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Pharmaceutical Research Division Takeda Chemical Industries Ltd. | 論文
- Identification of Prolactin-Releasing Peptide
- Synthesis of New Peptides with Prolactin-releasing Activity by a Combination of Recombinant DNA Technology and a Cysteine-specific Cyanylation Reaction
- IDENTIFICATION OF A CORTISTATIN-LIKE PEPTIDE IN HUMAN
- Chemistry and Anti-tumor Activity of Sperabillin Polymers
- Chemical Modification of Ansamitocins. III. Synthesis and Biological Effects of 3-Acyl Esters of Maytansinol
- Cyanine Dyes, New Potent Antitumor Agents
- Identification of Neuromedin U Receptors
- Renaturation of Recombinant Human Neurotrophin-3 from Inclusion Bodies
- An Efficient Chemical Method for Removing N-terminal Extra Methionine from Recombinant Methionylated Human Growth Hormone
- Microbial Enantioselective Ester Hydrolysis for the Preparation of Optically Active 4, 1-Benzoxazepine-3-acetic Acid Derivatives as Squalene Synthase Inhibitors^
- Role of Capsaicin-Sensitive Sensory Neurons and Nitric Oxide in the Protective Effect of Lansoprazole,a Proton Pump Inhibitor,on the Gastric Mucosa in Rats
- Optically Active Antifungal Azoles. III. Synthesis and Antifungal Activity of Sulfide and Sulfonamide Derivatives of (2R, 3R)-2-(2,4-Difluorophenyl)-3-mercapto-1-(1H, 1,2,4-triazol-1-yl)-2-butanol
- Optically Active Antifungal Azoles. I. Synthesis and Antifungal Activity of (2R, 3R)-2-(2,4-Difluorophenyl)-3-mercapto-1-(1H-1,2,4-triazol-1-yl)-2-butanol and Its Stereoisomers
- Effects of Serotonin_ Agonists on Anoxia-Induced Impairment of Protein Synthesis in Rat Brain Slices
- Microbial Conversion of EM574 and EM523, Gastrointestinal motor Stimulating Agents
- Bioactive Metabolites of EM574 and EM523, Erythromycin Derivatives Having Strong Gastrointestinal Motor Stimulating Activity
- Vagus-Dependent and Vagus-Independent Mechanisms of Action of the Erythromycin Derivative EM574 and Motilin in Dogs
- In Vivo Evaluation of Carborane Gadolinium-DTPA Complex as an MR Imaging Boron Carrier
- 新しい天然生理活性物質の研究--天然由来ペプチド研究の動向(総説シリ-ズ--現代医学の焦点-46-)
- New Protecting Groups for the Indole Ring of Tryptophan in Peptide Synthesis : 2,4,6-Trimethoxybenzenesulfonyl and 4-Methoxy-2,3,6-trimethylbenzenesulfonyl Groups
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