HK1199838A1 - Macrocyclic lrrk2 kinase inhibitors lrrk2 - Google Patents
Macrocyclic lrrk2 kinase inhibitors lrrk2Info
- Publication number
- HK1199838A1 HK1199838A1 HK15100389.2A HK15100389A HK1199838A1 HK 1199838 A1 HK1199838 A1 HK 1199838A1 HK 15100389 A HK15100389 A HK 15100389A HK 1199838 A1 HK1199838 A1 HK 1199838A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- lrrk2
- macrocyclic
- kinase inhibitors
- lrrk2 kinase
- inhibitors
- Prior art date
Links
Classifications
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/504—Pyridazines; Hydrogenated pyridazines forming part of bridged ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/529—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim forming part of bridged ring systems
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- 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
- C07D487/12—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 three hetero rings
- C07D487/16—Peri-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
- C07D487/12—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 three hetero rings
- C07D487/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D515/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D515/18—Bridged systems
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP2011067086 | 2011-09-30 | ||
PCT/IB2012/002318 WO2013046029A1 (fr) | 2011-09-30 | 2012-09-28 | Inhibiteurs macrocycliques de la kinase lrrk2 |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1199838A1 true HK1199838A1 (en) | 2015-07-24 |
Family
ID=47326223
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15100389.2A HK1199838A1 (en) | 2011-09-30 | 2015-01-14 | Macrocyclic lrrk2 kinase inhibitors lrrk2 |
Country Status (18)
Country | Link |
---|---|
US (2) | US9096609B2 (fr) |
EP (1) | EP2760453B1 (fr) |
JP (1) | JP6082397B2 (fr) |
KR (1) | KR20140095477A (fr) |
CN (1) | CN104023728B (fr) |
AU (1) | AU2012314035B2 (fr) |
BR (1) | BR112014007654A8 (fr) |
CA (1) | CA2850350A1 (fr) |
DK (1) | DK2760453T3 (fr) |
ES (1) | ES2583477T3 (fr) |
HK (1) | HK1199838A1 (fr) |
HU (1) | HUE029728T2 (fr) |
MX (1) | MX342177B (fr) |
PL (1) | PL2760453T3 (fr) |
PT (1) | PT2760453T (fr) |
RU (1) | RU2622104C2 (fr) |
UA (1) | UA113186C2 (fr) |
WO (1) | WO2013046029A1 (fr) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2849999A1 (fr) * | 2011-09-30 | 2013-04-04 | Oncodesign S.A. | Inhibiteurs de kinase flt3 macrocycliques |
MD20140130A2 (ro) | 2012-06-29 | 2015-04-30 | Pfizer Inc. | 4-(amino-substituite)-7H-pirolo[2,3-d]pirimidine noi ca inhibitori de LRRK2 |
EP2970333B1 (fr) * | 2013-03-15 | 2017-05-03 | Ipsen Pharma S.A.S. | Inhibiteurs macrocycliques de la kinase lrrk2 |
US20160024114A1 (en) * | 2013-03-15 | 2016-01-28 | Oncodesign S.A. | Macrocyclic rip2 kinase inhibitors |
CA2906262A1 (fr) | 2013-03-15 | 2014-09-18 | Oncodesign S.A. | Inhibiteurs macrocycliques de la kinase inductible par un sel |
EP2994471B1 (fr) * | 2013-05-06 | 2017-05-17 | Merck Patent GmbH | Macrocycles utilisés en tant qu'inhibiteurs de kinases |
CA2933767C (fr) | 2013-12-17 | 2018-11-06 | Pfizer Inc. | Nouvelles 1h-pyrrolo[2,3- b]pyridines 3,4-disubstituees et 7h-pyrrolo[2,3-c]pyridazines 4,5-disubstituees en tant qu'inhibiteurs de la lrrk2 |
WO2015136073A1 (fr) * | 2014-03-14 | 2015-09-17 | Oncodesign Sa | Inhibiteurs macrocycliques de la kinase tgf-br2 |
EP3166637B1 (fr) | 2014-07-10 | 2020-01-29 | The J. David Gladstone Institutes | Compositions et méthodes pour le traitement d'une infection par le virus de la dengue |
BR112017004035B1 (pt) | 2014-09-17 | 2023-11-14 | Oncodesign Precision Medicine (OPM) | Inibidores macrocíclicos de rip2 quinase e composições farmacêuticas |
ES2717510T3 (es) * | 2014-09-17 | 2019-06-21 | Oncodesign Sa | Inhibidores macrocíclicos de cinasa LRRK2 |
WO2016146651A1 (fr) | 2015-03-16 | 2016-09-22 | Oncodesign Sa | Inhibiteurs macrocycliques de récepteur kinase de type activine |
AU2016322813B2 (en) | 2015-09-14 | 2021-04-01 | Pfizer Inc. | Novel imidazo (4,5-c) quinoline and imidazo (4,5-c)(1,5) naphthyridine derivatives as LRRK2 inhibitors |
AU2017302019A1 (en) * | 2016-07-28 | 2019-02-07 | Turning Point Therapeutics, Inc. | Macrocycle kinase inhibitors |
KR101923852B1 (ko) * | 2017-02-24 | 2018-11-29 | 재단법인 대구경북첨단의료산업진흥재단 | 혈액 뇌관문을 통과할 수 있는 화합물을 유효성분으로 함유하는 뇌암의 예방 또는 치료용 약학적 조성물 |
CN110891954A (zh) * | 2017-07-14 | 2020-03-17 | 葛兰素史密斯克莱知识产权发展有限公司 | 富含亮氨酸的重复激酶2的抑制剂 |
CN110627812B (zh) | 2018-06-25 | 2022-10-11 | 北京诺诚健华医药科技有限公司 | 作为trk抑制剂的杂环化合物 |
EP3870579A4 (fr) | 2018-10-22 | 2022-10-19 | Alumis Inc. | Inhibiteurs de tyk2 et leurs utilisations |
US20230357269A1 (en) * | 2020-05-06 | 2023-11-09 | Les Laboratoires Servier | New macrocyclic lrrk2 kinase inhibitors |
JP2024512449A (ja) * | 2021-03-18 | 2024-03-19 | レ ラボラトワール セルヴィエ | 大環状lrrk2キナーゼ阻害剤 |
WO2023076404A1 (fr) | 2021-10-27 | 2023-05-04 | Aria Pharmaceuticals, Inc. | Méthodes de traitement de lupus érythémateux disséminé |
US11780851B2 (en) | 2021-10-27 | 2023-10-10 | H. Lundbeck A/S | LRRK2 inhibitors |
CN117425660A (zh) * | 2022-05-18 | 2024-01-19 | 上海翊石医药科技有限公司 | 一种芳杂环类化合物及其中间体、药物组合物和用途 |
WO2023224894A1 (fr) * | 2022-05-20 | 2023-11-23 | Merck Sharp & Dohme Llc | Macrocycles servant d'inhibiteurs de lrrk2, compositions pharmaceutiques et leurs utilisations |
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IS2334B (is) | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
BR9407686A (pt) | 1993-10-01 | 1997-02-04 | Astra Ab | Processo e aparelho para o tratamento de um medicamento em pó finamente dividido uso do aparelho e aglomerados |
EP0729758A3 (fr) | 1995-03-02 | 1997-10-29 | Pfizer | Pyrazolopyrimidines et pyrrolopyrimidines pour traiter les troubles neuronaux et autres maladies |
US6043358A (en) | 1995-11-01 | 2000-03-28 | Merck & Co., Inc. | Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases |
ES2294800T3 (es) | 1996-07-24 | 2008-04-01 | Bristol-Myers Squibb Pharma Company | Azolo triazinas y pirimidinas. |
GB9718913D0 (en) | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
US6194410B1 (en) | 1998-03-11 | 2001-02-27 | Hoffman-La Roche Inc. | Pyrazolopyrimidine and pyrazolines and process for preparation thereof |
US6369087B1 (en) | 1999-08-26 | 2002-04-09 | Robert R. Whittle | Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same |
ATE526330T1 (de) | 2000-12-28 | 2011-10-15 | Ono Pharmaceutical Co | Heterotrizyklische verbindungen als antagonisten des crf-rezeptors |
DE10239042A1 (de) * | 2002-08-21 | 2004-03-04 | Schering Ag | Makrozyclische Pyrimidine, deren Herstellung und Verwendung als Arzneimittel |
EA013904B1 (ru) * | 2003-12-18 | 2010-08-30 | Янссен Фармацевтика Н.В. | Пиридо- и пиримидопиримидиновые производные в качестве антипролиферативных агентов |
WO2006045392A2 (fr) | 2004-10-21 | 2006-05-04 | GSF-Forschungszentrum für Umwelt und Gesundheit GmbH | Gene kaspp (lrrke), production de ce gene et utilisation de ce gene pour la detection et le traitement de troubles neurodegeneratifs |
NO323175B1 (no) | 2004-12-23 | 2007-01-15 | Jan O Aasly | Framgangsmate for a pavise en mutasjon som forarsaker arvelig parkinsonisme |
FI123725B (fi) | 2005-08-01 | 2013-10-15 | Reijo Viljanen | Menetelmä sahalaitteen terän jännittämiseksi ja ohjaamiseksi sekä ohjaus- ja jännityslaitteet |
DE102005042742A1 (de) * | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
US7750000B2 (en) * | 2005-09-02 | 2010-07-06 | Bayer Schering Pharma Ag | Substituted imidazo[1,2b]pyridazines as kinase inhibitors, their preparation and use as medicaments |
KR101576159B1 (ko) * | 2005-11-16 | 2015-12-09 | 에스*바이오 피티이 리미티드 | 헤테로알킬이 결합된 피리미딘 유도체 |
NZ576234A (en) * | 2006-11-06 | 2011-06-30 | Supergen Inc | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
WO2008060248A1 (fr) * | 2006-11-15 | 2008-05-22 | S*Bio Pte Ltd. | Pyrimidines substituées par indole, et leur utilisation dans le traitement d'un cancer |
WO2008075103A1 (fr) * | 2006-12-20 | 2008-06-26 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Indoles antiviraux |
US7732434B2 (en) * | 2007-04-20 | 2010-06-08 | Bristol-Myers Squibb Company | Macrocyclic acyl guanidines as beta-secretase inhibitors |
JP5536647B2 (ja) * | 2007-07-27 | 2014-07-02 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ピロロピリミジン |
DK2283024T3 (da) * | 2008-03-10 | 2013-08-05 | Janssen Pharmaceutica Nv | 4-aryl-2-anilinpyrimidiner som PLK-kinaseinhibitorer |
DE102008019146A1 (de) | 2008-04-16 | 2009-11-05 | Airbus Deutschland Gmbh | Enteisungssystem für ein Flugzeug |
CN102428084B (zh) * | 2009-03-19 | 2016-05-18 | 医疗技术研究局 | 化合物 |
CA2771176A1 (fr) * | 2009-09-21 | 2011-03-24 | F. Hoffmann-La Roche Ag | Inhibiteurs macrocycliques de jak |
EA021437B1 (ru) | 2009-09-29 | 2015-06-30 | Глэксо Груп Лимитед | Соединения, ингибирующие lrrk2 киназную активность |
EP2710018B8 (fr) * | 2011-05-19 | 2022-02-23 | Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Composés macrocycliques en tant qu'inhibiteurs des protein kinases |
WO2013001310A1 (fr) * | 2011-06-30 | 2013-01-03 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Composés macrocycliques et leur utilisation en tant qu'inhibiteurs de cdk8 |
CA2849999A1 (fr) * | 2011-09-30 | 2013-04-04 | Oncodesign S.A. | Inhibiteurs de kinase flt3 macrocycliques |
-
2012
- 2012-09-28 HU HUE12798824A patent/HUE029728T2/en unknown
- 2012-09-28 KR KR1020147011284A patent/KR20140095477A/ko not_active Application Discontinuation
- 2012-09-28 MX MX2014003557A patent/MX342177B/es active IP Right Grant
- 2012-09-28 EP EP12798824.4A patent/EP2760453B1/fr not_active Not-in-force
- 2012-09-28 AU AU2012314035A patent/AU2012314035B2/en not_active Ceased
- 2012-09-28 RU RU2014117515A patent/RU2622104C2/ru not_active IP Right Cessation
- 2012-09-28 PT PT127988244T patent/PT2760453T/pt unknown
- 2012-09-28 WO PCT/IB2012/002318 patent/WO2013046029A1/fr active Application Filing
- 2012-09-28 UA UAA201404562A patent/UA113186C2/uk unknown
- 2012-09-28 US US14/348,138 patent/US9096609B2/en not_active Expired - Fee Related
- 2012-09-28 BR BR112014007654A patent/BR112014007654A8/pt not_active IP Right Cessation
- 2012-09-28 PL PL12798824.4T patent/PL2760453T3/pl unknown
- 2012-09-28 JP JP2014532498A patent/JP6082397B2/ja not_active Expired - Fee Related
- 2012-09-28 ES ES12798824.4T patent/ES2583477T3/es active Active
- 2012-09-28 CA CA2850350A patent/CA2850350A1/fr not_active Abandoned
- 2012-09-28 CN CN201280058430.8A patent/CN104023728B/zh not_active Expired - Fee Related
- 2012-09-28 DK DK12798824.4T patent/DK2760453T3/en active
-
2015
- 2015-01-14 HK HK15100389.2A patent/HK1199838A1/xx not_active IP Right Cessation
- 2015-06-23 US US14/747,882 patent/US9370520B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2014528405A (ja) | 2014-10-27 |
MX342177B (es) | 2016-09-20 |
PL2760453T3 (pl) | 2016-11-30 |
AU2012314035B2 (en) | 2016-12-15 |
CN104023728A (zh) | 2014-09-03 |
PT2760453T (pt) | 2016-08-02 |
RU2014117515A (ru) | 2015-11-10 |
WO2013046029A1 (fr) | 2013-04-04 |
US9096609B2 (en) | 2015-08-04 |
CN104023728B (zh) | 2016-11-02 |
AU2012314035A1 (en) | 2014-05-15 |
RU2622104C2 (ru) | 2017-06-13 |
BR112014007654A8 (pt) | 2018-06-12 |
ES2583477T3 (es) | 2016-09-21 |
HUE029728T2 (en) | 2017-03-28 |
EP2760453A1 (fr) | 2014-08-06 |
CA2850350A1 (fr) | 2013-04-04 |
EP2760453B1 (fr) | 2016-05-25 |
US20150290198A1 (en) | 2015-10-15 |
KR20140095477A (ko) | 2014-08-01 |
UA113186C2 (xx) | 2016-12-26 |
JP6082397B2 (ja) | 2017-02-15 |
MX2014003557A (es) | 2014-11-26 |
BR112014007654A2 (pt) | 2018-04-17 |
US20140206683A1 (en) | 2014-07-24 |
US9370520B2 (en) | 2016-06-21 |
DK2760453T3 (en) | 2016-08-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20200930 |