http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2415022-A1

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filingDate 2001-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_163c7d5c94cf3ca4fcc69468e2c0175b
publicationDate 2002-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2415022-A1
titleOfInvention Cinnoline compounds
abstract The invention relatest to compounds of the formula (I) wherein either any one of G¿1?, G¿2?, G¿3?, G¿4? and G¿5? is nitrogen and the other four are -CH-, or G¿1?, G¿2?, G¿3?, G¿4? and G¿5? are all -CH-; Z is -O-, -NH-, -S-, -CH¿2?- or a direct bond; Z is linked to any one of G¿1?, G¿2?, G¿3? and G¿4? which is a free carbon atom; n is an integer from 0 to 5; any of the substitutents R?1¿ may be attached at any free carbon atom of the indole, azaindole or indazole group; m is an integer from 0 to 3; R?a¿ represents hydrogen; R?b¿ represents hydrogen or another value as defined herien; R?1¿ represents hydrogen, oxo, hydroxy, halogeno, C¿1-4?alkyl, C¿1-4?alkoxy, C¿1-4?alkoxyC¿1-4?alkyl, aminoC¿1-4?alkyl, C¿1-3?alkylaminoC¿1-4?alkyl, di(C¿1-3?alkyl)aminoC¿1-4?alkyl, -C¿1-5?alkyl(ring B) wherein ring B is selected from azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, N-methylpiperazinly, N-ethylpiperazinyl, morpholino and thiomorpholino; R?2¿ represents hydrogen, hydroxy, halogeno, cyano, nitro, trifluoromethyl, C¿1-3?alkyl, C¿1-3?alkoxy, C¿1-3?aklylsulphanyl, -NR?3¿R?4¿ (wherein R?3¿ and R?4¿, which may be the same or different, each represents hydrogen or C¿1-3?alkyl), or R?5¿X?1¿-(wherein R?5¿ and X?1¿ are as defined herein) and salts thereof, processes for the preparation of such compounds, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and the use of a compound of formula I in the manufacture of medicament for the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals.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.
priorityDate 2000-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 433.