http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2542326-T3

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filingDate 2001-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de0fb6ce5e0b1f01b01258f2235ec391
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publicationDate 2015-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2542326-T3
titleOfInvention HIV replication inhibitors
abstract A compound of the formula: ** Formula ** an N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine, and a stereochemically isomeric form thereof, where -b1> = b2-C (R2a)> = b3- b4> = represents a bivalent radical of the formula: -CH> = CH-C (R2a10)> = CH-CH> = (b-1); -N> = CH-C (R2a)> = CH-CH> = (b-2); -CH> = N-C (R2a)> = CH-CH> = (b-3); -N> = CH-C (R2a)> = N-CH> = (b-4); -N> = CH-C (R2a)> = CH-N> = (b-5); -CH> = N-C (R2a20)> = N-CH> = (b-6); -N> = N-C (R2a)> = CH-CH> = (b-7); R1 is hydrogen; aryl; formyl; C1-6alkylcarbonyl; C1-6alkyl; C1-6 alkyloxycarbonyl; formyl-substituted C1-6alkyl, C1-6alkylcarbonyl, C1-6alkyloxycarbonyl, C1-6alkylcarbonyloxy; C1-6 alkyloxy-C1-6 alkylcarbonyl substituted with C1-6 alkyloxycarbonyl; q is 0, 1, 2; or when possible q is 3 or 4; R2a is cyano, aminocarbonyl, mono- or di- (methyl) aminocarbonyl, C1-6 alkyl substituted with cyano, aminocarbonyl or mono- or di- (methyl) aminocarbonyl, C2-6 alkenyl substituted with cyano or C2-6 alkynyl substituted with cyano; each R2 is independently hydroxy, halo, C1-6 alkyl optionally substituted with cyano or -C (> = O) R6, C3-7 cycloalkyl, C2-6 alkenyl optionally substituted with one or more halogen or cyano atoms , C2-6 alkynyl optionally substituted with one or more halogen or cyano atoms, C1-6 alkyloxy, C1-6 alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di- (C1-6alkyl) amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, -S (> = O) pR6, -NHS (> = O) pR6, -C (> = O) R6, -NHC (> = O) H, -C (> = O) NHNH2, - NHC (> = O) R6, -C (> = NH) R6 or a radical of the formula: ** Formula ** in which: each A1 is, independently, N, CH or CR6; and A2 is NH o, S or NR6; p is 1 or 2; L is C1-10 alkyl, C2-10 alkenyl, C2-10 alkynyl, C3-7 cycloalkyl, each of said groups being substituted with one or two substituents independently selected from: * C3-7 cycloalkyl, * indolyl or isoindolyl, each optionally substituted with one, two, three or four substituents each independently selected from halo, C1-6 alkyl, hydroxy, C1-6 alkyloxy, cyano, aminocarbonyl, nitro, amino, polyhalomethyl, polyhalomethyloxy and C1-6alkylcarbonyl, * phenyl, pyridyl, pyrimidinyl, pyrazinyl or pyridazinyl, each of said aromatic rings being optionally substituted with one, two, three, four or five substituents each independently selected among the defined substituents at R2; or L is -X1-R3 or -X2-Alk-R4, wherein: R3 is 2,4,6-trisubstituted phenyl, each of the substituents being independently selected from the substituents defined in R2; Alk is C1-4 alcanediĆ­lo; R4 is phenyl, pyridyl, pyrimidinyl, pyrazinyl or pyridazinyl, each of said aromatic rings being optionally substituted with one, two, three, four or five substituents each independently selected from among the substituents defined in R2; and X1 or X2 is each, independently, -NR7-, -NH-NH-, -N> = N-, -O-, -C (> = O) -, -CHOH-, -S-, -S (> = O) p-.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419493831
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID64143
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9PTS1
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458427722
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP25227
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448149292
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414879459
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Total number of triples: 379.