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filingDate 2001-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d17549541f1976275941abe9aee9a68e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35f10a782c3b826056d476deab901363
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_619f7e0867db5ecea27bf5aeae59bc90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c54a71aef4ca2874e27ceaa532a70a01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f603111897bfbcfcb693f05667ee64d3
publicationDate 2002-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20020002249-A
titleOfInvention New diphenylurea compounds, a process for their preparation and pharmaceutical compositions containing them
abstract The present invention relates to compounds of formula (I) and to medicaments:n n n n n n n n Wheren n n R 1 , R 2 , R 3 and R 4 are independently hydrogen atom, halogen atom, or alkyl, alkoxy, hydroxy, cyano, optionally substituted amino, nitro, carboxy, alkoxycarbonyl, optionally substituted amino Carbonyl or carbonyl group,n n n L 1 and L 2 each represent a hydrogen atom or combine together to form a -CH 2 -CH 2 -group,n n n X 1 bonded to the 2 or 3 position of the aromatic ring represents a single bond, in which case X 2 represents a hydrogen atom, a halogen atom or an alkyl, alkoxy, hydroxy, nitro, cyano or optionally substituted amino group Or X 1 and X 2 combine with two adjacent carbon atoms to which they are bonded at the 2, 3 or 4 position of the aromatic ring to form a (C 4 -C 7 ) cycloalkyl group, wherein one of the cycloalkyl rings Or two-CH 2 -groups are optionally substituted by an oxygen atom or an NH group,n n n X 3 represents a hydrogen, a halogen atom or an alkyl, alkoxy, hydroxy, nitro, cyano or optionally substituted amino group,n n n G represents a group selected from the following formula:n n n n n n n n Wheren n n The dashed line represents an optionally present double bond,n n n Alk represents a linear or branched (C 1 -C 6 ) alkylene group,n n n n is 0 or 1,n n n T 3 represents an alkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl or optionally substituted heteroarylalkyl group,n n n T 4 represents an alkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl or optionally substituted heteroarylalkyl group.
priorityDate 2000-06-29-04:00^^<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/substance/SID419559526
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420429135
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID55669
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419703018
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19670
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69583705
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423007769
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID40426
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11528408
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22186064
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413515407
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11116341
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453754492
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449756655
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454973655
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424339778
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID131724571
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21584533
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421268171
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID101807
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
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Total number of triples: 343.