http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SV-2003001054-A
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classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-496 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5383 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P21-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4709 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P27-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-28 |
filingDate | 2002-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a08a4b2bd07ed2701691df5d7d4e35f2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ceb2cd72fb39262353b0dc8ed42226b0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ca498cc5b86a7878ce26dd4061072da http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e919262e22de20870e2ebb76ee4729db http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e4261e9adc3d08c2af2ba1780da9eb0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59990f1a77210e84851dd4c51e7d769a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e43ca7e3b6cc9dea4097b1f2480ba1a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbe6d4e2edebe797a64eb5c6b22e64e5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f1fe15307387be2adc4ec4d6eeb1628 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_526199ebca1f2301937fa9a933b1f6e9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4383ed53bc15a770159ae0aec55c34b7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf7c9189948d1f7f5a0255e0d2c026fb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40b3c809471123956d31edb8ed58cd58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad6a9fb2a989d6332173e32a66b2e1da |
publicationDate | 2003-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | SV-2003001054-A |
titleOfInvention | DERIVATIVES OF NEW PIRROLES AS PHARMACEUTICAL AGENTS REF. X-15017 |
abstract | THIS INVENTION REFERS TO A COMPOSITE OF THE STRUCTURE, SEE STRUCTURE, WHERE X IS A RING OF FOUR, FIVE OR SIX MEMBERS AND X IS C, OR OR S; R1 IS PHENYLL, OR OPTIONALLY REPLACED PHENYL; PYRIDINE, OR OPTIONALLY REPLACED PYRIDINY; PIRIDINE N-OXIDE, OR OPTIONALLY REPLACED PIRIDINE N-OXIDE; QUINOLINE, OR OPTIONALLY REPLACED KINOLINE; QUINOLNA N-OXIDE, OR OPTIONALLY REPLACED; OPTIONALLY REPLACED QUINOLINE N-OXIDE; NAFTIRIDINE; PIRAZONA; OR THIOPHEN; IN DODNE THE REPLACEMENT MAY BE ONE OR MORE OF THE FOLLOWING: HYDROGEN (C1-C6) RENT, (C2-C6) ALQUENILO, (C2-C6) ALQUINILO (C1-C6) ALCOXI (C2-C6) ALQUENILOXI (C2-C6-C6) ) ALQUINILOXI (C1-C6) ALQUILTIO, (c1-C6) ALQUILSULFINILO (C1-C6) ALQUILSULFONILO (C1-C6) ALQUILAMINO, DI - [(C1-C6) ALQUILO] AMINO, (C1-C6) ALCOXICARBONILO ( c1-C6) ALQUILCARBONILO, N- (C1-C6) ALQUILCARBOILO, N, N-DI - [(C1-C6) ALQUILO] CARBAMOIL, (C2-C6) ALCANOILO, (C2-C6) ALCANOILO, (C2-C6) ALCANOILOXI (C2-C6) ALCANOILAMINO, N- (C1-C6) RENT (C2-C6) ALCANOILAMINO, (C3-C6) ALQUENOILAMINO, N- (C1-C6) ALQUIL- (C3-C6) ALQUENOILAMINO, (C3-C6 ) ALQUINOILAMINO, N- (c1-C6) ALQUIL- (C3-C6) ALQUINOILAMINO, N- (C1-C6) ALQUILSULFAMOILO, N, N-DI - [(C1-C6) ALQUILO] SULFAMOILO, (C1-C6) ALCANOSULFONILAMINO , N- (C1-C6) alkyl- (C1-C6) alkanesulfonylamino, carboxamide, ethylene, thiophenyl, aminophenyl, trifluorophenyl, halo, trifluoromethoxy, HIDROXIEMTILO, N-pyrrolidinyl, N-MOROFOLINO, phenylthio, dialkylaminomethyl, EMTOXIFENILO, aMINO, hYDROXY , CARBOXYL, PHENYL, ARYALKYL; R2 IS OPTIONALLY REPLACED KINOLINE; QUINOLIN N-OXIDE, OR OPTIONALLY REPLACED KINOLINE N-OXIDE; PHENYLL, OR OPTIONALLY REPLACED PHENYL; NAFTALENE, OR OPTIONALLY REPLACED NAFTALENE; PIRIDINE OR PIRIDINE OPTIONALLY REPLACED; N-OXIDE OF PIRIDINE, OR N-OXIDE OF PIRIDINE OPTIONALLY REPLACED; QUINAZOLINE, OR OPTIONALLY REPLACED KINAZOLINE; OPTIONALLY REPLACED CINOLINE CINOLINE; BENZODIOXOL, OR OPTIONALLY REPLACED BENZODIOXOL; BENZODIOXANE, OR OPTIONALLY REPLACED BENZODIOXANE; PYRIMIDINE, OR OPTIONALLY REPLACED PYRIMIDINE; BENZOTIOFENO, OR OPTIONALLY REPLACED BENZOTIOFEN; OR FENANTROLENO, WHERE THE SUBSTITUTION MAY BE, INDEPENDENTLY ONE OR MORE OF THE FOLLOWING; HYDROGEN, (C1-C6) ALQUILO, (C2-C6) ALQUENILO, (C2-C6) ALQUINILO, (C1-C6) ALQUILHALURO, (C1-C6) ALCOXI (C2-C6) ALQUENILOXI (C2-C6) -ALQUINYL C1-C6) ALQUILTIO, (C1-C6) ALQUILSULFONILO (C1-C6) ALQUILSULFONILO, (c1-C6) ALQUILAMINO, DI - [(C1-C6) ALQUILO] AMINO, (C1-C6) ALCOXICARBONILO, N- (C1- C6) RENT] CARBAMOIL, AMINOOXI, N- (C1-C6) RENT, AMINOOXI, N, N-DI - [(C1-C6) RENT] AMINOOXI, (c2-C6) ALCANOYL, (c2-C6) ALCANOILOXI, ( C2-C) ALCANOILAMINO, N- (C1-C6) ALQUKL- (C2-C6) ALCANOILAMINO, (c3-C6) ALQUENOILAMINO, N- (C1-C6) ALQUIL- (C3-C6) ALQUENOILAMINO, (C3-C6) ALQUINOILAMINO, N- (C1-C6) ALQUIL (C3-C6) ALQUINOILAMINO, SULFAMOILO, N- (C1-6C) ALQUILSULFAMOILKO, N, N-DI - [(C1-C6) ALQULO] SULFAMOILO, (c1-C6) ALCAMOSUL , N- (C1-C6) ALQUIL- (c1-C6) ALCANOSULFONILAMIONO, CARBOXAMIDA, ETILENIO, THIOFENILO, AMINOFENILO, PHENILTIO, HALO, CYANO, PIRIDINILO, HYDROXI, N-PIRROLIDINO, N-MORFXEN 1,2,4-OXADIAZOL-3-ILO] METOXI, (5-OXO-PIRROLIDINO) METOXI, 2- (4,5-DIHIDRO-1H-IMIDAZOLILO), N, N-DIALQUILCARBAMOILOXI, 1-HDIROXI-1 -METILETILO, 4-FLUOROFENILO, 3,4-METHYLENDIOXYPHENYL, TRIFLUOROMETILO, TRIFLUOROMETOXI, SEE DODNE FORMULAS: X1 ES O, N, S, SO2NR13, C (O), OR LINK; Q1 IS HYDROGEN, PHENYLL, 5- (2,2-DIFLUORO-1,3-BENZODIOXOLILO), C (O) Q5, OR PIRIDYL NOTEBOOK M AND N ARE INDEPENDENTLY 0-2; Q1 ES OR11NR11NR11R12, HALO, N-MORFOLINO, N-PIPERAZINO-N'TRIAZOLILO, N- (4-PIPERIDINYLPIPERIDINE), SO2R14, SOR14, NHSO2R15, ACETAMIDO, N-FTALIMIDO, N-OXADOZID-NIDOLZROLINE N (N'-METHYLBENCIMIDAZOLINO, N, N- (C1-C4) ALCOXI, N-BENZIMIDAZOLINO; WHEN MYN IS INDEPENDENTLY 0-2, BUT ONE OF THE TWO IS ALREADY NOT 0, Q5 E SHDIROXI, METOXI, AMINO , DIETILAMINO, DIEMTILAMINO, R10 IS HYDROGEN, HALO, (C1-C6) RENT; R11 AND R12 ARE INDEPENDENTLY HYDROGEN, (c1-C6) RENT, (C1-C6) ALCOXI, ARILALQUILO, CYCLOALKYL (4- METHYLIPIPERIDINE, PIRIDILE, OR R11 AND R10 CAN BE JOINED TO FORM A RING OF 4,5,6 OR 7 MEMBERS, OR R11 AND R12 CAN BE JOINED TO FORM A RING OF 3,4,5,6 OR 7 MEMBERS; R13 EN HYDROGEN, (C1-C6) RENT, 2-METOXYPHENYL, R14 E S2-PYRIDIMIDINYL, N-METHYL-2-IMIDAZOLYL, 4-CHLOROPHENYL, 2-PYRIDYL METHYL; R15 ES (C1-C6) RENT, N-METHYL-4- IMIDAZOLIL; R16 IS HYDROGEN, HALO, RENT, ARILO, SEE FORMULA, WHERE; Q2 IS HYDROGEN, 4-IMIDAZOLIL, OR C (O) NR24R25 WHEN O AND P ARE INDEPENDENTLY 0-2; Q2 IS OR23, NR24R25, OR N-MORPHOLINE, WHEN O AND P ARE INDEPENDENTLY 0-2 BUT ONE OF THEM ALREADY OR OR P DON'T BE 0; R20 IS HYDROGEN, OR (C1-C6) RENT; R21 IS HYDROGEN, (C1-C6) RENT, OR R21 AND R20 CAN BE JOINED TO FORM A RING OF 4,5,6 OR 7 MEMBERS; R22 IS HYDROGEN, (C1-C6) RENT, ARIALQUIL, ARILO, OR R21 AND R22 CAN JOIN TO FORM A RING OF 4,5,6,7 MEMBERS; R23 IS HYDROGEN OR (c1-C6) RENT; R24 IS HYDROGEN, (C1-C6) RENT, OR R24 AND R25 CAN BE TAKEN TOGETHER TO FORM A RING OF 3,4,5,6, OR 7 MEMBERS, OR R24 AND R20 MAY BE TAKEN TO FORM A RING OF 6 OR 7 MEMBERS ; R25 IS HYDROGNEUM (C1-C6) RENT OR ACETYLL, OR A FORMULA GROUP SEE FORMULA, WHERE R30 IS HYDROGEN, OR (C1-C6) RENT, R31 IS HYDROGEN, (C1-C6) RENT, 2-PIRIDYL, PIRIDYL , AMINO OR HYDROXY, OR A FORMULA GROUP SEE FORMULA, WHERE R32 AND R33 ARE EACH INDEPENDENTLY HYDROGEN, (C1-C6) RENT, A CETILO, RENT SULFONYL, OR R32 AND R33 CAN BE GATHERED TO FORM A RING 5.6 OR 7 MIEM, BROS, SEE FORMULA, WHERE X2 IS CH2, OR, ON; Q IS 2- * 3 EXCEPT THAT Q3 IS A LINK, Q IS 0-3; Q3 IS NR36R37, OR38, OR A LINK; R35 IS HDIROGEN, OR R35 AND Q3 IS A LINK Q3 IS A LINK Q IS 0-3; Q3 IS NR36R37, OR38, OR A LINK; R35 IS HYDROGEN, OR R35 AND Q3 (WHEN Q3 IS A LINK, THEY CAN JOIN TO FORM A RING OF 5 MEMBERS; R36, R37 AND R3 EACH ARE INDEPENDENTLY HYDROGEN, OR (C1-C6) RENT, OR A FORMULA GROUP, EVR FORMULA, WHERE X3 IS CYAN, CARBOXAMIDE, N, N-DIEMTILCARBOXAMIDA, N, N-DIEMTILCARBOXAMIDA, N, N-DIEMTILAMINOMETILO, 4-MERILPIPERAZIN-1ILO-EMTILO OR CARBOXYLATE, OR A GROUP OF Q42 IN R42; EN 2-3; R40 E SHDIROGEN, OR (C1-C6) = RENT; R41 AND R42 ARE HYDROGEN, (C1-C6) RENT, OR R41 AND R40 CAN BE TAKEN TO FORM A RING OF 6 OR 7 MEMBERS, A GROUP FORMULA SEE FORM IN WHERE: Q7 IS HYDROXY, METOXI, OR N-PIPERIDINYL; WITH THE CONDITION THAT R1 AND R2 CANNOT BE BOTH PHENYLL OR PHENYL OPTIONALLY REPLACED, AND WITH THE CONDITION THAT WHEN IT IS ALREADY R1 OR R2 PHENYLL OR PHENYL OPTIONALLY REPLACED, THE OTHER CANNOT BE THIOFEN-2-ILO AND ALWAYS AND NOTEBOOK R2 BE QUINOLINA-4-ILO, REPLACEMENT IN POSITION 7 OF QUINOLINE CANNOT INCLUDE ARILO, HETER OARILO, ARILO FUSIONADO, NI HETEROARILO FUSIONADO.K IS 1-8; R3 ONE OR MORE OF THE FOLLOWING: HDIROGEN; (C1-C4) RENT; (C1-C4) ALQUILHIDORXI; HYDROXY; HYDROXY; N, N-DI (C1-C4) ALKYLAMINE (C1-C4) ALCOXI; BENCILO OXIEMTILO; Phenyloxymethyl, OXO, CARBOXYL (C1-C4) RENT; BENCILOXI, ACETOXI, AMINO (C1-C4) RENT; (C1-C4) ALKYLENE; HALO; -O- (C1-C4) CHLOROPHENYL; ACETONITRILE; PHENYLL, OR AN OPTIONALLY REPLACED PHENYL; WHERE THE REPLACEMENT MAY BE ONE OR MORE OF THE FOLLOWING: (C1-C6) ALCOXI, HALO, CARBOXI, OR (C1-C6) ALCOXICARBONILO; AND THE PHARMACEUTICALLY ACCEPTABLE, ESTERS AND PRODROGAS SALTS OF THEM. |
priorityDate | 2001-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 106.