AR034203A1 - Derivados de 1-aril- o 1-alquilsulfonilbenzazol como ligandos de 5-hidroxitriptamina-6, un metodo para su preparacion, composicion farmaceutica y el uso de los mismos para la fabricacion de un medicamento - Google Patents

Derivados de 1-aril- o 1-alquilsulfonilbenzazol como ligandos de 5-hidroxitriptamina-6, un metodo para su preparacion, composicion farmaceutica y el uso de los mismos para la fabricacion de un medicamento

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Publication number
AR034203A1
AR034203A1 ARP020100210A ARP020100210A AR034203A1 AR 034203 A1 AR034203 A1 AR 034203A1 AR P020100210 A ARP020100210 A AR P020100210A AR P020100210 A ARP020100210 A AR P020100210A AR 034203 A1 AR034203 A1 AR 034203A1
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Argentina
Prior art keywords
alkyl
optionally substituted
aryl
independently
heteroaryl group
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ARP020100210A
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Wyeth Corp
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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Indole Compounds (AREA)

Abstract

Derivados de 1-aril- ó 1-alquilsulfonilbenzazol, que comprenden un compuesto de fórmula (1), en donde: W es SO2, CO, CONH, CSNH ó CH2; X es CR7 ó N; Y es CR8 ó N, con la condición que cuando X es N, entonces Y debe ser CR8; Z es O, SOp ó NR9; R1 y R2 son cada uno de manera independiente H o alquilo C1-6; n es un entero de 2, 3, ó 4; R3 y R4 son cada uno de manera independiente H, CNR10NR11R12 o un grupo alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloheteroalquilo, arilo o heteroarilo, cada uno opcionalmente sustituido, o R3 y R4 pueden tomarse junto con el átomo al cual están unidos, para formar un anillo de 3 a 6 miembros, opcionalmente sustituido, que contiene opcionalmente un heteroátomo adicional seleccionado entre O, N ó S; R5 es H, halógeno, CN, OR13, CO2R14, CONR15R16, CNR17NR18R19, SO2NR20R21, SOpR22, o un grupo alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloheteroalquilo, fenilo o heteroarilo, cada uno opcionalmente sustituido; m es un entero de 1, 2, ó 3; p y q son cada uno de manera independiente 0 ó un entero de 1 ó 2; R6 es un grupo alquilo C1-6 opcionalmente sustituido, arilo o heteroarilo; R7 y R8 son cada uno de manera independiente H, halógeno, o un grupo alquilo C1-6, arilo, heteroarilo, o alcoxi C1-6, cada uno opcionalmente sustituido; R9 es H, o un grupo alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloheteroalquilo, arilo o heteroarilo, cada uno opcionalmente sustituido; R10, R11, R12, R15, R16, R17, R18 y R19 son cada uno de manera independiente H, o alquilo C1-4; R13 es H, COR23, o un grupo alquilo C1-6, alquenilo C2-6, alquinilo C2-6, arilo o heteroarilo, cada uno opcionalmente sustituido; R14 es H, o un grupo alquilo C1-6, arilo o heteroarilo, cada uno opcionalmente sustituido; R20 y R21 son cada uno de manera independiente H o un grupo alquilo C1-6, arilo o heteroarilo, cada uno opcionalmente sustituido; y R22 y R23 son cada uno de manera independiente un grupo alquilo C1-6 opcionalmente sustituido, arilo o heteroarilo; o una sal farmacéuticamente aceptable del mismo; un método para su preparación, una composición farmacéutica y el uso del mismo para el tratamiento terapéutico de desórdenes relacionados con, o afectados por el receptor de 5-HT6.
ARP020100210A 2001-01-23 2002-01-22 Derivados de 1-aril- o 1-alquilsulfonilbenzazol como ligandos de 5-hidroxitriptamina-6, un metodo para su preparacion, composicion farmaceutica y el uso de los mismos para la fabricacion de un medicamento AR034203A1 (es)

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US26342501P 2001-01-23 2001-01-23

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AR034203A1 true AR034203A1 (es) 2004-02-04

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Country Status (23)

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US (4) US6509357B1 (es)
EP (1) EP1353904B9 (es)
JP (1) JP4208573B2 (es)
KR (1) KR20030068591A (es)
CN (1) CN1273450C (es)
AR (1) AR034203A1 (es)
AT (1) ATE312078T1 (es)
AU (1) AU2002251811B2 (es)
BR (1) BR0206633A (es)
CA (1) CA2435566A1 (es)
DE (1) DE60207815T2 (es)
DK (1) DK1353904T3 (es)
EA (1) EA006057B1 (es)
ES (1) ES2250638T3 (es)
HU (1) HUP0401009A3 (es)
IL (1) IL157059A0 (es)
MX (1) MXPA03006479A (es)
NO (1) NO20033300L (es)
NZ (1) NZ527051A (es)
PL (1) PL364568A1 (es)
TW (1) TW593278B (es)
WO (1) WO2002059088A1 (es)
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112847099A (zh) * 2021-03-08 2021-05-28 王佳丽 一种有效调节进给量实现自动切割的砂轮切割机

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1293072C (zh) * 2001-04-20 2007-01-03 惠氏公司 作为5-羟色胺-6配体的杂环基氧基-、-硫代-和-氨基吲哚衍生物
AU2002309585B2 (en) * 2001-04-20 2008-01-31 Wyeth Heterocyclylalkoxy-, -alkylthio- and -alkylaminobenzazole derivatives as 5-hydroxytryptamine-6 ligands
JP4187642B2 (ja) * 2001-06-07 2008-11-26 エフ.ホフマン−ラ ロシュ アーゲー 5−ht6受容体親和性を有する新規インドール誘導体
WO2003068740A1 (en) * 2002-02-14 2003-08-21 Wyeth Pyrrolylalkylidene-hydrazinecarboximidamide derivatives as 5-hydroxytryptamine-6 ligands
CN1293053C (zh) 2002-06-05 2007-01-03 弗·哈夫曼-拉罗切有限公司 作为5-ht6-受体调节剂用于治疗cns-病症的1-磺酰基-4-氨基烷氧基吲哚衍生物
US20060167046A1 (en) * 2002-09-18 2006-07-27 Eli Lilly And Company Patent Division Histamine h3 receptor antagonists, preparation and therapeutic uses
ES2291722T3 (es) * 2002-12-03 2008-03-01 Hoffmann La Roche Aminoalcoxiindoles como ligandos 5-ht6-receptores para el tratamiento de transtornos del snc.
BRPI0407253A (pt) * 2003-02-14 2006-01-31 Wyeth Corp Heterociclil-3-sulfonilindazóis como ligandos 5-hidroxitriptamina-6 processo de preparação dos mesmos, seus usos na preparação de uma composição farmacêutica e composição farmacêutica compreendendo os referidos compostos
US7135575B2 (en) 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
SE0302760D0 (sv) * 2003-10-20 2003-10-20 Biovitrum Ab New compounds
RU2006134022A (ru) 2004-02-27 2008-04-10 Ф.Хоффманн-Ля Рош Аг (Ch) Производные индазола и содержащие их фармацевтические композиции
CA2558109A1 (en) 2004-02-27 2005-09-15 F. Hoffmann-La Roche Ag Heteroaryl-fused pyrazolo derivatives
CA2557575A1 (en) 2004-02-27 2005-09-15 F. Hoffmann-La Roche Ag Fused derivatives of pyrazole
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
CA2523026C (en) * 2004-10-08 2014-03-25 I-Con Systems, Inc. Diaphragm valve with mechanical pressure relief
ATE417830T1 (de) 2004-11-02 2009-01-15 Pfizer Sulfonylbenzimidazolderivate
US7538113B2 (en) 2005-02-18 2009-05-26 Wyeth 4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
US7534796B2 (en) 2005-02-18 2009-05-19 Wyeth Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor
US7582634B2 (en) 2005-02-18 2009-09-01 Wyeth 7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
US7531542B2 (en) 2005-05-18 2009-05-12 Wyeth Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor
US7582636B2 (en) 2005-05-26 2009-09-01 Wyeth Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor
NZ565872A (en) * 2005-08-15 2011-06-30 Wyeth Corp Substituted-3-sulfonylindazole derivatives as 5-hydroxytryptamine-6 ligands
WO2007023111A2 (en) 2005-08-25 2007-03-01 F. Hoffmann-La Roche Ag P38 map kinase inhibitors and methods for using the same
PE20070427A1 (es) 2005-08-30 2007-04-21 Novartis Ag Compuestos derivados de benzimidazoles sustituidos como inhibidores de tirosina quinasas
SI1981851T1 (sl) 2006-01-31 2012-05-31 Array Biopharma Inc Kinazni inhibitorji in postopki za njihovo uporabo
EP2001865A1 (en) * 2006-04-05 2008-12-17 Wyeth a Corporation of the State of Delaware Sulfonyl-3-heterocyclylindazole derivatives as 5-hydroxytryptamine-6 ligands
WO2007120596A1 (en) * 2006-04-12 2007-10-25 Wyeth DIHYDRO[1,4]DIOXINO[2,3-e]INDAZOLE DERIVATIVES AS 5-HYDROXYTRYPTAMINE-6 LIGANDS
JP2009538910A (ja) * 2006-06-01 2009-11-12 ワイス 5−ヒドロキシトリプタミン−6リガンドとしての1−スルホニルインダゾリルアミン誘導体および1−スルホニルインダゾリルアミド誘導体
WO2009006267A2 (en) * 2007-06-28 2009-01-08 Wyeth N'-(2-halobenzylidene)sulfonylhydrazides as intermediates in the manufacture of arylsulfonylindazoles
EP3170813B1 (en) 2010-10-06 2018-12-12 GlaxoSmithKline LLC Benzimidazole derivatives as pi3 kinase inhibitors
CN104725295B (zh) 2013-12-20 2019-05-24 广东东阳光药业有限公司 芳杂环类衍生物及其在药物上的应用
CA2953004C (en) 2014-07-08 2023-02-21 Sunshine Lake Pharma Co., Ltd. Aromatic heterocyclic derivatives and pharmaceutical applications thereof
AU2017336074A1 (en) 2016-09-30 2019-03-28 Epizyme, Inc. Substituted fused bi- or tri- heterocyclic compounds as ehmt2 inhibitors
CN118021814A (zh) 2017-04-21 2024-05-14 Epizyme股份有限公司 用ehmt2抑制剂进行的组合疗法
IL274444B2 (en) 2017-11-06 2024-06-01 Rapt Therapeutics Inc Chemokine receptor modulators for the treatment of Epstein-Barr virus-positive cancer

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2905877A1 (de) * 1979-02-16 1980-08-28 Boehringer Mannheim Gmbh Neue aminopropanolderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
US5889022A (en) 1993-12-21 1999-03-30 Smithkline Beecham, P.L.C. Indole, indoline and quinoline derivatives with 5HT1D (anti-depressive) activity
GB9416972D0 (en) * 1994-08-23 1994-10-12 Smithkline Beecham Plc Carbon side chain/indole/indolene
CA2242579A1 (en) * 1996-01-09 1997-07-17 Eli Lilly And Company Benzimidzolyl neuropeptide y receptor antagonists
GB9600344D0 (en) 1996-01-09 1996-03-13 Lilly Co Eli Benzimidzolyl neuropeptide y receptor antagonists
AU2139097A (en) * 1996-03-01 1997-09-16 Eli Lilly And Company Methods of treating or preventing sleep apnea
WO1998030548A1 (en) 1997-01-13 1998-07-16 Yamanouchi Pharmaceutical Co., Ltd. 5-HT2c RECEPTOR AGONISTS AND AMINOALKYLINDAZOLE DERIVATIVES
US6127380A (en) 1997-02-18 2000-10-03 American Home Products Corporation 4-aminoalkoxy-1H-benzoimidazoles
US5872144A (en) 1997-02-18 1999-02-16 American Home Products Corporation 4-aminoethoxyindazole derivatives
EA200001007A1 (ru) 1998-03-31 2001-04-23 Дюпон Фармасьютикалз Компани Фармацевтические препараты для визуализации ангиогенных расстройств
GB9820113D0 (en) * 1998-09-15 1998-11-11 Merck Sharp & Dohme Therapeutic agents
ATE362772T1 (de) * 1998-12-18 2007-06-15 Bristol Myers Squibb Pharma Co Vitronektin rezeptor antagonist arzneimitteln oder diagnostika
GB9902452D0 (en) * 1999-02-05 1999-03-24 Zeneca Ltd Chemical compounds
GB0019950D0 (en) * 2000-08-12 2000-09-27 Smithkline Beecham Plc Compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112847099A (zh) * 2021-03-08 2021-05-28 王佳丽 一种有效调节进给量实现自动切割的砂轮切割机

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EP1353904B9 (en) 2006-05-03
IL157059A0 (en) 2004-02-08
JP4208573B2 (ja) 2009-01-14
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NO20033300L (no) 2003-09-03
CN1498209A (zh) 2004-05-19
ES2250638T3 (es) 2006-04-16
CA2435566A1 (en) 2002-08-01
DE60207815D1 (de) 2006-01-12
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DK1353904T3 (da) 2006-02-20
WO2002059088A1 (en) 2002-08-01
AU2002251811B2 (en) 2007-06-21
TW593278B (en) 2004-06-21
US20040092564A1 (en) 2004-05-13
ATE312078T1 (de) 2005-12-15
EA200300829A1 (ru) 2003-12-25
JP2004521116A (ja) 2004-07-15
US6710069B2 (en) 2004-03-23
US6509357B1 (en) 2003-01-21
US20030149018A1 (en) 2003-08-07
DE60207815T2 (de) 2006-08-24
KR20030068591A (ko) 2003-08-21
EP1353904A1 (en) 2003-10-22

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