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Takeda Chemical Industries Ltd. Pharmaceutical Research Division | 論文
- The Chemokine Receptor CXCR4 as a Therapeutic Target for Several Diseases Including AIDS, Cancer and Rheumatoid Arthritis
- CXCR4 Antagonists Identified as Anti-Cancer-Metastatic Agents
- Studies on Antidiabetic Agents. VII. : Synthesis and Hypoglycemic Activity of 4-Oxazoleacetic Acid Derivatives
- Studies on Antidiabetic Agents. X. Synthesis and Biological Activities of Pioglitazone and Related Compounds
- Studies on Antidiabetic Agents. IX. : A New Aldose Reductase Inhibitor, AD-5467,and Related 1,4-Benzoxazine and 1,4-Benzothiazine Derivatives : Synthesis and Biological Activity
- Microbial Enantioselective Ester Hydrolysis for the Preparation of Optically Active 4, 1-Benzoxazepine-3-acetic Acid Derivatives as Squalene Synthase Inhibitors^
- Syntheses of(4, 1-Benzoxazepine-3-ylidene)acetic Acid Derivatives and Their Inhibition of Squalene Synthase^
- Reaction of Trifluoromethyl Ketones. III. : The Aluminum Chloride Assisted Ene Reaction of 1,1,1-Trifluoro-2-hexanone and α, α, α-Trifluoroacetophenone
- Antihyperglycemic Effect of T-1095 via Inhibition of Renal Na^+ -Glucose Cotransporters in Streptozotocin-Induced Diabetic Rats
- Selevtive Nonpeptidic Inhibitors of Herpes Simplex Virus Type 1 and Human Cytomegalovirus Proteases
- A Wild-type Japanese Measles Virus Strain Inducing Predominant Early Down-regulation of CD46
- Preparation of Rapidly Disintegrating Tablet Using New Types of Microcrystalline Cellulose(PH-M Series)and Low Substituted-Hydroxypropylcellulose or Spherical Sugar Granules by Direct Compression Method
- Preparation of Griseofulvin for Topical Application Using N-Methyl-2-pyrrolidone
- Potent NK_1 Receptor Antagonists : Synthesis and Antagonistic Activity of Various Heterocycles with an N-[3,5-Bis(trifluoromethyl)benzyl]-N-methylcarbamoyl Substituent
- Purification and functional properties of soluble forms of membrane cofactor protein (CD46) of complement: identification of forms increased in cancer patients' sera
- Orally Active CCR5 Antagonists as Anti-HIV-1 Agents : Synthesis and Biological Activity of 1-Benzothiepine 1, 1-Dioxide and 1-Benzazepine Derivatives Containing a Tertiary Amine Moiety
- Preparation and Evaluation of Tablets Rapidly Disintegrating in Salive Containing Bitter-Taste-Masked Granules by the Compression Method
- Orally Active CCR5 Antagonists as Anti-HIV-1 Agents 2 : Synthesis and Biological Activities of Anilide Derivatives Containing a Pyridine N-Oxide Moiety
- Synthesis of 1-Benzothiepine and 1-Benzazepine Derivatives as Orally Active CCR5 Antagonists
- CCR5 Antagonists as Anti-HIV-1 Agents.1. Synthesis and Biological Evaluation of 5-Oxopyrrolidine-3-carboxamide Derivatives
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