AP2516A - 2-Pyridine carboxamide derivatives as sodium channel modulators - Google Patents

2-Pyridine carboxamide derivatives as sodium channel modulators

Info

Publication number
AP2516A
AP2516A AP2009005009A AP2009005009A AP2516A AP 2516 A AP2516 A AP 2516A AP 2009005009 A AP2009005009 A AP 2009005009A AP 2009005009 A AP2009005009 A AP 2009005009A AP 2516 A AP2516 A AP 2516A
Authority
AP
ARIPO
Prior art keywords
sodium channel
channel modulators
carboxamide derivatives
pyridine carboxamide
pyridine
Prior art date
Application number
AP2009005009A
Other languages
English (en)
Other versions
AP2009005009A0 (en
Inventor
Sharanjeet Kaur Bagal
Stephen Martin Denton
Karl Richard Gibson
Original Assignee
Pfizer Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of AP2009005009A0 publication Critical patent/AP2009005009A0/xx
Application granted granted Critical
Publication of AP2516A publication Critical patent/AP2516A/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—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
    • 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
    • C07D213/60—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 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AP2009005009A 2007-05-03 2008-04-21 2-Pyridine carboxamide derivatives as sodium channel modulators AP2516A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US91574507P 2007-05-03 2007-05-03
US95753607P 2007-08-23 2007-08-23
PCT/IB2008/001050 WO2008135826A2 (fr) 2007-05-03 2008-04-21 Dérivés de la pyridine

Publications (2)

Publication Number Publication Date
AP2009005009A0 AP2009005009A0 (en) 2009-10-31
AP2516A true AP2516A (en) 2012-11-26

Family

ID=39855225

Family Applications (1)

Application Number Title Priority Date Filing Date
AP2009005009A AP2516A (en) 2007-05-03 2008-04-21 2-Pyridine carboxamide derivatives as sodium channel modulators

Country Status (33)

Country Link
US (1) US8134007B2 (fr)
EP (1) EP2183241B1 (fr)
JP (1) JP4657384B2 (fr)
KR (1) KR20100007956A (fr)
CN (1) CN101675040A (fr)
AP (1) AP2516A (fr)
AR (1) AR070636A1 (fr)
AU (1) AU2008247102B2 (fr)
BR (1) BRPI0810202A2 (fr)
CA (1) CA2684105C (fr)
CL (1) CL2008001268A1 (fr)
CO (1) CO6251367A2 (fr)
CR (1) CR11061A (fr)
CU (1) CU23846B1 (fr)
DO (1) DOP2009000254A (fr)
EA (1) EA015952B1 (fr)
EC (1) ECSP099710A (fr)
ES (1) ES2398606T3 (fr)
GE (1) GEP20125379B (fr)
GT (1) GT200900280A (fr)
IL (1) IL201569A0 (fr)
MA (1) MA31419B1 (fr)
MX (1) MX2009011816A (fr)
NI (1) NI200900192A (fr)
NZ (1) NZ581614A (fr)
PA (1) PA8779201A1 (fr)
PE (1) PE20090730A1 (fr)
SV (1) SV2009003400A (fr)
TN (1) TN2009000450A1 (fr)
TW (1) TWI375675B (fr)
UY (1) UY31063A1 (fr)
WO (1) WO2008135826A2 (fr)
ZA (1) ZA200907609B (fr)

Families Citing this family (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104478875B (zh) 2008-08-06 2017-04-12 麦迪韦逊科技有限公司 聚(adp‑核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂
PE20120008A1 (es) 2009-01-12 2012-01-24 Icagen Inc Derivados de fenoxi bencenosulfonamida
CN101638352B (zh) * 2009-08-14 2011-08-31 大连理工大学 一种芳基取代的氮杂环化合物的制备方法
WO2011077313A1 (fr) 2009-12-22 2011-06-30 Pfizer Inc. Pipéridinecarboxamides en tant qu'inhibiteurs de mpges - 1
TW201139406A (en) * 2010-01-14 2011-11-16 Glaxo Group Ltd Voltage-gated sodium channel blockers
CN101768036B (zh) * 2010-01-23 2013-05-08 大连理工大学 一种在醇溶剂中制备芳基取代的氮杂芳环化合物的方法
EP2531033A4 (fr) 2010-02-03 2013-07-31 Biomarin Pharm Inc Inhibiteurs à base de dihydropyridophtalazinone de la poly(adp-ribose) polymérase (parp) utilisables dans le cadre du traitement de maladies associées à un déficit en pten
KR101826652B1 (ko) 2010-02-08 2018-02-07 메디베이션 테크놀로지즈, 인크. 디히드로피리도프탈라지논 유도체의 합성 방법
WO2011104649A1 (fr) 2010-02-25 2011-09-01 Pfizer Limited Analogues peptidiques
ES2526675T3 (es) 2010-07-09 2015-01-14 Pfizer Limited N-sulfonilbenzamidas como inhibidores de los canales de sodio dependientes de voltaje
CA2804593C (fr) 2010-07-09 2015-11-24 Pfizer Limited Derives de biphenyloxybenzensulphonamide utiles en tant qu'inhibiteurs du canal sodique
JP2013532185A (ja) 2010-07-12 2013-08-15 ファイザー・リミテッド 化合物
JP2013532184A (ja) 2010-07-12 2013-08-15 ファイザー・リミテッド 電位開口型ナトリウムチャネル阻害剤として有用なｎ−スルホニルベンズアミド誘導体
JP2013531030A (ja) 2010-07-12 2013-08-01 ファイザー・リミテッド 電位開口型ナトリウムチャネルの阻害剤としてのｎ−スルホニルベンズアミド
CA2804351A1 (fr) 2010-07-12 2012-01-19 Pfizer Limited Composes chimiques
JP2013536165A (ja) 2010-07-12 2013-09-19 ファイザー・リミテッド 痛みの処置のためのｎａｖ１．７阻害薬としてのスルホンアミド誘導体
JP2013531687A (ja) 2010-07-16 2013-08-08 パーデュー、ファーマ、リミテッド、パートナーシップ ナトリウムチャネル遮断剤としてのピリジン化合物
CN103249721B (zh) * 2010-10-18 2016-10-12 拉夸里亚创药株式会社 作为ttx-s阻滞剂的芳胺衍生物
KR20190120458A (ko) 2010-10-21 2019-10-23 메디베이션 테크놀로지즈 엘엘씨 결정질의 (8s,9r)-5-플루오로-8-(4-플루오로페닐)-9-(1-메틸-1h-1,2,4-트리아졸-5-일)-8,9-디하이드로-2h-피리도[4,3,2-de]프탈라진-3(7h)-온 토실레이트 염
WO2012095781A1 (fr) 2011-01-13 2012-07-19 Pfizer Limited Dérivés d'indazole comme inhibiteurs des canaux sodiques
WO2012120398A1 (fr) 2011-03-04 2012-09-13 Pfizer Limited Dérivés de carboxamide substitués par aryle en tant que modulateurs de trpm8
PH12013502020A1 (en) 2011-04-05 2018-04-11 Pfizer Ltd Pyrrolo [2,3-d] pyrimidine derivatives as inhibitors of tropomyosin-related kinases
EP2731959B1 (fr) 2011-07-13 2016-02-03 Pfizer Limited Analogues d'encéphaline
WO2013054185A1 (fr) 2011-10-13 2013-04-18 Pfizer, Inc. Dérivés de pyrimidine et de pyridine utiles en thérapie
CA2850925C (fr) 2011-10-26 2017-01-10 Pfizer Limited Derives de (4-phenylimidazol-2-yl) ethylamine utiles comme modulateurs de canal de sodium
WO2013061297A1 (fr) 2011-10-28 2013-05-02 Pfizer Limited Dérivés de pyridazine utiles en thérapie
WO2013088315A1 (fr) 2011-12-15 2013-06-20 Pfizer Limited Dérivés de sulfonamide
WO2013093688A1 (fr) 2011-12-19 2013-06-27 Pfizer Limited Dérivés sulfonamides et leur utilisation en tant qu'inhibiteurs de vgsc
US20150291514A1 (en) 2012-01-04 2015-10-15 Pfizer Limted N-Aminosulfonyl Benzamides
JP6002785B2 (ja) 2012-02-03 2016-10-05 ファイザー・インク ナトリウムチャネルモジュレーターとしてのベンゾイミダゾールおよびイミダゾピリジン誘導体
WO2013136170A1 (fr) 2012-03-16 2013-09-19 Purdue Pharma L.P. Pyridines substituées en tant que bloqueurs des canaux sodiques
IN2014MN01982A (fr) * 2012-04-25 2015-07-10 Raqualia Pharma Inc
US20150218172A1 (en) 2012-10-04 2015-08-06 Pfizer Limited Pyrrolo[2,3-D]Pyrimidine Tropomyosin-Related Kinase Inhibitors
JP2015531395A (ja) 2012-10-04 2015-11-02 ファイザー・リミテッドＰｆｉｚｅｒ Ｌｉｍｉｔｅｄ ピロロ［３，２−ｃ］ピリジントロポミオシン関連キナーゼ阻害剤
JP2015531393A (ja) 2012-10-04 2015-11-02 ファイザー・リミテッドＰｆｉｚｅｒ Ｌｉｍｉｔｅｄ トロポミオシン関連キナーゼ阻害剤
ES2661585T3 (es) * 2012-10-31 2018-04-02 Raqualia Pharma Inc Derivados de pirazolopiridina como bloqueadores de TTX-S
EP2935257B1 (fr) 2012-12-20 2018-02-07 Purdue Pharma LP Sulfonamides cycliques en tant que bloquants des canaux sodiques
RS56015B1 (sr) 2013-01-31 2017-09-29 Vertex Pharma Piridon amidi kao modulatori natrijumovih kanala
RU2683788C2 (ru) 2013-01-31 2019-04-02 Вертекс Фармасьютикалз Инкорпорейтед Амиды хинолина и хиназолина, полезные в качестве модуляторов натриевых каналов
MX374512B (es) 2013-03-08 2025-03-06 Amgen Inc Compuestos de 1,3-oxazin-2-amina fusionados con ciclopropilo perfluorado como inhibidores de beta-secretasa y métodos de uso.
UA119147C2 (uk) 2013-07-19 2019-05-10 Вертекс Фармасьютікалз Інкорпорейтед Сульфонаміди як модулятори натрієвих каналів
JP6320523B2 (ja) 2013-10-15 2018-05-09 ヤンセン ファーマシューティカ エヌ．ベー． ＲＯＲγＴの第二級アルコールキノリニルモジュレータ
CN105916846A (zh) * 2013-11-07 2016-08-31 麦迪韦逊科技有限公司 用于合成经保护的n-烷基三唑甲醛的三唑中间体
CA2931550C (fr) 2013-12-13 2023-09-26 Vertex Pharmaceuticals Incorporated Promedicaments d'amides de pyridone utiles en tant que modulateurs des canaux sodiques
US10730866B2 (en) 2014-04-07 2020-08-04 Purdue Pharma L.P. Indole derivatives and use thereof
JP2017526706A (ja) * 2014-09-10 2017-09-14 エピザイム，インコーポレイティド イソオキサゾールカルボキサミド化合物
CN106674264A (zh) * 2016-12-20 2017-05-17 苏州汉德创宏生化科技有限公司 (2,2,2‑三氟乙氧基)苯硼酸类化合物的合成方法
EP3625214B1 (fr) 2017-05-16 2022-07-06 Vertex Pharmaceuticals Incorporated Amides de pyridone deutérés et leurs promédicaments utilisés en tant que modulateurs de canaux sodiques
AU2018300150A1 (en) 2017-07-11 2020-01-30 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
BR112020003116A2 (pt) * 2017-08-17 2020-08-04 Ikena Oncology, Inc. inibidores de ahr e usos dos mesmos
CA3086668A1 (fr) * 2018-02-05 2019-08-08 Universite De Strasbourg Composes et compositions pour le traitement de la douleur
US11529337B2 (en) 2018-02-12 2022-12-20 Vertex Pharmaceuticals Incorporated Method of treating pain
CN109053434A (zh) * 2018-07-18 2018-12-21 上海华堇生物技术有限责任公司 一种2,4-二甲氧基苯甲酰氯的新制备方法
CN108794328A (zh) * 2018-08-03 2018-11-13 上海华堇生物技术有限责任公司 3,4-二甲氧基苯甲酰氯的制备方法
US12440481B2 (en) 2019-01-10 2025-10-14 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
WO2020146682A1 (fr) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides utilisés en tant que modulateurs de canaux sodiques
WO2020176763A1 (fr) 2019-02-27 2020-09-03 Vertex Pharmaceuticals Incorporated Forme posologique comprenant un promédicament inhibiteur de canal sodique na 1,8
WO2020219867A1 (fr) 2019-04-25 2020-10-29 Vertex Pharmaceuticals Incorporated Compositions de co-cristaux d'amide de pyridone pour le traitement de la douleur
KR20220044721A (ko) 2019-08-06 2022-04-11 도메인 테라퓨틱스 신경펩타이드 ff 수용체 길항제로서의 5-헤테로아릴-피리딘-2-아민 화합물
BR112022010924A2 (pt) 2019-12-06 2022-09-06 Vertex Pharma Tetra-hidrofuranos substituídos como moduladores de canais de sódio
US12029718B2 (en) 2021-11-09 2024-07-09 Cct Sciences, Llc Process for production of essentially pure delta-9-tetrahydrocannabinol
CN113248455A (zh) * 2021-05-25 2021-08-13 湖北科技学院 一种3,5-二取代异噁唑类衍生物及其合成方法
AU2022283934A1 (en) 2021-06-04 2023-11-30 Vertex Pharmaceuticals Incorporated Substituted tetrahydrofuran-2-carboxamides as modulators of sodium channels
CA3221938A1 (fr) 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Analogues de tetrahydrofurane substitues utiles en tant que modulateurs de canaux sodiques
US20240400544A1 (en) 2021-06-04 2024-12-05 Vertex Pharmaceuticals Incorporated N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamide analogs as modulators of sodium channels
WO2022256842A1 (fr) 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Tétrahydrofuranes à substitution hydroxy et (halo)alkoxy utiles en tant que modulateurs de canaux sodiques
HRP20260068T1 (hr) 2021-06-04 2026-02-27 Vertex Pharmaceuticals Incorporated Čvrsti farmaceutski oblici i režimi doziranja koji obuhvaćaju (2r,3s,4s,5r)-4-[[3-(3,4-difluor-2-metoksifenil)-4,5-dimetil-5-(trifluormetil)tetrahidrofuran-2-karbonil]amino]piridin-2-karboksamid
SMT202500481T1 (it) 2021-06-04 2026-01-12 Vertex Pharma N-(idrossialchil(etero)aril)tetraidrofuran carbossammidi come modulatori di canali del sodio
CN115703719B (zh) * 2021-08-03 2024-04-30 联化科技股份有限公司 一种溴化肟类化合物的制备方法
US20230382910A1 (en) 2022-04-22 2023-11-30 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
WO2023205463A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
CA3256248A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
CA3257285A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
WO2024123815A1 (fr) 2022-12-06 2024-06-13 Vertex Pharmaceuticals Incorporated Procédé de synthèse de modulateurs de tétrahydrofurane substitués de canaux sodiques
WO2025090511A1 (fr) 2023-10-23 2025-05-01 Vertex Pharmaceuticals Incorporated Procédés de préparation de modulateurs de canaux sodiques et formes solides de ceux-ci pour le traitement de la douleur
WO2025090516A1 (fr) 2023-10-23 2025-05-01 Vertex Pharmaceuticals Incorporated Procédés de préparation de composés pour le traitement de la douleur et de formes solides de ceux-ci
WO2025090480A1 (fr) 2023-10-23 2025-05-01 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
WO2025090465A1 (fr) 2023-10-23 2025-05-01 Vertex Pharmaceuticals Incorporated Composés hétéroaryle pour le traitement de la douleur
US20250186419A1 (en) 2023-12-07 2025-06-12 Vertex Pharmaceuticals Incorporated Dosing regimens for treating pain
US20260001877A1 (en) 2024-06-28 2026-01-01 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
WO2026013449A2 (fr) 2024-07-11 2026-01-15 Sea4Us - Biotecnologia E Recursos Marinhos, Sa Composés dérivés d'oxazolidone et leur utilisation dans le traitement de la douleur chronique et aiguë
WO2026030525A1 (fr) 2024-07-31 2026-02-05 Vertex Pharmaceuticals Incorporated Formes galéniques et schémas posologiques de zilvétrigine pour le traitement de la douleur

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001057024A1 (fr) * 2000-02-04 2001-08-09 University College London Blocage de canaux sodiques dependant de la tension
WO2003037274A2 (fr) * 2001-11-01 2003-05-08 Icagen, Inc. Pyrazole-amides et -sulfonamides
WO2006011050A2 (fr) * 2004-07-23 2006-02-02 Pfizer Limited Derives de pyridine

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2102367T3 (es) 1990-05-18 1997-08-01 Hoechst Ag Amidas de acidos isoxazol-4-carboxilicos y amidas de acidos hidroxialquiliden-cianoaceticos, medicamentos que contienen estos compuestos y su utilizacion.
EP0674627A1 (fr) 1992-12-18 1995-10-04 The Wellcome Foundation Limited Derives de pyrimidine, de pyridine, de pteridinone et d'indazole utilises comme inhibiteurs enzymatiques
AU4515896A (en) 1994-12-12 1996-07-03 Merck & Co., Inc. Substituted 2-acylamino-pyridines as inhibitors of nitric oxide synthase
WO1996018616A1 (fr) 1994-12-12 1996-06-20 Merck & Co., Inc. 2-aminopyridines substituees utilisees comme inhibiteurs de synthase d'oxyde d'azote
US6011051A (en) 1996-07-31 2000-01-04 Hoechst Aktiengesellschaft Use of isoxazole and crotonamide derivatives for the modulation of apoptosis
US6020357A (en) 1996-12-23 2000-02-01 Dupont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
US6060491A (en) 1997-06-19 2000-05-09 Dupont Pharmaceuticals 6-membered aromatics as factor Xa inhibitors
DE19857009A1 (de) 1998-12-10 2000-06-15 Aventis Pharma Gmbh Zubereitung mit verbesserter therapeutischer Breite, enthaltend Nukleotidsyntheseinhibitoren
US6458789B1 (en) 1999-09-29 2002-10-01 Lion Bioscience Ag 2-aminopyridine derivatives and combinatorial libraries thereof
AR029489A1 (es) 2000-03-10 2003-07-02 Euro Celtique Sa Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento
AU5889701A (en) 2000-06-05 2001-12-17 Dong A Pharm Co Ltd Novel oxazolidinone derivatives and a process for the preparation thereof
US6849660B1 (en) 2000-08-01 2005-02-01 Isis Pharmaceuticals, Inc. Antimicrobial biaryl compounds
DE10132308A1 (de) 2001-07-06 2003-01-30 Aventis Behring Gmbh Kombinationspräparat zur Therapie von immunologischen Erkrankungen
AR037233A1 (es) 2001-09-07 2004-11-03 Euro Celtique Sa Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento
AR036873A1 (es) 2001-09-07 2004-10-13 Euro Celtique Sa Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento
JP2003086564A (ja) * 2001-09-14 2003-03-20 Mitsubishi Electric Corp 遠心乾燥装置および半導体装置の製造方法ならびに半導体製造装置
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
ATE375980T1 (de) 2002-02-12 2007-11-15 Smithkline Beecham Corp Nicotinamide und deren verwendung als p38 inhibitoren
WO2004080999A1 (fr) 2003-03-14 2004-09-23 Biolipox Ab Composes de pyrazole utilises dans le traitement de l'inflammation
MXPA05012081A (es) 2003-05-09 2006-02-22 Pharmacia & Upjohn Co Llc Derivados de pirimidina sustituidos.
TWI287010B (en) 2003-06-12 2007-09-21 Euro Celtique Sa Therapeutic agents useful for treating pain
SI1664016T1 (sl) 2003-09-22 2009-04-30 Euro Celtique Sa Terapevtska sredstva, uporabna za zdravljenje bolečine
JP2007526332A (ja) 2004-03-02 2007-09-13 ニューロジェン・コーポレーション ヘテロアルキル置換ビフェニル−４−カルボン酸アリールアミド類縁体
US20060106011A1 (en) 2004-11-12 2006-05-18 Bock Mark G 2-(Bicyclo)alkylamino-derivatives as mediators of chronic pain and inflammation
WO2006051311A1 (fr) 2004-11-12 2006-05-18 Galapagos Nv Composés hétéroaromatiques de l'azote qui se lient au site actif d'enzymes de type protéines kinases
US8211919B2 (en) 2005-09-02 2012-07-03 Astellas Pharma Inc. Amide derivatives as rock inhibitors
EA013909B1 (ru) 2005-09-09 2010-08-30 Смитклайн Бичам Корпорейшн Пиридиновые производные и их применение для лечения психотических расстройств
EP1764095A1 (fr) 2005-09-20 2007-03-21 Revotar Biopharmaceuticals AG Nouveaux derivés de nitrocatéchol ayant activité de ligande de selectine
EP1764093A1 (fr) 2005-09-20 2007-03-21 Revotar Biopharmaceuticals AG Nouveaux composés aromatiques et leur application médical
ES2274712B1 (es) 2005-10-06 2008-03-01 Laboratorios Almirall S.A. Nuevos derivados imidazopiridina.
TW200732320A (en) 2005-10-31 2007-09-01 Biolipox Ab Pyrazoles useful in the treatment of inflammation
TWI385169B (zh) 2005-10-31 2013-02-11 Eisai R&D Man Co Ltd 經雜環取代之吡啶衍生物及含有彼之抗真菌劑
EP1943234A1 (fr) 2005-10-31 2008-07-16 Biolipox AB Utilisation de triazoles comme inhibiteurs de la lipoxygenase
NL2000284C2 (nl) 2005-11-04 2007-09-28 Pfizer Ltd Pyrazine-derivaten.
EP1945632B1 (fr) 2005-11-08 2013-09-18 Vertex Pharmaceuticals Incorporated Modulateurs hétérocycliques de transporteurs à cassette liant l' atp
WO2007058990A2 (fr) 2005-11-14 2007-05-24 Kemia, Inc. Therapie a base d’inhibiteurs de cytokine
CA2629964A1 (fr) 2005-11-30 2007-06-07 Astellas Pharma Inc. Derive de 2-aminobenzamide
WO2007083239A1 (fr) 2006-01-23 2007-07-26 Pfizer Limited Dérivés de pyridine en tant que modulateurs du canal sodium
TW200806290A (en) 2006-01-25 2008-02-01 Synta Pharmaceuticals Corp Substituted biaryl compounds for inflammation and immune-related uses
US20070254926A1 (en) 2006-01-31 2007-11-01 Jun Jiang Pyridylphenyl compounds for inflammation and immune-related uses
JP2009528989A (ja) 2006-02-17 2009-08-13 ファイザー・リミテッド Ｔｌｒ７変調剤としての３−デアザプリン誘導体
EP2418202B1 (fr) 2006-03-31 2014-01-29 Novartis AG Dérivés (4-[4-[5-(substituted amino)-pyridin-2-yl]phenyl]-cyclohexyl)-acetic acid en tant qu'inhibiteurs de DGAT
PE20080906A1 (es) 2006-08-17 2008-07-05 Kemia Inc Derivados heteroarilo como inhibidores de citocina
US7795249B2 (en) 2006-12-22 2010-09-14 Millennium Pharmaceuticals, Inc. Certain pyrazoline derivatives with kinase inhibitory activity
AU2008205252B2 (en) 2007-01-09 2013-02-21 Amgen Inc. Bis-aryl amide derivatives useful for the treatment of cancer
CA2679659C (fr) 2007-03-01 2016-01-19 Novartis Ag Inhibiteurs de pim kinase et procedes de leur utilisation
WO2008135830A1 (fr) 2007-05-03 2008-11-13 Pfizer Limited Dérivés de pyrazine

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001057024A1 (fr) * 2000-02-04 2001-08-09 University College London Blocage de canaux sodiques dependant de la tension
WO2003037274A2 (fr) * 2001-11-01 2003-05-08 Icagen, Inc. Pyrazole-amides et -sulfonamides
WO2006011050A2 (fr) * 2004-07-23 2006-02-02 Pfizer Limited Derives de pyridine

Also Published As

Publication number Publication date
TWI375675B (en) 2012-11-01
CL2008001268A1 (es) 2008-11-03
ES2398606T3 (es) 2013-03-20
DOP2009000254A (es) 2009-11-30
EA015952B1 (ru) 2011-12-30
BRPI0810202A2 (pt) 2014-10-21
PA8779201A1 (es) 2009-01-23
NZ581614A (en) 2011-06-30
WO2008135826A3 (fr) 2009-02-05
AP2009005009A0 (en) 2009-10-31
US20090048306A1 (en) 2009-02-19
GEP20125379B (en) 2012-01-10
JP4657384B2 (ja) 2011-03-23
GT200900280A (es) 2011-08-29
CA2684105C (fr) 2011-09-06
MX2009011816A (es) 2009-11-19
JP2010526050A (ja) 2010-07-29
AR070636A1 (es) 2010-04-28
IL201569A0 (en) 2010-05-31
WO2008135826A2 (fr) 2008-11-13
PE20090730A1 (es) 2009-07-11
EA200970913A1 (ru) 2010-04-30
CA2684105A1 (fr) 2008-11-13
TN2009000450A1 (fr) 2011-03-31
CO6251367A2 (es) 2011-02-21
US8134007B2 (en) 2012-03-13
CU20090180A7 (es) 2011-05-27
CR11061A (es) 2009-11-03
UY31063A1 (es) 2009-01-05
SV2009003400A (es) 2010-08-17
ZA200907609B (en) 2011-04-28
EP2183241A2 (fr) 2010-05-12
CN101675040A (zh) 2010-03-17
TW200906403A (en) 2009-02-16
KR20100007956A (ko) 2010-01-22
EP2183241B1 (fr) 2012-12-19
AU2008247102B2 (en) 2011-11-24
NI200900192A (es) 2010-07-15
AU2008247102A1 (en) 2008-11-13
CU23846B1 (es) 2012-10-15
ECSP099710A (es) 2009-11-30
MA31419B1 (fr) 2010-06-01

Similar Documents

Publication Publication Date Title
AP2516A (en) 2-Pyridine carboxamide derivatives as sodium channel modulators
IL201202A0 (en) Imidazolidine carboxamide derivatives as p2x7 modulators
IL193173A0 (en) 3-deazapurine derivatives as tlr7 modulators
IL205759A0 (en) Isoxazolo-pyridine derivatives
IL200501A0 (en) Purinyl derivatives and their use as potassium channel modulators
IL205753A0 (en) Isoxazolo-pyridazine derivatives
IL192627A0 (en) Prolinamide derivatives as sodium channel modulators
IL206276A0 (en) Pyridine derivatives
IL202020A0 (en) Spiroindolinone derivatives
EP2178373A4 (fr) Hétérocycle en tant que modulateur de canaux potassiques
ZA200905796B (en) Purinyl derivatives and their use as potassium channel modulators
IL193176A0 (en) Benzoyl-piperidine derivatives as 5ht2/d3 modulators
IL202830A0 (en) Indazolamide derivatives
IL205755A0 (en) Isoxazolo-pyrazine derivatives
EP2175728A4 (fr) Inhibiteurs de canaux sodiques
IL200618A0 (en) Aza-pyridopyrimidinone derivatives
EP2097384A4 (fr) Dérivés d'indozalyl sulfomnamide utiles comme modulateurs des glucocorticoïdes
IL208837A0 (en) Novel heteroaryl carboxamide derivatives
ZA200806811B (en) 3-Deazapurine derivatives as TLR7 Modulators
EP2141168A4 (fr) Dérivés hétéroarylé
IL202667A0 (en) Isoxazole-imidazole derivatives
PL2220060T3 (pl) Pochodne tetrahydrobenzotiazolu
PL2170861T3 (pl) Pochodne 4-(N-azacykloalkilo)anilidów jako modulatory kanałów sodowych
ZA201007615B (en) Aminopyridine derivatives
ZA200901055B (en) Oxazolidone derivatives as PR modulators