スポンサーリンク
Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd. | 論文
- Identification of Arginine Analogues as Antagonists and Agonists for the Melanocortin-4 Receptor
- A Novel Fungal Metabolite NG-061 Enhances and Mimics Neurotrophic Effect of Nerve Growth Factor (NGF) on Neurite Outgrowth in PC12 Cells
- Bassiatin, a New Platelet Aggregation Inhibitor Produced by Beauveria bassiana K-717
- A Novel Bioactive δ lactone FD-211 Taxonomy, Isolation and Characterization
- Synthesis of 2-Methyl 16-Membered Macrolide Derived from Tylosin
- Microbial Glycosylation of Macrolide Antibiotics by Streptomyces hygroscopicus ATCC 31080 and Distribution of a Macrolide Glycosyl Transferase in Several Streptomyces Strains
- In Vitro and In Vivo Antibacterial Activities of the Tricyclic Ketolide TE-802 and Its Analogs
- The Synthesis and Antibacterial Activity of Tetracycyclic Macrolides
- Synthesis and Antibacterial Activity of the Tricyclic Ketolides TE-802 and Its Analogs
- PI-220, a New Platelet Aggregation Inhibitor
- Increased Excretion of Urinary 20-HETE in Rats With Cyclosporine-Induced Nephrotoxicity
- Conformational Analysis of Tricyclic Ketolide TE-802 and Its Analogues
- Role of 20-hydroxyeicosatetraenoic acid (20-HETE) in vascular system
- Elevated Post-Translational Modification of Proteins by O-Linked N-Acetylglucosamine in Various Tissues of Diabetic Goto-Kakizaki Rats Accompanied by Diabetic Complications
- Synthesis of Diphenylmethyl Analogues and Their Affinity for the Melanocortin-4 Receptor and the Serotonin Transporter
- Stachybotrin C and Parvisporin, Novel Neuritogenic Compounds II. Structure Determination
- Stachybotrin C and Parvisporin, Novel Neuritogenic Compouds I. Taxonomy, Isolation, Physico-chemical and Biological Properties
- Isolation and Characterization of a New Pyrano[4', 3': 6, 7]naphtho[1, 2-b]xanthene Antibiotic FD-594
- Cytochrome P450 4A Isoform Inhibitory Profile of N-Hydroxy-N'-(4-butyl-2-methylphenyl)-formamidine (HET0016), a Selective Inhibitor of 20-HETE Synthesis(Pharmacology)
- A Practical Procedure for the Synthesis of Esonarimod, (R, S)-2-Acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic Acid, an Antirheumatic Agent (Part 1)
スポンサーリンク