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Research Laboratories, Chugai Pharmaceutical Co., Ltd. | 論文
- Synthesis of Antibacterial Agents having both Sulfanilamido- and Nitrofuryl- Groups in the Molecules. II.
- Synthesis of Antibacterial Agents having both Sulfanilamido- and Nitrofuryl- Groups in the Molecules. I
- Borate Complex of Hydroxamic Acids
- Pyrimidine Derivatives. III. The Preparation and Bacteriostatic Activity of Benzamidopyrimidines
- Crystalline Salts of Sucrose Octasulfate
- Pyridazine Derivatives. X. 10H-Benzo[b]pyridazino[3,4-e][1,4]thiazine and 5H-Benao[b]pyridazino[4,3-e][1,4]thiazine
- Pyridazine Derivatives. VII. Syntheses of 1,2- and 2,3-Diazaphenothiazines
- Protein Bindings. I. Binding of 2-(4'-Hydroxyphenylazo) benzoic Acid to Bovine Serum Albumin
- Quantum Chemical Considerations on the Stability of Aqueous Solution of an Electron Acceptor such as Menadione
- Syntheses and Biological Activities of N^1-(2-Formylethyl)-5-fluorouracil and Related Compounds
- Studies on Analgesics of Aniline Series. III. Preparation and Properties of N, N-Dialkyl 3-(Substituted anilino) butyramide Series
- Studies on Analgesics of Aniline Series. II. Preparation and Properties of N-Alkyl or N, N-Dialkyl 3-(N'-Acyl- or N'-Benzyl-substituted anilino) propionamide Series and N-Alkyl or N, N-Dialkyl 3-(Substituted anilino) propylamine Series
- Studies on Analgesics of Aniline Series. I. Preparation and Properties of β-Alaninamide Series
- Studies on Steroids. III. The Preparation of Steroid-21-yl-glucopyranosiduronamides.
- The Convenient Synthesis of 25-Hydroxycholesterol
- Synthesis of 1α, 24 (R)- and 1α, 24 (S)-Dihydroxycholesterol from Cholic Acid Derivatives
- The Relationship between the Hydroxylated Position of Aromatic Compounds by Monooxygenase and Various Electronic Reactivity Indices
- Studies on Antiviral Agents. V. Synthesis and Antiviral Activity of N-Chloro Compounds.
- Studies on Antiviral Agents. IV. Biological Activity of Tenuazonic Acid Derivatives.
- Studies on Antiviral Agents. I. Relationship between Chemical Reactivity of Sulfhydryl Reagents and Their Inactivating Activity of Adenovirus Type 5
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