ATE276751T1 - Therapeutische verwendung als histamin-h3- rezeptor liganden von alkylaminen, die kein imidazole enthalten - Google Patents
Therapeutische verwendung als histamin-h3- rezeptor liganden von alkylaminen, die kein imidazole enthaltenInfo
- Publication number
- ATE276751T1 ATE276751T1 AT99941543T AT99941543T ATE276751T1 AT E276751 T1 ATE276751 T1 AT E276751T1 AT 99941543 T AT99941543 T AT 99941543T AT 99941543 T AT99941543 T AT 99941543T AT E276751 T1 ATE276751 T1 AT E276751T1
- Authority
- AT
- Austria
- Prior art keywords
- histamine
- alkylamines
- therapeutic use
- receptor ligands
- contain imidazole
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title abstract 4
- 239000003446 ligand Substances 0.000 title abstract 2
- 102000004384 Histamine H3 receptors Human genes 0.000 title 1
- 108090000981 Histamine H3 receptors Proteins 0.000 title 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 title 1
- 150000003973 alkyl amines Chemical class 0.000 title 1
- 230000001225 therapeutic effect Effects 0.000 title 1
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 1
- 229960001340 histamine Drugs 0.000 abstract 1
- -1 imidazole alkylamine Chemical class 0.000 abstract 1
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- A61K31/396—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having three-membered rings, e.g. aziridine
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- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
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- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98401944A EP0978512A1 (de) | 1998-07-29 | 1998-07-29 | Aryloxy- (oder Arylthio)alkylamine ohne Imidazolring als Histamin-H3-Antagonisten und deren therapeutische Anwendung |
| EP98403351A EP0982300A3 (de) | 1998-07-29 | 1998-12-31 | Alkylamine ohne Imidazolring als Histamin-H3-antagonisten und deren therapeutische Anwendung |
| PCT/EP1999/005744 WO2000006254A2 (en) | 1998-07-29 | 1999-07-29 | Non-imidazole alkylamines as histamine h3-receptor ligands and their therapeutic applications |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE276751T1 true ATE276751T1 (de) | 2004-10-15 |
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| Application Number | Title | Priority Date | Filing Date |
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| AT99941543T ATE276751T1 (de) | 1998-07-29 | 1999-07-29 | Therapeutische verwendung als histamin-h3- rezeptor liganden von alkylaminen, die kein imidazole enthalten |
| AT04003944T ATE326446T1 (de) | 1998-07-29 | 1999-07-29 | Therapeutische verwendung als histamin-h3- rezeptor liganden von alkylaminen, die kein imidazole enthalten |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
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| AT04003944T ATE326446T1 (de) | 1998-07-29 | 1999-07-29 | Therapeutische verwendung als histamin-h3- rezeptor liganden von alkylaminen, die kein imidazole enthalten |
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| EP (4) | EP0982300A3 (de) |
| JP (2) | JP4553487B2 (de) |
| AT (2) | ATE276751T1 (de) |
| AU (1) | AU5511999A (de) |
| BE (1) | BE2016C048I2 (de) |
| CA (1) | CA2321881C (de) |
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| DE (2) | DE69931409T2 (de) |
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| LU (1) | LU93229I2 (de) |
| PT (2) | PT1100503E (de) |
| WO (1) | WO2000006254A2 (de) |
Families Citing this family (68)
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| EP0982300A3 (de) * | 1998-07-29 | 2000-03-08 | Societe Civile Bioprojet | Alkylamine ohne Imidazolring als Histamin-H3-antagonisten und deren therapeutische Anwendung |
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| GB0224557D0 (en) | 2002-10-22 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
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| GB0229820D0 (en) * | 2002-12-20 | 2003-01-29 | Glaxo Group Ltd | Novel compounds |
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| EP1611902A4 (de) * | 2003-04-03 | 2006-04-12 | Kyowa Hakko Kogyo Kk | Mittel zur prävention und/oder behandlung von neuropathischen schmerzen |
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| FR2874215B1 (fr) * | 2004-08-11 | 2006-09-29 | Sanofi Synthelabo | Derives de cyclopropylmethanones, leur preparation et leur utilisation en therapeutique |
| EP1720861A2 (de) | 2004-02-25 | 2006-11-15 | Eli Lilly And Company | Antagonisten des histamin-h3-rezeptors, herstellung und therapeutische anwendungen |
| US7456164B2 (en) | 2004-05-07 | 2008-11-25 | Pfizer, Inc | 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands |
| EP1595881A1 (de) | 2004-05-12 | 2005-11-16 | Pfizer Limited | Tetrahydronaphthyridin-Derivate, verwendbar als Histamin H3 Rezeptor-Liganden |
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| EP1717233A1 (de) * | 2005-04-29 | 2006-11-02 | Bioprojet | Liganden für den Histamin H3-Rezeptor und ihre therapeutische Anwendung |
| EP1717235A3 (de) * | 2005-04-29 | 2007-02-28 | Bioprojet | Phenoxypropylpiperidine und -pyrrolidine und ihre Verwendung als Liganden für den Histamin H3-Rezeptor |
| EP1717234A1 (de) * | 2005-04-29 | 2006-11-02 | Bioprojet | Phenoxypropylpiperidine und -pyrrolidine und ihre Verwendung als Liganden für den Histamin H3-Rezeptor |
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| KR102678074B1 (ko) | 2012-05-17 | 2024-06-26 | 제넨테크, 인크. | 무정형 형태의 akt 저해성 피리미디닐 - 사이클로펜탄 화합물, 조성물 및 이들의 방법 |
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| EP3239138A1 (de) * | 2016-04-25 | 2017-11-01 | Sandoz Ag | Wasserstofffumaratsalz von 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidin |
| EP3378477A1 (de) * | 2017-03-21 | 2018-09-26 | BIOPROJET Pharma | Neue therapeutische verwendungen von h3-liganden |
| DK3598975T3 (da) | 2018-07-27 | 2020-11-02 | Bioprojet Soc Civ | Hidtil ukendte kombinationer af en H3-antagonist og en noradrenalin-genoptagelseshæmmer, og de terapeutiske anvendelser deraf |
| WO2020092604A1 (en) * | 2018-10-30 | 2020-05-07 | Concert Pharmaceuticals, Inc. | Deuterated pitolisant |
| KR102669877B1 (ko) * | 2019-12-19 | 2024-05-29 | 삼성전자주식회사 | 통신 장치 및 통신 방법 |
| EP4251148A1 (de) | 2020-11-27 | 2023-10-04 | Richter Gedeon Nyrt. | Histamin-h3-rezeptorantagonisten/inversagonisten zur behandlung von autismusspektrumsstörungen |
| US11623920B2 (en) | 2021-06-07 | 2023-04-11 | Nuray Chemicals Private Limited | Process for preparing pitolisant hydrochloride and solid-state forms thereof |
| US11945788B2 (en) | 2021-06-07 | 2024-04-02 | Nuray Chemicals Private Limited | Process for preparing pitolisant hydrochloride and solid-state forms thereof |
| EP4374854A1 (de) | 2022-11-28 | 2024-05-29 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Pharmazeutische mischung mit amorphem pitolistant |
| WO2024201139A1 (en) | 2023-03-31 | 2024-10-03 | Bioprojet Pharma | Polymorph form of pitolisant hydrochloride |
| WO2025082974A1 (en) | 2023-10-16 | 2025-04-24 | Bioprojet Pharma | New formulations of pitolisant and methods of use |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2870151A (en) * | 1959-01-20 | Mqrpholine -ethers | ||
| DE184968C (de) * | ||||
| DE965813C (de) * | 1950-09-29 | 1957-06-19 | Abbott Lab | Verfahren zur Herstellung von AEthern von Morpholinoalkanolen |
| DE1007774B (de) * | 1954-09-08 | 1957-05-09 | Hoffmann La Roche | Verfahren zur Herstellung von substituierten therapeutisch wirksamen 2, 6, 6-Trimethylcyclohexen-(1)-yl-(1)-propyl- oder -butylaminen bzw. deren Salzen oder quaternaerenAmmoniumverbindungen |
| FR558M (de) * | 1959-03-13 | 1961-05-29 | ||
| DE1269134B (de) * | 1962-12-18 | 1968-05-30 | Hydrierwerk Rodleben Veb | Verfahren zur Herstellung von Dialkylaminoalkylaethern von Phenolen |
| US3312696A (en) * | 1964-02-20 | 1967-04-04 | Turbanti Luigi | 2-tertiary amino alkoxy-betaphenyl-propiophenones |
| US3947434A (en) * | 1973-06-06 | 1976-03-30 | Morton-Norwich Products, Inc. | 9-(P-phenylazoanilino)-7-methyl-1H-imidazo[4,5-f]quinolines |
| DE2408530A1 (de) * | 1974-02-22 | 1975-09-04 | Basf Ag | Verfahren zur herstellung von betahalogenalkylaminosulfonylhalogeniden |
| GB1513092A (en) * | 1975-06-05 | 1978-06-07 | Bottu | O-aminophenol derivatives |
| NL188944C (nl) * | 1975-06-19 | 1992-11-16 | Mitsubishi Chem Ind | Werkwijze voor het bereiden van omega-aminoalkoxybenzeenderivaten alsmede werkwijze voor het bereiden van farmaceutische preparaten met toepassing daarvan, als werkzame verbinding. |
| DE3381617D1 (de) * | 1982-03-17 | 1990-07-05 | Asahi Chemical Ind | Indazol-derivate. |
| DK368687A (da) * | 1986-11-21 | 1988-05-22 | Cheminova As | Aminoalkylerede hydroxyforbindelser og deres anvendelse som fungicider |
| US5348964A (en) * | 1990-07-25 | 1994-09-20 | Merrell Dow Pharmaceuticals Inc. | Piperidyl ethers and thioethers as inhibitors of cholesterol biosynthesis |
| EP0982300A3 (de) * | 1998-07-29 | 2000-03-08 | Societe Civile Bioprojet | Alkylamine ohne Imidazolring als Histamin-H3-antagonisten und deren therapeutische Anwendung |
| FR2788775B1 (fr) * | 1999-01-22 | 2001-04-13 | Pf Medicament | Nouvelles n-alcoyl-n-[1-(omega-(arylalcoyloxy)alcoyl] piperidin-4-yl]-4h-3,1-benzo(thia/oxa)zines-2-amines substituees, leur preparation et leur application en therapeutique |
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1998
- 1998-12-31 EP EP98403351A patent/EP0982300A3/de not_active Withdrawn
-
1999
- 1999-07-29 EP EP04003944A patent/EP1428820B1/de not_active Expired - Lifetime
- 1999-07-29 EP EP99941543A patent/EP1100503B1/de not_active Expired - Lifetime
- 1999-07-29 WO PCT/EP1999/005744 patent/WO2000006254A2/en not_active Ceased
- 1999-07-29 DK DK04003944T patent/DK1428820T3/da active
- 1999-07-29 DE DE69931409T patent/DE69931409T2/de not_active Expired - Lifetime
- 1999-07-29 DK DK99941543T patent/DK1100503T3/da active
- 1999-07-29 ES ES99941543T patent/ES2226423T3/es not_active Expired - Lifetime
- 1999-07-29 EP EP06002726A patent/EP2000462A3/de not_active Withdrawn
- 1999-07-29 AU AU55119/99A patent/AU5511999A/en not_active Abandoned
- 1999-07-29 PT PT99941543T patent/PT1100503E/pt unknown
- 1999-07-29 DE DE69920472T patent/DE69920472T2/de not_active Expired - Lifetime
- 1999-07-29 AT AT99941543T patent/ATE276751T1/de active
- 1999-07-29 JP JP2000562103A patent/JP4553487B2/ja not_active Expired - Lifetime
- 1999-07-29 AT AT04003944T patent/ATE326446T1/de active
- 1999-07-29 US US09/622,199 patent/US7138413B1/en not_active Expired - Lifetime
- 1999-07-29 PT PT04003944T patent/PT1428820E/pt unknown
- 1999-07-29 CA CA2321881A patent/CA2321881C/en not_active Expired - Lifetime
- 1999-07-29 ES ES04003944T patent/ES2260703T3/es not_active Expired - Lifetime
-
2004
- 2004-06-01 US US10/856,838 patent/US7169928B2/en not_active Expired - Lifetime
-
2006
- 2006-07-03 US US11/478,682 patent/US7910605B2/en not_active Expired - Fee Related
-
2010
- 2010-06-02 JP JP2010127067A patent/JP5301501B2/ja not_active Expired - Lifetime
- 2010-12-15 US US12/968,807 patent/US20110281844A1/en not_active Abandoned
-
2016
- 2016-09-21 LU LU93229C patent/LU93229I2/fr unknown
- 2016-09-23 BE BE2016C048C patent/BE2016C048I2/fr unknown
- 2016-09-26 FR FR16C0038C patent/FR16C0038I2/fr active Active
- 2016-09-28 CY CY2016032C patent/CY2016032I2/el unknown
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