http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2330125-T3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
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filingDate 2005-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00f7d34cb64de0361650fd98df484066
publicationDate 2009-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2330125-T3
titleOfInvention DERIVATIVES OF AZETIDINE COM ANTAGONIST RECEIVER CCR-3.
abstract A compound of formula I ** (See formula) ** in free or salt form, wherein Ar is a phenyl optionally substituted by a halo, C1-C8 alkyl, C1-C8 alkoxy, cyano, nitro, -SO2-alkyl C1-C8, -SO2-NH-C1-C8 alkyl or -SO2-N- (C1-C8 alkyl) 2; X is a bond or -CO-CH2-NH-; Y is -CO-R1-, -CO-R2-S-, -CO-NH- or -SO2-; T is a cyclic group selected from C1-C8 cycloalkyl, phenyl optionally substituted by a halo, C1-C8 alkyl, C1-C8 alkoxy or cyano, and a heterocyclic group having a ring of 5 to 10 atoms wherein at least one of those ring atoms is a nitrogen, oxygen or sulfur atom, said heterocyclic group being optionally substituted by a halo, C1-C8 alkyl optionally substituted by an R3, C1-C8 alkoxy optionally substituted by an R3, phenyl or by a heterocyclic ring 5 or 6 members having at least one ring of nitrogen, oxygen or sulfur atom; R1 and R2 are each a bond or C1-C8 alkylene; and R3 is a 5 or 6 membered phenyl or a heterocyclic ring having at least one nitrogen, oxygen or sulfur atom ring
priorityDate 2004-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID657308
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2779290
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID519716

Total number of triples: 309.