AR068503A1 - Derivados de amidas sustituidas, composicion farmaceutica y usos. - Google Patents
Derivados de amidas sustituidas, composicion farmaceutica y usos.Info
- Publication number
- AR068503A1 AR068503A1 ARP080104094A ARP080104094A AR068503A1 AR 068503 A1 AR068503 A1 AR 068503A1 AR P080104094 A ARP080104094 A AR P080104094A AR P080104094 A ARP080104094 A AR P080104094A AR 068503 A1 AR068503 A1 AR 068503A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- cyclic ring
- och3
- formula
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
Abstract
Se describen composiciones farmacéuticas que comprenden al menos un compuesto de Formula 1, junto con al menos un vehículo farmacéuticamente aceptable seleccionado de portadores, adyuvantes y excipientes. Se describen métodos para tratar pacientes que padecen ciertas enfermedades que responden a la inhibicion de actividad de Btk y/o actividad de célula B. Se describen métodos para determinar la presencia de Btk en una muestra. Reivindicacion 1: Un compuesto de formula (1), o una sal o solvato farmacéuticamente aceptable del mismo, caracterizado porque X es N o CR2; Y es N o CR3'; Z es N o CR3, siempre que solamente uno de X, Y y Z sea N a la vez; W es N o CH; V es CH o N; siempre que uno de W y V deban ser N, y W y V no sean ambos N; R1 se selecciona del grupo de formulas (2), R2 se selecciona de H, CH3, F, CI, CN y OCH3; R2' se selecciona de H y F; R3 se selecciona de H, CH3, F, Cl, CN y OCH3; R3' se selecciona de H, CH3, F, CI, CN y OCH3; R4 es como formula (3), m es 0 o 1, n es 0 o 1; R5 es H o alquilo C1-6 opcionalmente sustituido con OH; R6 es H o alquilo C1-6; o R5 y R6 se toman opcionalmente junto con el átomo de nitrogeno al cual están unidos para formar un anillo cíclico de 4 a 6 miembros que tiene 0-1 N, S u O adicional, en donde el nitrogeno de anillo adicional opcional está opcionalmente sustituido con alquilo C1-3 y dicho anillo cíclico está opcionalmente sustituido con OH; R7 es H o alquilo C1-6 en donde dicho alquilo está opcionalmente sustituido con uno o más sustituyentes seleccionados de OH y O(alquilo C1-4); o R6 y R7 se toman opcionalmente junto con el grupo -N(R5)C(R9)(CH2)nC(=O)N(R8)- a través de los respectivos átomos de nitrogeno a los cuales están directamente unidos para formar un anillo cíclico de 6 miembros; R8 es H o alquilo C1-6; o R7 y R8 se toman opcionalmente junto con el átomo de nitrogeno al cual están unidos para formar un anillo cíclico de 4 a 6 miembros que tiene 0-1 N, S u O adicional, en donde el nitrogeno de anillo adicional opcional está opcionalmente sustituido con alquilo C1-3 y dicho anillo cíclico está opcionalmente sustituido con OH; R9 es H o CH3; y R10 es H o alquilo C1-3 opcionalmente sustituido con N(R9)2; y R11 es H o CH3.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97399507P | 2007-09-20 | 2007-09-20 | |
US5077708P | 2008-05-06 | 2008-05-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR068503A1 true AR068503A1 (es) | 2009-11-18 |
Family
ID=40377565
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080104094A AR068503A1 (es) | 2007-09-20 | 2008-09-19 | Derivados de amidas sustituidas, composicion farmaceutica y usos. |
Country Status (14)
Country | Link |
---|---|
US (2) | US7884108B2 (es) |
EP (1) | EP2188267B1 (es) |
JP (1) | JP5485894B2 (es) |
KR (1) | KR20100072032A (es) |
CN (1) | CN101861307B (es) |
AR (1) | AR068503A1 (es) |
AU (1) | AU2008302099B2 (es) |
BR (1) | BRPI0817130A2 (es) |
CA (1) | CA2700443A1 (es) |
CL (1) | CL2008002793A1 (es) |
PE (1) | PE20091201A1 (es) |
RU (1) | RU2470923C2 (es) |
TW (1) | TWI423966B (es) |
WO (1) | WO2009039397A2 (es) |
Families Citing this family (76)
Publication number | Priority date | Publication date | Assignee | Title |
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AR063706A1 (es) * | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden. |
US7838523B2 (en) * | 2006-09-11 | 2010-11-23 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
US7683064B2 (en) | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
UA103319C2 (en) | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
CA2723237A1 (en) * | 2008-05-06 | 2009-11-12 | Peter A. Blomgren | Substituted amides, method of making, and use as btk inhibitors |
BRPI0914657A2 (pt) | 2008-06-24 | 2019-09-24 | F Hoffmann La Roche | piridin-2-onae piridazin-3-onas substituídas |
ES2420854T3 (es) | 2008-07-02 | 2013-08-27 | F. Hoffmann-La Roche Ag | Nuevas fenilpirazinonas como inhibidores de quinasas |
JP5832524B2 (ja) | 2010-05-07 | 2015-12-16 | ジーアイリード コネチカット インコーポレーテッドGilead Connecticut,Inc. | ピリドン及びアザピリドン化合物、並びにそれらの使用方法 |
CN106220614B (zh) * | 2010-09-01 | 2019-07-16 | 吉利德康涅狄格有限公司 | 吡啶酮/吡嗪酮、其制备方法及使用方法 |
EP2773640B1 (en) | 2011-11-03 | 2015-08-19 | Hoffmann-La Roche AG | Bicyclic piperazine compounds |
BR112014010439A2 (pt) | 2011-11-03 | 2017-04-18 | F Hoffmann - La Roche Ag | compostos, composição farmacêutica, processo de produção, método de tratamento de uma doença ou distúrbio, métodos, kit e uso de uma composição farmacêutica |
UA111756C2 (uk) * | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона |
TWI553004B (zh) * | 2011-11-03 | 2016-10-11 | 建南德克公司 | 8-氟基呔-1(2h)-酮化合物 |
WO2013097052A1 (en) | 2011-12-30 | 2013-07-04 | Abbott Laboratories | Bromodomain inhibitors |
JP6248048B2 (ja) | 2012-01-09 | 2017-12-13 | エックス−アールエックス,インコーポレーテッド | キナーゼ阻害活性を有するトリプトリン誘導体及びその使用 |
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CA2903288C (en) * | 2013-03-15 | 2021-09-21 | Deciphera Pharmaceuticals, Llc | N-acyl-n'-(pyridin-2-yl) ureas and analogs exhibiting anti-cancer and anti-proliferative activities |
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US9789072B2 (en) * | 2013-06-19 | 2017-10-17 | Som Innovation Biotech, S.L. | Therapeutic agents for use in the propylaxis and/or treatment of hyperkinetic movement disorders |
EP3016943B1 (en) | 2013-07-03 | 2019-08-21 | F. Hoffmann-La Roche AG | Heteroaryl pyridone and aza-pyridone amide compounds |
MX2016001304A (es) | 2013-07-30 | 2016-04-07 | Gilead Connecticut Inc | Polimorfo de inhibidores de syk. |
MD4684B1 (ro) | 2013-07-30 | 2020-03-31 | Gilead Connecticut INc. | Formulări pe bază de imidazopirazine în calitate de inhibitori SYK |
PL3702373T3 (pl) | 2013-09-13 | 2022-12-05 | Beigene Switzerland Gmbh | Przeciwciała anty-PD1 i ich zastosowanie jako środki terapeutyczne i diagnostyczne |
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AR042586A1 (es) * | 2001-02-15 | 2005-06-29 | Sugen Inc | 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa |
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JP2008533032A (ja) | 2005-03-10 | 2008-08-21 | シージーアイ ファーマシューティカルズ,インコーポレイティド | 或る種の置換アミド、その製造方法及び使用方法 |
AR063706A1 (es) * | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden. |
EP2270200A3 (en) * | 2006-09-11 | 2011-07-13 | CGI Pharmaceuticals, Inc. | Kinase inhibitors, and methods of using and identifying kinase inhibitors |
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2008
- 2008-09-17 CL CL2008002793A patent/CL2008002793A1/es unknown
- 2008-09-19 RU RU2010115574/04A patent/RU2470923C2/ru active
- 2008-09-19 KR KR1020107008468A patent/KR20100072032A/ko not_active Application Discontinuation
- 2008-09-19 WO PCT/US2008/077054 patent/WO2009039397A2/en active Application Filing
- 2008-09-19 PE PE2008001640A patent/PE20091201A1/es not_active Application Discontinuation
- 2008-09-19 AR ARP080104094A patent/AR068503A1/es unknown
- 2008-09-19 US US12/234,281 patent/US7884108B2/en active Active
- 2008-09-19 BR BRPI0817130 patent/BRPI0817130A2/pt not_active Application Discontinuation
- 2008-09-19 TW TW097136216A patent/TWI423966B/zh not_active IP Right Cessation
- 2008-09-19 AU AU2008302099A patent/AU2008302099B2/en not_active Ceased
- 2008-09-19 EP EP08832237.5A patent/EP2188267B1/en active Active
- 2008-09-19 CA CA2700443A patent/CA2700443A1/en not_active Abandoned
- 2008-09-19 JP JP2010526003A patent/JP5485894B2/ja active Active
- 2008-09-19 CN CN2008801161200A patent/CN101861307B/zh active Active
-
2010
- 2010-11-04 US US12/939,518 patent/US8247550B2/en active Active
Also Published As
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US7884108B2 (en) | 2011-02-08 |
BRPI0817130A2 (pt) | 2015-03-31 |
AU2008302099B2 (en) | 2013-03-28 |
EP2188267A2 (en) | 2010-05-26 |
EP2188267B1 (en) | 2016-08-03 |
WO2009039397A2 (en) | 2009-03-26 |
CN101861307B (zh) | 2013-05-01 |
US8247550B2 (en) | 2012-08-21 |
RU2010115574A (ru) | 2011-10-27 |
RU2470923C2 (ru) | 2012-12-27 |
US20110059944A1 (en) | 2011-03-10 |
CN101861307A (zh) | 2010-10-13 |
KR20100072032A (ko) | 2010-06-29 |
CA2700443A1 (en) | 2009-03-26 |
WO2009039397A3 (en) | 2009-05-22 |
US20090082330A1 (en) | 2009-03-26 |
JP5485894B2 (ja) | 2014-05-07 |
TWI423966B (zh) | 2014-01-21 |
PE20091201A1 (es) | 2009-09-13 |
TW200914446A (en) | 2009-04-01 |
JP2010540452A (ja) | 2010-12-24 |
CL2008002793A1 (es) | 2009-09-04 |
AU2008302099A1 (en) | 2009-03-26 |
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