AR058919A1 - Compuestos de heteroarilo biciclicos como inhibidores de pde10, composiciones farmaceuticas que los contienen y su uso en la preparacion de medicamentos para el tratamiento de enfermedades del snc. - Google Patents
Compuestos de heteroarilo biciclicos como inhibidores de pde10, composiciones farmaceuticas que los contienen y su uso en la preparacion de medicamentos para el tratamiento de enfermedades del snc.Info
- Publication number
- AR058919A1 AR058919A1 ARP070100041A ARP070100041A AR058919A1 AR 058919 A1 AR058919 A1 AR 058919A1 AR P070100041 A ARP070100041 A AR P070100041A AR P070100041 A ARP070100041 A AR P070100041A AR 058919 A1 AR058919 A1 AR 058919A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- cycloalkyl
- alkenyl
- alkynyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 12
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 8
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 abstract 2
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 210000003169 central nervous system Anatomy 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000006546 (C4-C10) cycloalkyl group Chemical group 0.000 abstract 1
- -1 -NR8R8 Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- 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
- A61P25/18—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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
- 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
- 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
-
- 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
- C07D471/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen 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 two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Compuestos de heteroarilo bicíclicos que sirven como inhibidores eficaces de la fosfodiesterasa (PDE), en particular son inhibidores selectivos de PDE-10; composiciones farmacéuticas que comprenden dichos compuestos; y al uso de dichos compuestos en la preparacion de medicamentos para tratar ciertos trastornos del sistema nervioso central (SNC) u otros trastornos. Reivindicacion 1: Un compuesto de formula 1 o su sal farmacéuticamente aceptable, en la que HET1 se selecciona del grupo que consiste en un heteroarilo monocíclico y un heteroarilo bicíclico, en el que dicho HET1 puede estar opcionalmente sustituido con por lo menos un R4; HET2 es un heteroarilo monocíclico, en el que dicho HET3 lo puede estar opcionalmente sustituido con por lo menos un R5; HET3 es un heteroarilo bicíclico de 8 o 9 miembros, en el que dicho HET3 puede estar opcionalmente sustituido con por lo menos un R6; R1 se selecciona del grupo que consiste en halogeno, hidroxilo, ciano, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-8, haloalquilo C1-8, cicloalquilo C3-8, heterocicloalquilo C2-7, alquiltio C1-8, -NR3R3, -O-CF3, -S (O)n-R3, -C (O)-NR3R3 y alquilo C1-8 sustituido con un heteroátomo en el que el heteroátomo se selecciona del grupo que consiste en nitrogeno, oxígeno y azufre, y en el que el heteroátomo puede estar además sustituido con uno o más sustituyentes seleccionados del grupo que consiste en hidrogeno, alquilo C1-8, cicloalquilo C3-8, alquenilo C2-8, alquinilo C2-8 y haloalquilo C1-8; Cada R2 se selecciona independientemente del grupo que consiste en hidrogeno, alquilo C1-8, cicloalquil C3-8-alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alquenilo C2-8, haloalquilo C1-8 y cicloalquilo C3-8; cada R3 se selecciona independientemente del grupo que consiste en hidrogeno, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, haloalquilo C1-8, cicloalquilo C3-8; cada R4 se selecciona independientemente del grupo que consiste en halogeno, hidroxilo, ciano, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-8, cicloalquilo C3-8, alquiltio C1-8, haloalquilo C1-8 y alquilo C1-8 sustituido con uno o más sustituyentes seleccionados del grupo que consiste en -OR8, -NR8R8 y -SR8; R5 se selecciona independientemente del grupo que consiste en halogeno, hidroxilo, ciano, -NR8R8, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-8, cicloalquilo C3-8, alquiltio C1-8 y haloalquilo C1-8; B1 y B2 son átomos adyacentes en Het1 que se seleccionan independientemente del grupo que consiste en C y N; B3 y B4 son átomos adyacentes en Het3 donde B3 es C y B4 es N; X y X1 se seleccionan cada uno independientemente del grupo que consiste en o, S, -C(R2) y -NR2, siempre que por lo menos uno de X o X1 sea -C(R2)2; donde cada R6 se selecciona independientemente del grupo que consiste en halogeno, hidroxilo, ciano, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, alcoxi C1-8, cicloalquilo C1-8, alquiltio C1-8, haloalquilo C3-8, NR7R7, -O-CF3, - S(O)L,,-R' y -C(O)NR7R7, alquilo C1-8 sustituido con un heteroátomo, en el que el heteroátomo se selecciona del grupo que consiste en nitrogeno, oxígeno y azufre, y en donde el heteroátomo puede además estar sustituido con un sustituyente seleccionado del grupo que consiste en hidrogeno, alquilo C1-8, cicloalquilo C1-8, alquenilo C2-8, alquinilo C2-8 y haloalquilo C1-8; o dos R6, junto con los átomos a los que están unidos, pueden opcionalmente formar un cicloalquilo C4-10, cicloalquenilo C4-10, anillo heterocicloalquilo (4-10 miembros) o anillo heterocicloalquenilo (4-10 miembros); donde cada R7 se selecciona independientemente del grupo que consiste en hidrogeno y alquilo C1-8; donde cada R8 se selecciona independientemente del grupo que consiste en hidrogeno, alquilo C1-8, alquenilo C2-8 y alquinilo C2-8; n = 0, 1 o 2; m = 0, 1 o 2; y p= 0, 1, 2, 3 o 4.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75645006P | 2006-01-05 | 2006-01-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR058919A1 true AR058919A1 (es) | 2008-03-05 |
Family
ID=38131538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070100041A AR058919A1 (es) | 2006-01-05 | 2007-01-04 | Compuestos de heteroarilo biciclicos como inhibidores de pde10, composiciones farmaceuticas que los contienen y su uso en la preparacion de medicamentos para el tratamiento de enfermedades del snc. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20070155779A1 (es) |
| EP (1) | EP1979343A2 (es) |
| JP (1) | JP2009522346A (es) |
| AR (1) | AR058919A1 (es) |
| CA (1) | CA2636264A1 (es) |
| NL (1) | NL2000397C2 (es) |
| PE (1) | PE20071116A1 (es) |
| TW (1) | TW200736246A (es) |
| UY (1) | UY30080A1 (es) |
| WO (1) | WO2007077490A2 (es) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2650976A1 (en) * | 2006-05-02 | 2007-11-15 | Pfizer Products Inc. | Bicyclic heteroaryl compounds as pde10 inhibitors |
| PE20091953A1 (es) * | 2008-05-08 | 2010-01-09 | Du Pont | Azoles sustituidos como fungicidas |
| TWI501965B (zh) * | 2008-06-20 | 2015-10-01 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之新穎苯基咪唑衍生物 |
| US8133897B2 (en) | 2008-06-20 | 2012-03-13 | H. Lundbeck A/S | Phenylimidazole derivatives as PDE10A enzyme inhibitors |
| RU2506260C2 (ru) * | 2008-06-25 | 2014-02-10 | Энвиво Фармасьютикалз, Инк. | 1,2-дизамещенные гетероциклические соединения |
| KR20110031355A (ko) | 2008-06-25 | 2011-03-25 | 엔비보 파마슈티칼즈, 인코퍼레이티드 | 1,2―이치환된 헤테로사이클릭 화합물 |
| US9061984B2 (en) * | 2008-08-15 | 2015-06-23 | University Of Louisville Research Foundation, Inc. | Compounds related to chalcones and benzothienopyrimidines, their synthesis, and uses to treat diseases |
| TW201030001A (en) | 2008-11-14 | 2010-08-16 | Amgen Inc | Pyridine and pyrimidine derivatives as phosphodiesterase 10 inhibitors |
| AU2009333214B2 (en) * | 2008-12-17 | 2013-09-26 | Amgen Inc. | Aminopyridine and carboxypyridine compounds as phosphodiesterase 10 inhibitors |
| HUE026238T2 (en) * | 2009-05-07 | 2016-06-28 | Forum Pharmaceuticals Inc | Phenoxymethyl heterocyclic compounds |
| BRPI1009637A2 (pt) | 2009-06-05 | 2019-04-30 | Cephalon, Inc | composto, composição e uso de um composto |
| WO2011053559A1 (en) * | 2009-10-30 | 2011-05-05 | Merck Sharp & Dohme Corp. | Aryl aminopyridine pde10 inhibitors |
| AU2010311493B2 (en) * | 2009-10-30 | 2014-06-05 | Janssen Pharmaceutica Nv | Radiolabelled PDE10 ligands |
| TWI487705B (zh) * | 2009-12-17 | 2015-06-11 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之雜芳香族芳基三唑衍生物 |
| TWI485151B (zh) | 2009-12-17 | 2015-05-21 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之雜芳香族苯基咪唑衍生物 |
| AR081810A1 (es) | 2010-04-07 | 2012-10-24 | Bayer Cropscience Ag | Piridinilpirazoles biciclicos |
| US8969349B2 (en) | 2010-05-26 | 2015-03-03 | Sunovion Pharmaceuticals Inc. | Substituted quinoxalines and quinoxalinones as PDE-10 inhibitors |
| TW201215607A (en) | 2010-07-02 | 2012-04-16 | Lundbeck & Co As H | Aryl-and heteroarylamid derivatives as PDE10A enzyme inhibitor |
| JP5973990B2 (ja) * | 2011-03-16 | 2016-08-23 | 武田薬品工業株式会社 | 縮合複素環化合物 |
| JP2014122161A (ja) * | 2011-03-31 | 2014-07-03 | Astellas Pharma Inc | ピラゾール化合物 |
| EP2714041B1 (en) | 2011-05-24 | 2016-10-19 | Merck Sharp & Dohme Corp. | Aryloxymethyl cyclopropane derivatives as pde10 inhibitors |
| US9938269B2 (en) | 2011-06-30 | 2018-04-10 | Abbvie Inc. | Inhibitor compounds of phosphodiesterase type 10A |
| ME02419B (me) * | 2011-08-25 | 2016-09-20 | Merck Sharp & Dohme | Inhibitori pirimidina pde10 |
| KR101584925B1 (ko) * | 2011-09-19 | 2016-01-12 | 에프. 호프만-라 로슈 아게 | Pde10a 억제제로서의 트라이아졸로피리딘 화합물 |
| KR20140090665A (ko) | 2011-11-09 | 2014-07-17 | 아비에 도이치란트 게엠베하 운트 콤파니 카게 | 포스포디에스테라제 타입 10a의 억제제로서 유용한 헤테로사이클릭 카복스아미드 |
| US20130116241A1 (en) | 2011-11-09 | 2013-05-09 | Abbvie Inc. | Novel inhibitor compounds of phosphodiesterase type 10a |
| US9138494B2 (en) * | 2011-12-23 | 2015-09-22 | Abbvie Inc. | Radiolabeled PDE10A ligands |
| EP2841070B1 (en) * | 2012-04-24 | 2018-07-25 | Board Of Trustees Of Northern Illinois University | Design and synthesis of novel inhibitors of isoprenoid biosynthesis |
| CN104540835B (zh) | 2012-04-26 | 2017-08-08 | 百时美施贵宝公司 | 用于治疗血小板聚集的作为蛋白酶激活受体4(par4)抑制剂的咪唑并噻二唑衍生物 |
| CN104583218B (zh) | 2012-04-26 | 2018-04-24 | 百时美施贵宝公司 | 作为蛋白酶活化受体4(par4)抑制剂用于治疗血小板聚集的咪唑并噻二唑和咪唑并吡嗪的衍生物 |
| CA2871599A1 (en) | 2012-04-26 | 2013-10-31 | Bristol-Myers Squibb Company | Imidazothiadiazole and imidazopyridazine derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation |
| UY34980A (es) | 2012-08-17 | 2014-03-31 | Abbvie Inc | Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a |
| HK1206728A1 (en) | 2012-09-17 | 2016-01-15 | AbbVie Deutschland GmbH & Co. KG | Novel inhibitor compounds of phosphodiesterase type 10a |
| US20140206667A1 (en) | 2012-11-14 | 2014-07-24 | Michela Gallagher | Methods and compositions for treating schizophrenia |
| US9790203B2 (en) | 2012-11-26 | 2017-10-17 | Abbvie Inc. | Inhibitor compounds of phosphodiesterase type 10A |
| US9200005B2 (en) | 2013-03-13 | 2015-12-01 | AbbVie Deutschland GmbH & Co. KG | Inhibitor compounds of phosphodiesterase type 10A |
| WO2014140184A1 (en) | 2013-03-14 | 2014-09-18 | AbbVie Deutschland GmbH & Co. KG | Novel inhibitor compounds of phosphodiesterase type 10a |
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| US4681940A (en) * | 1985-11-19 | 1987-07-21 | American Home Products Corporation | 5-[3-[[2-quinolyl]methoxy]phenyl]-1,3-oxazoles |
| US5843958A (en) * | 1996-11-27 | 1998-12-01 | Ortho Pharmaceutical Corporation | Arylpyrazoles as leukotriene inhibitors |
| MXPA06014236A (es) * | 2004-06-07 | 2007-02-14 | Pfizer Prod Inc | Inhibicion de la fosfodiesterasa 10 como tratamiento para las afecciones relacionadas con el sindrome metabolico y con la obesidad. |
| BRPI0518508A2 (pt) * | 2005-01-07 | 2008-11-25 | Pfizer Prod Inc | compostos de quinolina heteroaromÁticos e seu uso como inibidores de pde10 |
-
2006
- 2006-12-21 NL NL2000397A patent/NL2000397C2/nl not_active IP Right Cessation
- 2006-12-27 CA CA002636264A patent/CA2636264A1/en not_active Abandoned
- 2006-12-27 JP JP2008549069A patent/JP2009522346A/ja not_active Withdrawn
- 2006-12-27 EP EP06831852A patent/EP1979343A2/en not_active Withdrawn
- 2006-12-27 WO PCT/IB2006/003875 patent/WO2007077490A2/en not_active Ceased
-
2007
- 2007-01-03 PE PE2007000001A patent/PE20071116A1/es not_active Application Discontinuation
- 2007-01-03 US US11/619,218 patent/US20070155779A1/en not_active Abandoned
- 2007-01-03 UY UY30080A patent/UY30080A1/es not_active Application Discontinuation
- 2007-01-04 AR ARP070100041A patent/AR058919A1/es unknown
- 2007-01-04 TW TW096100305A patent/TW200736246A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1979343A2 (en) | 2008-10-15 |
| JP2009522346A (ja) | 2009-06-11 |
| WO2007077490A2 (en) | 2007-07-12 |
| TW200736246A (en) | 2007-10-01 |
| CA2636264A1 (en) | 2007-07-12 |
| NL2000397A1 (nl) | 2007-07-06 |
| US20070155779A1 (en) | 2007-07-05 |
| PE20071116A1 (es) | 2007-11-17 |
| NL2000397C2 (nl) | 2007-10-30 |
| UY30080A1 (es) | 2007-08-31 |
| WO2007077490A3 (en) | 2007-10-04 |
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