MX342177B - Inhibidores de cinasa 2 de repeticion rica en leucina (lrrk2) macrociclica. - Google Patents
Inhibidores de cinasa 2 de repeticion rica en leucina (lrrk2) macrociclica.Info
- Publication number
- MX342177B MX342177B MX2014003557A MX2014003557A MX342177B MX 342177 B MX342177 B MX 342177B MX 2014003557 A MX2014003557 A MX 2014003557A MX 2014003557 A MX2014003557 A MX 2014003557A MX 342177 B MX342177 B MX 342177B
- Authority
- MX
- Mexico
- Prior art keywords
- kinase inhibitors
- compounds
- disease
- lrrk2 kinase
- lrrk2
- 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
Abstract
La presente invención se refiere a nuevos compuestos macrocíclicos y composiciones que contienen tales compuestos que actúan como inhibidores de cinasa, en particular como inhibidores de LRRK2 (Cinasa 2 de Repetición Rica en Leucina). Sin embargo, la presente invención proporciona procesos para la preparación de los compuestos descritos, así como también métodos para usarlos, por ejemplo como un medicamento o agente de diagnóstico, en particular para el tratamiento y/o diagnóstico de enfermedades caracterizadas por actividad de cinasa LRRK2 tales como trastornos neurológicos que incluyen enfermedad de Parkinson y enfermedad de Alzheimer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP2011067086 | 2011-09-30 | ||
PCT/IB2012/002318 WO2013046029A1 (en) | 2011-09-30 | 2012-09-28 | Macrocyclic lrrk2 kinase inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2014003557A MX2014003557A (es) | 2014-11-26 |
MX342177B true MX342177B (es) | 2016-09-20 |
Family
ID=47326223
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2014003557A MX342177B (es) | 2011-09-30 | 2012-09-28 | Inhibidores de cinasa 2 de repeticion rica en leucina (lrrk2) macrociclica. |
Country Status (18)
Country | Link |
---|---|
US (2) | US9096609B2 (es) |
EP (1) | EP2760453B1 (es) |
JP (1) | JP6082397B2 (es) |
KR (1) | KR20140095477A (es) |
CN (1) | CN104023728B (es) |
AU (1) | AU2012314035B2 (es) |
BR (1) | BR112014007654A8 (es) |
CA (1) | CA2850350A1 (es) |
DK (1) | DK2760453T3 (es) |
ES (1) | ES2583477T3 (es) |
HK (1) | HK1199838A1 (es) |
HU (1) | HUE029728T2 (es) |
MX (1) | MX342177B (es) |
PL (1) | PL2760453T3 (es) |
PT (1) | PT2760453T (es) |
RU (1) | RU2622104C2 (es) |
UA (1) | UA113186C2 (es) |
WO (1) | WO2013046029A1 (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112014007622A2 (pt) * | 2011-09-30 | 2017-04-04 | Oncodesign Sa | inibidores de flt3 cinase macrocíclicos |
SG11201408044QA (en) | 2012-06-29 | 2015-01-29 | Pfizer | NOVEL 4-(SUBSTITUTED-AMINO)-7H-PYRROLO[2,3-d]PYRIMIDINES AS LRRK2 INHIBITORS |
CA2906262A1 (en) | 2013-03-15 | 2014-09-18 | Oncodesign S.A. | Macrocyclic salt-inducible kinase inhibitors |
BR112015022982A2 (pt) * | 2013-03-15 | 2017-07-18 | Oncodesign Sa | inibidores macrocíclicos de rip2 quinase |
KR20150129016A (ko) * | 2013-03-15 | 2015-11-18 | 입센 파마 에스.에이.에스 | 마크로시클릭 lrrk2 키나제 억제제 |
AU2014264973B2 (en) * | 2013-05-06 | 2018-01-18 | Merck Patent Gmbh | Macrocycles as kinase inhibitors |
US9695171B2 (en) | 2013-12-17 | 2017-07-04 | Pfizer Inc. | 3,4-disubstituted-1 H-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7H-pyrrolo[2,3-c]pyridazines as LRRK2 inhibitors |
WO2015136073A1 (en) * | 2014-03-14 | 2015-09-17 | Oncodesign Sa | Macrocyclic tgf-br2 kinase inhibitors |
EP3166637B1 (en) | 2014-07-10 | 2020-01-29 | The J. David Gladstone Institutes | Compositions and methods for treating dengue virus infection |
EA032872B1 (ru) | 2014-09-17 | 2019-07-31 | Онкодизайн С.А. | Макроциклические ингибиторы rip2-киназы |
DK3194405T3 (en) * | 2014-09-17 | 2019-04-15 | Oncodesign Sa | MACROCYCLIC LRRK2 KINase INHIBITORS |
WO2016146651A1 (en) | 2015-03-16 | 2016-09-22 | Oncodesign Sa | Macrocyclic activin-like receptor kinase inhibitors |
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 |
EP3490564A4 (en) * | 2016-07-28 | 2020-02-26 | Turning Point Therapeutics, Inc. | MACRO CYCLE Kinase Inhibitors |
WO2018155947A1 (ko) * | 2017-02-24 | 2018-08-30 | 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 (en) | 2018-10-22 | 2022-10-19 | Alumis Inc. | TYK2 INHIBITORS AND THEIR USES |
CN115996932A (zh) * | 2020-05-06 | 2023-04-21 | 法国施维雅药厂 | 新的大环lrrk2激酶抑制剂 |
EP4308570A1 (en) * | 2021-03-18 | 2024-01-24 | Les Laboratoires Servier | Macrocyclic lrrk2 kinase inhibitors |
WO2023076404A1 (en) | 2021-10-27 | 2023-05-04 | Aria Pharmaceuticals, Inc. | Methods for treating systemic lupus erythematosus |
TW202330549A (zh) * | 2021-10-27 | 2023-08-01 | 丹麥商H 朗德貝克公司 | Lrrk2抑制劑 |
WO2023222005A1 (zh) * | 2022-05-18 | 2023-11-23 | 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 (en) * | 2022-05-20 | 2023-11-23 | Merck Sharp & Dohme Llc | Macrocycles as lrrk2 inhibitors, pharmaceutical compositions, and uses thereof |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IS2334B (is) | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
SG48049A1 (en) | 1993-10-01 | 1998-04-17 | Astra Ab | Process i |
EP0729758A3 (en) | 1995-03-02 | 1997-10-29 | Pfizer | Pyrazolopyrimidines and pyrrolopyrimidines to treat neuronal disorders and other diseases |
US6043358A (en) | 1995-11-01 | 2000-03-28 | Merck & Co., Inc. | Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases |
EP1908764A1 (en) | 1996-07-24 | 2008-04-09 | Bristol-Myers Squibb Pharma Company | Azolo triazines and pyrimidines |
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 |
ES2369837T3 (es) | 2000-12-28 | 2011-12-07 | Ono Pharmaceutical Co., Ltd. | Compuestos triheterocíclicos como antagonistas de receptor cfr. |
DE10239042A1 (de) * | 2002-08-21 | 2004-03-04 | Schering Ag | Makrozyclische Pyrimidine, deren Herstellung und Verwendung als Arzneimittel |
US7799772B2 (en) * | 2003-12-18 | 2010-09-21 | Janssen Pharmaceutica N.V. | Pyrido-and pyrimidopyrimidine derivatives as anti-profilerative agents |
CA2584489C (en) | 2004-10-21 | 2014-07-22 | Gsf-Forschungszentrum Fur Umwelt Und Gesundheit Gmbh | Kaspp (lrrke) gene, its production and use for the detection and treatment of neurodegenerative disorders |
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 |
TWI506029B (zh) * | 2005-11-16 | 2015-11-01 | Cti Biopharma Corp | 氧連接之嘧啶衍生物 |
EP2086979B1 (en) * | 2006-11-06 | 2015-06-03 | Tolero Pharmaceuticals, Inc. | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
WO2008060248A1 (en) * | 2006-11-15 | 2008-05-22 | S*Bio Pte Ltd. | Indole sustituted pyrimidines and use thereof in the treatment of cancer |
US8101595B2 (en) * | 2006-12-20 | 2012-01-24 | Istituto di Ricerche di Biologia Molecolare P. Angletti SpA | Antiviral indoles |
US7732434B2 (en) * | 2007-04-20 | 2010-06-08 | Bristol-Myers Squibb Company | Macrocyclic acyl guanidines as beta-secretase inhibitors |
EP2185562B1 (en) * | 2007-07-27 | 2015-12-02 | Janssen Pharmaceutica, N.V. | Pyrrolopyrimidines useful for the treatment of proliferative diseases |
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 |
PE20120506A1 (es) * | 2009-03-19 | 2012-05-14 | Medical Res Council Technology | Derivados de pirazolopiridina como inhibidores de quinasas |
MX2012002385A (es) * | 2009-09-21 | 2012-04-02 | Hoffmann La Roche | Inhibidores macrociclicos de cinasa janus. |
EP2483254B1 (en) | 2009-09-29 | 2014-08-13 | Glaxo Group Limited | Novel compounds |
HRP20220319T1 (hr) * | 2011-05-19 | 2022-05-13 | Fundación Del Sector Público Estatal Centro Nacional De Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Makrociklički spojevi kao inhibitori protein kinaze |
WO2013001310A1 (en) * | 2011-06-30 | 2013-01-03 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Macrocyclic compounds and their use as cdk8 inhibitors |
BR112014007622A2 (pt) * | 2011-09-30 | 2017-04-04 | Oncodesign Sa | inibidores de flt3 cinase macrocíclicos |
-
2012
- 2012-09-28 CA CA2850350A patent/CA2850350A1/en not_active Abandoned
- 2012-09-28 ES ES12798824.4T patent/ES2583477T3/es active Active
- 2012-09-28 US US14/348,138 patent/US9096609B2/en not_active Expired - Fee Related
- 2012-09-28 WO PCT/IB2012/002318 patent/WO2013046029A1/en active Application Filing
- 2012-09-28 UA UAA201404562A patent/UA113186C2/uk unknown
- 2012-09-28 HU HUE12798824A patent/HUE029728T2/en unknown
- 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 PT PT127988244T patent/PT2760453T/pt unknown
- 2012-09-28 RU RU2014117515A patent/RU2622104C2/ru not_active IP Right Cessation
- 2012-09-28 CN CN201280058430.8A patent/CN104023728B/zh not_active Expired - Fee Related
- 2012-09-28 KR KR1020147011284A patent/KR20140095477A/ko not_active Application Discontinuation
- 2012-09-28 BR BR112014007654A patent/BR112014007654A8/pt not_active IP Right Cessation
- 2012-09-28 MX MX2014003557A patent/MX342177B/es active IP Right Grant
- 2012-09-28 DK DK12798824.4T patent/DK2760453T3/en active
- 2012-09-28 AU AU2012314035A patent/AU2012314035B2/en not_active Ceased
- 2012-09-28 EP EP12798824.4A patent/EP2760453B1/en not_active Not-in-force
-
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 |
---|---|
HUE029728T2 (en) | 2017-03-28 |
PT2760453T (pt) | 2016-08-02 |
RU2014117515A (ru) | 2015-11-10 |
US9096609B2 (en) | 2015-08-04 |
PL2760453T3 (pl) | 2016-11-30 |
CA2850350A1 (en) | 2013-04-04 |
EP2760453A1 (en) | 2014-08-06 |
DK2760453T3 (en) | 2016-08-15 |
BR112014007654A2 (pt) | 2018-04-17 |
AU2012314035B2 (en) | 2016-12-15 |
BR112014007654A8 (pt) | 2018-06-12 |
AU2012314035A1 (en) | 2014-05-15 |
CN104023728B (zh) | 2016-11-02 |
US20150290198A1 (en) | 2015-10-15 |
JP2014528405A (ja) | 2014-10-27 |
JP6082397B2 (ja) | 2017-02-15 |
CN104023728A (zh) | 2014-09-03 |
EP2760453B1 (en) | 2016-05-25 |
US9370520B2 (en) | 2016-06-21 |
KR20140095477A (ko) | 2014-08-01 |
MX2014003557A (es) | 2014-11-26 |
UA113186C2 (xx) | 2016-12-26 |
WO2013046029A1 (en) | 2013-04-04 |
ES2583477T3 (es) | 2016-09-21 |
RU2622104C2 (ru) | 2017-06-13 |
HK1199838A1 (en) | 2015-07-24 |
US20140206683A1 (en) | 2014-07-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX342177B (es) | Inhibidores de cinasa 2 de repeticion rica en leucina (lrrk2) macrociclica. | |
MX2017003470A (es) | Inhibidores macrociclicos de cinasa lrrk2. | |
SG179120A1 (en) | Novel compounds | |
WO2012162254A8 (en) | Inhibitors of lrrk2 kinase activity | |
TN2013000285A1 (en) | Novel heterocyclic derivatives and their use in the treatment of neurological disorders | |
MX2012001070A (es) | Derivados de oxazina y su uso como inhibidores de bace para el tratamiento de trastornos neurologicos. | |
MX2012007273A (es) | Pteridinonas como inhibidores de la quinasa tipo polo. | |
CL2012001073A1 (es) | Compuestos derivados de pirido[4,3-d]pirimidin-5-ona, sus composiciones farmaceuticas y su uso como inhibidores de quinasa para tratar asma, epoc, colitis ulcerante, bronquitis, lupus, cancer de mamas, enfermedad de alzheimer, enfermedad de parkinson, osteoporosis, esclerosis multiple, diabetes, trastornos oculares, restenosis, enfermedades inflamatorias. | |
EA025086B9 (ru) | Производные индоламида и родственные соединения для использования при лечении нейродегенеративных заболеваний | |
TN2012000249A1 (en) | Pyrazine derivatives and their use in the treatment of neurological disorders | |
PH12015500211B1 (en) | 4-methyl-2,3,5,9,9b-pentaaza-cyclopenta[a]naphthalenes | |
WO2012048129A3 (en) | Inhibitors of polo-like kinase | |
MX2009004908A (es) | Compuestos quimicos. | |
MX2008013212A (es) | 4-anilinquinolina-3-carboxamidas como inhibidores de la cinsa csf-1r. | |
MX2009010407A (es) | Derivados fluorados de deferiprona. | |
WO2013061004A8 (fr) | Nouveaux composés di-substitués de la diamino-3,4-cyclobutène-3-dione-1,2 utiles dans le traitement de pathologies médiées par des chimiokines | |
JOP20130213B1 (ar) | معارضات لمستقبلht3-5 | |
PH12015500860A1 (en) | 2-phenyl -5- heterocyclyl -tetrahydro-2h- pyran-3-amine compounds for use in the treatment of diabetes and its associated disorders | |
MX2015011359A (es) | Inhibidores macrociclicos de cinasa 2 de repeticion rica en leucina (lrrk2). | |
MX2015012528A (es) | Inhibidores macrociclicos de cinasa inducibles por sal. | |
PH12014501195A1 (en) | Novel 2h-indazoles as ep2, receptor antagonists | |
WO2012103282A3 (en) | Methods and compositions for treating alzheimer's disease | |
TN2012000191A1 (en) | Quinuclidine compounds as alpha-7nicotinic acetylcholine receptor ligands | |
MY182553A (en) | Pharmaceutical compositions comprising 7-(1h-imidazol-4-ylmethyl)-5,6,7,8-tetrahydro-quinoline for treating skin diseases and conditions | |
MY186523A (en) | Macrocyclic rip2 kinase inhibitors |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant or registration |