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
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- 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
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- 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)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Addiction (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (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) | JP2004509894A (es) |
| AR (2) | AR034264A1 (es) |
| AU (2) | AU2001292898A1 (es) |
| PE (2) | PE20020443A1 (es) |
| WO (2) | WO2002024700A2 (es) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7198911B2 (en) * | 2001-02-16 | 2007-04-03 | Bristol-Myers Squibb Company | Identification and cloning of a novel human gene, RET16, involved in the intracellular signaling cascade |
| 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 |
| DE60206636T2 (de) | 2001-08-08 | 2006-06-22 | Pharmacia & Upjohn Co. Llc, Kalamazoo | THERAPEUTISCHE 1H-PYRIDO[4,3-b]INDOLE |
| US7595311B2 (en) * | 2002-05-24 | 2009-09-29 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
| TWI329111B (en) * | 2002-05-24 | 2010-08-21 | X Ceptor Therapeutics Inc | Azepinoindole and pyridoindole 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 |
| ES2398694T3 (es) * | 2004-06-30 | 2013-03-21 | Athersys, Inc. | Derivados de azepina sustituidos como moduladores de receptores de serotonina |
| JP5173190B2 (ja) | 2004-08-25 | 2013-03-27 | 武田薬品工業株式会社 | 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 |
| AU2007207508B2 (en) | 2006-01-19 | 2011-08-18 | Athersys, Inc. | Thiophenyl and pyrrolyl azepines as serotonin 5-HT2c receptor ligands and uses thereof |
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| EP2476680B1 (en) | 2008-01-11 | 2014-08-27 | Albany Molecular Research, Inc. | (1-Azinone)-Substituted Pyridoindoles |
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| US9625475B2 (en) | 2008-09-29 | 2017-04-18 | Abbvie Inc. | Indole and indoline derivatives and methods of use thereof |
| BRPI0919948A2 (pt) | 2008-10-31 | 2015-08-25 | Madivation Technologies Inc | Pirido[4,3-b]indois contendo porções rígidas |
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| 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 |
| US8618299B2 (en) | 2009-07-01 | 2013-12-31 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle MCH-1 antagonists, methods of making, and use thereof |
| 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 |
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| JPWO2011071136A1 (ja) | 2009-12-11 | 2013-04-22 | アステラス製薬株式会社 | 線維筋痛症治療剤 |
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| US20140303144A1 (en) * | 2011-02-18 | 2014-10-09 | Medivation Technologies, Inc. | Compounds and methods of treating hypertension |
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| WO2018064465A1 (en) | 2016-09-29 | 2018-04-05 | 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 |
| IL304026B2 (en) | 2017-03-24 | 2024-11-01 | Intra Cellular Therapies Inc | A pharmaceutical preparation containing 1-(4-fluoro-phenyl)-4-((Sa10,Rb6)-3-D2-2,2-methyl-2, 3, a10, 10, 9, b6- hexahydro-H7, H1- Pyrido[3',4',:4,5]pyrrolo[3,2,1-de]quioxalin-8-yl)-butan-1-one and its uses |
| JPWO2019131902A1 (ja) | 2017-12-27 | 2020-12-10 | 武田薬品工業株式会社 | 腹圧性尿失禁および便失禁の治療薬 |
| WO2020047241A1 (en) | 2018-08-29 | 2020-03-05 | Intra-Cellular Therapies, Inc. | Novel compositions and methods |
| CN118873536A (zh) | 2018-08-31 | 2024-11-01 | 细胞内治疗公司 | 新方法 |
| BR112021003655A2 (pt) | 2018-08-31 | 2021-05-18 | Intra-Cellular Therapies, Inc. | métodos novos |
| AU2020229779B9 (en) * | 2019-02-27 | 2025-09-18 | The Regents Of The University Of California | Azepino-indoles and other heterocycles for treating brain disorders |
| JP7636796B2 (ja) | 2019-02-27 | 2025-02-27 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | 脳障害を治療するためのn-置換インドール及び他の複素環化合物 |
| 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 |
| WO2023092045A1 (en) | 2021-11-17 | 2023-05-25 | Terran Biosciences, Inc. | Salt and solid forms of tabernanthalog |
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| JP2025502614A (ja) * | 2021-12-15 | 2025-01-28 | デリックス セラピューティクス,インク. | 縮合ピロリジンサイコプラストゲンとその使用 |
| US20250145638A1 (en) * | 2021-12-22 | 2025-05-08 | Kuleon Llc | Serotonin Receptor Agonists and Methods of Making and Using the Same |
| WO2023212811A1 (en) * | 2022-05-06 | 2023-11-09 | Bright Minds Biosciences Inc. | Azepinoindoles and methods of preparation thereof |
| 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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
| GR35044B (el) * | 1966-05-10 | 1968-07-31 | The Upjohn Company | Μεθοδος παρασκευης οργανικων ενωσεων. |
| US3839357A (en) | 1966-05-10 | 1974-10-01 | Upjohn Co | 1,2,3,4,5,6-hexahydroazepino(4,5-b)indoles |
| 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. |
| PE20010052A1 (es) | 1999-04-23 | 2001-01-27 | Upjohn Co | Compuestos de azepinindol tetraciclico como agonistas o antagonistas del receptor de 5-ht |
| ES2228549T3 (es) * | 1999-06-15 | 2005-04-16 | Bristol-Myers Squibb Pharma Company | Gamma-carbolinas condensadas con heterociclo sustituido. |
| 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 |
| WO2002004456A1 (en) * | 2000-07-06 | 2002-01-17 | Pharmacia & Upjohn Company | SUBSTITUTED 2,3,7,8,9,10,11,12-OCTAHYDROAZEPINO[4,5-b]PYRANO[3,2-e]INDOLES |
-
2001
- 2001-09-20 WO PCT/US2001/029447 patent/WO2002024700A2/en not_active Ceased
- 2001-09-20 AU AU2001292898A patent/AU2001292898A1/en not_active Abandoned
- 2001-09-20 JP JP2002529111A patent/JP2004509894A/ja not_active Withdrawn
- 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 US US09/957,625 patent/US6583135B2/en not_active Expired - Fee Related
- 2001-09-20 EP EP01973304A patent/EP1319004A2/en not_active Withdrawn
- 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/US2001/029535 patent/WO2002024701A2/en not_active Ceased
- 2001-09-20 AU AU2001294606A patent/AU2001294606A1/en not_active Abandoned
- 2001-09-20 AR ARP010104450A patent/AR034264A1/es unknown
- 2001-09-20 AR ARP010104449A patent/AR035493A1/es not_active Application Discontinuation
-
2003
- 2003-03-20 US US10/393,968 patent/US6903090B2/en not_active Expired - Fee Related
- 2003-03-20 US US10/394,676 patent/US6828314B2/en not_active Expired - Fee Related
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| Publication number | Publication date |
|---|---|
| EP1319005A2 (en) | 2003-06-18 |
| EP1319004A2 (en) | 2003-06-18 |
| US20030225058A1 (en) | 2003-12-04 |
| JP2004509894A (ja) | 2004-04-02 |
| US20030220321A1 (en) | 2003-11-27 |
| PE20020510A1 (es) | 2002-06-12 |
| US6903090B2 (en) | 2005-06-07 |
| WO2002024701A2 (en) | 2002-03-28 |
| WO2002024701A3 (en) | 2002-06-13 |
| US6828314B2 (en) | 2004-12-07 |
| WO2002024700A3 (en) | 2002-06-13 |
| PE20020443A1 (es) | 2002-05-16 |
| US20020107278A1 (en) | 2002-08-08 |
| AU2001292898A1 (en) | 2002-04-02 |
| AU2001294606A1 (en) | 2002-04-02 |
| JP2004509893A (ja) | 2004-04-02 |
| WO2002024700A2 (en) | 2002-03-28 |
| AR034264A1 (es) | 2004-02-18 |
| US20020077318A1 (en) | 2002-06-20 |
| US6586421B2 (en) | 2003-07-01 |
| US6583135B2 (en) | 2003-06-24 |
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