MX2014012945A - Derivados de pirazol aminopirimidina como moduladores de cinasa 2 de repeticion rica en leucina (lrrk2). - Google Patents
Derivados de pirazol aminopirimidina como moduladores de cinasa 2 de repeticion rica en leucina (lrrk2).Info
- Publication number
- MX2014012945A MX2014012945A MX2014012945A MX2014012945A MX2014012945A MX 2014012945 A MX2014012945 A MX 2014012945A MX 2014012945 A MX2014012945 A MX 2014012945A MX 2014012945 A MX2014012945 A MX 2014012945A MX 2014012945 A MX2014012945 A MX 2014012945A
- Authority
- MX
- Mexico
- Prior art keywords
- aminopyrimidine derivatives
- lrrk2
- pyrazole
- modulators
- lrrk2 modulators
- Prior art date
Links
Classifications
-
- 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
- C07D403/02—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 two hetero rings
- C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 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
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Psychology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente invención se relaciona con compuestos de pirazol que son moduladores de LRRK2, con métodos para elaborar los compuestos, y con métodos para usar los compuestos para el tratamiento de enfermedades asociadas con el receptor LRRK2, tal como la enfermedad de Parkinson.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261642019P | 2012-05-03 | 2012-05-03 | |
PCT/EP2013/058939 WO2013164321A1 (en) | 2012-05-03 | 2013-04-30 | Pyrazole aminopyrimidine derivatives as lrrk2 modulators |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2014012945A true MX2014012945A (es) | 2015-02-10 |
MX363118B MX363118B (es) | 2019-03-11 |
Family
ID=48325675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2014012945A MX363118B (es) | 2012-05-03 | 2013-04-30 | Derivados de pirazol aminopirimidina como moduladores de cinasa 2 de repeticion rica en leucina (lrrk2). |
Country Status (11)
Country | Link |
---|---|
US (1) | US9212173B2 (es) |
EP (1) | EP2844652B1 (es) |
JP (1) | JP6218808B2 (es) |
KR (1) | KR102091894B1 (es) |
CN (2) | CN106220615A (es) |
BR (1) | BR112014026952B1 (es) |
CA (1) | CA2870049C (es) |
HK (1) | HK1200820A1 (es) |
MX (1) | MX363118B (es) |
RU (1) | RU2637947C2 (es) |
WO (1) | WO2013164321A1 (es) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
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JP6211061B2 (ja) * | 2012-05-03 | 2017-10-11 | ジェネンテック, インコーポレイテッド | パーキンソン病の処置における使用のためのlrrk2モジュレーターとしてのピラゾールアミノピリミジン誘導体 |
GEP201706620B (en) | 2012-06-29 | 2017-02-10 | Pfizer | NOVEL 4-(SUBSTITUTED-AMINO)-7H-PYRROLO[2,3-d]PYRIMIDINES AS LRRK2 INHIBITORS |
WO2015092592A1 (en) | 2013-12-17 | 2015-06-25 | Pfizer Inc. | Novel 3,4-disubstituted-1h-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7h-pyrrolo[2,3-c]pyridazines as lrrk2 inhibitors |
ES2812605T3 (es) | 2013-12-20 | 2021-03-17 | Signal Pharm Llc | Compuestos de diaminopirimidilo sustituidos, composiciones de los mismos y procedimientos de tratamiento con ellos |
RU2016134751A (ru) | 2014-01-29 | 2018-03-02 | Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед | Соединения |
KR20160106622A (ko) | 2014-01-29 | 2016-09-12 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 화합물 |
JP2017521465A (ja) * | 2014-07-24 | 2017-08-03 | バイエル・ファルマ・アクティエンゲゼルシャフト | グルコース輸送阻害剤 |
EP3350178B1 (en) | 2015-09-14 | 2021-10-20 | Pfizer Inc. | Novel imidazo [4,5-c]quinoline and imidazo [4,5-c][1,5]naphthyridine derivatives as lrrk2 inhibitors |
WO2017087905A1 (en) * | 2015-11-20 | 2017-05-26 | Denali Therapeutics Inc. | Compound, compositions, and methods |
CN108934162A (zh) * | 2015-12-16 | 2018-12-04 | 南方研究所 | 吡咯并嘧啶化合物、作为激酶lrrk2抑制剂的用途及其制备方法 |
US11028080B2 (en) | 2016-03-11 | 2021-06-08 | Denali Therapeutics Inc. | Substituted pyrimidines as LRKK2 inhibitors |
PE20190395A1 (es) * | 2016-06-16 | 2019-03-13 | Denali Therapeutics Inc | Pirimidin-2-ilamino-1h-pirazoles como inhibidores de lrrk2 para el uso en el tratamiento de trastornos neurodegenerativos |
CN106588884B (zh) * | 2016-11-10 | 2019-04-09 | 浙江大学 | 2-多取代芳环-嘧啶类衍生物及制备和医药用途 |
GB201705263D0 (en) * | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
KR101798840B1 (ko) | 2017-05-17 | 2017-11-17 | 주식회사 레고켐 바이오사이언스 | 신규 오토탁신 저해 화합물 및 이를 함유하는 약제학적 조성물 |
EP3645518B1 (en) * | 2017-06-30 | 2021-05-19 | Amgen Inc. | Synthesis of omecamtiv mecarbil |
ES2975319T3 (es) * | 2017-11-21 | 2024-07-04 | Denali Therapeutics Inc | Polimorfos y formas sólidas de un compuesto de pirimidinilamino-pirazol y métodos de producción |
ES2975958T3 (es) * | 2017-12-20 | 2024-07-18 | Denali Therapeutics Inc | Procedimiento para la preparación de compuestos de pirimidinil-4-aminopirazol |
KR102501982B1 (ko) | 2018-02-14 | 2023-02-20 | 오사카 유키가가쿠고교 가부시키가이샤 | 내열성과 용이 박리성의 경화수지막을 형성하는 경화성 수지 조성물 및 그의 제조 방법 |
WO2019160037A1 (ja) * | 2018-02-14 | 2019-08-22 | 国立大学法人 東京大学 | 酸ハロゲン化物による化合物の製造方法 |
IL281765B2 (en) * | 2018-09-25 | 2024-04-01 | Cardurion Pharmaceuticals Inc | Aminopyrimidine compound |
WO2020068846A1 (en) * | 2018-09-25 | 2020-04-02 | Heterocyclic Compound | Heterocyclic compound |
CN111718332B (zh) * | 2019-03-19 | 2021-08-17 | 北京赛特明强医药科技有限公司 | 2-取代吡唑氨基-4-取代氨基-5-嘧啶甲酰胺类化合物、组合物及其应用 |
EP3980412A4 (en) * | 2019-06-06 | 2023-05-31 | Merck Sharp & Dohme LLC | INDAZOLE 5-, 6-DISUBSTITUTED, 1-PYRAZOLYL DERIVATIVES AS LRRK2 INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF |
EP4232040A1 (en) | 2020-10-20 | 2023-08-30 | F. Hoffmann-La Roche AG | Combination therapy of pd-1 axis binding antagonists and lrrk2 inhitibors |
WO2023076404A1 (en) | 2021-10-27 | 2023-05-04 | Aria Pharmaceuticals, Inc. | Methods for treating systemic lupus erythematosus |
WO2024097394A1 (en) | 2022-11-03 | 2024-05-10 | Denali Therapeutics Inc. | Solid and co-crystal forms of a pyrimidine triazole compound |
TW202434571A (zh) | 2022-11-22 | 2024-09-01 | 美商戴納立製藥公司 | 嘧啶胺基吡唑化合物之製備方法及中間物 |
CN115819405A (zh) * | 2022-12-20 | 2023-03-21 | 沪渝人工智能研究院 | 嘧啶氨基吡唑衍生物及其作为富亮氨酸重复激酶2抑制剂的应用 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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RU2340611C2 (ru) * | 2000-09-15 | 2008-12-10 | Вертекс Фармасьютикалз Инкорпорейтед | Производные пиразола, используемые в качестве ингибиторов протеинкиназы |
PT1317448E (pt) * | 2000-09-15 | 2005-08-31 | Vertex Pharma | Compostos de pirazole uteis como inibidores de proteina-quinase |
JP5208516B2 (ja) * | 2004-12-30 | 2013-06-12 | エグゼリクシス, インコーポレイテッド | キナーゼモジュレーターとしてのピリミジン誘導体および使用方法 |
WO2009145814A2 (en) * | 2008-03-10 | 2009-12-03 | Vertex Pharmaceuticals Incorporated | Pyrimidines and pyridines useful as inhibitors of protein kinases |
WO2010144468A1 (en) * | 2009-06-10 | 2010-12-16 | Abbott Laboratories | 2- ( lh-pyrazol-4 -ylamino ) -pyrimidine as kinase inhibitors |
PT2576541T (pt) * | 2010-06-04 | 2016-07-08 | Hoffmann La Roche | Derivados de aminopirimidina como moduladores de lrrk2 |
CA2809836C (en) * | 2010-09-01 | 2019-01-15 | Gilead Connecticut, Inc. | Pyridinones/pyrazinones, method of making, and method of use thereof for the treatment of disorders mediated by bruton's tyrosine kinase |
RS59106B1 (sr) * | 2010-11-10 | 2019-09-30 | Genentech Inc | Derivati pirazol aminopirimidina kao lrrk2 modulatori |
US8637537B2 (en) * | 2011-08-25 | 2014-01-28 | Genentech, Inc. | Serine/threonine kinase inhibitors |
US8669251B2 (en) * | 2011-11-03 | 2014-03-11 | Genentech, Inc. | 8-fluorophthalazin-1(2H)-one compounds |
PT2820009T (pt) * | 2012-03-01 | 2018-04-12 | Array Biopharma Inc | Inibidores de serina/treonina quinases |
MX2015003513A (es) * | 2012-09-26 | 2015-07-17 | Hoffmann La Roche | Compuestos ciclicos eter pirazol-4-il-heterociclil-carboxamida y metodos de utilizacion. |
MA38624A1 (fr) * | 2013-05-01 | 2017-02-28 | Hoffmann La Roche | Composés bihétéroaryle et leurs utilisations |
-
2013
- 2013-04-30 RU RU2014147381A patent/RU2637947C2/ru active
- 2013-04-30 BR BR112014026952-1A patent/BR112014026952B1/pt active IP Right Grant
- 2013-04-30 WO PCT/EP2013/058939 patent/WO2013164321A1/en active Application Filing
- 2013-04-30 CA CA2870049A patent/CA2870049C/en active Active
- 2013-04-30 KR KR1020147033695A patent/KR102091894B1/ko active IP Right Grant
- 2013-04-30 EP EP13720901.1A patent/EP2844652B1/en active Active
- 2013-04-30 JP JP2015509410A patent/JP6218808B2/ja active Active
- 2013-04-30 MX MX2014012945A patent/MX363118B/es unknown
- 2013-04-30 CN CN201610580911.5A patent/CN106220615A/zh active Pending
- 2013-04-30 CN CN201380023403.1A patent/CN104271569B/zh active Active
-
2014
- 2014-11-03 US US14/531,271 patent/US9212173B2/en active Active
-
2015
- 2015-02-05 HK HK15101249.0A patent/HK1200820A1/zh unknown
Also Published As
Publication number | Publication date |
---|---|
CN104271569A (zh) | 2015-01-07 |
RU2014147381A (ru) | 2016-06-27 |
KR102091894B1 (ko) | 2020-03-20 |
JP6218808B2 (ja) | 2017-10-25 |
BR112014026952B1 (pt) | 2022-03-15 |
WO2013164321A1 (en) | 2013-11-07 |
EP2844652B1 (en) | 2019-03-13 |
CN104271569B (zh) | 2016-08-24 |
CN106220615A (zh) | 2016-12-14 |
US20150051238A1 (en) | 2015-02-19 |
CA2870049C (en) | 2020-12-29 |
CA2870049A1 (en) | 2013-11-07 |
KR20150016532A (ko) | 2015-02-12 |
BR112014026952A2 (pt) | 2017-06-27 |
EP2844652A1 (en) | 2015-03-11 |
BR112014026952A8 (pt) | 2021-06-15 |
HK1200820A1 (zh) | 2015-08-14 |
US9212173B2 (en) | 2015-12-15 |
RU2637947C2 (ru) | 2017-12-08 |
MX363118B (es) | 2019-03-11 |
JP2015515966A (ja) | 2015-06-04 |
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