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filingDate 1985-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bfbb9476c8024a0a5afb50269baa83cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c841b9fb0c4b3979d9ef1a1b89c7e65d
publicationDate 1988-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4794188-A
titleOfInvention Certain unsymmetrical quinolinyl ethers having anti-inflammatory and anti-allergic activity
abstract Compounds of the formula: Ar1-X-Ar-Z-(R)n' and salts thereof, wherein Ar1 is a nitrogen, sulfur or oxygen heterocyclic ring; Ar is a phenyl ring or a nitrogen, oxygen or sulfur heterocyclic ring; Ar and Ar1 may be fully substituted or less than fully substituted with H, CH3, lower alkyl, aryl, aralkyl, halo, hydroxy, lower alkoxy, CF3, carboxy, alkylcarboxy, arylcarboxy, alkylcarbalkoxy, alkanoyl, formyl, oxo, nitrilo, amino, aminoalkyl, alkylamine, carboxamide, aryloxy, nitro, sulfonyl, sulfonamide, thio, alkylthio, hydroxyalkyl or oxyalkylcarbalkoxy; X= <IMAGE> of up to 2 carbon atoms in the principal chain and up to a total of 4 carbon atoms, <IMAGE> +TR <IMAGE> Z is an alkylene chain containing up to 10 carbon atoms in the principal chain and a total of up to 12 carbon atoms and from 0 to 2 double bonds and the said alkylene chain may be attached to Ar through an oxygen, sulfur or amino nitrogen atom, and when n'=2, one of the R substituents may be halogen on an omega carbon of the alkylene chain Z; when n'=1, R is a substituent attached to one of the carbon atoms of Z selected from the group consisting of =O, OR3, SR3, N(R2)2 and R1, -COR4 and when n'=2 one R is previously defined and the additional R is a substituent attached to one of the carbon atoms of Z selected from the group consisting of =O, OR3, SR3, N(R2)2, -COR4, lactone and halo; R1 is H or CH3; R2 is H, lower alkyl, aryl or aralkyl; R3 is H, lower alkyl, lower alkanoyl, aryl, aralkyl or substituted aryl in which the substituent is halo, lower alkyl or lower alkoxy; R4 is OR2 or N(R2)2; n=0 or 1; n'=1 to 7; and n''=0, 1 or 2.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23692255
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID236070653
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235907017
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127417364
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235907021
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395085
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5055
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136057721
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7221
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID347917584
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235907003
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127412993
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9223
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235907015
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223948431
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127400281
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54476566
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127409548
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128445809
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21280489
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21280490
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128970588
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21280488
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21280485

Total number of triples: 933.