SYNTHESIS OF BIOLOGICALLY ACTIVE TETRAACETYL-3-DEOXY-D-MANNO-2-OCTULOSONIC ACID(KDO)-(α2→6)-D-GLUCOSAMINE ANALOGS OF LIPID A
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概要
- 論文の詳細を見る
Novel synthesis of tetraacetyl-KDO-(α2→6)-monosaccharide analogs of lipid A is described. Also a preliminary analysis of their biological activity is presented.
- 公益社団法人日本薬学会の論文
- 1986-05-25
著者
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阿知波 一雄
Shizuoka College of Pharmacy
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中本 信一
Fuji Chemical Industries
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中本 信一
Shizuoka College of Pharmacy
関連論文
- Antitumor Activity and Lethal Toxicity of Chemically Synthesized Tetraacetyl-2-keto-3-deoxyoctonic Acid-(α2→6)-D-glucosamine Analogues of Lipid A(Biological)
- Comparison of Biological Activities of Chemically Synthesized Monosaccharide Analogues of Reducing and Nonreducing Sugar Moieties of Lipid A(Blological)
- MITOGENIC ACTIVITY OF CHEMICALLY SYNTHESIZED TETRAACETYL-2-KETO-3-DEOXYOCTONIC ACID-(α 2→6)-D-GLUCOSAMINE ANALOGUES OF LIPID A
- ANTITUMOR ACTIVITY AND BIOLOGICAL EFFECTS OF CHEMICALLY SYNTHESIZED MONOSACCHARIDE ANALOGUES OF LIPID A IN MICE
- 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
- Pyrrolidine-Forming 1,3-Dipolar Cycloaddition of N-(Phenylthiomethyl)-α-amino Acid Esters
- 1,3-DIPOLAR CYCLOADDITION LEADING TO N-ALKYLPYRROLIDINES
- 1,3-Dipolar Cycloaddition Leading to N-Acylated Pyrrolidines and 2,5-Dihydropyrroles
- Decarboxylation Reaction. X. Introduction of a Carbon Unit at the α-Position of Amines by Reaction of Hexahydro-1,3,5-triazines with Carboxylic Acids
- A 1,3-Dipolar Cycloaddition of Alicyclic Methylene Iminium Ylide to form Pyrrolizidine Nuclei and Its Application to Synthesis of Pyrrolizidine Alkaloids
- Mitogenic Activity and Lethal Toxicity of Lipid A Analogs, Glucosamine-phosphate Carrying Aromatic Alkyl Groups, in Mice
- Biological Activities of Chemically Synthesized Derivatives of Lipid A : Tetraacetyl-monosaccharides Linked to 2,3-Acyloxyacylglucosamine-4-phosphate
- TOTAL SYNTHESIS OF PROTEUS MIRABILIS LIPID A(Communication to the Editor)
- Thiocarbonyl Ylides. VI, New Generation of Thiocarbonyl Ylides from Organosilicon Compounds Containing Sulfur and Their 1,3-Cycloadditions(Organic,Chemical)
- 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
- Enzymes and Catalysts. I. Pig Liver Esterase-Catalyzed Hydrolysis of Heterocyclic Diesters(Organic,Chemical)
- Synthesis of Proline Derivatives by 1,3-Dipolar Cycloaddition of Azomethine Ylide Generated from an Organosilicon Compound(Organic,Chemical)
- Evidence for Ambivalent Azomethine Ylide Intermediate in the 1, 3-Cycloaddition of Trimethylsilylmethylamine Derivatives(Organic,Chemical)
- Trifluoroacetic Acid-Catalyzed 1,3-Cycloaddition of the Simplest Iminium Ylide Leading to 3-or 3,4-Substituted Pyrrolidines and 2,5-Dihydropyrroles
- A DEFINITE EVIDENCE ON THE AMBIVALENT AZOMETHINE YLIDE INTERMEDIATE IN TRIFLUOROACETIC ACID- AND FLUORIDE ANION-PROMOTED 1,3-CYCLO-ADDITIONS INVOLVING THE SILICON-CARBON BOND CLEAVAGE
- Highly Regioselective Synthesis of Trisubstituted Pyrrolidines by 1,3-Cydoaddition(Organic,Chemical)
- One-Pot Synthesis of N-Alkylpyrrolidines by 1,3-Dipolar Cycloaddition(Organic,Chemical)
- Trimethylsilyl Triflate-Catalyzed 1,3-Dipolar Cycloaddition Leading to N-Unsubstituted Pyrrolidines
- 1,3-Dipolar Cycloaddition of the Simplest N-Acylazomethine Ylide Leading to 3- or 3,4-Substituted N-Acylpyrrolidines
- Lipid A and Related Compounds. XVII. : Synthesis of 3- Deoxy-D-manno-2-octulosonic Acid (KDO)-(α2→6)-D-Glucosamine-4-phosphates, Analogs of the Biologically Active Moiety of Lipopolysaccharide from Escherichia coli Re Mutant
- Lipid A and Related Compounds. XVI. Synthesis of Biologically Active Tetraacetyl-3-deoxy-D-manno-2-octulosonic Acid (KDO)-(α2→6)-D-Glucosamine-4-phosphates, Novel Analogs of the Nonreducing Sugar Moiety of Lipid A(Medicinal Chemistry,Chemical)
- SYNTHESIS OF BIOLOGICALLY ACTIVE TETRAACETYL-3-DEOXY-D-MANNO-2-OCTULOSONIC ACID(KDO)-(α2→6)-D-GLUCOSAMINE ANALOGS OF LIPID A