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Volumn 876, Issue 1-2, 2000, Pages 75-86
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Stereoselective binding of 2,3-substituted 3-hydroxypropionic acids on an immobilised human serum albumin chiral stationary phase: Stereochemical characterisation and quantitative structure-retention relationship study
a a a a a a b c |
Author keywords
3 Hydroxypropionic acid; Chiral stationary phases, LC; Enantiomer separation; Human serum albumin; Quantitative structure retention relationship
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Indexed keywords
ANTIINFLAMMATORY AGENT;
HUMAN SERUM ALBUMIN;
HYDRACRYLIC ACID DERIVATIVE;
ANALYTIC METHOD;
ARTICLE;
CHIRAL CHROMATOGRAPHY;
CIRCULAR DICHROISM;
CONTROLLED STUDY;
DRUG CONFORMATION;
ENANTIOMER;
LIPOPHILICITY;
MOLECULAR MODEL;
PARTITION COEFFICIENT;
PHYSICAL CHEMISTRY;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN IMMOBILIZATION;
QUANTITATIVE STRUCTURE ACTIVITY RELATION;
REGRESSION ANALYSIS;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
STATIONARY PHASE;
STEREOCHEMISTRY;
STEREOISOMERISM;
TECHNIQUE;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
HUMANS;
LACTIC ACID;
MODELS, MOLECULAR;
SERUM ALBUMIN;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0034697230
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/S0021-9673(00)00195-3 Document Type: Article |
Times cited : (54)
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References (33)
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