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Faculty Of Pharmaceutical Sciences Osaka University | 論文
- Pharmacological Activity of Chemically Modified Subfragment from Human Serum IgG. XI. Increment of Tumor Necrosis Factor (TNF) Activity in Mouse Sera by Carboxamide-Methylated Light Chain
- Studies on Thermophile Products. VI. Activation of Mouse Peritoneal Macrophages by Bis(2-hydroxyethyl) Trisulfide
- Studies on Pharmacological Activation of Human Immunoglobulin G by Chemical Modification and Active Subfragments. X. Effect of Carboxamidemethylated Fc Fragment (CM-Fc) from Human Immunoglobulin G on Delayed Type Hypersensitivity
- Characterization of Capacitation Inhibitory Protein from Rabbit Seminal Plasma : Homology with Human Annexins
- Studies on Pharmacological Activation of Human Serum Immunoglobulin G by Chemical Modification and Active Subfragments. IX. Anti-inflammatory Activity of Completely Alkylated Heavy Chain (C.Fr.I-H)
- Studies on Thermophile Products. V. Immunosuppressive Profile in Vitro of Bacillus stearothermophilus Component, Fr.5-B
- Studies on tRNA and Related Compounds. XXXVII. Synthesis and Physical Properties of 2'- or 3'-O-(o-Nitrobenzyl) nucleosides : the Use of o-Nitrophenyldiazomethane as a Synthetic Reagent
- Polynucleotides. XLVIII. Synthesis and Template-Directed Polymerization of Tri-(adenylic Acid) having a 2'-O-(o-nitrobenzyl) Group at the 3'-End
- Studies on Transfer Ribonucleic Acids and Related Compounds. XVI. Synthesis of Ribooligonucleotides using a Photosensitive o-Nitrobenzyl Protection for the 2'-Hydroxyl Group
- Micelle/Water Partition Properties of Phenols Determined by Liquid Chromatographic Method. Proposal for Versatile Measure of Hydrophobicity
- Thermochemical Aspects of Partition. Quantitative Structure Activity Relationships of Benzyldimethylalkylammonium Chlorides
- Synthetic Studies on Spiroketal Natural Products. V. Total Synthesis of (+)-Talaromycin A and (-)-talaromycin B
- Synthetic Studies on Spiroketal Natural Products. IV.A Stereoselective Synthesis of (3S, 5S, 6R, 9R, R_S)-3-Benzyloxymethyl-9-hydroxymethyl-5-(p-tolyl)sulfinyl-1,7-dioxaspiro[5.5]undecane, a Key Intermediate for Talaromycins
- Synthetic Studies on Spiroketal Natural Products. II. An Enantioselective Synthesis of (R)- and (S)-1,7-Dioxaspiro[5.5]undecane
- Synthetic Studies on Spiroketal Natural Products. I. : A Stereoselective Synthesis of (2R^*, 5R^*)- and (2R^*, 5S^*)-2-Methyl-1,6-dioxaspiro[4.5]decane
- Double Stereodifferentiation in Intramolecular C-H Insertion Reaction toward the Synthesis of 1β-Methylcarbapenem Antibiotics
- ロジウム(II)錯体触媒を用いる不斉C-H挿入反応 (生物活性天然物の合成--複雑な構造をいかにして構築するか) -- (骨格構築法)
- Novel Annelations of Xanthines by the Reaction of 8-Aminoxanthines with Dimethyl Acetylene-dicarboxylate
- P-130 都市大気粉塵の免疫毒性メカニズムに関する基礎的検討(ポスターセッション)
- P-064 非結晶性ナノシリカの物性と有害性発現との連関評価(2)(ポスターセッション)
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