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Faculty of Pharmaceutical Sciences, Kobe Gakuin University | 論文
- Cellular Antioxidant Defense by a Ubiquinol-Regenerating System Coupled with Cytosolic NADPH-Dependent Ubiquinone Reductase : Protective Effect against Carbon Tetrachloride-Induced Hepatotoxicity in the Rat
- Studies on the Bacterial Gall of Myrica rubra : Isolation of a New [7,0]-Metacyclophan from the Gall and DL-β-Phenyllactic Acid from the Culture of Gall-Forming Bacteria(Pharmacognosy,Chemical)
- Differential Receptor Recognition by Dmt-Containing Enkephalin Dimers Cross-Linked by Phenylenediamines
- Synthesis of Furan Derivatives. LIX. Synthesis of 5-Substituted-2-(2-furyl)-1,3,4-oxadiazoles from 1-Furoyl-2-arylidenehydrazine with Lead Tetraacetate
- Deprotection of the Indole (N^)_Formyl (For) Group on Tryptophan Employing a New Reagent, N,N'-Dimethylethylendiamine (DMEDA) in an Aqueous Solution
- Development of μ-Receptor Selective Opioid Mimetics Derived from Endomorphin Sequences
- Development of New Safety Tests for Environmental Chemicals at Low Contaminant Levels (Regular Presentations) (Proceedings of the 10 th Symposium on Environmental Pollutants and Toxicology)
- Inhibition in Vitro Fertilization of Mouse Gametes by Sulfated Sialic Acid Polymers
- SYNTHESIS OF EGLIN C AND DEVELOPMENT OF INHIBITORS AGAINST HUMAN LEUKOCYTE ELASTASE AND CATHEPSIN G
- Synthesis of Peptide Chloromethyl Ketones and Examination of Their Inhibitory Effects on Human Spleen Fibrinolytic Proteinase (SFP) and Human Leukocyte Elastase (LE)(Organic,Chemical)
- Anti-Mouse Sperm Monoclonal Antibody, A-1,Inhibits Sperm Capacitation, Acrosome Reaction and Calcium Influx into Spermatocytes
- Structures of Euglobals-G1,-G2,-G3,-G4,and -G5 from Eucalyptus gradis
- STRUCTURES OF EUGLOBAL-G1,-G2,AND -G3 FROM EUCALYPTUS GRANDIS, THREE NEW INHIBITORS OF EPSTEIN- BARR VIRUS ACTIVATION
- Syntheses and ^1H- and ^C-Nuclear Magnetic Resonance Spectra of All Positional Isomers of Tetra-O-acetyl-D-glucopyranoses, and Their Monobenzyl and Monotrityl Derivatives
- Evaluation of a New N-Protecting Group, 2-(4-Sulfophenylsulfonyl)ethoxycarbonyl Group, for Solid Phase Peptide Synthesis in Water
- Peptide Synthesis in Water IV. Preparation of N-Ethanesulfonylethoxycarbonyl (Esc) Amino Acids and Their Application to Solid Phase Peptide Synthesis
- Solid Phase Synthesis in Water : Application of the Ethanesulfonylethoxycaronyl (Esc) Group
- Amino Acids and Peptides. XXXV. Facile Preparation of p-Nitroanilide Analogs by the Solid-Phase Method
- A Facile Solid-Phase Synthesis of Peptide ρ-Nitroanilide Analogs
- Synthesis of Some Pseudo-Peptide Analogs of Thiol Proteinase Inhibitors
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