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Volumn 360, Issue , 2012, Pages 56-68
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Synthesis of pentasaccharides corresponding to the glycoform II of the outer core region of the Pseudomonas aeruginosa lipopolysaccharide
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Author keywords
Cystic fibrosis; Lipopolysaccharide; Outer core region; Pentasaccharide; Pseudomonas aeruginosa; Synthesis
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Indexed keywords
CORE REGION;
CYSTIC FIBROSIS;
LIPOPOLYSACCHARIDES;
PENTASACCHARIDES;
PSEUDOMONAS AERUGINOSA;
CELL MEMBRANES;
CHLORINE COMPOUNDS;
GENES;
PROTEINS;
SYNTHESIS (CHEMICAL);
BACTERIA;
1,2 5,6 DI O ISOPROPYLIDENE 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL) ALPHA DEXTRO GLUCOFURANOSE;
1,2 O ISOPROPYLIDENE 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL ALPHA DEXTRO GLUCOFURANOSE;
1,2,4 TRI O ACETYL 6 O CHLOROACETYL 3 O (2,3,4-TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL) DEXTRO GLUCOPYRANOSE;
2,4 DI O ACETYL 6 O CHLOROACETYL 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL) ALPHA DEXTRO GLUCOPYRANOSYL BROMIDE;
2,4 DI O ACETYL 6 O CHLOROACETYL 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL) ALPHA DEXTRO GLUCOPYRANOSYL TRICHLOROACETIMIDATE;
2,4 DI O ACETYL 6 O CHLOROACETYL 3 O (2,3,4 TRI O BENZOYL BETA LEVO RHAMNOPYRANOSYL) DEXTRO GLUCOPYRANOSE;
6 O CHLOROACETYL 1,2 O ISOPROPYLIDENE 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL) ALPHA DEXTRO GLUCOFURANOSE;
6 O CHLOROACETYL 3 O (2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL DEXTRO GLUCOPYRANOSE;
BACTERIUM LIPOPOLYSACCHARIDE;
CARBOHYDRATE DERIVATIVE;
ETHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 2 O BENZOYL 4 O BENZYL 1 THIO BETA DEXTRO GLUCOPYRANOSIDE;
ETHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 2 O BENZOYL 4,6 O BENZYLIDENE 1 THIO BETA DEXTRO GLUCOPYRANOSIDE;
ETHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 4,6 O BENZYLIDENE 1 THIO BETA DEXTRO GLUCOPYRANOSIDE;
ETHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 6 O ACETYL 2 O BENZOYL 4 O BENZYL 1 THIO BETA DEXTRO GLUCOPYRANOSIDE;
GALACTOSAMINE;
METHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 2,4 DI O ACETYL 6 O CHLOROACETYL BETA DEXTRO GLUCOPYRANOSYL (1 3) 2 AZIDO 4,6 O BENZYLIDENE 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 2,4 DI O ACETYL 6 O CHLOROACETYL BETA DEXTRO GLUCOPYRANOSYL (1 3) 2 AZIDO 6 O BENZYL 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL 2,3,4 TRI O BENZOYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) 6 O ACETYL 2 O BENZOYL 4 O BENZYL BETA DEXTRO DEXTRO GLUCOPYRANOSYL (1 3) 2 AZIDO 4,6 O BENZYLIDENE 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) [2,4 DI O BENZYL ALPHA DEXTRO GLUCOPYRANOSYL) (1 3) [2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSYL (1 4)] 2 AMINO 6 O BENZYL 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 6)] BETA DEXTRO DEXTRO GLUCOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 4)] 2 ACETAMIDO 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 6)] BETA DEXTRO GLUCOPYRANOSYL (1 3) [ALPHA DEXTRO DEXTRO GLUCOPYRANOSYL (1 4)] 2 (LEVO ALANYLAMINO) 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 6)] BETA DEXTRO GLUCOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 4)] 2 [N (TERT BUTOXYCARBONYL) LEVO ALANYLAMINO] 2 DEOXY ALPHA DETXRO GALACTOPYRANOSIDE;
METHYL ALPHA LEVO RHAMNOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL(1 6)] BETA DEXTRO GLUCOPYRANOSYL (1 3) [ALPHA DEXTRO GLUCOPYRANOSYL (1 4)] 2 (N ACETYL LEVO ALANYLAMINO) 2 DEOXY ALPHA DEXTRO GALACTOPYRANOSIDE;
PENTASACCHARIDE;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
UNCLASSIFIED DRUG;
ARTICLE;
BINDING AFFINITY;
CARBOHYDRATE ANALYSIS;
CARBOHYDRATE SYNTHESIS;
CARBON NUCLEAR MAGNETIC RESONANCE;
DEACETYLATION;
GLYCOSYLATION;
HYDROLYSIS;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
PSEUDOMONAS AERUGINOSA;
ALANINE;
CARBOHYDRATE CONFORMATION;
CARBOHYDRATE SEQUENCE;
GALACTOSAMINE;
LIPOPOLYSACCHARIDES;
OLIGOSACCHARIDES;
PSEUDOMONAS AERUGINOSA;
BACTERIA (MICROORGANISMS);
PSEUDOMONAS AERUGINOSA;
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EID: 84865556083
PISSN: 00086215
EISSN: 1873426X
Source Type: Journal
DOI: 10.1016/j.carres.2012.07.019 Document Type: Article |
Times cited : (15)
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References (39)
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