Elucidation and Total Synthesis of WA8242B
- WA8242A_1, A_2 and B, Novel Secrtory Phospholipase A_2 Inhibitors Produced by Streptomyces violaceusniger II. Biological Properties
- SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF NOVEL CEPHALOSPORINS. CEPHALOSPORINS WITH AMINOHETEROAROMATICS AT THE 7-POSITION
- Transition Metal-Catalyzed Intramolecular Cyclization of 1,5- and 1,6- Dienes via Direct Cleavage and Addition of the Carbon-Hydrogen Bond
- Asymmetric Intramolecular C-H/Olefin Coupling : Asymmetric Cyclization Reactions of 1, 5-Dienes Catalyzed by Rhodium Complexes
- Transition Metal-Catalyzed Intramolecular C-H/Olefin Coupling
- WS75624 A and B, New Endothelin Converting Enzyme Inhibitors Isolated from Saccharothrix sp.No.75624 II.Structure Elucidation of WS75624 A and B
- Synthesis and Antibacterial Activity of Novel 4-Pyrrolidinylthio Carbapenems II: 2-Alkyl and -2Arylthiomethyl Derivatives
- Pharmacological Characterization of FR194921, a New Potent, Selective, and Orally Active Antagonist for Central Adenosine A1 Receptors
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