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Analytical and Metabolic Research Laboratories, Sankyo Co., Ltd. | 論文
- THE RELATION BETWEEN STRUCTURE AND DISTRIBUTION OF QUATERNARY AMMONIUM IONS IN MICE AND RATS. SIMPLE TETRAALKYLAMMONIUM AND A SERIES OF m-SUBSTITUTED TRIMETHYLPHENYLAMMONIUM IONS
- Tissue and Organ Expression of Catalase in Acatalasemic Beagle Dogs
- A-72363 A-1, A-2, and C, Novel Heparanase Inhibitors from Streptomyces nobilis SANK 60192 I. Taxonomy of Producing Organism, Fermentation, Isolation, and Structure Elucidation
- Structure of HV-toxin M, a Host-specific Toxin-related Compound Produced by Helminthosporium victoriae(Organic Chemistry)
- Structure of HV-toxin M, a Host-specific Toxin-related Compound Produced by Helminthosporium victoriae
- A-53930A and B, Novel N-Type Ca^ Channel Blockers
- Trachyspic Acid, a New Metabolite Produced by Talaromyces trachyspermus, that Inhibits Tumor Cell Heparanase:Taxonomy of the Producing Strain, Fermentation, Isolation, Structural Elucidation, and Biological Activity
- Formation of [M-H]^+ Ions under Fast Atom Bombardment Conditions : Trolox and α-Tocopherol
- INDENTIFICATION OF MAJOR URINARY METABOLITES OF ACNU, 3-[(4-AMINO-2-METHYL-5-PYRIMIDINYL) METHYL]-1-(2-CHLOROETHYL)-1-NITROSOUREA HYDROCHLORIDE IN RATS
- PA84 APPLICATION OF CONSECUTIVE REACTION MASS SPECTROMETRY (MS/MS/MS) ON PEPTIDE SEQUENCING : A SOLUTION FOR THE LEUCINE/ISOLEUCINE PROBLEM
- Mixture of Caesium Iodide, Sodium Iodide, and Glycerol as a Calibrant for Routine Fast Atom Bombardment Mass Analysis
- Amino Acid Sequence Determination of Cyclic Peptides by Tandem Mass Spectrometry Coupled with Fast Atom Bombardment Ionization
- S-adenosyl-L-methionine ameliorates reduced local cerebral glucose utilization following brain ischemia in the rat.
- The 2.0.ANGS. crystal structure of cyanide metmyoglobin reconstituted with 5,10,15,20-tetrapropylhemin.
- Protective Effect of N-Acyl Amino Acids (NAAs) on Cephaloridine (CER) Nephrotoxicity in Rabbits.
- Preparation of polyoxa-1,n-dithia(n)(1,1')ruthenocenophanes and the structural studies of their metal complexes.
- Reduction of aryl halides and N-hydroxy nitrogen compounds in fast atom bombardment mass spectrometry.
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