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Volumn 44, Issue 18, 2001, Pages 3031-3038
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S(+)-4-(1-phenylethylamino)quinazolines as inhibitors of human immunoglobuline E synthesis: Potency is dictated by stereochemistry and atomic point charges at N-1
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Author keywords
[No Author keywords available]
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Indexed keywords
ARALKYLAMINE;
IMMUNOGLOBULIN E;
INTERLEUKIN 4;
PHENETHYLAMINE DERIVATIVE;
PYRIMIDINE DERIVATIVE;
QUINAZOLINE DERIVATIVE;
ALLERGIC DISEASE;
ARTICLE;
CELL VIABILITY;
DOSE RESPONSE;
DRUG POTENCY;
DRUG STRUCTURE;
ENANTIOMER;
ENZYME LINKED IMMUNOSORBENT ASSAY;
GENE EXPRESSION;
HUMAN;
HUMAN CELL;
LIPOPHILICITY;
QUANTUM MECHANICS;
STEREOCHEMISTRY;
ANIMALS;
ANTIBODIES, MONOCLONAL;
ANTIGENS, CD40;
B-LYMPHOCYTES;
BLOTTING, NORTHERN;
CELL LINE;
DEPRESSION, CHEMICAL;
ENZYME-LINKED IMMUNOSORBENT ASSAY;
FEMALE;
GENES, REPORTER;
GERM CELLS;
HUMANS;
IMMUNOGLOBULIN E;
INTERLEUKIN-4;
LUCIFERASES;
MICE;
MICE, INBRED BALB C;
PHOSPHORYLATION;
PROMOTER REGIONS (GENETICS);
QUINAZOLINES;
RECEPTOR, EPIDERMAL GROWTH FACTOR;
REPRODUCIBILITY OF RESULTS;
SPLEEN;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
TYROSINE;
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EID: 0035974653
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm010888h Document Type: Article |
Times cited : (40)
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References (44)
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