Neutral, acidic, and basic derivatives of anthranilamide that confer different formal charge to reducing oligosaccharides

Carbohydrate Research

Volumn 339, Issue 2, 2004, Pages 221-231

  Locke, Darren ^a   Bevans, Carville G ^b   Wang, Lai Xi ^c   Zhang, Ye ^d   Harris, Andrew L ^a   Lee, Yuan C ^d  

^a RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^b MAX PLANCK INSTITUTE OF BIOPHYSICS   (Germany)

^c INSTITUTE OF HUMAN VIROLOGY   (United States)

^d JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Anthranilic acid; Carbohydrate; Channel; Glycoconjugate; Maltosaccharide; Reductive amination

Indexed keywords

AMINES; CHROMATOGRAPHIC ANALYSIS; DERIVATIVES; FLUORESCENCE; POROSITY;

ACID DERIVATIVES; FLUORESCENT MOIETIES;

SACCHARIFICATION;

2 AMINOBENZAMIDE; AMIDE; ANTHRANILIC ACID DERIVATIVE; N (2 AMINOBENZOYL)GLYCINAMIDE; N (2 AMINOBENZOYL)GLYCINE; N,N METHYL N' (2 AMINOBENZOYL)ETHYLENEDIAMINE; OLIGOSACCHARIDE; UNCLASSIFIED DRUG;

ACIDITY; ALKALINITY; AMINATION; ANALYTIC METHOD; ARTICLE; CARBOHYDRATE SYNTHESIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONJUGATION; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PH; PRIORITY JOURNAL; REDUCTION; SYNTHESIS;

EID: 0348047431     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2003.10.020     Document Type: Article

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