AR039957A1 - Derivados de 1-sulfonil-4-aminoalcoxi indol, metodos de preparacion y composicion farmaceutica - Google Patents
Derivados de 1-sulfonil-4-aminoalcoxi indol, metodos de preparacion y composicion farmaceuticaInfo
- Publication number
- AR039957A1 AR039957A1 ARP030101981A ARP030101981A AR039957A1 AR 039957 A1 AR039957 A1 AR 039957A1 AR P030101981 A ARP030101981 A AR P030101981A AR P030101981 A ARP030101981 A AR P030101981A AR 039957 A1 AR039957 A1 AR 039957A1
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- compound
- group
- lower alkyl
- produce
- Prior art date
Links
Classifications
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
-
- 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
- A61P25/24—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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Se provee, una composición farmacéutica que comprende el compuesto de fórmula 1 y métodos para preparar estos compuestos, y uso de los mismos en la preparación de medicamentos. Estos compuestos son útiles como moduladores del 5-HT6 con los que se pueden tratar enfermedades del SNC y también enfermedades del tracto gastrointestinal. Entre las del primer grupo se pueden mencionar: estados de psicosis, esquizofrenia, trastornos maníaco-depresivos, trastornos de la memoria, y enfermedad de Parkinson y Alzheimer. Reivindicación 1: Un compuesto de la fórmula 1: una sal farmacéuticamente aceptable o una prodroga del mismo caracterizado porque: n es 2 o 3; cada uno de R1 y R2 es independientemente hidrógeno, alquilo inferior, o R1 y R2 junto con el átomo de nitrógeno al cual están unidos pueden formar un grupo heterociclilo; cada R3 es independientemente hidrógeno o alquilo, o R3 y R1 junto con el átomo de nitrógeno al cual R1 está unido puede formar una aprte de anillo de cuatro a siete miembros con R1 y R3 juntos formando un grupo alquileno; R4 es hidrógeno, alquilo inferior, o halaoalquilo; R5 es hidrógeno, alquilo inferior, halo, alcoxi o haloalquilo; y R6 es arilo opcionalmente sustituido o heteroarilo opcionalmente sustituido. Reivindicación 18: Un procedimiento para producir un compuesto de fórmula 1 de acuerdo con la reivindicación 1, procedimiento caracterizado porque comprende poner en contacto un compuesto 4-hidroxil-1-sulfonil indol de la fórmula 2, (i) con un compuesto alquilante de la fórmula 3 para obtener un compuesto de fórmula 1; o (ii) (a) con un compuesto ciano de la fórmula: Y-CH2-CN; y (b) reducir el grupo ciano con un agente reductor para producir un compuesto 4-aminoalcoxi-1-sulfonil indol de la fórmula (4); (c) y opcionalmente alquilar el grupo amino con uno o más grupos alquilantes de la fórmula R1-X1 y R2-X2 para producir el compuesto de fórmula (5), en donde R1, R2, R4, R5, R6 y n son aquellos definidos en la reivindicación 1; y cada uno de X1, X2 e Y es independientemente un grupo saliente. Reivindicación 19: Un procedimiento para producir un compuesto de fórmula 1 de acuerdo con la reivindicación 1, caracterizado porque dicho método comprende: (a) poner en contacto un compuesto 4-aminoalcoxi indol de la fórmula (6) con un agente sulfonilante de la fórmula R6-SO2-X para producir el compuesto de fórmula 1 de acuerdo con la reivindicación 1, en donde R1, R2, R3, R4, R5, R6 y n son aquellos definidos en la reivindicación 1; y X es un grupo activante de sulfonilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38604902P | 2002-06-05 | 2002-06-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR039957A1 true AR039957A1 (es) | 2005-03-09 |
Family
ID=29736132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030101981A AR039957A1 (es) | 2002-06-05 | 2003-06-04 | Derivados de 1-sulfonil-4-aminoalcoxi indol, metodos de preparacion y composicion farmaceutica |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6774241B2 (es) |
| EP (1) | EP1513809A1 (es) |
| JP (1) | JP4390698B2 (es) |
| KR (1) | KR100657056B1 (es) |
| CN (1) | CN1293053C (es) |
| AR (1) | AR039957A1 (es) |
| AU (1) | AU2003237705B2 (es) |
| BR (1) | BR0311593A (es) |
| CA (1) | CA2485725A1 (es) |
| MX (1) | MXPA04012122A (es) |
| PL (1) | PL374401A1 (es) |
| RU (1) | RU2323927C2 (es) |
| WO (1) | WO2003104193A1 (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2309154C9 (ru) | 2002-03-27 | 2016-09-27 | Глэксо Груп Лимитед | 3-фенилсульфонил-8-пиперазин-1-ил-хинолины, обладающие аффинностью к 5-нт6 рецептору, способы их получения (варианты) |
| RU2324693C2 (ru) * | 2002-10-18 | 2008-05-20 | Ф.Хоффманн-Ля Рош Аг | 4-пиперазинилбензолсульфонилиндолы, характеризующиеся сродством к рецептору 5-нт6 |
| DE602004000260T2 (de) | 2003-07-22 | 2006-08-24 | Arena Pharmaceuticals, Inc., San Diego | Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen |
| SE0302760D0 (sv) * | 2003-10-20 | 2003-10-20 | Biovitrum Ab | New compounds |
| CN102114244A (zh) | 2004-09-30 | 2011-07-06 | 弗·哈夫曼-拉罗切有限公司 | 治疗认知障碍的组合物和方法 |
| US7713954B2 (en) * | 2004-09-30 | 2010-05-11 | Roche Palo Alto Llc | Compositions and methods for treating cognitive disorders |
| RU2294325C2 (ru) * | 2005-04-04 | 2007-02-27 | Государственное образовательное учреждение высшего профессионального образования "Кубанский государственный технологический университет" (ГОУВПО "КубГТУ") | Способ получения 4-[1-(толил-4-сульфонил)-1h-индолил-2]-бут-3-ен-2-онов |
| BRPI0520579B8 (pt) | 2005-08-12 | 2021-05-25 | Suven Life Sciences Ltd | composto, processo para a preparação de um composto e composição farmacêutica |
| KR101250820B1 (ko) * | 2005-08-16 | 2013-04-04 | 수벤 라이프 사이언시스 리미티드 | 개선된 로사르탄 제조 방법 |
| CA2655694C (en) | 2006-07-03 | 2014-12-16 | Biovitrum Ab (Publ) | 1,4-substituted indoles useful for modulation of the 5-ht6 receptor |
| CA2679346A1 (en) * | 2007-03-13 | 2008-09-18 | Biovitrum Ab (Publ) | Tricyclic isoquinoline derivatives for treatment of obesity |
| US8507469B2 (en) * | 2007-03-23 | 2013-08-13 | Abbott Gmbh & Co. Kg | Azetidin compounds suitable for treating disorders that respond to modulation of the serotonin 5-HT6 receptor |
| UA97837C2 (ru) | 2007-03-23 | 2012-03-26 | Эбботт Гмбх Унд Ко. Кг | Соединения хинолина для лечения нарушений, которые реагируют на модуляцию рецептора серотонина 5-ht6 |
| EP2195656A4 (en) * | 2007-08-21 | 2011-10-19 | Senomyx Inc | HUMAN T2R BITTERITY RECEPTORS AND USES THEREOF |
| US8076491B2 (en) | 2007-08-21 | 2011-12-13 | Senomyx, Inc. | Compounds that inhibit (block) bitter taste in composition and use thereof |
| EP2508177A1 (en) | 2007-12-12 | 2012-10-10 | Glaxo Group Limited | Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-quinoline |
| US20110021538A1 (en) | 2008-04-02 | 2011-01-27 | Arena Pharmaceuticals, Inc. | Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor |
| US9126946B2 (en) | 2008-10-28 | 2015-09-08 | Arena Pharmaceuticals, Inc. | Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto |
| CN102344402B (zh) * | 2010-07-30 | 2015-01-07 | 中国人民解放军军事医学科学院毒物药物研究所 | 苯并氮杂环羟乙基胺类化合物、其制备方法和用途 |
| EP3083588B1 (en) | 2013-12-20 | 2020-12-09 | Sunshine Lake Pharma Co., Ltd. | Aromatic heterocyclic compounds and their application in pharmaceuticals |
| EP3166924B1 (en) | 2014-07-08 | 2019-02-20 | Sunshine Lake Pharma Co., Ltd. | Aromatic heterocyclic derivatives and pharmaceutical applications thereof |
| US10022355B2 (en) | 2015-06-12 | 2018-07-17 | Axovant Sciences Gmbh | Diaryl and arylheteroaryl urea derivatives as modulators of the 5-HT2A serotonin receptor useful for the prophylaxis and treatment of REM sleep behavior disorder |
| BR112018000728A2 (pt) | 2015-07-15 | 2018-09-04 | Axovant Sciences Gmbh | resumo método para a profilaxia e/ou tratamento de alucinações visuais em um sujeito com necessidade do mesmo |
| CN115894325B (zh) * | 2022-09-20 | 2025-05-27 | 徐州医科大学 | 一种含有芳基哌嗪结构的衍生物、组合物及其应用 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1139760A (en) | 1979-03-07 | 1983-01-18 | Makiko Sakai | 1,4-dioxaspiro¬4,5| decene compounds |
| JPH04134064A (ja) | 1990-09-25 | 1992-05-07 | Otsuu Kenkyusho | 4―アルコキシインドール誘導体の製造方法 |
| JPH09506885A (ja) | 1993-12-21 | 1997-07-08 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | 5ht▲下1d▼(抗うつ作用)活性を有するインドール、インドリンおよびキノリン誘導体 |
| EP0871442A1 (en) | 1996-01-09 | 1998-10-21 | Eli Lilly And Company | Benzimidzolyl neuropeptide y receptor antagonists |
| US5958965A (en) | 1996-08-27 | 1999-09-28 | American Home Products Corporation | 4-aminoethoxy indoles |
| GB9820113D0 (en) * | 1998-09-15 | 1998-11-11 | Merck Sharp & Dohme | Therapeutic agents |
| JP2000247949A (ja) * | 1999-02-26 | 2000-09-12 | Eisai Co Ltd | スルホンアミド含有インドール化合物 |
| KR100823908B1 (ko) * | 2000-10-20 | 2008-04-21 | 바이오비트럼 에이비(피유비엘) | 2-, 3-, 4-, 또는 5-치환-n1-(벤젠술포닐)인돌 및 이의치료 용도 |
| JP4184077B2 (ja) * | 2000-11-02 | 2008-11-19 | ワイス | 5−ヒドロキシトリプトアミン−6リガンドとしての1−アリールまたは1−アルキルスルホニル−ヘテロシクリルベンザゾール |
| WO2002041889A2 (en) * | 2000-11-24 | 2002-05-30 | Smithkline Beecham P.L.C. | Indolsulfonyl compounds useful in the treatment of cns disorders |
| TW593278B (en) * | 2001-01-23 | 2004-06-21 | Wyeth Corp | 1-aryl-or 1-alkylsulfonylbenzazole derivatives as 5-hydroxytryptamine-6 ligands |
| CN1293072C (zh) * | 2001-04-20 | 2007-01-03 | 惠氏公司 | 作为5-羟色胺-6配体的杂环基氧基-、-硫代-和-氨基吲哚衍生物 |
| CN1293073C (zh) * | 2001-04-20 | 2007-01-03 | 惠氏公司 | 作为5-羟色胺-6配体的杂环基烷氧基-、-烷硫基-和-烷基氨基吲哚衍生物 |
-
2003
- 2003-05-28 CA CA002485725A patent/CA2485725A1/en not_active Abandoned
- 2003-05-28 BR BR0311593-3A patent/BR0311593A/pt not_active IP Right Cessation
- 2003-05-28 RU RU2004139050/04A patent/RU2323927C2/ru not_active IP Right Cessation
- 2003-05-28 EP EP03735482A patent/EP1513809A1/en not_active Withdrawn
- 2003-05-28 CN CNB038128489A patent/CN1293053C/zh not_active Expired - Fee Related
- 2003-05-28 WO PCT/EP2003/005604 patent/WO2003104193A1/en not_active Ceased
- 2003-05-28 KR KR1020047019737A patent/KR100657056B1/ko not_active Expired - Fee Related
- 2003-05-28 PL PL03374401A patent/PL374401A1/xx not_active Application Discontinuation
- 2003-05-28 JP JP2004511263A patent/JP4390698B2/ja not_active Expired - Fee Related
- 2003-05-28 MX MXPA04012122A patent/MXPA04012122A/es active IP Right Grant
- 2003-05-28 AU AU2003237705A patent/AU2003237705B2/en not_active Ceased
- 2003-06-04 AR ARP030101981A patent/AR039957A1/es unknown
- 2003-06-04 US US10/454,050 patent/US6774241B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR20050010861A (ko) | 2005-01-28 |
| JP4390698B2 (ja) | 2009-12-24 |
| PL374401A1 (en) | 2005-10-17 |
| BR0311593A (pt) | 2005-04-26 |
| CN1659141A (zh) | 2005-08-24 |
| CN1293053C (zh) | 2007-01-03 |
| US20030229069A1 (en) | 2003-12-11 |
| RU2004139050A (ru) | 2005-09-10 |
| JP2005533048A (ja) | 2005-11-04 |
| EP1513809A1 (en) | 2005-03-16 |
| RU2323927C2 (ru) | 2008-05-10 |
| MXPA04012122A (es) | 2005-04-19 |
| US6774241B2 (en) | 2004-08-10 |
| CA2485725A1 (en) | 2003-12-18 |
| AU2003237705B2 (en) | 2009-07-30 |
| KR100657056B1 (ko) | 2006-12-13 |
| WO2003104193A1 (en) | 2003-12-18 |
| AU2003237705A1 (en) | 2003-12-22 |
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