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Volumn 46, Issue 1, 2003, Pages 49-63

Synthesis and structure-activity relationships of 6,7-disubstituted 4-anilinoquinoline-3-carbonitriles. The design of an orally active, irreversible inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor-2 (HER-2)

Author keywords

[No Author keywords available]

Indexed keywords

ACID ANHYDRIDE; AMIDE; CHLORIDE; EPIDERMAL GROWTH FACTOR RECEPTOR; PELITINIB; PROTEIN TYROSINE KINASE INHIBITOR; QUINOLONE DERIVATIVE; RECEPTOR SUBTYPE;

EID: 0037413550     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm020241c     Document Type: Article
Times cited : (260)

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