Bioorganic and Medicinal Chemistry Letters p. 2723 - 2728 (1997)
Update date:2022-08-29
Topics:
Gibson
Grundy
Godfrey
Woodburn
Ashton
Curry
Scarlett
Barker
Brown
Investigation of structure-activity relationships of novel quinazolines has identified 4-(4-isoquinolylamino)-quinazoline and a 4-(trans-2-phenylcyclopropylamino)-quinazoline as potent inhibitors of EGF-receptor tyrosine kinase in vitro. Further modificatons of the latter compound have identified a derivative which shows anti-tumour activity against a tumour xenograft model when dosed orally once per day.
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