AR035493A1 - Derivados de azepino (4,5b) indolina sustituidos, composicion farmaceutica y el uso de dichos derivados para preparar un medicamento - Google Patents
Derivados de azepino (4,5b) indolina sustituidos, composicion farmaceutica y el uso de dichos derivados para preparar un medicamentoInfo
- Publication number
- AR035493A1 AR035493A1 ARP010104449A ARP010104449A AR035493A1 AR 035493 A1 AR035493 A1 AR 035493A1 AR P010104449 A ARP010104449 A AR P010104449A AR P010104449 A ARP010104449 A AR P010104449A AR 035493 A1 AR035493 A1 AR 035493A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- hydrocarbylene
- hydrogen
- independently
- het
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940126601 medicinal product Drugs 0.000 title 1
- 125000000743 hydrocarbylene group Chemical group 0.000 abstract 12
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 10
- 239000001257 hydrogen Substances 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 150000002431 hydrogen Chemical class 0.000 abstract 8
- -1 Het Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 108091032151 5-hydroxytryptamine receptor family Proteins 0.000 abstract 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 1
- 102000014630 G protein-coupled serotonin receptor activity proteins Human genes 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 229910003827 NRaRb Inorganic materials 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 210000003169 central nervous system Anatomy 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000003387 indolinyl group Chemical class N1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 238000002483 medication Methods 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 125000005505 thiomorpholino group Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D487/02—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 two hetero rings
- C07D487/04—Ortho-condensed 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
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Child & Adolescent Psychology (AREA)
- Anesthesiology (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
Abstract
Derivados de azepino[4,5b]indolina sustituidos, que comprenden un compuesto de Fórmula (1) en la cual R1 está seleccionado del grupo que consiste en hidrógeno, alquilo C1-8 y hidrocarbileno C1-8 Ar, cada R2 independientemente está seleccionado del grupo que consiste en alquilo C1-8, y OH; R3 es hidrógeno, alquilo C1-8, Ar, Het, R7C(=O)-, R7OC(=O)-, R5R6NC(=O)-, R7C(=S)-, R7SC(=O)-, R5R6NC(=S)-, R7SO2-, R5R6NSO2, R7S(=O)-, R5R6NS(=O)-, Rc hidrocarbileno C1-8, o Rc hidrocarbileno C1-8 C(=O)-; cada R4, independientemente , esta seleccionado del grupo que consiste en Ar, alquilo C1-8, ArO-, alcoxi C1-8, Het, halo, OH, CN, NO2, CF3, CF3O, NRaRb, N=CRaRb, R7S, hidrocarbileno C1-8 Ar, e hidrocarbileno C1-8 ORa; cada R5 y R6 es independientemente hidrógeno, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, haloalquilo C1-8, cicloalquenilo C3-8, Ar, o hidrocarbileno C1-8 Ar; o R5 y R6 conjuntamente con el nitrógeno al cual están unidos forman un anillo pirrolidino, piperidino, morfolino, o tiomorfolino, cada R7 es independientemente hidrógeno, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, haloalquilo C1-8, cicloalquenilo C3-8, Ar, o hidrocarbileno C1-8 Ar, Ra y Rb, independientemente, están seleccionados del grupo que consiste en hidrógeno, alquilo C1-8, Ar, hidrocarbileno C1-3 Ar, SO2Ar, SO2 alquilo C1-4, (cicloalquilo C3-8) alquilo C1-8, y Het; Rc es Ar, Het, R7CO2-, R7C(=O)-, R7OC(=O)-, R7O-, R7 alquileno C1-8 O-, R7S-, R7C(=S)-, R7S(=O)-, R7S(=O)2-, R7SC(=O)-, R7C(=O)N(R7)-, R7C(=S)N(R7)-, R5R6N-, R5R6NC(=O)-, R5R6NC(=S)-, R5R6NS(=O)-, R5R6NSO2-, R7S(=O)N(R7)-, R7SO2N(R7)-, o R7N(R7)C(=O)N(R7)-; cada Ar es independientemente arilo o heteroarilo; p es 0, 1, 2, 3, o 4; y q es 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 o 10; donde Ar de R1, R3- R7, Ra, Rb y Rc está opcionalmente sustituido con uno o más (por ejemplo 1, 2, 3, 4 o 5) sustituyentes independientemente seleccionados de halo, CN, NO2, ORe, metilendioxi, etilendioxi, CF3, OCF3, SRe, SO2Re, NRfRg, CONRfRg, CORe, Re e hidrocarbileno Rd C1-8, cada Rd es independientemente hidroxi, alcoxi C1-8, ciano, SRh o C(=O)Rh, cada Re está independientemente seleccionado del grupo que consiste en hidrógeno, alquilo C1-8, Ar, hidrocarbileno Ar C1-3, SO2Ar, SO2alquilo C1-4, (cicloalquilo C3-8) alquilo C1-8 y Het; donde cualquier Ar de Re está opcionalmente sustituido con uno o más (por ejemplo 1, 2, 3, 4 o 5) sustituyentes independientemente seleccionados de halo, CN, NO2, ORd, metilendioxi, etilendioxi, CF3, OCF3, SRf, SO2Rf, NRfRg, CONRfRg, CORf, Rf e hidrocarbileno Rd C1-8; cada Rf y Rg está independientemente seleccionado del grupo que consiste en hidrógeno, alquilo C1-8, Ar, hidrocarbileno Ar C1-3, SO2Ar, SO2 alquilo C1-4, (cicloalquilo C3-8) alquilo C1-8 y Het; y cada Rh es independientemente hidrógeno, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, halolaquilo C1-8, cicloalquenilo C3-8, fenilo o hidrocarbileno (fenilo) C1-8; o una sal farmacéuticamente aceptable del mismo; con la condición de que cuando (a) R1 es metilo; y (b) R3 hidrógeno o -(CH2)3NR5R6, donde, R5 y R6 son cada uno metilo; entonces p y q no son cada uno 0, y composiciones farmacéuticas que contienen dichos compuestos o sales. Los compuestos y sales son ligandos 5-HT y son útiles para tratar enfermedades, desórdenes, y/o condiciones de un mamífero en el cual está implicada la actividad de un receptor 5-HT. Los compuestos y sales son particularmente útiles para tratar enfermedades del sistema nervioso central. También se refiere al uso de dichos derivados para preparar medicamentos útiles para tratar una enfermedad del sistema nervioso central.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23437600P | 2000-09-20 | 2000-09-20 | |
| US26604701P | 2001-02-01 | 2001-02-01 | |
| US30196401P | 2001-06-29 | 2001-06-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035493A1 true AR035493A1 (es) | 2004-06-02 |
Family
ID=27398561
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010104450A AR034264A1 (es) | 2000-09-20 | 2001-09-20 | Derivados azepino(4,5-b)indol sustituidos y composiciones farmaceuticas |
| ARP010104449A AR035493A1 (es) | 2000-09-20 | 2001-09-20 | Derivados de azepino (4,5b) indolina sustituidos, composicion farmaceutica y el uso de dichos derivados para preparar un medicamento |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010104450A AR034264A1 (es) | 2000-09-20 | 2001-09-20 | Derivados azepino(4,5-b)indol sustituidos y composiciones farmaceuticas |
Country Status (7)
| Country | Link |
|---|---|
| US (4) | US6583135B2 (es) |
| EP (2) | EP1319004A2 (es) |
| JP (2) | JP2004509893A (es) |
| AR (2) | AR034264A1 (es) |
| AU (2) | AU2001292898A1 (es) |
| PE (2) | PE20020510A1 (es) |
| WO (2) | WO2002024701A2 (es) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004532619A (ja) * | 2001-02-16 | 2004-10-28 | ブリストル−マイヤーズ スクイブ カンパニー | 細胞内シグナル伝達カスケードに関与する新規なヒト遺伝子ret16の同定およびクローニング |
| EP1281700A1 (en) * | 2001-07-31 | 2003-02-05 | Resolution Research Nederland B.V. | Manufacturing process for the preparation of alpha, alpha-branched alkane carboxylic acids providing esters with an improved softness |
| EP1414819B1 (en) | 2001-08-08 | 2005-10-12 | Pharmacia & Upjohn Company LLC | THERAPEUTIC 1H-PYRIDO[4,3-b]INDOLES |
| TWI329111B (en) * | 2002-05-24 | 2010-08-21 | X Ceptor Therapeutics Inc | Azepinoindole and pyridoindole derivatives as pharmaceutical agents |
| US7595311B2 (en) * | 2002-05-24 | 2009-09-29 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
| AU2002950217A0 (en) | 2002-07-16 | 2002-09-12 | Prana Biotechnology Limited | 8- Hydroxy Quinoline Derivatives |
| US7592454B2 (en) * | 2004-04-14 | 2009-09-22 | Bristol-Myers Squibb Company | Substituted hexahydro-pyridoindole derivatives as serotonin receptor agonists and antagonists |
| CN1980710B (zh) * | 2004-06-30 | 2013-06-12 | 阿特西斯公司 | 作为5-羟色胺受体调节剂的取代的氮杂环庚烯衍生物 |
| WO2006022420A1 (ja) | 2004-08-25 | 2006-03-02 | Takeda Pharmaceutical Company Limited | 腹圧性尿失禁の予防・治療剤及びそのスクリーニング方法 |
| EP1747779A1 (en) * | 2005-07-28 | 2007-01-31 | Laboratorios Del Dr. Esteve, S.A. | Tetrahydro-b-carbolin-sulfonamide derivatives as 5-HT6 ligands |
| EP1981337B1 (en) * | 2006-01-19 | 2015-09-02 | Athersys, Inc. | Thiophenyl azepines as serotonin 5-ht2c receptor ligands and uses thereof |
| WO2007132841A1 (ja) | 2006-05-16 | 2007-11-22 | Takeda Pharmaceutical Company Limited | 縮合複素環化合物およびその用途 |
| WO2009035574A1 (en) * | 2007-09-10 | 2009-03-19 | Merck & Co., Inc. | Method for measuring mitochondrial membrane potential in vertebrate cells |
| US7816435B2 (en) * | 2007-10-31 | 2010-10-19 | Momentive Performance Materials Inc. | Halo-functional silane, process for its preparation, rubber composition containing same and articles manufactured therefrom |
| JP5520051B2 (ja) | 2007-11-15 | 2014-06-11 | 武田薬品工業株式会社 | 縮合ピリジン誘導体およびその用途 |
| WO2009089482A1 (en) | 2008-01-11 | 2009-07-16 | Albany Molecular Research, Inc. | (1-azinone) -substituted pyridoindoles as mch antagonists |
| AR073701A1 (es) | 2008-09-29 | 2010-11-24 | Abbott Lab | Derivados de indol y de indolicina, metodos para su preparacion, una composicion farmaceutica que los comprende y su uso en el tratamiento de enfermedades neurodegenerativas. |
| US9625475B2 (en) | 2008-09-29 | 2017-04-18 | Abbvie Inc. | Indole and indoline derivatives and methods of use thereof |
| EP2348847A4 (en) * | 2008-10-31 | 2012-05-23 | Medivation Technologies Inc | AZEPINO [4, 5-B] INDOLE AND USE PROCESS |
| CA2742320A1 (en) | 2008-10-31 | 2010-05-06 | Medivation Technologies, Inc. | Pyrido[4,3-b]indoles containing rigid moieties |
| WO2011003007A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
| WO2011003012A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle mch-1 antagonists, methods of making, and use thereof |
| JP2012532144A (ja) * | 2009-07-01 | 2012-12-13 | アルバニー モレキュラー リサーチ, インコーポレイテッド | アジノン置換アゼピノ[b]インドールおよびピリド−ピロロ−アゼピンmch−1拮抗薬、ならびにその作製方法および使用 |
| WO2011003021A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
| WO2011071136A1 (ja) | 2009-12-11 | 2011-06-16 | アステラス製薬株式会社 | 線維筋痛症治療剤 |
| US9034865B2 (en) | 2010-02-18 | 2015-05-19 | Medivation Technologies, Inc. | Pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use |
| WO2011103460A1 (en) | 2010-02-18 | 2011-08-25 | Medivation Technologies, Inc. | Fused tetracyclic pyrido[4,3-b]indole and pyrido[3,4-b]ondole derivatives and methods of use |
| US20130172320A1 (en) * | 2010-02-18 | 2013-07-04 | Sarvajit Chakravarty | Pyrido [4,3-b] indole and pyrido [3,4-b] indole derivatives and methods of use |
| US9040519B2 (en) | 2010-02-18 | 2015-05-26 | Medivation Technologies, Inc. | Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use |
| WO2011103430A1 (en) * | 2010-02-19 | 2011-08-25 | Medivation Technologies, Inc. | Pyrido[4,3-b]indole and pyrido[3,4-b]indole derivatives and methods of use |
| US8993765B2 (en) | 2010-12-21 | 2015-03-31 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof |
| US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
| WO2012112963A1 (en) | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods for treatment of hypertension |
| WO2012112965A1 (en) * | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods of treating diabetes |
| JP2014505737A (ja) | 2011-02-18 | 2014-03-06 | メディベイション テクノロジーズ, インコーポレイテッド | 糖尿病を処置する化合物および方法 |
| US20130178618A1 (en) * | 2012-01-10 | 2013-07-11 | William Allen Boulanger | Novel pharmaceutical intermediates and methods for preparing the same |
| WO2014031165A1 (en) * | 2012-08-22 | 2014-02-27 | Medivation Technologies, Inc. | Compounds and methods of treating diabetes |
| EP3519816A4 (en) | 2016-09-29 | 2020-05-06 | The Regents of the University of California | Compounds for increasing neural plasticity |
| EP3525763B1 (en) | 2016-10-12 | 2025-03-05 | Intra-Cellular Therapies, Inc. | Amorphous solid dispersions |
| MX395214B (es) | 2017-03-24 | 2025-03-25 | Intra Cellular Therapies Inc | Composiciones novedosas y metodos |
| EP3733204A4 (en) | 2017-12-27 | 2021-09-15 | Takeda Pharmaceutical Company Limited | THERAPEUTIC AGENT FOR URINARY INCONTINENCE OF STRESS AND FECAL INCONTINENCE |
| US12144808B2 (en) | 2018-08-29 | 2024-11-19 | Intra-Cellular Therapies, Inc. | Compositions and methods |
| US10695345B2 (en) | 2018-08-31 | 2020-06-30 | Intra-Cellular Therapies, Inc. | Pharmaceutical capsule compositions comprising lumateperone mono-tosylate |
| EP3843738A4 (en) | 2018-08-31 | 2022-06-01 | Intra-Cellular Therapies, Inc. | NEW METHODS |
| EP3930708A4 (en) | 2019-02-27 | 2023-02-15 | The Regents Of The University Of California | N-SUBSTITUTED INDOLES AND OTHER HETEROCYCLES FOR THE TREATMENT OF BRAIN DISORDERS |
| BR112021016620A2 (pt) | 2019-02-27 | 2021-11-03 | Univ California | Azepino-indóis e outros heterociclos para o tratamento de distúrbios cerebrais |
| CN111053789A (zh) * | 2019-11-26 | 2020-04-24 | 湖南营养树生物科技有限公司 | 调节免疫系统的方法和组合物 |
| US20230257385A1 (en) | 2021-11-17 | 2023-08-17 | Terran Biosciences Inc. | Salt and solid forms of tabernanthalog |
| IL313457A (en) * | 2021-12-15 | 2024-08-01 | Delix Therapeutics Inc | Compressed pyrrolidine psychoplastogens and their uses |
| TW202333668A (zh) * | 2021-12-15 | 2023-09-01 | 美商德利克斯醫療公司 | 經苯氧基及苄氧基取代之精神成形素(psychoplastogen)及其用途 |
| US20250145638A1 (en) * | 2021-12-22 | 2025-05-08 | Kuleon Llc | Serotonin Receptor Agonists and Methods of Making and Using the Same |
| JP2025515146A (ja) * | 2022-05-06 | 2025-05-13 | ブライト マインズ バイオサイエンスィズ インコーポレイテッド | アゼピノインドール及びその調製方法 |
| US12116372B1 (en) | 2023-12-14 | 2024-10-15 | William Allen Boulanger | Process for preparing methyl 3-bromo-2-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)propanoate |
| CN120607526A (zh) * | 2024-05-31 | 2025-09-09 | 和径医药科技(上海)有限公司 | 三并环类化合物、其药物组合物及应用 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR6699E (fr) | 1905-09-25 | 1907-01-31 | Maurice Honore Firmin Muraire | Machine à enfiler les cocons de vers à soie |
| DE1062840B (de) | 1953-03-03 | 1959-08-06 | Siemens Reiniger Werke Ag | Eirichtung zur Sichtbarmachung usichtbarer, bzw. zur Verstaerkung sichtbarer,durch Korpuskular- oder Wellenstrahlung hervorgerufener Bilder, insbesondere fuer Roentgendurchleuchtungen |
| CH445508A (de) * | 1964-12-03 | 1967-10-31 | Geigy Ag J R | Verfahren zur Herstellung von neuen Indolderivaten |
| US3839357A (en) | 1966-05-10 | 1974-10-01 | Upjohn Co | 1,2,3,4,5,6-hexahydroazepino(4,5-b)indoles |
| GR35044B (el) | 1966-05-10 | 1968-07-31 | The Upjohn Company | Μεθοδος παρασκευης οργανικων ενωσεων. |
| US3525750A (en) | 1966-05-31 | 1970-08-25 | Geigy Chem Corp | 1,2,3,4,5,6-hexahydro-azepino(4,5-b) indole derivatives |
| US3553232A (en) | 1967-08-25 | 1971-01-05 | Upjohn Co | 4-(1,4,5,6-tetrahydroazepine(4,5-b)indole-3(2h)-yl)butyrophenones |
| US3622673A (en) | 1968-11-14 | 1971-11-23 | Upjohn Co | 4-(1,4,5,6-TETRAHYDROZEPINO 4,5-b INDOL-3(2H)-YL-BUTYROPHENON COMPOSITIONS AND PROCESS OF TREATMENT MENTAL OR EMOTIONAL DISORDERS |
| US3652588A (en) | 1969-10-23 | 1972-03-28 | Upjohn Co | 6-alkyl-1 2 3 4 5 6-hexahydroazepino(4 5-b)indoles |
| US3676558A (en) | 1970-08-28 | 1972-07-11 | Upjohn Co | Anorexigenic compositions comprising 6-alkyl-1,2,3,4,5,6-hexahydroazepino 4,5-indoles as active ingredient and process of treatment |
| US3776922A (en) | 1972-03-24 | 1973-12-04 | J Epstein | Indole carboxaldehydes |
| DE3070467D1 (en) | 1979-11-02 | 1985-05-15 | Sandoz Ag | Azepinoindoles, process for their production and pharmaceutical compositions containing them |
| CH649553A5 (de) | 1982-05-06 | 1985-05-31 | Sandoz Ag | Azepinoindole und verfahren zu deren herstellung. |
| JPS63163347A (ja) | 1986-12-25 | 1988-07-06 | Konica Corp | 有機着色物質の光褪色防止方法 |
| EP0377238A1 (en) | 1988-12-22 | 1990-07-11 | Duphar International Research B.V | New annelated indolo (3,2-c)-lactams |
| FR2663935A1 (fr) | 1990-06-27 | 1992-01-03 | Adir | Nouveaux 1,2,3,4,5,6-hexahydroazepino [4,5-b] indoles et 1,2,3,4-tetrahydrobethacarbolines, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent. |
| AR023574A1 (es) | 1999-04-23 | 2002-09-04 | Pharmacia & Upjohn Co Llc | Compuestos de azepinindol tetraciclico,composiciones farmaceuticas y el uso de dichos compuestos para preparar un medicamento, e intermediarios |
| AU5737900A (en) | 1999-06-15 | 2001-01-02 | Du Pont Pharmaceuticals Company | Substituted heterocycle fused gamma-carbolines |
| DE19929076A1 (de) | 1999-06-25 | 2000-12-28 | Aventis Pharma Gmbh | Indanylsubstituierte Benzolcarbonamide, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament sowie sie enthaltende pharmazeutische Zubereitungen |
| MY122278A (en) | 1999-07-19 | 2006-04-29 | Upjohn Co | 1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position |
| AU2001269781A1 (en) * | 2000-07-06 | 2002-01-21 | Pharmacia And Upjohn Company | Substituted 2,3,7,8,9,10,11,12-octahydroazepino(4,5-b)pyrano(3,2-e) indoles |
-
2001
- 2001-09-20 AU AU2001292898A patent/AU2001292898A1/en not_active Abandoned
- 2001-09-20 WO PCT/US2001/029535 patent/WO2002024701A2/en not_active Ceased
- 2001-09-20 US US09/957,625 patent/US6583135B2/en not_active Expired - Fee Related
- 2001-09-20 AR ARP010104450A patent/AR034264A1/es unknown
- 2001-09-20 AU AU2001294606A patent/AU2001294606A1/en not_active Abandoned
- 2001-09-20 EP EP01973304A patent/EP1319004A2/en not_active Withdrawn
- 2001-09-20 AR ARP010104449A patent/AR035493A1/es not_active Application Discontinuation
- 2001-09-20 US US09/957,319 patent/US6586421B2/en not_active Expired - Fee Related
- 2001-09-20 PE PE2001000944A patent/PE20020510A1/es not_active Application Discontinuation
- 2001-09-20 EP EP01975267A patent/EP1319005A2/en not_active Withdrawn
- 2001-09-20 WO PCT/US2001/029447 patent/WO2002024700A2/en not_active Ceased
- 2001-09-20 PE PE2001000945A patent/PE20020443A1/es not_active Application Discontinuation
- 2001-09-20 JP JP2002529110A patent/JP2004509893A/ja active Pending
- 2001-09-20 JP JP2002529111A patent/JP2004509894A/ja not_active Withdrawn
-
2003
- 2003-03-20 US US10/394,676 patent/US6828314B2/en not_active Expired - Fee Related
- 2003-03-20 US US10/393,968 patent/US6903090B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2004509893A (ja) | 2004-04-02 |
| US20030225058A1 (en) | 2003-12-04 |
| EP1319004A2 (en) | 2003-06-18 |
| US6903090B2 (en) | 2005-06-07 |
| WO2002024701A2 (en) | 2002-03-28 |
| JP2004509894A (ja) | 2004-04-02 |
| AU2001292898A1 (en) | 2002-04-02 |
| US20020077318A1 (en) | 2002-06-20 |
| AR034264A1 (es) | 2004-02-18 |
| WO2002024701A3 (en) | 2002-06-13 |
| PE20020510A1 (es) | 2002-06-12 |
| PE20020443A1 (es) | 2002-05-16 |
| US6828314B2 (en) | 2004-12-07 |
| US6586421B2 (en) | 2003-07-01 |
| US6583135B2 (en) | 2003-06-24 |
| AU2001294606A1 (en) | 2002-04-02 |
| WO2002024700A2 (en) | 2002-03-28 |
| US20030220321A1 (en) | 2003-11-27 |
| US20020107278A1 (en) | 2002-08-08 |
| EP1319005A2 (en) | 2003-06-18 |
| WO2002024700A3 (en) | 2002-06-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR035493A1 (es) | Derivados de azepino (4,5b) indolina sustituidos, composicion farmaceutica y el uso de dichos derivados para preparar un medicamento | |
| AR082152A1 (es) | Derivados de n-(metilsulfonil)benzamida, composiciones farmaceuticas que los comprenden y su uso en la preparacion de medicamentos para el tratamiento de enfermedades mediadas por la inhibicion de nav1.7 | |
| ES2230884T3 (es) | Uso de antagosnistas de 5ht-6 para el tratamiento del trastorno de hiperactividad con deficit de atencion (adhd). | |
| AR036939A1 (es) | Antagonistas de la hormona de concentracion de melanina (mch) composiciones farmaceuticas, un proceso para su elaboracion y el uso de dichos compuestos, solos o en combinacion, para la elaboracion de un medicamento para el tratamiento de obesidad | |
| AR058362A1 (es) | Derivados de isoquinolina - aminopirazol su obtencion y su utilizacion como agentes farmaceuticos | |
| AR063602A1 (es) | Derivados de espiroindolinona, formulaciones farmaceuticas que los contienen y su uso en la obtencion de un medicamento para el tratamiento de trastornos oncologicos. | |
| AR030596A1 (es) | Derivados de quinolina y quinazolina, un procedimiento para su preparacion, composicion farmaceutica que los comprende, uso de los mismos para la elaboracion de medicamentos | |
| CO6251254A2 (es) | Uso de inhibidores de piridopirimidinona de pi3k en el tratamiento del cancer | |
| AR043938A1 (es) | Compuesto heterociclico derivado de quinolina o naftiridina, composicion farmaceutica que lo comprende y su uso para preparar esta ultima | |
| AR037731A1 (es) | Uso de ureas de benzotiazoles | |
| AR044719A1 (es) | Derivados de fenilo y piridinilo, su uso, un proceso para prepararlos, y medicamentos que los contienen | |
| RU2008110913A (ru) | НОВЫЕ ПРОИЗВОДНЫЕ ИМИДАЗО[4,5-b]ПИРИМИДИНА В КАЧЕСТВЕ ИНГИБИТОРОВ КИНАЗЫ ГЛИКОГЕНСИНТАЗЫ 3 ДЛЯ ПРИМЕНЕНИЯ В ЛЕЧЕНИИ ДЕМЕНЦИИ И НЕЙРОДЕГЕНЕРАТИВНЫХ РАССТРОЙСТВ | |
| AR069524A1 (es) | Derivados de isoxazolo - pirazina, un procedimiento para la preparacion del compuesto, medicamento en base al compuesto y uso del compuesto para preparar un medicamento | |
| AR064389A1 (es) | Derivados heterociclicos de nicotinamida utiles en el tratamiento de afecciones y enfermedades alergicas y respiratorias, y composiciones farmaceuticas que los contienen. | |
| CO5031253A1 (es) | Antagonistas receptores y5 de neuropeptidos composiciones farmaceuticas que las contienen | |
| AR067396A1 (es) | Compuesto derivado de imidazo(1,2-a)piridin-2-ilmetil piperidina sustituida sal hidrocloruro del mismo uso del compuesto o de la sal hidrocloruro para la preparacion de un medicamento y composiciones farmaceuticas que los comprende | |
| AR055395A1 (es) | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c | |
| AR030244A1 (es) | Carboxamidas heterociclicas, composiciones farmaceuticas, el uso de las mismas para la manufactura de medicamentos antivirales y un metodo in vitro para inhibir la polimerasa de adn viral | |
| AR071300A1 (es) | Compuestos; composiciones farmaceuticas en base al compuesto y uso del mismo para la manufactura de un medicamento | |
| AR058073A1 (es) | Derivados de imidazol 5-il-pirimidina, procesos de obtencion, composiciones farmaceuticas y usos | |
| AR030563A1 (es) | N-[5-[[[5-alquil-2-oxazolil]metil]tio]-2-tiazolil]carboxamidas inhibidoras de cinasas dependientes de la ciclina y composiciones farmaceuticas que las contienen | |
| AR057835A1 (es) | Derivados de 9- azabiciclo (3.3.1)nonano y composicion farmaceutica | |
| AR040928A1 (es) | Compuestos de acidos sulfona-hidroxamicos aromaticos, composiciones farmaceuticas y su uso en la preparacion de medicamentos utiles como inhibidores de proteasas | |
| AR074700A1 (es) | Derivados heterociclicos fusionados con oxadiazola, composiciones farmaceuticas, procesos de preparacion y su uso en el tratamiento de esclerosis multiple y otras enfermedades | |
| AR012436A1 (es) | Compuestos de 4-aminopirido[2,3-d]pirimidina 5,7-disustituidos, composicion farmaceutica que los comprende, el uso de los mismos para lamanufactura de medicamentos, un procedimiento para su preparacion. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal | ||
| FB | Suspension of granting procedure |