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filingDate 1996-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d69bd73ca38f97ce25210285c2c1d230
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d26b0c243147f9004a80ee7aff4d8b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46c5d33aa219ae25a894167af9d28327
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a09219fa08b4a60130ee5a1feb0462b3
publicationDate 2000-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-9904125-A2
titleOfInvention 1- (1,2-Disubstituted piperidinyl) -4-substituted piperidine derivatives having tachykinin receptor antagonist activity
abstract Compounds of general formula (I) wherein n is 0, 1 or 2; m is 1 or 2 with the proviso that if m is 2, the value of the stone is 1; p is 0, 1 or 2; = Q is = O or = NR 3; X is a covalent bond, -O-, -S-, or -NR 3 -; R1 is Ar1-, Ar1- (C1-C6) alkyl or di (Ar1) -C1-6 alkyl piperidine, of which C1-6 alkyl pipettors are optionally hydroxy (C1-C4) alkyl-oxy; aryl, heteroaryl, heteroaryl, heteroaryl, aryl, heteroaryl, heteroaryl, aryl, heteroaryl, heteroaryl, heteroaryl, heteroaryl, heteroaryl, aryl, heteroaryl, or Het (1-6szénatőmős) alkyl; R 4 is hydrogen, C 1-4 alkyl, (C 1-4) alkyloxy (C 1-4) alkyl, hydroxy (C 1-4) alkyl, carboxyl, (C 1-4) alkyloxy - carbonyl or Ar3; R5 is hydrogen; OH; Ar 3; Ar3- (C1-C6) alkyl-oxy; di (Ar 3) - (C 1-6) alkyl-oxy, Ar 3 - (C 1-6) -alkylthio; di (Ar 3) - (C 1-6) alkylthio; Ar3- (C 1-6 alkyl) alkylphenoxy; di- (Ar 3) - (C 1-6) alkylcarbonyl; Ar 3 C (1-6szénatőmős) alkylsulfonyl; di (Ar 3) - (C 1-6) alkylsulfonyl-1- (C 6 -alkyl) phenyl substituted with a diphenyl substituent of the general formula NR 7 R 8, -NR 7 R 8; or a tube of general formula (a-1) or (a-2); or R 4 and R 5 together form a divalent aromatic moiety of the formula -O-CH 2 -CH 2 -O- or -C (= O) -NR 3 -CH 2 - NR 7; and R6 is selected from the group consisting of Hydrogen, Hydroxyl Powder, (C 1-6) Alkoxy-Peak, C 1-6 Alkyl Powder and Ar 3 (C 1-6) Alkyl Pyrene having Tachykinin Antagonist Activity. The preparation of the above compounds and pharmaceutical compositions containing them are described. ŕ
priorityDate 1995-12-27-04:00^^<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/anatomy/ANATOMYID9606
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527255
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419840560
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419535600
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394866
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID79341
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426078412
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419652197
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419493463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70221472
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410393697
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426205585

Total number of triples: 295.