重水素標識化合物 (安定同位体の医・薬学,生物学への応用) -- (安定同位元素標識化合物)
スポンサーリンク
概要
著者
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川添 豊
Faculty of Pharmaceutical Sciences, Nagoya City University
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川添 豊
Faculty Of Pharmaceutical Sciences Nagoya City University
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前田 満和
National Cancer Center Research Institute
関連論文
- LIGNIFIED MATERIALS AS MEDICINAL RESOURCES. VI. ANTI-HIV ACTIVITY OF DEHYDROGENATION POLYMER OF p-COUMARIC ACID, A SYNTHETIC LIGNIN, IN A QUASI-IN-VIVO ASSAY SYSTEM AS AN INTERMEDIARY STEP TO CLINICAL TRIALS
- Lignified Materials as Medicinal Resources. V. Anti-HIV (Human Immunodeficiency Virus) Activity of Some Synthetic Lignins)
- Studies on Chemical Carcinogens and Mutagens. XXXIX. : Effects of Silicon and Germanium Substitutions on Physicochemical Properties and Cytotoxicity of N-Alkyl-N-nitrosoureas
- Some Cytotoxicological Aspects of Ethyl and Fluoroethyl Alkanesulfonates in Escherichia coli : Role of Fluorine Substitution
- Lignified Materials as a Potential Medicinal Resource. IV. Dehydrogenation Polymers of Some Phenylpropenoids and Their Capacity to Stimulate Polymorphonuclear Cell Iodination
- Formation of O^6,7-Dimethylguanine Residues in Calf Thymus Deoxyribonucleic Acid Treated with Carcinogenic N-Methyl-N-nitrosourea in Vitro
- Singlet Oxygen Takes Part in 8-Hydroxydeoxyguanosine Formation in Deoxyribonucleic Acid Treated with the Horseradish Peroxidase-H_2O_2 System
- LIGNIFIED NATURAL PRODUCTS AS POTENTIAL MEDICAL RESOURCES. : I POTENTIATION OF HEMOLYTIC PLAQUE-FORMING CELL PRODUCTION IN MICE
- Enhanced Cytotoxicity in Simultaneous and Sequential Drug-Heat Treatments of Cultured Chinese Hamster V79 Cells
- Deoxyribonucleic Acid (DNA) Damage Induced by Bleomycin-Fe(II) in Vitro : Formation of 8-Hydroxyguanine Residues in DNA
- DEPRIVATION OF THE MUTAGENIC PROPERTY OF QUINOLINE : INHIBITION OF MUTAGENIC METABOLISM BY FLUORINE SUBSTITUTION
- Potentiation of the Cytotoxic Activity of Anti-cancer Drugs against Cultured L1210 Cells by Bacillus thuringiensis subsp. israelensis Toxin
- Cytotoxicity of Fluorine-Containing Alkyl Alkanesulfonates to Cultured Leukemia L1210 Cells
- SYNERGISTIC EFFECT OF GLYCEROL ON CYTOTOXICITY OF BLEOMYCIN IN CULTURED CHINESE HAMSTER V79 CELLS
- Spontaneous and Enzymatic Activations of Carcinogenic N-Butyl-N',N'-dimethyl-N-nitrosourea(Biological)
- Studies on Chemical Carcinogens and Mutagens. XL. : Chemoselectivity of Acylating Agents toward Aniline in Aqueous Medium
- SYNTHESIS OF 7-AMINOGUANOSINE AND ITS CONVERSION TO 8-SUBSTITUTED DERIVATIVES
- Studies on Chemical Carcinogens and Mutagens. XXXVII. : A Simple Method to Predict Ultimate Structures of Chemical Mutagens, and Probably Carcinogens
- Spontaneous and Enzymatic Activations of Carcinogenic N-Butyl-N',N'-dimethyl-N-nitrosourea(Biological)
- Spontaneous and Enzymatic Activations of Carcinogenic N-Butyl-N',N'-dimethyl-N-nitrosourea(Biological)
- Studies on Chemical Carcinogens. XVIII. Acetylation of Carcinogenic 4-(N-Hydroxy-N-methylamino) quinoline 1-Oxide
- Interaction of Antidepressant Drugs with Lipid Bilayers Studied by High-Resolution Carbon-13 (^C-) and High-Power Deuterium Nuclear Magnetic Resonance (^2H-NMR) Spectroscopy : The Manner of Binding as Deduced from the Differential Line-Broadening of ^
- The Structure of Nobilonine. The Second Alkaloid from Dendrobium nobile
- The Structure of Dendrobine
- Voltammetric and Spectroscopic Studies on the Carcinogen 4-(Hydroxyamino)quinoline N-Oxide and Its Analogues(Physical,Chemical)
- Metabolism of Mutagenicity-Deprived 3-Fluoroquinoline : Comparison with Mutagenic Quinoline
- Effect of Metal Ions on Transcription of the ada Gene Which Encodes O^6-Methylguanine-DNA Methyltransferase of Escherichia coli
- Studies on Chemical Carcinogens. XXIV. mutagenic Potency of Alkylated 4-Nitroquinoline 1-Oxides : Its Dependence on the Rate of Metabolic Activation
- METABOLITES OF QUINOLINE, A HEPATOCARCINOGEN, IN A SUBCELLULAR MICROSOMAL SYSTEM
- Studies on Chemical Carcinogens. XXI. Quantitative Structure-Mutagenicity Relationship among Substituted Styrene Oxides
- Studies on Chemical Carcinogens. XX. Inhibitory Effect of Alkyl Isocyanates and Isothiocyanates on Mutagenesis in E. coli by Ultraviolet Radiation
- On the Relationship between C-13 Nuclear Magnetic Resonance Chemical Shift and Stability of Molecule in Methyl-Substituted N, N-Dimethylpiperidinium Salts
- Radical Methylation and Radical Hydroxymethylation of N-Substituted Quinoline Derivatives
- Studies on Hydrogen Exchange. XIV. Selective Hydrogen-Deuterium Exchange in Aliphatic Amines and Amino Acids catalyzed by Platinum
- Chemical Structure of QA_, One of the Covalently Bound Adducts of Carcinogenic 4-Nitroquinoline 1-Oxide with Nucleic Acid Bases of Cellular Nucleic Acids
- Studies on Chemical Alterations of Nucleic Acids and Their Components. X. syntheses and Reactivties of 3-Aminopyrimidine Nucleosides
- Selective Substitution Reactions of Quinoline Derivatives by Redox Systems Nucleophilic Character of Hydroxyalkyl Radicals
- 重水素標識化合物 (安定同位体の医・薬学,生物学への応用) -- (安定同位元素標識化合物)
- Studies on Chemical Alterations of Nucleic Acids and Their Components. VIII. Alkaline Rearrangement of 1-Aminoadenosine to 5-Amino-1-β-D-ribofuranosyl-4-(1,2,4-triazol-3-yl) imidazole
- Solvent-and Concentration-Dependent Shifts in Proton Magnetic Resonance of Quaternary Ammonium Salts
- Direct C-Amination of Guanosine with Hydroxylamine-O-Sulfonic Acid. Simplest Model Reaction possibly involved in DNA Damage leading to Carcinogenesis by N-Arylhydroxylamines
- Application of NMR to Stereochemistry. (I). The Spatial Interaction Effect of the Hydroxyl Group to Methyl Resonance.(53)
- Synthesis and Reactivities of 1-Methyl-2-trichloromethyl-1,2-dihydroquinolines
- Studies on the Metabolism of D-and L-Isomers of 3,4-Dihydroxyphenylalanine (DOPA). VI. Metabolism of D-DOPA in Rat Kidney
- Homolytic C-Methylation of Guanine, Guanosine, and Guanylic Acid
- Studies on Hydrogen Exchange. XII. Reaction Mechanism for Hydrogen Exchange of C-8 Hydrogen of Purine Ribosides
- The Correlation between the Antitumor Activities and Chemical Structures of Thiocyanato Derivatives of Purines and Their Ribonucleosides
- Proton and Carbon-13 Nuclear Magnetic Resonance Chemical Shift Data for Nitroquinolines and Their N-Oxides
- Studies on Chemical Carcinogens and Mutagens. XXVI. Chemical Properties and Mutagenicity of Alkyl Alkanesulfonates on Salmonella typhimurium TA100
- Studies on Chemical Carcinogens and Mutagens. XXV. Chemoselectivity of Alkyl Sulfonates toward 4-(p-Nitrobenzyl) pyridine (NBP) in Phosphate Buffer
- Studies on Chemical Carcinogens and Mutagens. XXXII. Chemoselectivity of Alkylating Agents toward Pyridine in Aqueous Media-A Simple Procedure for Evaluation of Swain-Scott's Substrate Constants
- Lignified Materials as Potential Medicinal Resources.III. : Diversity of Biological Activity and Possible Molecular Species Involved
- Studies on Chemical Carcinogens and Mutagens. XXXIII. : Mutation Frequencies Induced by Combinations of Methylating and/or Ethylating Mutagens
- Studies on Chemical Carcinogens. XXIII. A Simple Method for Characterization of the Alkylating Ability of Compounds by using 4-(p-Nitrobenzyl) pyridine
- Alkaloids of Root-bark of Orixa japonica THUNB. XII. Nuclear Magnetic Resonance Study of N-Methylorixidinine, N-Methylisoorixidinine, and N-Methylorixidine.
- Studies on Chemical Carcinogens and Mutagens. XXXVI. : Apparent Activation Energy for Mutagenic Modification Induced in E. coli by Alkylating Agents. Estimation from Mutation Frequency
- Studies on Chemical Carcinogens and Mutagens. XXXV. : Standardization of Mutagenic Capacities of Several Common Alkylating Agents Based on the Concentration-Time Integrated Dose
- Application of Nuclear Magnetic Resonance to Stereochemistry. II. Determination of the Conformation of Hydroxyl Groups by Nuclear Magnetic Resonance ; Androst-4-en-3-one and Pregn-4-en-3-one Series.