MA34465B1 - Inhibiteurs de tyrosine kinase de bruton - Google Patents
Inhibiteurs de tyrosine kinase de brutonInfo
- Publication number
- MA34465B1 MA34465B1 MA35658A MA35658A MA34465B1 MA 34465 B1 MA34465 B1 MA 34465B1 MA 35658 A MA35658 A MA 35658A MA 35658 A MA35658 A MA 35658A MA 34465 B1 MA34465 B1 MA 34465B1
- Authority
- MA
- Morocco
- Prior art keywords
- tyrosine kinase
- kinase inhibitors
- compounds
- useful
- diseases associated
- Prior art date
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
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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
- A61P11/04—Drugs for disorders of the respiratory system for throat disorders
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/14—Heterocyclic 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 three or more hetero rings
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
-
- 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
- C07D487/08—Bridged systems
-
- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE DES DÉRIVÉS DE 6-(2-HYDROXYMÉTHYL-PHÉNYL)-2-MÉTHYL-2H-PYRIDAZIN-3-ONE SELON LA FORMULE GÉNÉRIQUE (I) : DANS LAQUELLE LES VARIABLES X, R, ET Y4, SONT DÉFINIS COMME PRÉSENTEMENT DÉCRIT, QUI INHIBENT BTK. LES COMPOSÉS PRÉSENTEMENT DÉCRITS SONT UTILES POUR MODULER L'ACTIVITÉ DE BTK ET TRAITER DES MALADIES ASSOCIÉES À UNE ACTIVITÉ BTK EXCESSIVE. LES COMPOSÉS SONT ÉGALEMENT UTILES POUR TRAITER DES MALADIES INFLAMMATOIRES ET AUTO-IMMUNES ASSOCIÉES À UNE PROLIFÉRATION ABERRANTE DE LYMPHOCYTES B, TELLE 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.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37288710P | 2010-08-12 | 2010-08-12 | |
US201161497093P | 2011-06-15 | 2011-06-15 | |
PCT/EP2011/063657 WO2012020008A1 (fr) | 2010-08-12 | 2011-08-09 | Inhibiteurs de tyrosine kinase de bruton |
Publications (1)
Publication Number | Publication Date |
---|---|
MA34465B1 true MA34465B1 (fr) | 2013-08-01 |
Family
ID=45565273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA35658A MA34465B1 (fr) | 2010-08-12 | 2011-08-09 | Inhibiteurs de tyrosine kinase de bruton |
Country Status (21)
Country | Link |
---|---|
US (2) | US8481540B2 (fr) |
EP (1) | EP2603500B1 (fr) |
JP (1) | JP5823518B2 (fr) |
KR (1) | KR101546167B1 (fr) |
CN (1) | CN103153984B (fr) |
AR (1) | AR082590A1 (fr) |
AU (1) | AU2011288489A1 (fr) |
BR (1) | BR112013003114A2 (fr) |
CA (1) | CA2807634A1 (fr) |
CL (1) | CL2013000391A1 (fr) |
CO (1) | CO6620025A2 (fr) |
EA (1) | EA201390207A1 (fr) |
EC (1) | ECSP13012437A (fr) |
ES (1) | ES2528371T3 (fr) |
HK (1) | HK1186186A1 (fr) |
MA (1) | MA34465B1 (fr) |
MX (1) | MX2013001715A (fr) |
PE (1) | PE20131153A1 (fr) |
SG (1) | SG187747A1 (fr) |
WO (1) | WO2012020008A1 (fr) |
ZA (1) | ZA201300705B (fr) |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
DE102007032507A1 (de) * | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
DE102007038957A1 (de) * | 2007-08-17 | 2009-02-19 | Merck Patent Gmbh | 6-Thioxo-pyridazinderivate |
DE102007061963A1 (de) * | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
DE102008019907A1 (de) * | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
DE102008028905A1 (de) * | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
DE102008037790A1 (de) * | 2008-08-14 | 2010-02-18 | Merck Patent Gmbh | Bicyclische Triazolderivate |
NZ594172A (en) | 2008-12-22 | 2013-04-26 | Merck Patent Gmbh | Novel polymorphic forms of 6-(1-methyl-1h-pyrazol-4-yl)-2-{ 3-[5-(2-morpholin-4-yl-ethoxy)-pyrimidin-2-yl]-benzyl} -2h-pyridazin-3-one dihydrogenphosphate and processes of manufacturing thereof |
AU2012257802A1 (en) | 2011-05-17 | 2013-10-31 | F. Hoffmann-La Roche Ag | Inhibitors of Bruton's tyrosine kinase |
PE20140865A1 (es) * | 2011-08-17 | 2014-07-19 | Hoffmann La Roche | Inhibidores de la tirosina-quinasa de bruton |
WO2013067277A1 (fr) | 2011-11-03 | 2013-05-10 | Genentech, Inc. | Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk |
KR20140096100A (ko) | 2011-11-03 | 2014-08-04 | 에프. 호프만-라 로슈 아게 | 이환 피페라진 화합물 |
UA111756C2 (uk) * | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона |
CN104203937A (zh) * | 2011-11-03 | 2014-12-10 | 霍夫曼-拉罗奇有限公司 | 作为btk活性的抑制剂的8-氟酞嗪-1(2h)-酮化合物 |
CN104364239B (zh) * | 2012-06-13 | 2017-08-25 | 霍夫曼-拉罗奇有限公司 | 二氮杂螺环烷烃和氮杂螺环烷烃 |
AU2013293087B2 (en) | 2012-07-24 | 2017-08-31 | Pharmacyclics Llc | Mutations associated with resistance to inhibitors of Bruton's tyrosine kinase (BTK) |
CA2881519A1 (fr) | 2012-08-10 | 2014-02-13 | Boehringer Ingelheim International Gmbh | Composes heteroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk) |
CN104619696A (zh) * | 2012-09-13 | 2015-05-13 | 弗·哈夫曼-拉罗切有限公司 | 布鲁顿氏酪氨酸激酶抑制剂 |
AR092645A1 (es) | 2012-09-25 | 2015-04-29 | Hoffmann La Roche | Derivados biciclicos inhibidores de autotaxina (atx) |
RU2015120216A (ru) * | 2012-11-16 | 2017-01-10 | Ф. Хоффманн-Ля Рош Аг | Ингибиторы тирозинкиназы брутона |
CN104968346B (zh) * | 2012-11-30 | 2017-06-27 | 弗·哈夫曼-拉罗切有限公司 | 酪氨酸蛋白激酶抑制剂 |
JP2016510051A (ja) * | 2013-03-05 | 2016-04-04 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ブルトン型チロシンキナーゼの阻害剤 |
AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
SI2989106T1 (sl) | 2013-04-25 | 2017-07-31 | Beigene, Ltd. | Zlite heterociklične spojine kot inhibitorji beljakovinske kinaze |
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 |
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RU2646758C2 (ru) | 2013-12-05 | 2018-03-07 | Ф. Хоффманн-Ля Рош Аг | Гетероарил пиридоны и азапиридоны с электрофильной функциональностью |
EP3080098B1 (fr) | 2013-12-13 | 2017-12-06 | F. Hoffmann-La Roche AG | Inhibiteurs de la tyrosine kinase de bruton |
RU2016139697A (ru) | 2014-03-12 | 2018-04-12 | Новартис Аг | Комбинация, содержащая ингибитор btk и ингибитор akt |
CR20160418A (es) | 2014-03-26 | 2016-11-07 | Hoffmann La Roche | Nuevos compuestos biciclicos de 7 eslabones |
HUE046820T2 (hu) | 2014-03-26 | 2020-03-30 | Hoffmann La Roche | Biciklusos vegyületek autotaxin (ATX) és lizofoszfatidsav (LPA) termelésgátlókként |
US9982265B2 (en) * | 2014-03-28 | 2018-05-29 | Board Of Regents, The University Of Texas System | Inhibition of Bruton's tyrosine kinase (Btk) in the lung to treat severe lung inflammation and lung injury |
TWI687438B (zh) | 2014-07-03 | 2020-03-11 | 英屬開曼群島商百濟神州生物科技有限公司 | 抗pd-l1抗體及其作為治療及診斷之用途 |
MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
WO2016209996A1 (fr) | 2015-06-23 | 2016-12-29 | University Of Oregon | Hétérocycles contenant du phosphore et procédé de production et d'utilisation |
RU2746481C1 (ru) | 2015-09-04 | 2021-04-14 | Ф. Хоффманн-Ля Рош Аг | Феноксиметильные производные |
PE20180451A1 (es) | 2015-09-24 | 2018-03-05 | Hoffmann La Roche | Nuevos compuestos biciclicos como inhibidores de atx |
CA2983782A1 (fr) | 2015-09-24 | 2017-03-30 | F. Hoffmann-La Roche Ag | Composes bicycliques utilises en tant qu'inhibiteurs d'atx |
CN107614505B (zh) | 2015-09-24 | 2021-05-07 | 豪夫迈·罗氏有限公司 | 作为双重atx/ca抑制剂的新型二环化合物 |
EP3353178B1 (fr) | 2015-09-24 | 2021-07-14 | F. Hoffmann-La Roche AG | Composés bicycliques comme inhibiteurs mixtes de atx/ca |
NZ749997A (en) | 2016-07-05 | 2022-11-25 | Beigene Ltd | Combination of a pd-l antagonist and a raf inhibitor for treating cancer |
EP3500575A4 (fr) | 2016-08-16 | 2020-04-08 | BeiGene, Ltd. | Forme cristalline de (s)-7-(1-acryloylpipéridin-4-yl)-2-(4-phénoxyphényle)-4,5,6,7-tétra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide, sa préparation et ses utilisations |
EP4353747A3 (fr) | 2016-08-19 | 2024-06-26 | BeiGene Switzerland GmbH | Combinaison de zacuturinib avec un anticorps anti-cd20 ou anti-pd-1 pour une utilisation dans le traitement du cancer |
US20190201409A1 (en) | 2016-09-19 | 2019-07-04 | Mei Pharma, Inc. | Combination therapy |
EP3573989A4 (fr) | 2017-01-25 | 2020-11-18 | Beigene, Ltd. | Formes cristallines de (s) -7- (1- (but-2-ynoyl) pipéridin-4-yl) -2- (4-phénoxyphényl) -4, 5, 6, 7-tétrahy dropyrazolo [1, 5-a]pyrimidine-3-carboxamide, préparation et utilisations associées |
EP3596060B1 (fr) | 2017-03-16 | 2023-09-20 | F. Hoffmann-La Roche AG | Nouveaux composés bicycliques utilisés en tant qu'inhibiteurs d'atx |
JP7157755B2 (ja) | 2017-03-16 | 2022-10-20 | エフ.ホフマン-ラ ロシュ アーゲー | 二重atx/ca阻害剤として有用な複素環式化合物 |
JP2020525411A (ja) | 2017-06-26 | 2020-08-27 | ベイジーン リミテッド | 肝細胞癌のための免疫療法 |
WO2019034009A1 (fr) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | Inhibiteur de btk ayant une double sélectivité améliorée |
TWI694995B (zh) * | 2017-11-06 | 2020-06-01 | 美商美國禮來大藥廠 | Btk抑制劑化合物 |
CN111801334B (zh) | 2017-11-29 | 2023-06-09 | 百济神州瑞士有限责任公司 | 使用包含btk抑制剂的组合治疗惰性或侵袭性b-细胞淋巴瘤 |
US11479556B1 (en) | 2018-10-15 | 2022-10-25 | Nurix Therapeutics, Inc. | Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway |
CN109438377B (zh) * | 2018-12-13 | 2020-06-09 | 天津利安隆新材料股份有限公司 | 一种低温法制备含有醚键的长碳链三嗪类紫外线吸收剂的方法 |
BR112021019722A2 (pt) | 2019-04-09 | 2021-12-14 | Nurix Therapeutics Inc | Compostos de piperidina 3-substituídos para inibição de cbl-b, e uso de inibidor de cbl-b em combinação com vacina contra câncer e/ou vírus oncolítico |
EP3969447A1 (fr) | 2019-05-17 | 2022-03-23 | Nurix Therapeutics, Inc. | Composés cyano-cyclobutyle pour l'inhibition de cbl-b et leurs utilisations |
CN113939289A (zh) | 2019-06-10 | 2022-01-14 | 百济神州瑞士有限责任公司 | 一种含有布鲁顿氏酪氨酸激酶抑制剂的口服固体片剂及其制备方法 |
JP2022538174A (ja) | 2019-06-26 | 2022-08-31 | ニューリックス セラピューティクス,インコーポレイテッド | Cbl-b阻害のための置換ベンジル-トリアゾール化合物、及びそのさらなる使用 |
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WO2021110142A1 (fr) * | 2019-12-04 | 2021-06-10 | Henan Normal University | Imidazolecarboxamide substitué utilisé comme inhibiteurs de la tyrosine kinase de bruton |
CA3214729A1 (fr) | 2021-04-08 | 2022-10-13 | Marilena GALLOTTA | Polytherapies comprenant des composes inhibiteurs de cbl-b |
US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
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WO2004022562A1 (fr) | 2002-09-09 | 2004-03-18 | Cellular Genomics, Inc. | 6-arykl-imidazo[1,2-a]pyrazin-8-ylamines, procede de preparation et procede d'utilisation correspondants |
MY141521A (en) | 2002-12-12 | 2010-05-14 | Hoffmann La Roche | 5-substituted-six-membered heteroaromatic glucokinase activators |
WO2005014599A1 (fr) | 2003-06-04 | 2005-02-17 | Cellular Genomics, Inc. | Imidazo[1,2-a]pyrazin-8-ylamines et methodes d'inhibition de la tyrosine kinase de bruton par de tels composes |
AU2006223409B2 (en) | 2005-03-10 | 2011-07-21 | Gilead Connecticut, Inc. | Certain substituted amides, method of making, and method of use thereof |
WO2006124731A2 (fr) | 2005-05-12 | 2006-11-23 | Irm Llc | Composes et compositions utilise(e)s en tant qu'inhibiteurs de proteines-kinases |
ES2351939T3 (es) | 2005-08-09 | 2011-02-14 | Irm Llc | Compuestos y composiciones como inhibidores de proteínas cinasas. |
ATE528302T1 (de) | 2005-08-29 | 2011-10-15 | Vertex Pharma | 3,5-disubstituierte pyrid-2-one, die als hemmer der tec-familie von nicht-rezeptor tyrosin- kinasen nützlich sind |
WO2007027528A2 (fr) | 2005-08-29 | 2007-03-08 | Vertex Pharmaceuticals Incorporated | Utilisation de pyridones en tant qu'inhibiteurs de kinases |
AU2006285038A1 (en) | 2005-08-29 | 2007-03-08 | Vertex Pharmaceuticals Incorporated | 3,5-disubstituted pyrid-2-ones useful as inhibitors of Tec family of non-receptor tyrosine kinases |
EP2018167A4 (fr) | 2006-05-15 | 2010-07-14 | Irm Llc | Compositions et procédés utilisés en tant qu'inhibiteurs des kinases réceptrices fgf |
AU2007278261A1 (en) | 2006-07-24 | 2008-01-31 | F. Hoffmann-La Roche Ag | Pyrazoles as glucokinase activators |
US7838523B2 (en) | 2006-09-11 | 2010-11-23 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
WO2008033858A2 (fr) | 2006-09-11 | 2008-03-20 | Cgi Pharmaceuticals, Inc. | Inhibiteurs de kinase et procédés d'utilisation et d'identification des inhibiteurs de kinase |
AR063707A1 (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 farmacéuticas que las comprenden. |
PE20080839A1 (es) | 2006-09-11 | 2008-08-23 | Cgi Pharmaceuticals Inc | Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas |
EP2426109B1 (fr) * | 2007-10-23 | 2013-12-18 | F. Hoffmann-La Roche AG | Nouveaux inhibiteurs de kinase |
ES2462642T3 (es) | 2007-12-14 | 2014-05-26 | F. Hoffmann-La Roche Ag | Nuevos derivados de imidazo[1,2-a]piridina e imidazo[1,2-b]piridazina |
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US7683064B2 (en) * | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
US7741327B2 (en) | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
UA103327C2 (en) * | 2008-06-24 | 2013-10-10 | Ф. Хоффманн-Ля Рош Аг | Substituted pyridin-2-ones and pyridazin-3-ones |
CA2728683C (fr) * | 2008-07-02 | 2017-05-02 | F.Hoffmann-La Roche Ag | Nouvelles phenylpyrazinones en tant qu'inhibiteurs de kinases |
US8299077B2 (en) * | 2009-03-02 | 2012-10-30 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
EP2421854B1 (fr) * | 2009-04-24 | 2014-07-23 | F.Hoffmann-La Roche Ag | Inhibiteurs de la tyrosien kinase de bruton |
ES2537190T3 (es) * | 2010-09-01 | 2015-06-03 | Gilead Connecticut, Inc. | Piridazinonas, procedimiento de preparación y procedimientos de utilización de las mismas |
AU2012257802A1 (en) * | 2011-05-17 | 2013-10-31 | F. Hoffmann-La Roche Ag | Inhibitors of Bruton's tyrosine kinase |
-
2011
- 2011-08-08 AR ARP110102870A patent/AR082590A1/es unknown
- 2011-08-09 WO PCT/EP2011/063657 patent/WO2012020008A1/fr active Application Filing
- 2011-08-09 ES ES11746518.7T patent/ES2528371T3/es active Active
- 2011-08-09 PE PE2013000232A patent/PE20131153A1/es not_active Application Discontinuation
- 2011-08-09 MA MA35658A patent/MA34465B1/fr unknown
- 2011-08-09 MX MX2013001715A patent/MX2013001715A/es unknown
- 2011-08-09 CA CA2807634A patent/CA2807634A1/fr not_active Abandoned
- 2011-08-09 AU AU2011288489A patent/AU2011288489A1/en not_active Abandoned
- 2011-08-09 EP EP11746518.7A patent/EP2603500B1/fr not_active Not-in-force
- 2011-08-09 EA EA201390207A patent/EA201390207A1/ru unknown
- 2011-08-09 JP JP2013523591A patent/JP5823518B2/ja not_active Expired - Fee Related
- 2011-08-09 CN CN201180048444.7A patent/CN103153984B/zh not_active Expired - Fee Related
- 2011-08-09 BR BR112013003114A patent/BR112013003114A2/pt active Search and Examination
- 2011-08-09 SG SG2013009246A patent/SG187747A1/en unknown
- 2011-08-09 KR KR1020137006162A patent/KR101546167B1/ko not_active IP Right Cessation
- 2011-08-11 US US13/207,481 patent/US8481540B2/en not_active Expired - Fee Related
-
2013
- 2013-01-25 ZA ZA2013/00705A patent/ZA201300705B/en unknown
- 2013-01-31 CO CO13018558A patent/CO6620025A2/es not_active Application Discontinuation
- 2013-02-08 CL CL2013000391A patent/CL2013000391A1/es unknown
- 2013-02-08 EC ECSP13012437 patent/ECSP13012437A/es unknown
- 2013-03-01 US US13/781,815 patent/US8940741B2/en not_active Expired - Fee Related
- 2013-12-10 HK HK13113723.2A patent/HK1186186A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
SG187747A1 (en) | 2013-03-28 |
AU2011288489A1 (en) | 2013-02-07 |
ES2528371T3 (es) | 2015-02-09 |
ECSP13012437A (es) | 2013-03-28 |
JP2013533300A (ja) | 2013-08-22 |
CN103153984A (zh) | 2013-06-12 |
US8940741B2 (en) | 2015-01-27 |
KR20130038420A (ko) | 2013-04-17 |
PE20131153A1 (es) | 2013-10-05 |
JP5823518B2 (ja) | 2015-11-25 |
BR112013003114A2 (pt) | 2016-06-28 |
EA201390207A1 (ru) | 2013-08-30 |
US20120040949A1 (en) | 2012-02-16 |
WO2012020008A1 (fr) | 2012-02-16 |
MX2013001715A (es) | 2013-03-22 |
US20130178461A1 (en) | 2013-07-11 |
US8481540B2 (en) | 2013-07-09 |
EP2603500A1 (fr) | 2013-06-19 |
CO6620025A2 (es) | 2013-02-15 |
AR082590A1 (es) | 2012-12-19 |
CN103153984B (zh) | 2015-04-22 |
CA2807634A1 (fr) | 2012-02-16 |
EP2603500B1 (fr) | 2014-11-19 |
KR101546167B1 (ko) | 2015-08-20 |
ZA201300705B (en) | 2014-06-25 |
CL2013000391A1 (es) | 2013-09-23 |
HK1186186A1 (en) | 2014-03-07 |
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