MX2012004157A - 8-etil-6-(aril)pirido[2.3-d]pirimidin-7(8h)-onas para el tratamiento de trastornos del snc. - Google Patents
8-etil-6-(aril)pirido[2.3-d]pirimidin-7(8h)-onas para el tratamiento de trastornos del snc.Info
- Publication number
- MX2012004157A MX2012004157A MX2012004157A MX2012004157A MX2012004157A MX 2012004157 A MX2012004157 A MX 2012004157A MX 2012004157 A MX2012004157 A MX 2012004157A MX 2012004157 A MX2012004157 A MX 2012004157A MX 2012004157 A MX2012004157 A MX 2012004157A
- Authority
- MX
- Mexico
- Prior art keywords
- treatment
- pyrido
- pyrimidin
- aryl
- ones
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 abstract 2
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D403/02—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Se proveen aquí inhibidores de PAK y métodos de utilización de inhibidores de PAK para el tratamiento de trastornos del sistema nervioso central tales como trastornos neurosiquiátricos.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25026209P | 2009-10-09 | 2009-10-09 | |
| US35305410P | 2010-06-09 | 2010-06-09 | |
| PCT/US2010/052106 WO2011044535A2 (en) | 2009-10-09 | 2010-10-08 | 8-ethyl-6-(aryl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012004157A true MX2012004157A (es) | 2012-08-03 |
Family
ID=43857425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012004157A MX2012004157A (es) | 2009-10-09 | 2010-10-08 | 8-etil-6-(aril)pirido[2.3-d]pirimidin-7(8h)-onas para el tratamiento de trastornos del snc. |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US8372970B2 (es) |
| EP (1) | EP2486037A4 (es) |
| JP (1) | JP2013507395A (es) |
| KR (1) | KR20120104200A (es) |
| CN (1) | CN102648200A (es) |
| AR (1) | AR078609A1 (es) |
| AU (1) | AU2010303218A1 (es) |
| BR (1) | BR112012007935A2 (es) |
| CA (1) | CA2776770A1 (es) |
| EA (1) | EA201270498A1 (es) |
| IL (1) | IL219078A0 (es) |
| MX (1) | MX2012004157A (es) |
| PH (1) | PH12012500692A1 (es) |
| TW (1) | TW201118095A (es) |
| WO (1) | WO2011044535A2 (es) |
| ZA (1) | ZA201202688B (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10164139A1 (de) | 2001-12-27 | 2003-07-10 | Bayer Ag | 2-Heteroarylcarbonsäureamide |
| US20110217280A1 (en) * | 2007-12-19 | 2011-09-08 | Vollrath Benedikt | Methods for treating neuropsychiatric conditions |
| US20100317715A1 (en) * | 2007-12-21 | 2010-12-16 | Vollrath Benedikt | Methods for treating neuropsychiatric conditions |
| WO2010071846A2 (en) | 2008-12-19 | 2010-06-24 | Afraxis, Inc. | Compounds for treating neuropsychiatric conditions |
| EP2504011A4 (en) * | 2009-11-23 | 2013-07-31 | Afraxis Inc | METHOD FOR TREATING EASY COGNITIVE IMPAIRMENT |
| PT3029039T (pt) | 2010-05-17 | 2017-11-28 | Forum Pharmaceuticals Inc | Formulações farmacêuticas que compreendem formas cristalinas de cloridrato de (r)-7-cloro-n-(quinuclidin-3-il)benzo(b)tiofeno-2-carboxamida mono-hidratado |
| US8912203B2 (en) | 2010-06-09 | 2014-12-16 | Afraxis Holdings, Inc. | 6-(sulfonylaryl)pyrido[2,3-D]pyrimidin-7(8H)-ones for the treatment of CNS disorders |
| EP2582374A4 (en) * | 2010-06-16 | 2014-03-19 | Afraxis Holdings Inc | METHOD FOR TREATING NERVOUS ELEMENTS |
| RU2013149800A (ru) * | 2011-04-08 | 2015-05-20 | Афраксис Холдингз, Инк. | 8-этил-6-(арил)пиридо[2,3-d]пиримидин-7(8h)-оны для лечения расстройств нервной системы и рака |
| SG11201401996TA (en) * | 2011-11-04 | 2014-05-29 | Afraxis Holdings Inc | Pak inhibitors for the treatment of fragile x syndrome |
| BR112014020173A8 (pt) | 2012-03-16 | 2017-07-11 | Hoffmann La Roche | Métodos para o tratamento de um melanoma, utilizações de um inibidor, composições, conjunto, método de inibição, método de identificação, método de ajuste do tratamento e invenção |
| EP2846796A4 (en) | 2012-05-08 | 2015-10-21 | Forum Pharmaceuticals Inc | METHODS OF MAINTAINING, PROCESSING OR ENHANCING COGNITIVE FUNCTION |
| WO2014056082A1 (en) * | 2012-10-12 | 2014-04-17 | University Of Prince Edward Island | Method for measuring symptoms of autism spectrum disorders and comorbid conditions |
| US8974365B2 (en) * | 2012-11-25 | 2015-03-10 | Steven Richard Devore Best | Treatment of thalamocortical dysrhythmia |
| WO2014127112A1 (en) * | 2013-02-13 | 2014-08-21 | Baylor College Of Medicine | Memory enhancer and actin dynamics |
| WO2015011252A1 (en) * | 2013-07-26 | 2015-01-29 | F. Hoffmann-La Roche Ag | Pyrimidine-pyridinone serine/threonine kinase inhibitors |
| EP2905024A1 (en) | 2014-02-07 | 2015-08-12 | Institut Quimic De Sarriá Cets, Fundació Privada | Pyrido[2,3-d]pyrimidine-7(8H)-one derivatives for the treatment of infections caused by Flaviviridae |
| WO2016015597A1 (en) | 2014-07-26 | 2016-02-04 | Sunshine Lake Pharma Co., Ltd. | Compounds as cdk small-molecule inhibitors and uses thereof |
| TWI511868B (zh) * | 2014-10-27 | 2015-12-11 | Nat Univ Tsing Hua | A Method for Instantaneous Measurement of Local Permeability Coefficient of Injection Molding |
| WO2017144546A1 (en) | 2016-02-23 | 2017-08-31 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of nasopharyngeal carcinoma |
| WO2017192228A1 (en) * | 2016-05-06 | 2017-11-09 | Albert Einstein College Of Medicine, Inc. | Pak1 inhibitors and uses thereof |
| CA3191481A1 (en) | 2017-01-20 | 2018-07-26 | Polaris Industries Inc. | Diagnostic systems and methods of a continuously variable transmission |
| CN108191857B (zh) * | 2017-01-24 | 2020-10-23 | 晟科药业(江苏)有限公司 | 6-取代的吡啶并[2,3-d]嘧啶类化合物作为蛋白激酶抑制剂 |
| CN110914267B (zh) * | 2017-07-19 | 2022-07-12 | 江苏奥赛康药业有限公司 | 嘧啶并吡啶酮或者吡啶并吡啶酮类化合物及其应用 |
| CN109813912B (zh) * | 2019-01-04 | 2021-12-28 | 深圳大学 | 一组血清差异蛋白组合在制备用于检测孤独症的试剂中的应用 |
| US20220220480A1 (en) | 2019-04-17 | 2022-07-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and compositions for treatment of nlrp3 inflammasome mediated il-1beta dependent disorders |
| EP4065578A1 (en) | 2019-11-26 | 2022-10-05 | Theravance Biopharma R&D IP, LLC | Fused pyrimidine pyridinone compounds as jak inhibitors |
| CN118767143A (zh) | 2019-12-12 | 2024-10-15 | 听治疗有限责任公司 | 用于预防和治疗听力损失的组合物和方法 |
| WO2021198511A1 (en) | 2020-04-03 | 2021-10-07 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and compositions for treatment of sars-cov-2 infection |
| WO2022008597A1 (en) | 2020-07-08 | 2022-01-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical composition for the treatment of infectious diseases |
| CN116271206B (zh) * | 2023-04-10 | 2025-02-25 | 温州市工业科学研究院 | 一种镓卟啉配合物/丝素蛋白抗菌敷料及其制作方法 |
| WO2024261302A1 (en) | 2023-06-22 | 2024-12-26 | Institut National de la Santé et de la Recherche Médicale | Nlrp3 inhibitors, pak1/2 inhibitors and/or caspase 1 inhibitors for use in the treatment of rac2 monogenic disorders |
| WO2025078334A1 (en) | 2023-10-09 | 2025-04-17 | Institut National de la Santé et de la Recherche Médicale | Combination of pak1 inhibitors and clk inhibitors for preventing resistance to chemotherapy in patients suffering from acute myeloid leukemia |
| CN118084902B (zh) * | 2024-01-16 | 2024-10-29 | 赣南师范大学 | 2-氨基噻唑嘧啶并吡啶酮类化合物或药学上可接受的盐或立体异构体及制备方法和应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL117923A (en) * | 1995-05-03 | 2000-06-01 | Warner Lambert Co | Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds |
| US5620981A (en) * | 1995-05-03 | 1997-04-15 | Warner-Lambert Company | Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation |
| US5945422A (en) | 1997-02-05 | 1999-08-31 | Warner-Lambert Company | N-oxides of amino containing pyrido 2,3-D! pyrimidines |
| CA2394650A1 (en) | 1999-12-17 | 2001-06-21 | Chi B. Vu | Novel heterocycles |
| DZ3308A1 (fr) * | 2000-03-06 | 2001-09-27 | Warner Lambert Co | Inhibiteurs de tyrosine kinase a base de 5-alkylpyrido [2,3-d] pyrimidines |
| WO2001098775A1 (en) * | 2000-06-16 | 2001-12-27 | The Board Of Trustees Of The University Of Arkansas | Regulation of the p21 gene and uses thereof |
| CA2420122A1 (en) * | 2000-08-31 | 2002-03-07 | F. Hoffmann-La Roche Ag | 7-oxo pyridopyrimidines |
| ATE305303T1 (de) | 2001-02-12 | 2005-10-15 | Hoffmann La Roche | 6-substituierte pyridopyrimidine |
| GEP20063909B (en) * | 2002-01-22 | 2006-08-25 | Warner Lambert Co | 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d] PYRIMIDIN-7-ONES |
| CA2542105C (en) | 2003-10-08 | 2011-08-02 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| EP1718645A1 (en) | 2004-02-18 | 2006-11-08 | Warner-Lambert Company LLC | 2-(pyridin-3-ylamino)-pyrido 2,3-d pyrimidin-7-ones |
| EP1846403A1 (en) | 2005-02-02 | 2007-10-24 | Ranbaxy Laboratories Limited | Azabicyclo derivatives as anti-inflammatory agents |
| US7989461B2 (en) | 2005-12-23 | 2011-08-02 | Amgen Inc. | Substituted quinazolinamine compounds for the treatment of cancer |
| US8188113B2 (en) | 2006-09-14 | 2012-05-29 | Deciphera Pharmaceuticals, Inc. | Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
| EP2076513A1 (en) | 2006-10-20 | 2009-07-08 | Irm Llc | Compositions and methods for modulating c-kit and pdgfr receptors |
| CN101535308A (zh) * | 2006-11-09 | 2009-09-16 | 霍夫曼-拉罗奇有限公司 | 作为激酶抑制剂的取代的6-苯基-吡啶并[2,3-d]嘧啶-7-酮衍生物及其使用方法 |
| WO2010071846A2 (en) | 2008-12-19 | 2010-06-24 | Afraxis, Inc. | Compounds for treating neuropsychiatric conditions |
-
2010
- 2010-10-08 JP JP2012533373A patent/JP2013507395A/ja active Pending
- 2010-10-08 MX MX2012004157A patent/MX2012004157A/es not_active Application Discontinuation
- 2010-10-08 EP EP10822806A patent/EP2486037A4/en not_active Withdrawn
- 2010-10-08 AU AU2010303218A patent/AU2010303218A1/en not_active Abandoned
- 2010-10-08 US US13/500,295 patent/US8372970B2/en not_active Expired - Fee Related
- 2010-10-08 WO PCT/US2010/052106 patent/WO2011044535A2/en not_active Ceased
- 2010-10-08 CN CN2010800549894A patent/CN102648200A/zh active Pending
- 2010-10-08 BR BR112012007935A patent/BR112012007935A2/pt not_active IP Right Cessation
- 2010-10-08 EA EA201270498A patent/EA201270498A1/ru unknown
- 2010-10-08 PH PH1/2012/500692A patent/PH12012500692A1/en unknown
- 2010-10-08 CA CA2776770A patent/CA2776770A1/en not_active Abandoned
- 2010-10-08 KR KR1020127011904A patent/KR20120104200A/ko not_active Abandoned
- 2010-10-11 TW TW099134663A patent/TW201118095A/zh unknown
- 2010-10-12 AR ARP100103719A patent/AR078609A1/es unknown
-
2012
- 2012-04-05 IL IL219078A patent/IL219078A0/en unknown
- 2012-04-13 ZA ZA2012/02688A patent/ZA201202688B/en unknown
- 2012-09-18 US US13/622,323 patent/US20130035335A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW201118095A (en) | 2011-06-01 |
| AR078609A1 (es) | 2011-11-23 |
| BR112012007935A2 (pt) | 2019-09-24 |
| JP2013507395A (ja) | 2013-03-04 |
| EP2486037A2 (en) | 2012-08-15 |
| WO2011044535A3 (en) | 2011-08-18 |
| EA201270498A1 (ru) | 2012-11-30 |
| US8372970B2 (en) | 2013-02-12 |
| KR20120104200A (ko) | 2012-09-20 |
| US20130035335A1 (en) | 2013-02-07 |
| WO2011044535A2 (en) | 2011-04-14 |
| ZA201202688B (en) | 2014-10-29 |
| PH12012500692A1 (en) | 2012-11-12 |
| CN102648200A (zh) | 2012-08-22 |
| US20120270866A1 (en) | 2012-10-25 |
| IL219078A0 (en) | 2012-06-28 |
| AU2010303218A1 (en) | 2012-05-10 |
| EP2486037A4 (en) | 2013-01-16 |
| CA2776770A1 (en) | 2011-04-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2012004157A (es) | 8-etil-6-(aril)pirido[2.3-d]pirimidin-7(8h)-onas para el tratamiento de trastornos del snc. | |
| MX2013011518A (es) | 8-etil-6-(aril)pirido[2,3-d]pirimidin-7(8h)-onas para el tratamiento de desordenes del sistema nervioso y cancer. | |
| EP2580213A4 (en) | 8- (HETEROARYLMETHYL) PYRIDO [2,3-D] PYRIMIDIN-7 (8H) -ONES FOR THE TREATMENT OF CNS DISORDERS | |
| EP2580214A4 (en) | 8- (SULFONYLARYL) PYRIDO [2,3-D] PYRIMIDIN-7 (8H) -ONES FOR THE TREATMENT OF CNS DISORDERS | |
| WO2011156780A3 (en) | 8-(sulfonylbenzyl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders | |
| LT2945632T (lt) | Heterociklo-pakeisti-[1,2,4]triazolo[1,5-c]chinazolin-5-amino junginiai, tinkami centrinės nervų sistemos sutrikimų gydymui arba prevencijai | |
| CU24522B1 (es) | PIRIDO[2,3-d]PIRIMIDIN-7(8H)-ONAS 6-FLUOROALQUIL-2-(ALQUILSULFONILPIPERIDIN-4-IL)AMINO SUSTITUIDAS | |
| WO2011156786A3 (en) | 6-(ethynyl)pyrido[2,3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders | |
| BR112013019354A2 (pt) | derivados de (1,2,4)triazolo[4,3-a]quinoxalina como inibidores de fosfodiesterases | |
| WO2011156775A3 (en) | 8-(2'-heterocycyl)pyrido[2.3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders | |
| HUE064667T2 (hu) | Pirido[3',4':4,5]pirrolo[1,2,3-de]kinoxalin származékok központi idegrendszeri betegségek kezelésében történõ alkalmazásra | |
| GT201300206A (es) | Imidazo(5,1-f)(1,2,4)triazinas para el tratamiento de transtornos neurológicos | |
| UY33801A (es) | COMPUESTOS SUSTITUIDOS DE N-(1H-INDAZOL-4IL)IMIDAZO[1,2-a]PIRIDIN-3-CARBOXAMIDA COMO INHIBIDORES DE LA TIROSINA QUINASA RECEPTORA DE TIPO III | |
| PH12014500995A1 (en) | Pak inhibitors for the treatment of cell proliferative disorders | |
| EA201290744A1 (ru) | Имидазо[1,2-b][1,2,4]триазины в качестве c-met ингибиторов | |
| MX362855B (es) | Derivados de quinazolinona como inhidores poli (adp-ribosa) polimerasa (parp). | |
| CL2011001947A1 (es) | Compuestos derivados de fenil-{1,2,4}triazolo[1,5-a]piridin-fenilamino sustituidos, inhibidores de cinasa; utiles para tratar trastornos asociados con la permeabilidad vascular. | |
| BRPI0909628A2 (pt) | compostos de azaindol para o tratamento de distúrbios do sistema nervosos central | |
| MX2014006015A (es) | Derivados de 3-fenil-isoquinolin-1 (2h) -ona como inhibidores de parp-1. | |
| PE20150965A1 (es) | Azaindolinas | |
| MX2014014808A (es) | Compuestos triciclicos como inhibidores de kat ii. | |
| BR112014014560A8 (pt) | subpopulação de monócitos humanos para tratamento de lesões do sistema nervoso central | |
| IL244619A0 (en) | Pyrido[3-b,4]pyrazine-2-carboxamides as neurogenic agents for the treatment of neurodegenerative disorders | |
| EA201390620A1 (ru) | ОКСАЗОЛО[5,4-b]ПИРИДИН-5-ИЛЬНЫЕ СОЕДИНЕНИЯ | |
| IL229791A0 (en) | Indoleamine derivatives for the treatment of diseases of the central nervous system |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |