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|Title:||Quinazoline derivatives useful for treatment of neoplastic disease|
|Abstract:||The invention concerns quinazoline derivatives of the formula I ##STR1## wherein m is 1, 2 or 3 and each R.sup.1 includes hydroxy, amino, carboxy, carbamoyl, ureido, (1-4C)alkoxycarbonyl, N-(1-4C)alkylcarbamoyl, N,N-di-[(1-4C)alkyl]carbamoyl, hydroxyamino, (1-4C)alkoxyamino, (2-4C)alkanoyloxyamino, trifluoromethoxy, (1-4C)alkyl, (1-4C)alkoxy and (1-3C)alkylenedioxy; n is 1 or 2 and each R.sup.2 includes hydrogen, hydroxy, halogeno, trifluoromethyl, amino, nitro, cyano and (1-4C)alkyl; or a pharmaceutically-acceptable salt thereof; processes for their preparation; pharmaceutical compositions containing them; and the use of the receptor tyrosine kinase inhibitory properties of the compounds in the treatment of cancer.|
|Inventor(s):||Barker; Andrew J. (Macclesfield, GB2)|
|Assignee:||Zeneca Limited (London, GB2)|
Patent Claim Types:|
see list of patent claims
|Compound; Composition; Use;|
|Country||Document Number||Publication Date||Supplementary Protection Certificate||SPC Country||SPC Expiration|
|Norway||930178||Jan 19, 1993|
|Spain||2078798||Dec 16, 1995|
|Canada||2086968||Jul 21, 1993|
|European Patent Office||0566226||Nov 08, 1995|
|Austria||130000||Nov 15, 1995|
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