AR051921A1 - Acidos sustituidos utiles como compuestos farmaceuticos para tratar trastornos respiratorios, composiciones farmaceuticas que los contienen, y procesos para su preparacion - Google Patents
Acidos sustituidos utiles como compuestos farmaceuticos para tratar trastornos respiratorios, composiciones farmaceuticas que los contienen, y procesos para su preparacionInfo
- Publication number
- AR051921A1 AR051921A1 ARP050102853A ARP050102853A AR051921A1 AR 051921 A1 AR051921 A1 AR 051921A1 AR P050102853 A ARP050102853 A AR P050102853A AR P050102853 A ARP050102853 A AR P050102853A AR 051921 A1 AR051921 A1 AR 051921A1
- Authority
- AR
- Argentina
- Prior art keywords
- halogen
- alkyl
- cycloalkyl
- optionally substituted
- hydrogen
- Prior art date
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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Abstract
Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) o una sal aceptable para uso farmacéutico del mismo, en el cual: T es un enlace, S(O)n (donde n es 0, 1 o 2), CR1R2, NR13; W es O, S(O)n (donde n es 0, 1 o 2), NR13, CR1OR2 o CR1R2; X es hidrogeno, halogeno, ciano, nitro, S(O)nR6, OR12 o C1-6 alquilo que puede ser sustituido por uno o más átomos de halogeno; Y se selecciona entre hidrogeno, halogeno, CN, nitro, SO2R3, OR4, SR4, SOR3, SO2NR4R5, CONR4R5, NR4R5, NR6SO2R3, NR6CO2R6, NR6COR3, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7 o alquilo C1-6, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, OR6 y NR6R7, S(O)nR6 donde n es 0, 1 o 2; Z es arilo o heteroarilo, sustituido optativamente por uno o más sustituyentes seleccionados en forma independiente entre hidrogeno, halogeno, CN, OH, SH, nitro, CO2R6, SO2R9, OR9, SR9, SOR9, SO2NR10R11, CONR10R11, NR10R11, NHSO2R9, NR9SO2R9, NR6CO2R6, NHCOR9, NR9COR9, NR6CONR4R5, NR6SO2NR4R5, arilo, heteroarilo, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6, NR6R7, S(O)nR6 (donde n es 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R1 y R2 representan en forma independiente un átomo de hidrogeno, halogeno, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7 o un grupo alquilo C1-6, estando los ultimos cuatro grupos optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, NR6R7, OR6, S(O)nR6 (donde n es 0, 1 o 2); o R1 y R2 jun tos pueden formar un anillo de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S, NR6 y en sí mismo sustituido optativamente por uno o más alquilo C1-3 o halogeno; R3 representa cicloalquilo C3-7, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 todos los cuales pueden estar optativamente sustituidos por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R4 y R5 representan en forma independiente hidrogeno, cicloalquilo C3-7 o alquilo C1-6, estando los dos ultimos grupos sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R4 y R5 junto con el átomo de nitrogeno al cual están unidos pueden formar un anillo heterocíclico saturado de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S(O)n (donde n = 0, 1 o 2), NR8, y en sí mismo sustituido optativamente por halogeno o alquilo C1-3; R6 y R7 representan en forma independiente un átomo de hidrogeno o alquilo C1-6; R8 es hidrogeno, alquilo C1-4, -COalquiloC1-4, CO2alquiloC1-4 o CONR6alquiloC1-4; R9 representa arilo, heteroarilo, cicloalquilo C3-7 o alquilo C1-6, pudiendo los ultimos dos grupos estar sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, arilo heteroarilo, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; R10 y R11 representan en forma independiente arilo o heteroarilo, hidrogeno, cicloalquilo C3-7; o alquilo C1-6, estando los dos ultimos grupos sustituidos optativamente por uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, arilo, heteroarilo, OR6 y NR6R7, S(O)nR6 (donde n = 0, 1 o 2), CONR6R7, NR6COR7, SO2NR6R7 y NR6SO2R7; o R10 y R11 junto con el átomo de nitrogeno al cual están unidos pueden formar un anillo heterocíclico saturado de 3-8 miembros que contiene optativamente uno o más átomos seleccionados entre O, S(O)n (donde n = 0, 1 o 2), NR8, y en sí mismo sustituido optativamente por halogeno; o C1-3 alquilo; R12 representa un átomo de hidrogeno o alquilo C1-6 que puede ser sustituido por uno o más átomos de halogeno; y R13 representa un átomo de hidrogeno, alquilo C1-6 que puede ser sustituido por uno o más átomos de halogeno o cicloalquilo C3-7, SO2R6 o COalquiloC1-4, con las siguientes salvedades: cuanto T es carbono o un enlace, el sustituyente en el grupo Z no puede ser NR10R11, donde R10R11 son en forma independiente hidrogeno, arilo, o alquilo; y se excluyen los compuestos ácido 2-[(4-carboxifenil)amino]-4,5-dihidroxi-bencenpropanoico y ácido 4-cloro-2-[(4-clorofenil)tio]-bencenacético.
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AR042206A1 (es) * | 2002-11-26 | 2005-06-15 | Novartis Ag | Acidos fenilaceticos y derivados |
ES2401079T3 (es) * | 2002-12-20 | 2013-04-16 | Amgen Inc. | Moduladores del asma y de la inflamación alérgica |
EP1611105A1 (en) | 2003-03-28 | 2006-01-04 | Eli Lilly And Company | Isoquinoline-5-sulfonic acid amides as inhibitors of akt (protein kinase b) |
SE0301010D0 (sv) * | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
SE0301009D0 (sv) | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
DE60303238T2 (de) | 2003-04-25 | 2006-09-14 | Actimis Pharmaceuticals, Inc., La Jolla | Pyrimidin-Essigsäure Derivate geeignet zur Behandlung von CRTH2-bedingten Krankheiten |
SA04250253B1 (ar) | 2003-08-21 | 2009-11-10 | استرازينيكا ايه بي | احماض فينوكسي اسيتيك مستبدلة باعتبارها مركبات صيدلانية لعلاج الامراض التنفسية مثل الربو ومرض الانسداد الرئوي المزمن |
GB0324763D0 (en) | 2003-10-23 | 2003-11-26 | Oxagen Ltd | Use of compounds in therapy |
US7166738B2 (en) * | 2004-04-23 | 2007-01-23 | Roche Palo Alto Llc | Non-nucleoside reverse transcriptase inhibitors |
GB0409921D0 (en) | 2004-05-04 | 2004-06-09 | Novartis Ag | Organic compounds |
WO2005115382A1 (en) | 2004-05-29 | 2005-12-08 | 7Tm Pharma A/S | Crth2 receptor ligands for medicinal uses |
GB0415320D0 (en) | 2004-07-08 | 2004-08-11 | Astrazeneca Ab | Novel compounds |
GB0418830D0 (en) | 2004-08-24 | 2004-09-22 | Astrazeneca Ab | Novel compounds |
GB0422057D0 (en) | 2004-10-05 | 2004-11-03 | Astrazeneca Ab | Novel compounds |
ATE517085T1 (de) | 2004-11-23 | 2011-08-15 | Astrazeneca Ab | Zur behandlung von atemwegserkrankungen geeignete phenoxyessigsäurederivate |
GB0510584D0 (en) | 2005-05-24 | 2005-06-29 | Novartis Ag | Organic compounds |
TW200745003A (en) * | 2005-10-06 | 2007-12-16 | Astrazeneca Ab | Novel compounds |
JP5155171B2 (ja) | 2005-10-06 | 2013-02-27 | アストラゼネカ・アクチエボラーグ | 新規化合物 |
WO2007052023A2 (en) | 2005-11-05 | 2007-05-10 | Astrazeneca Ab | Novel compounds |
ATE545637T1 (de) | 2005-12-15 | 2012-03-15 | Astrazeneca Ab | Substituierte diphenylether, -amine, -sulfide und methane zur behandlung von atemwegserkrankungen |
UA100983C2 (ru) * | 2007-07-05 | 2013-02-25 | Астразенека Аб | Бифенилоксипропановая кислота как модулятор crth2 и интермедиаты |
-
2004
- 2004-07-08 GB GBGB0415320.1A patent/GB0415320D0/en not_active Ceased
-
2005
- 2005-07-06 US US11/571,707 patent/US8022248B2/en not_active Expired - Fee Related
- 2005-07-06 UY UY29004A patent/UY29004A1/es unknown
- 2005-07-06 JP JP2007519879A patent/JP4869225B2/ja not_active Expired - Fee Related
- 2005-07-06 WO PCT/GB2005/002650 patent/WO2006005909A1/en active Application Filing
- 2005-07-06 ES ES05758184.5T patent/ES2442677T3/es active Active
- 2005-07-06 EP EP05758184.5A patent/EP1765768B1/en not_active Not-in-force
- 2005-07-06 CN CN200580030192XA patent/CN101014564B/zh not_active Withdrawn - After Issue
- 2005-07-06 CN CN201210033516.7A patent/CN102557971B/zh not_active Expired - Fee Related
- 2005-07-08 AR ARP050102853A patent/AR051921A1/es unknown
- 2005-07-08 TW TW094123268A patent/TW200612892A/zh unknown
-
2012
- 2012-12-07 HK HK12112649.6A patent/HK1171736A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP1765768A1 (en) | 2007-03-28 |
US8022248B2 (en) | 2011-09-20 |
US20080114002A1 (en) | 2008-05-15 |
EP1765768B1 (en) | 2013-11-06 |
WO2006005909A1 (en) | 2006-01-19 |
ES2442677T3 (es) | 2014-02-12 |
HK1171736A1 (en) | 2013-04-05 |
JP4869225B2 (ja) | 2012-02-08 |
CN101014564B (zh) | 2012-05-09 |
CN102557971B (zh) | 2015-06-17 |
CN101014564A (zh) | 2007-08-08 |
GB0415320D0 (en) | 2004-08-11 |
UY29004A1 (es) | 2006-02-24 |
CN102557971A (zh) | 2012-07-11 |
TW200612892A (en) | 2006-05-01 |
JP2008505874A (ja) | 2008-02-28 |
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