<Abstract of published report>Kinetics of Hydrolysis of Micellar Substrates Catalyzed by Snake Venom Phospholipase A2.
スポンサーリンク
概要
著者
-
SAMEJIMA Yuji
Department of Hyginic Chemistry, Faculty of Pharmacy, Hoshi University
-
井上 晴嗣
大阪薬科大学第1生化学教室
-
Ikeda Kiyoshi
Department Of Biochemistry Osaka University Of Pharmaceutical Sciences
-
Hayashi Kyozo
Department Of Biochemistry Osaka University Of Pharmaceutical Sciences
-
Samejima Yuji
Department Of Hyginic Chemistry Faculty Of Pharmacy Hoshi University
-
池田 かおり
Developmental Research Laboratories Shionogi & Co. Ltd.
-
Inoue Seiji
Department Of Biochemistry Osaka University Of Pharmaceutical Sciences
関連論文
- Bacillus cereus菌由来PC-PLCによるLyso-PCの加水分解
- 5員環を持つリン脂質アナログによるホスホリパーゼA_2の阻害
- Comparison of Biological Activities of Chemically Synthesized Monosaccharide Analogues of Reducing and Nonreducing Sugar Moieties of Lipid A(Blological)
- ANTITUMOR ACTIVITY AND BIOLOGICAL EFFECTS OF CHEMICALLY SYNTHESIZED MONOSACCHARIDE ANALOGUES OF LIPID A IN MICE
- A Convenient Synthesis of N-Benzyloxy-β-lactams via N-Benzyloxyimines
- Trifluoromethanesulfonic Acid-Promoted Reaction of Hexahydro-1,3,5-triazines.Introduction of a Secondary Aminomethyl Grouping into Carboxylates at the α-Position through Ketene Silyl Acetals
- Low Mitogenic Activity of Synthetic Lipid A Analog, 2,3-Acyloxyacylgalactosamine-4-phosphate, in Cultured Murine Splenocytes
- Influence of Indomethacin and Isopropanol on Hydrophobic Interaction through Long-Chain Alkyl Groups of Hydrophobically-Modified Hydroxypropyl Methylcellulose
- Effect of Hydrophobically-Modified Hydroxypropyl Methylcellulose on the Crystallization from Supersaturated Solutions of Indomethacin
- IMMUNOHISTOCHEMICAL LOCALIZATION OF HUMAN EPIDERMAL GROWTH FACTOR/γ-UROGASTRONE IN SUBMANDIBULAR GLANDS AND IN THEIR OBSTRUCTIVE LESIONS
- Chromogenic Assay for the Activity of Sphingomyelinase from Bacillus cereus and Its Application to the Enzymatic Hydrolysis of Lysophospholipids(Analytical Biochemistry)
- His151 and His296 Are the Acid-Base Catalytic Residues of Bacillus cereus Sphingomyelinase in Sphingomyelin Hydrolysis
- Roles of Asp126 and Asp156 in the Enzyme Function of Sphingomyelinase from Bacillus cereus^1
- Mg^ Binding and Catalytic Function of Sphingomyelinase from Bacillus cereus
- Binding mode of Phospholipase A_2 with a New Type of Phospholipid Analog Having a Oxazolidinone Ring
- Role of Ca^ in the Substrate Binding and Catalytic Functions of Snake Venom Phospholipase A_2.
- Lipid A and Related Compounds. XXIX. Synthesis of Biologically Active N-Acylated L-Asparagine-Containing D-Glucosamine Derivatives Structurally Related to Lipid A
- Some Properties of Metallothioneins from Hepato-pancreas and Kidney in Carp (Cyprinus carpio)
- TOTAL SYNTHESIS OF PROTEUS MIRABILIS LIPID A(Communication to the Editor)
- 80 Proteus mirabilis lipid Aの全合成
- 毒ヘビ血液に存在する3種のホスホリパーゼA_2阻害タンパク質ファミリー
- Isolation and Amino Acid Sequence of a Phospholipase A_2 Inhibitor from the Blood Plasma of the sea Krait, Laticauda semifasciata
- II型塩基性PLA_2の特異的阻害タンパク質PLIβはLeucine-rich repeatをもつ
- 中国マムシ血漿由来PLA_2阻害タンパク質PLI_γのアミノ酸配列
- Isolation and Amino Acid Sequence of a Phospholipase A_2 Inhibitor from the Blood Plasma of Agikistrodon blomhoffii siniticus.
- Kinetics of Hydrolysis of Micellar Substrates Catalyzed by Snake Venom Phospholipase A2.
- Purification and Amino Acid Sequence of A Nerve Growth Factor from the Venom of Vipera russelli russelli.
- Amino Acid Sequence of Nerve Growth Factors Derived from Cobra Venoms.
- Amino Acid Sequences of Cytotoxin-Like Basic Proteins Derived from Cobra Venoms.
- Amino Acid Sequence of Nerve Growth Factor Purified from the Venom of the Formosan Cobra Naja naja atra.
- Amino Acid Sequences of Four Cytotoxins (Cytotoxins I, II, III and IV) Purified from the Venom of the Thailand Cobra, Naja naja siamensis.
- Amino Acid Sequece of a Cytotoxin-Like Basic Protein with Low Cytotoxic Activity from the Venom of the Thailand Cobra Naja naja siamensis.
- Lipid A and Related Compounds. XV. Efficient Synthesis of Novel Analogs of Glucosamine-4-phosphate, the Nonreducing Sugar Moiety of Lipid A(Medicinal Chemistry,Chemical)
- Lipid A and Related Compounds. XIV. A New Synthesis of Lipid Y, the Reducing Sugar Moiety of Salmonella- and Proteus-Type Lipid A(Organic,Chemical)
- Lipid A and Related Compounds. XI. New, Efficient Synthesis of Lipid X(Organic,Chemical)
- EFFICIENT SYNTHESIS OF NOVEL MONOSACCHARIDE ANALOGS OF LIPIDS A
- 4 Lipid X,YおよびSalmonella mutant Lipid Aの新合成
- A NEW METHODOLOGY FOR CHEMOSELECTION OF ONE AMINO AND FOUR HYDROXYL GROUPS OF GLUCOSAMINE DERIVATIVES AND ITS USE FOR SYNTHESIS OF LIPID X
- Neuraminic Acid and Related Compounds. I. : Syntheses of Biologically Active 4', 7', 8', 9'-Tetra-O-acetyl-sialyl- and Sialyl-(α2-6)-D-glucosamine-4-phosphate Analogues of Lipid A
- Effect of Benzyl Alcohol on Rat Skin as a Solvent of Liquid Droplet Dispersion Ointment
- Lipid A and Related Compounds. XXXVII. Determination of Favorable Binding Linkages of Lipid A Analog to Antigen Moiety for Synthetic Vaccines
- Synthesis of Cancer Peptide Antigen-Lipid A Analog Conjugates for Synthetic Vaccines
- Synthesis of Tn, Sialyl Tn and HIV-1-Derived Peptide Antigen Conjugates Having a Lipid A Analog as an Immunoadjuvant for Synthetic VAaccines
- 細菌内毒素リピドA類を免疫アジュバント部位とする癌,エイズ合成ワクチンヘの基礎研究
- SYNTHESIS OF TN AND SIALYL TN ANTIGEN-LIPID A ANALOG CONJUGATES FOR SYNTHETIC VACCINES
- Lipid A and Related Compounds. XXXIII.Synthesis and Structure-Activity Relationships of N-Acylated L-Serine or L-Threonine-Containing D-Glucosamine Derivatives as Mimics of Lipid A Disaccharide
- Lipid A and Related Compounds. XXXI.Synthesis of Biologically Active N-Acylated L-Serine-Containing D-Glucosamine 4-Phosphate Derivatives of Lipid A
- Lipid A and Related Compounds. XXX. Synthesis of Biologically Active N, N'-Diacyl Chitobiose Derivatives Structurally Related to Lipid A
- Synthesis of Ganglioside G_ and G_ Analogs Having Mimics of Ceramide Moieties and Their Binding Activities with Influenza Virus A
- Synthesis of Sulfated Cerebroside Analogs Having Mimicks of Ceramide and Their Anti-human Immunodeficiency Virus Type 1 Activities
- SYNTHESIS OF BIOLOGICALLY ACTIVE N-ACYLATED L-SERINE-CONTAINING D-GLUCOSAMINE-4-PHOSPHATE DERIVATIVES OF LIPID
- Lipid A and Related Compounds. XXVII. An Efficient Synthesis of D-Galactosamine-4-phosphate Analogs of Lipid A via a Novel Key Intermediate
- Lipid A and Related Compounds. XXVI. Syntheses of Biologically Active Penta-O-acetyl-N-glycoloylneuraminyl- and Penta-O-acetyl-3-deoxy-D-glycero-D-galacto-2-nonulopyranosonic Acid-(α2→6)-D-glucosamine-4-phosphate Analogs of Lipid A
- SYNTHESIS OF THE SEQUENCE OF HEPT-(α1→5)KDO-(α2→6)-D-GLUCOSAMINE-4-PHOSPHATE OF LIPOPOLYSACCHARIDE
- Lipid A and Related Compounds. XXIV. Efficient Synthesis of Several Lipid as via Common Disaccharide Intermediates
- SYNTHESIS OF BIOLOGICALLY ACTIVE DERIVATIVES OF D-GLUCOSAMINE-4-PHOSPHATE AND 1-THYMINYL-D-GLUCOSAMINE-4,6-DISULFATE
- Synthesis and Biological Evaluation of Peptide Mimics Derived from First Extracellular Loop of CCR5 toward HIV-1
- Synthesis of Peptides Mimicking Chemokine Receptor CCR5 and Their Inhibitory Effects against HIV-1 Infection
- A Facile Synthesis of 2-Deoxy-2,3-didehydroneuraminic Acid Derivatives
- Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (±)-N-[2-(3,4-Dichlorophenyl)-4-(spiro-substituted piperidin-1'-yl)butyl]-N-methylbenzamides and Evaluation of NK_1-NK_2 Dual Antagonistic Activities
- Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (±)-N-[2-(3,4-Dichlorophenyl)-4-(spiro[isobenzofuran-1(3H), 4'-piperidin]-1'-yl)butyl]-N-methylbenzamide, YM-35375,as a New Lead Compound for Novel Neurokinin Rec
- Kinetics of the Hydrolysis of Monodispersed Dihexanolyllecithin Catalyzed by a Cobra (Naja naja atra) Venom Phospholipase A_2
- Purification and Chracterization of a Membrane-Bound Sialidase from Pig Liver
- Orally Active NGF Synthesis Stimulators : Potential Therapeutic Agents in Alzheimer's Disease.
- hPIV-1 シアリダーゼ阻害活性をもつシアル酸誘導体の合成
- Binding of Cardiotoxin Analogue III from Formosan Cobra Venom to FL Cells.
- Amino Acid Sequence of A Cardiotoxin-Like Basic Polypeptide (CLBP) Isolated from the Venom of Formosan Cobra (Naja naja atra) with Low Cytotoxic Activity.
- Selective Muscarinic Antagonists. II. Synthesis and Antimuscarinic Properties of Biphenylylcarbamate Derivatives
- Selective Muscarinic Antagonists. I. Synthesis and Antimuscarinic Properties of 4-Piperidyl Benzhydrylcarbamate Derivatives
- Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. II. Syntheses and NK_2 Receptor-Antagonistic Activities of N-[2-Aryl-4-(spiro-substituted piperidin-1'-yl)butyl]carboxamides
- Oral administration of idebenone induces nerve growth factor in the brain and improves learning and memory in basal forebrain-lesioned rats.
- Nerve growth factor content in rat brains increases following basal-forebrain lesions induced by ibotenic acid, but not by electrolysis.
- Development of Plasticity of Brain Function with Repeated Trainings and Passage of Time after Basal Forebrain Lesions in Rats.
- Memory Impairment and Neural Dysfunction after Continuous Infusion of Anti-Nerve Growth Factor Antibody into the Septum in Adult Rats.
- Effects of Oral Administration of a Stimulator for Nerve Growth Factor Synthesis in Basal Forebrain-Lesioned Rats.
- Potentiation of Chemotactic Peptide-Induced Superoxide Generation by CD38 Ligation in Human Myeloid Cell Lines^1
- Carbohydrate in Nicotinic Acetylcholine Receptor : Effects of Exogenous, and of Removal of Endogenous Carbohydrate and Sialic Acid on Ligand Binding.
- Identification of Basic Fibroblast Growth Factor-like Immunoreactivity in Panax ginseng Extract: Investigation of Its Molecular Properties
- Therapeutic Effects of Aldose Reductase Inhibitor on Experimental Diabetic Neuropathy through Synthesis/Secretion of Nerve Growth Factor.
- Correlative regulation of nerve growth factor level and choline acetyltransferase activity by thyroxine in particular regions of infant rat brain.
- A Catechol Derivative (4-Methylcatechol) Accelerates the Recovery from Experimental Acrylamide-Induced Neuropathy
- Effects of 4-Methylcatechol, a Stimulator of Endogenous Nerve Growth Factor Synthesis, on Experimental Acrylamide-Induced Neuropathy in Rats.
- The therapeutic effects of 4-methylcatechol, a stimulator of endogenous nerve growth factor synthesis, on experimental diabetic neuropathy in rats.
- Changes in nerve growth factor content of the submaxillary gland in the genetically dystrophic (mdx) mouse.
- Alkylcatechols Regulate NGF Gene Expression in Astroglial Cells via Both Protein Kinase C- and cAMP-Independent Mechanisms.
- Interleukin-2 as a Neurotrophic Factor for Supporting the Survival of Neurons Cultured from Various Regions of Fetal Rat Brain.
- Interleukin-4 and -5 as Modulators of Nerve Growth Factor Synthesis/Secretion in Astrocytes.
- Tobacco Tar Components That Stimulate Nerve Growth Factor (NGF) Synthesis/Secretion of Mouse Astroglial Cells in Culture
- Purification and Characterization of the G203T Mutant α Subunit of GTP-Binding Protein Expressed in Baculovirus-Infected Sf9 Cells^1
- Nerve Growth Factor-like Immunoreactive Substance in Panax ginseng Extract
- Effects of Nerve Growth Factor (NGF) in Rats with Basal Forebrain Lesions.
- Synthesis of N-Acetylglucosaminyl- and N-Acetylgalactosaminylceramides as Cerebroside Analogs and Their Anti-human Immunodeficiency Virus Type 1 Activities
- NEUROMUSCULAR BLOCKING ACTIONS OF NEUROTOXINS ISOLATED FROM LATICAUDA SEMIFASCIATA, NAJA NAJA AND NAJA NAJA ATRA —A COMPARATIVE ASSAY—
- Imaging Corner
- hPIV-1シアリダーゼ阻害活性をもつシアル酸誘導体の合成
- A single amino acid mutation at position 170 of human parainfluenza virus type 1 fusion glycoprotein induces obvious syncytium formation and caspase-3-dependent cell death
- Effects of Nerve Growth Factor(NGF) in Rats with Basal Forebrain Lesions.
- Binding Mode of Phospholipase A2 with a New Type of Phospholipid Analog Having an Oxazolidinone Ring.
- Roles of Asp126 and Asp156 in the Enzyme Function of Sphingomyelinase from Bacillus cereus.
- Histochemical imaging of alkaline phosphatase using a novel fluorescent substrate.