ES2064973T3 - Nuevos derivados de indol. - Google Patents
Nuevos derivados de indol.Info
- Publication number
- ES2064973T3 ES2064973T3 ES91610055T ES91610055T ES2064973T3 ES 2064973 T3 ES2064973 T3 ES 2064973T3 ES 91610055 T ES91610055 T ES 91610055T ES 91610055 T ES91610055 T ES 91610055T ES 2064973 T3 ES2064973 T3 ES 2064973T3
- Authority
- ES
- Spain
- Prior art keywords
- hydrogen
- alkyl
- substituted
- elevated
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 title abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical class [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 4
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 229910052717 sulfur Chemical group 0.000 abstract 3
- 239000011593 sulfur Chemical group 0.000 abstract 3
- 241001282138 Antigonia capros Species 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical group [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- -1 METHYL GROUP Chemical group 0.000 abstract 1
- 208000019695 Migraine disease Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical class O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 1
- 230000036506 anxiety Effects 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- LPAGFVYQRIESJQ-UHFFFAOYSA-N indoline Chemical compound C1=CC=C2NCCC2=C1 LPAGFVYQRIESJQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000007774 longterm Effects 0.000 abstract 1
- 206010027599 migraine Diseases 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
- 229940076279 serotonin Drugs 0.000 abstract 1
- 208000019116 sleep disease Diseases 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/24—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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (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)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
SON 6-SUSTITUIDOS O 2-ALQUILO SUSTITUIDO INDOLE O DERIVADOS DEL 2, 3 -DIHIDROINDOLE QUE TIENEN LA FORMULA GENERAL I: DONDE AR ES FENIL OPCIONALMENTE SUSTITUIDO O UN GRUPO AROMATICO HETERO; X ES HIDROGENO, HALOGENO, ALQUILO, ALCOXI, HIDROXI, ALQUILTIO, ALQUILSULFONIL, ALQUILO UORMETIL, O TRIFLUOROMETILTIO; X'' ES UN SUSTITUYENTE TOMADO DE LOS X-SUSTITUYENTES; O X Y X'' ESTAN LIGADOS POR UN ANILLO CARBOCICLICO DE 5-7 MIEMBROS; R ELEVADO 1 ES HIDROGENO U OPCIONALMENTE ALQUILOS BAJO CON HIDROGENO SUSTITUIDO, SIEMPRE QUE CUANDO X ES HIDROGENO O FLUOR, R ELEVADO 1 NO PUEDE SER HIDROGENO; Y ES NITROGENO O CARBONO; LAS LINEAS DE PUNTOS INDICAN ENLACES OPCIONALES, SIEMPRE QUE LAS DOS LINEAS DE PUNTOS NO PUEDAN AL MISMO TIEMPO INDICAR ENLACES; R ES HIDROGENO, ALQUILO, ALQUENILO, CARBOALQUENILO O CICLOALQUILMETIL OPCIONALMENTE SUSTITUIDO POR HIDROXI, O R ES UN GRUPO TOMADO DE LAS ESTRUCTURAS 1A Y 1B: DONDE N ES UN NUMERO DEL 2 AL 6; W ES OXIGENO O AZUFRE; U ES NITROGENO O CARBONO; Z ES UNA CADENA DE CARBONO DIVALENTE DE 2 O 3 MIEMBROS OPCIONALMENTE SUSTITUIDA; V ES OXIGENO, AZUFRE, CH SUB 2 O NR (AL CUADRADO) DONDE R (AL CUADRADO) ES HIDROGENO, UN GRUPO ALQUILO O ALQUENILO OPCIONALMENTE HIDROXI SUSTITUIDO, O UN GRUPO CICLOALQUILO O CICLOALQUILMETIL; V ELEVADO 1 ES OXIGENO, AZUFRE, CH SUB 2 O N EFINIDO COMO ANTERIORMENTE LO HA SIDO R (AL CUADRADO) ; R ELEVADO 3 ES HIDROGENO, UN ALQUILO O ALQUENILO OPCIONALMENTE SUSTITUIDO HIDROXI O UN GRUPO CICLOALQUILO; Y R ELEVADO 4 ES UNO O DOS GRUPOS TOMADOS DE LOS SUSTITUYENTES DE R ELEVADO 3. TIENEN UNA ACTIVIDAD SEROTONIN DE LARGA DURACION CON UNION ESPECIFICA A LOS RECEPTORES DEL 5-HT SUB 2 EN CNS, SIENDO DE ESTA MANERA UTILIZABLES PARA EL TRATAMIENTO TERAPEUTICO DE LOS DESORDENES CNS TALES COMO ANSIEDAD , DEPRESION, DESARREGLOS DEL SUEÑO, MIGRAÑA, ESQUIZOFRENIA Y ENFERMEDAD DE PARKINSON.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK158590A DK158590D0 (da) | 1990-07-02 | 1990-07-02 | Indolderivater |
| SG19895A SG19895G (en) | 1990-07-02 | 1995-02-07 | Novel indole derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2064973T3 true ES2064973T3 (es) | 1995-02-01 |
Family
ID=26065925
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES91610055T Expired - Lifetime ES2064973T3 (es) | 1990-07-02 | 1991-06-24 | Nuevos derivados de indol. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US5216001A (es) |
| EP (1) | EP0465398B1 (es) |
| JP (1) | JP3057109B2 (es) |
| KR (1) | KR950010163B1 (es) |
| AT (1) | ATE115576T1 (es) |
| AU (1) | AU644186B2 (es) |
| CA (1) | CA2045955C (es) |
| DE (1) | DE69105839T2 (es) |
| DK (2) | DK158590D0 (es) |
| ES (1) | ES2064973T3 (es) |
| FI (1) | FI101223B (es) |
| GR (1) | GR3015286T3 (es) |
| HK (1) | HK52195A (es) |
| IE (1) | IE65339B1 (es) |
| IL (1) | IL98495A (es) |
| NO (1) | NO178191C (es) |
| NZ (1) | NZ238757A (es) |
| PT (1) | PT98168B (es) |
| SG (1) | SG19895G (es) |
| ZA (1) | ZA915110B (es) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK152090D0 (da) * | 1990-06-22 | 1990-06-22 | Lundbaek A S H | Piperidylsubstituerede indolderivater |
| US5559246A (en) * | 1990-10-15 | 1996-09-24 | Pfizer Inc. | Indole derivatives |
| US5578612A (en) * | 1990-10-15 | 1996-11-26 | Pfizer Inc. | Indole derivatives |
| US5607951A (en) * | 1990-10-15 | 1997-03-04 | Pfizer Inc | Indole derivatives |
| US5559129A (en) * | 1990-10-15 | 1996-09-24 | Pfizer Inc | Indole derivatives |
| US5545644A (en) * | 1990-10-15 | 1996-08-13 | Pfizer Inc. | Indole derivatives |
| US5643784A (en) * | 1990-12-04 | 1997-07-01 | H, Lundbeck A/S | Indan derivatives |
| DK36291D0 (da) * | 1991-03-01 | 1991-03-01 | Lundbeck & Co As H | Anvendelse af piperidylsubstituerede indolderivater til behandling af kognitive lidelser |
| NZ243065A (en) | 1991-06-13 | 1995-07-26 | Lundbeck & Co As H | Piperidine derivatives and pharmaceutical compositions |
| DK206591D0 (da) * | 1991-12-23 | 1991-12-23 | Lundbeck & Co As H | Behandling af psykoser |
| US5599774A (en) * | 1992-01-22 | 1997-02-04 | Imperial Chemical Industries Plc | N-arylindoles and their use as herbicides |
| DK55192D0 (da) * | 1992-04-28 | 1992-04-28 | Lundbeck & Co As H | 1-piperazino-1,2-dihydroindenderivater |
| US5240927A (en) * | 1992-05-19 | 1993-08-31 | Hoechst-Roussel Pharmaceuticals Incorporated | Benzo[β]thiophen-3-yl piperazines as antipsychotic agents |
| AU675964B2 (en) * | 1992-08-05 | 1997-02-27 | John Wyeth & Brother Limited | Amide derivatives |
| TW251284B (es) * | 1992-11-02 | 1995-07-11 | Pfizer | |
| AU686654B2 (en) * | 1993-08-31 | 1998-02-12 | Pfizer Inc. | 5-arylindole derivatives |
| DK139593D0 (da) * | 1993-12-16 | 1993-12-16 | Lundbeck & Co As H | Compounds |
| US5468768A (en) * | 1994-01-06 | 1995-11-21 | Bristol-Myers Squibb Company | Antimigraine derivatives of indolylcycloalkanylamines |
| GB9417310D0 (en) | 1994-08-27 | 1994-10-19 | Pfizer Ltd | Therapeutic agents |
| US5521196A (en) * | 1994-10-05 | 1996-05-28 | Eli Lilly And Company | 5-HT1F agonists for the treatment of migraine |
| US5521197A (en) * | 1994-12-01 | 1996-05-28 | Eli Lilly And Company | 3-<1-alkylenearyl>-4-<1,2,3,6-tetrahydropyridinyl>-and 3-<1-alkylenearyl>-4-piperidinyl-1h-indoles: new 5-HT1F agonists |
| KR19980703048A (ko) * | 1995-03-20 | 1998-09-05 | 피터쥐.스트링거 | 5-치환-3-(1,2,3,6-테트라히드로피리딘-4-일)- 및 3-(피페리딘-4-일)-1h-인돌: 신규한 5-ht1f 아고니스트 |
| JP4130700B2 (ja) * | 1996-02-26 | 2008-08-06 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 抗腫瘍剤含有組成物 |
| GB9700895D0 (en) * | 1997-01-17 | 1997-03-05 | Lilly Co Eli | Pharmaceutical compounds |
| DE19707628A1 (de) * | 1997-02-26 | 1998-08-27 | Merck Patent Gmbh | Oxazolidinone |
| AR013669A1 (es) * | 1997-10-07 | 2001-01-10 | Smithkline Beecham Corp | Compuestos y metodos |
| GB9805716D0 (en) * | 1998-03-17 | 1998-05-13 | Merck Sharp & Dohme | Therapeutic agents |
| GB9815317D0 (en) * | 1998-07-15 | 1998-09-16 | Merck Sharp & Dohme | Therapeutic agents |
| GB9816263D0 (en) | 1998-07-24 | 1998-09-23 | Merck Sharp & Dohme | Therapeutic agents |
| US5994352A (en) * | 1998-11-13 | 1999-11-30 | Pfizer Inc. | 5-arylindole derivatives |
| JP2002534426A (ja) * | 1999-01-07 | 2002-10-15 | ワイス | 鬱病の処置のための新規な1,4−二基置換されたシクロヘキサン誘導体 |
| US6200994B1 (en) | 1999-01-07 | 2001-03-13 | American Home Products Corp | 1,4-Disubstituted cyclohexane derivatives for the treatment of depression |
| EP1173432B9 (en) * | 1999-04-21 | 2008-10-15 | NPS Allelix Corp. | Piperidine-indole compounds having 5-ht6 affinity |
| US6281207B1 (en) * | 1999-09-15 | 2001-08-28 | Reed Richter | Treatment of movement disorders by administration of mirtazapine |
| US20050101788A1 (en) * | 2002-03-27 | 2005-05-12 | Jacopo Zanon | Method for manufacture of sertindole |
| JOP20210060A1 (ar) | 2018-10-05 | 2023-01-30 | Vertex Pharma | معدلات لمضاد تريبسين ألفا-1 |
| US11884672B2 (en) * | 2019-05-14 | 2024-01-30 | Vertex Pharmaceuticals Incorporated | Modulators of alpha-1 antitrypsin |
| AU2021247285A1 (en) | 2020-04-03 | 2022-10-27 | Vertex Pharmaceuticals Incorporated | Modulators of alpha-1 antitrypsin |
| JP7732999B2 (ja) | 2020-04-03 | 2025-09-02 | バーテックス ファーマシューティカルズ インコーポレイテッド | アルファ1-アンチトリプシンのモジュレーター |
| CN115697969B (zh) | 2020-04-03 | 2026-08-11 | 弗特克斯药品有限公司 | α-1抗胰蛋白酶调节剂 |
| EP4188931A2 (en) | 2020-07-27 | 2023-06-07 | Vertex Pharmaceuticals Incorporated | Processes for preparing modulators of alpha-1 antitrypsin |
| CA3229361A1 (en) * | 2021-08-20 | 2023-02-23 | Abdelmalik Slassi | 3-cycloamino-indole compounds as serotonergic agents useful for the treatment of disorders related thereto |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB944443A (es) * | 1959-09-25 | 1900-01-01 | ||
| DE2322470A1 (de) * | 1973-05-04 | 1974-11-21 | Boehringer Sohn Ingelheim | Neue indolyl-piperidino-(bzw. 1,2,5,6tetrahydro-pyridyl-)butyrophenone und verfahren zu ihrer herstellung |
| US4358456A (en) * | 1980-05-03 | 1982-11-09 | John Wyeth & Brother Limited | Antipsychotic piperidinomethyl-indole derivatives |
| FR2533924A1 (fr) * | 1982-10-05 | 1984-04-06 | Roussel Uclaf | Nouveaux derives du 4-(1h-indol-3-yl)a-methyl piperidine-1-ethanol, leurs sels, le procede de preparation, l'application a titre de medicaments et les compositions les renfermant |
| IE55972B1 (en) * | 1982-10-07 | 1991-03-13 | Kefalas As | Phenylindene derivatives,acid addition salts thereof,and methods of preparation |
| GB8427125D0 (en) * | 1984-10-26 | 1984-12-05 | Lundbeck & Co As H | Organic compounds |
| IE58370B1 (en) * | 1985-04-10 | 1993-09-08 | Lundbeck & Co As H | Indole derivatives |
-
1990
- 1990-07-02 DK DK158590A patent/DK158590D0/da not_active IP Right Cessation
-
1991
- 1991-06-12 IE IE200091A patent/IE65339B1/en not_active IP Right Cessation
- 1991-06-13 IL IL9849591A patent/IL98495A/en not_active IP Right Cessation
- 1991-06-14 NO NO912301A patent/NO178191C/no not_active IP Right Cessation
- 1991-06-24 DK DK91610055.5T patent/DK0465398T3/da active
- 1991-06-24 EP EP91610055A patent/EP0465398B1/en not_active Expired - Lifetime
- 1991-06-24 AT AT91610055T patent/ATE115576T1/de not_active IP Right Cessation
- 1991-06-24 DE DE69105839T patent/DE69105839T2/de not_active Expired - Fee Related
- 1991-06-24 ES ES91610055T patent/ES2064973T3/es not_active Expired - Lifetime
- 1991-06-26 KR KR1019910010711A patent/KR950010163B1/ko not_active Expired - Fee Related
- 1991-06-27 US US07/722,081 patent/US5216001A/en not_active Expired - Fee Related
- 1991-06-27 NZ NZ238757A patent/NZ238757A/xx unknown
- 1991-06-28 CA CA002045955A patent/CA2045955C/en not_active Expired - Fee Related
- 1991-07-01 PT PT98168A patent/PT98168B/pt active IP Right Grant
- 1991-07-01 FI FI913194A patent/FI101223B/fi active
- 1991-07-01 JP JP3160289A patent/JP3057109B2/ja not_active Expired - Fee Related
- 1991-07-02 AU AU80144/91A patent/AU644186B2/en not_active Ceased
- 1991-07-02 ZA ZA915110A patent/ZA915110B/xx unknown
-
1995
- 1995-02-07 SG SG19895A patent/SG19895G/en unknown
- 1995-03-03 GR GR950400464T patent/GR3015286T3/el unknown
- 1995-04-06 HK HK52195A patent/HK52195A/en not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NZ238757A (en) | Optionally heterocyclically-substituted 3-(piperidyl or piperazinyl)-indole derivatives and pharmaceutical compositions | |
| AR011229A1 (es) | Compuestos derivados de adenosina antagonistas en el receptor ai adenosina, procesos para su preparacion, composiciones farmaceuticas que los contieneny su uso en medicina. | |
| ES2149215T3 (es) | Bencilaminoquinuclidinas sustituidas como antagonistas de la sustancia p. | |
| PE46899A1 (es) | Derivados de n-fenil-sulfonamida | |
| ES2160596T3 (es) | Derivados de quinuclidina como antagonistas de la sustancia p. | |
| ES2127912T3 (es) | Benzoderivados condensados. | |
| PE20030039A1 (es) | Derivados de indol con afinidad por el receptor 5-ht6 | |
| ES2122289T3 (es) | Derivados de 5-arilindol. | |
| ES2165986T3 (es) | 3-cilindoles como agonistas del receptor cb2. | |
| CO4440628A1 (es) | Derivados de pirimidina condensados con un anillo heteroci- clico | |
| ES2143557T3 (es) | Agentes de tranferencia de cadena alilica. | |
| MX9102582A (es) | Derivados de indol 3,7-disubstituidos, procedimiento para su preparacion y composicion farmaceutica que los contiene. | |
| MX9206939A (es) | Derivados de piperazina, procedimiento para su preparacion y composicion farmaceutica que los comprende | |
| ES2110086T3 (es) | Indoles sustituidos como antagonistas de la angiotensina ii. | |
| ES2147183T3 (es) | Nuevos derivados de acido metilenobisfosfonico. | |
| ES2045126T3 (es) | Agentes terapeuticos. | |
| ES2103768T3 (es) | Procedimiento de preparacion de derivados sustituidos de benzofurano. | |
| ES2124896T3 (es) | Amidas del acido ciclohexancarboxilico sustituidas con n-(piperidinil-1-alquilo) como antagonistas de receptores t-ht1a. | |
| AR115228A1 (es) | DERIVADOS DE (AZA)INDOL SUSTITUIDOS, UN MÉTODO PARA SU PREPARACIÓN, INTERMEDIARIOS PARA SU SÍNTESIS, COMPOSICIÓN Y COMBINACIÓN FARMACÉUTICA QUE LOS COMPRENDEN Y EL USO DE LOS MISMOS EN EL TRATAMIENTO DE ENFERMEDADES ASOCIADAS AL RECEPTOR NICOTÍNICO DE ACETILCOLINA a7 | |
| ES2096265T3 (es) | Derivados aromaticos de hidroxiamidinas y su empleo como antagonistas del receptor leucotrieno b4. | |
| AR013836A1 (es) | Compuestos espiro [ciclohexil]piperazinilo y composiciones farmaceuticas que los contienen activos como ligandos de un subtipo de receptor de dopamina. | |
| ES8802149A1 (es) | Un procedimiento para la preparacion de derivados de piperazinilo 1,4-disustituidos | |
| ES2173435T3 (es) | Derivados condensados de 2,3-benzodiazepinas y su utilizacion como agentes inhibidores de receptores de ampa. | |
| AR022797A1 (es) | Benzoil indoles n-sustituidos como agentes estrogenicos | |
| AR039008A1 (es) | Derivados azabiciclicos, azatriciclicos y azaespirociclicos de aminociclohexano antagonistas de los receptores nmda, 5-ht3, y nicotinico neuronal |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
Ref document number: 465398 Country of ref document: ES |