MA35419B1 - Inhibiteurs de la tyrosine kinase de bruton - Google Patents

Inhibiteurs de la tyrosine kinase de bruton

Info

Publication number
MA35419B1
MA35419B1 MA36783A MA36783A MA35419B1 MA 35419 B1 MA35419 B1 MA 35419B1 MA 36783 A MA36783 A MA 36783A MA 36783 A MA36783 A MA 36783A MA 35419 B1 MA35419 B1 MA 35419B1
Authority
MA
Morocco
Prior art keywords
compounds
inhibitors
tyrosine kinase
diseases associated
present
Prior art date
Application number
MA36783A
Other languages
English (en)
Inventor
Christine Brotherton-Pleiss
Saul Jaime-Figueroa
Francisco Javier Lopez-Tapia
Yan Lou
Timothy D Owens
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46690498&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA35419(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA35419B1 publication Critical patent/MA35419B1/fr

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
    • C07D401/14—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 three or more hetero rings
    • 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
    • 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
    • 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
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Abstract

La présente invention concerne des composés selon la formule générique i : dans laquelle les variables sont telles que définies dans la description, et qui inhibent btk. Les composés décrits présentement sont utiles pour moduler l'activité de btk et traiter des maladies associées à une activité btk excessive. Les composés sont en outre utiles pour traiter des maladies inflammatoires et auto-immunes associées à une prolifération aberrante de lymphocytes b, telles que la polyarthrite rhumatoïde. La présente invention concerne en outre des compositions contenant des composés de formule i et au moins un véhicule, diluant ou excipient.
MA36783A 2011-08-17 2014-02-26 Inhibiteurs de la tyrosine kinase de bruton MA35419B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161524374P 2011-08-17 2011-08-17
US201261649991P 2012-05-22 2012-05-22
PCT/EP2012/065844 WO2013024078A1 (fr) 2011-08-17 2012-08-14 Inhibiteurs de la tyrosine kinase de bruton

Publications (1)

Publication Number Publication Date
MA35419B1 true MA35419B1 (fr) 2014-09-01

Family

ID=46690498

Family Applications (1)

Application Number Title Priority Date Filing Date
MA36783A MA35419B1 (fr) 2011-08-17 2014-02-26 Inhibiteurs de la tyrosine kinase de bruton

Country Status (22)

Country Link
US (1) US8889682B2 (fr)
EP (1) EP2744804B1 (fr)
JP (1) JP5823616B2 (fr)
KR (1) KR20140052032A (fr)
CN (1) CN103748088A (fr)
AR (1) AR087543A1 (fr)
AU (1) AU2012296888A1 (fr)
BR (1) BR112014003582A2 (fr)
CA (1) CA2841801A1 (fr)
CL (1) CL2014000350A1 (fr)
CO (1) CO6842020A2 (fr)
CR (1) CR20140027A (fr)
EA (1) EA024689B1 (fr)
EC (1) ECSP14013212A (fr)
HK (1) HK1197060A1 (fr)
IL (1) IL230561A0 (fr)
MA (1) MA35419B1 (fr)
MX (1) MX349372B (fr)
PE (1) PE20140865A1 (fr)
TW (1) TW201311669A (fr)
WO (1) WO2013024078A1 (fr)
ZA (1) ZA201400739B (fr)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5976828B2 (ja) 2011-11-03 2016-08-24 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Ｂｔｋ活性阻害剤としてのアルキル化ピペラジン化合物
JP5808869B2 (ja) 2011-11-03 2015-11-10 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト 二環式ピペラジン化合物
US8669251B2 (en) * 2011-11-03 2014-03-11 Genentech, Inc. 8-fluorophthalazin-1(2H)-one compounds
UA111756C2 (uk) 2011-11-03 2016-06-10 Ф. Хоффманн-Ля Рош Аг Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона
JP6182593B2 (ja) 2012-04-20 2017-08-16 アドヴィーナス セラピューティクス リミテッド 置換ヘテロ二環化合物、組成物及び医薬並びにそれらの用途
WO2013157021A1 (fr) 2012-04-20 2013-10-24 Advinus Therapeutics Limited Composés bicycliques, compositions et applications médicinales de ceux-ci
KR20150032340A (ko) 2012-07-24 2015-03-25 파마시클릭스, 인코포레이티드 브루톤 티로신 키나제(btk)의 억제제에 대한 내성과 관련된 돌연변이
EP2882741B1 (fr) 2012-08-10 2018-10-24 Boehringer Ingelheim International GmbH Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk)
RU2015120216A (ru) * 2012-11-16 2017-01-10 Ф. Хоффманн-Ля Рош Аг Ингибиторы тирозинкиназы брутона
KR20150075115A (ko) * 2012-11-30 2015-07-02 에프. 호프만-라 로슈 아게 브루톤 티로신 키나제의 억제제
CN105051028B (zh) * 2013-03-05 2017-06-09 豪夫迈·罗氏有限公司 布鲁顿氏酪氨酸激酶抑制剂
CN104177338B (zh) * 2013-05-22 2018-04-03 南京勇山生物科技有限公司 一类布鲁顿激酶抑制剂
KR101815360B1 (ko) * 2013-07-03 2018-01-04 에프. 호프만-라 로슈 아게 헤테로아릴 피리돈 및 아자-피리돈 아마이드 화합물
DK3026050T3 (en) 2013-07-26 2019-02-18 Carna Biosciences Inc NEW TRIAZINE DERIVATIVE
AU2014322239A1 (en) * 2013-09-20 2016-04-14 Carna Biosciences, Inc. Novel triazine derivative
EP3077384B1 (fr) 2013-12-05 2017-09-06 F. Hoffmann-La Roche AG Composés de pyridone hétéroarylique et d'aza-pyridone à fonctionnalité électrophile
EP3042903B1 (fr) 2015-01-06 2019-08-14 Impetis Biosciences Ltd. Composés hétéro-bicycliques substitués, compositions et leurs applications médicales
CN107428678B (zh) 2015-01-22 2021-01-01 赛诺菲-安万特德国有限公司 用于制备2-[4-(环丙烷羰基)苯基]-2-甲基-丙腈的方法
WO2017070708A1 (fr) 2015-10-23 2017-04-27 Array Biopharma, Inc. Composés de 2-pyridazin-3(2h)-one à substitution 2-aryle et 2-hétéroaryle utilisés en tant qu'inhibiteurs de fgfr tyrosine kinases
TW202204350A (zh) 2020-05-06 2022-02-01 美商雅捷可斯治療公司 作為ｊａｋ２抑制劑之６－雜芳基氧基苯并咪唑及氮雜苯并咪唑
WO2023009709A1 (fr) * 2021-07-29 2023-02-02 Ajax Therapeutics, Inc. Pyrazolo pipérazines en tant qu'inhibiteurs de jak2
WO2023086319A1 (fr) 2021-11-09 2023-05-19 Ajax Therapeutics, Inc. 6-hetero-aryloxy-benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2
CN115073299A (zh) * 2022-06-14 2022-09-20 爱斯特（成都）生物制药股份有限公司 一种制备2-氟-3-三氟甲基苯胺的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7683064B2 (en) * 2008-02-05 2010-03-23 Roche Palo Alto Llc Inhibitors of Bruton's tyrosine kinase
SI2242749T1 (sl) * 2008-02-05 2013-07-31 F.Hoffmann-La Roche Ag Novi piridinoni in piridazinoni
EP2297142B1 (fr) * 2008-06-24 2015-10-14 F. Hoffmann-La Roche AG Nouvelles pyridine-2-ones et pyridazine-3-ones substituées
US8299077B2 (en) * 2009-03-02 2012-10-30 Roche Palo Alto Llc Inhibitors of Bruton's tyrosine kinase
AR082590A1 (es) * 2010-08-12 2012-12-19 Hoffmann La Roche Inhibidores de la tirosina-quinasa de bruton
US8669251B2 (en) * 2011-11-03 2014-03-11 Genentech, Inc. 8-fluorophthalazin-1(2H)-one compounds
CA2853138A1 (fr) * 2011-12-05 2013-06-13 Immunomedics, Inc. Utilisation therapeutique d'anticorps anti-cd22 pour induire une trogocytose

Also Published As

Publication number Publication date
MX2014001653A (es) 2014-03-21
ZA201400739B (en) 2016-01-27
JP2014521734A (ja) 2014-08-28
EA024689B1 (ru) 2016-10-31
BR112014003582A2 (pt) 2017-03-14
CR20140027A (es) 2014-03-13
IL230561A0 (en) 2014-03-31
US20130045965A1 (en) 2013-02-21
KR20140052032A (ko) 2014-05-02
US8889682B2 (en) 2014-11-18
WO2013024078A1 (fr) 2013-02-21
EA201490452A1 (ru) 2014-05-30
JP5823616B2 (ja) 2015-11-25
AU2012296888A1 (en) 2014-01-23
TW201311669A (zh) 2013-03-16
CO6842020A2 (es) 2014-01-20
AR087543A1 (es) 2014-04-03
PE20140865A1 (es) 2014-07-19
CN103748088A (zh) 2014-04-23
HK1197060A1 (en) 2015-01-02
ECSP14013212A (es) 2014-03-31
CL2014000350A1 (es) 2014-08-22
CA2841801A1 (fr) 2013-02-21
EP2744804B1 (fr) 2017-05-17
MX349372B (es) 2017-07-26
EP2744804A1 (fr) 2014-06-25

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