摘要 |
The invention relates to the use of compounds of formula (I) wherein: R<2> represents hydroxy, halogeno, C1-3alkyl, C1-3alkoxy, C1-3alkanoyloxy, trifluoromethyl, cyano, amino or nitro; n is an integer from 0 to 5; Z represents -O-, -NH-, -S- or -CH2-; G<1> represents phenyl or a 5-10 membered heteroaromatic cyclic or bicyclic group; Y<1>, Y<2>, Y<3> and Y<4> each independently represents carbon or nitrogen; R<1> represents fluoro or hydrogen; m is an integer from 1 to 3; R<3> represents hydrogen, hydroxy, halogeno, cyano, nitro, trifluoromethyl; C1-3alkyl, -NR<4>R<5> (wherein R<4> and R<5> can each be hydrogen or C1-3alkyl), or a group R<6>-X<1>- wherein X<1> represents -CH2- or a heteroatom linker group and R<6> is an alkyl, alkenyl or alkynyl chain optionally substituted by for example hydroxy, amino, nitro, alkyl, cycloalkyl, alkoxyalkyl, or an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring, which alkyl, alkenyl or alkynyl chain may have a heteroatom linker group, or R<6> is an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals such as humans, processes for the preparation of such derivatives, pharmaceutical compositions containing a compound of formula (I) or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula (I). The compounds of formula (I) and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis. |
申请人 |
ZENECA LIMITED;ZENECA PHARMA S.A.;THOMAS, ANDREW, PETER;HENNEQUIN, LAURENT, FRANCOIS, ANDRE;PLE, PATRICK, ALAN |
发明人 |
THOMAS, ANDREW, PETER;HENNEQUIN, LAURENT, FRANCOIS, ANDRE;PLE, PATRICK, ALAN |