MA29399B1 - Nouveaux ligands du recepteur h3 de l'histamine et leurs applications therapeutiques - Google Patents
Nouveaux ligands du recepteur h3 de l'histamine et leurs applications therapeutiquesInfo
- Publication number
- MA29399B1 MA29399B1 MA30309A MA30309A MA29399B1 MA 29399 B1 MA29399 B1 MA 29399B1 MA 30309 A MA30309 A MA 30309A MA 30309 A MA30309 A MA 30309A MA 29399 B1 MA29399 B1 MA 29399B1
- Authority
- MA
- Morocco
- Prior art keywords
- therapeutic applications
- receptor ligands
- novel histamine
- novel
- histamine
- Prior art date
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- C07D213/24—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 with substituted hydrocarbon radicals attached to ring carbon atoms
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/20—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Abstract
LA PRÉSENTE INVENTION SE RAPPORTE À DE NOUVEAUX COMPOSÉS REPRÉSENTÉS PAR LA FORMULE (I), À LEUR PROCÉDÉ DE PRÉPARATION ET À LEUR UTILISATION THÉRAPEUTIQUE.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05290950A EP1717234A1 (fr) | 2005-04-29 | 2005-04-29 | Phenoxypropylpiperidines and -pyrrolidines et leur utilisation comme ligands du récepteur histaminique H3 |
| US67824305P | 2005-05-06 | 2005-05-06 | |
| EP05291793A EP1717235A3 (fr) | 2005-04-29 | 2005-08-26 | Phenoxypropylpiperidines and -pyrrolidines et leur utilisation comme ligands du récepteur histaminique H3 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29399B1 true MA29399B1 (fr) | 2008-04-01 |
Family
ID=37024927
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30309A MA29399B1 (fr) | 2005-04-29 | 2007-10-23 | Nouveaux ligands du recepteur h3 de l'histamine et leurs applications therapeutiques |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8076329B2 (fr) |
| EP (2) | EP1717235A3 (fr) |
| JP (1) | JP5693814B2 (fr) |
| KR (1) | KR101291575B1 (fr) |
| CN (1) | CN101258138B (fr) |
| AU (1) | AU2006242950B2 (fr) |
| BR (1) | BRPI0612957B8 (fr) |
| CA (1) | CA2606262C (fr) |
| DK (1) | DK1874746T3 (fr) |
| EA (1) | EA019594B1 (fr) |
| ES (1) | ES2563065T3 (fr) |
| HU (1) | HUE026549T2 (fr) |
| MA (1) | MA29399B1 (fr) |
| MX (1) | MX2007013384A (fr) |
| NO (1) | NO340728B1 (fr) |
| NZ (1) | NZ562873A (fr) |
| PL (1) | PL1874746T3 (fr) |
| PT (1) | PT1874746E (fr) |
| SG (1) | SG162732A1 (fr) |
| SI (1) | SI1874746T1 (fr) |
| TN (1) | TNSN07393A1 (fr) |
| WO (1) | WO2006117609A2 (fr) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2653062A1 (fr) * | 2006-05-23 | 2007-11-29 | Transtech Pharma, Inc. | Nouveaux medicaments |
| EP2502918B1 (fr) | 2006-07-25 | 2015-03-25 | Cephalon, Inc. | Dérivés de pyridazinone |
| US8115005B2 (en) * | 2006-08-04 | 2012-02-14 | Decode Genetics Ehf. | Pyrazolylphenyl and pyrrolylphenyl inhibitors of LTA4H for treating inflammation |
| EP2250176B1 (fr) | 2008-01-30 | 2012-08-01 | Cephalon, Inc. | Dérivés de pipéridine spirocyclique substitués en tant que ligands de récepteur d'histamine-3 (h3) |
| CA2712885A1 (fr) * | 2008-01-30 | 2009-08-06 | Cephalon, Inc. | Derives de pyridazine substitues a activite antagoniste des recepteurs h3 de l'histamine |
| KR101719550B1 (ko) | 2008-07-02 | 2017-03-24 | 브리티쉬 콜롬비아 캔써 에이전시 브랜치 | 디글리시드 에테르 유도체 치료법 및 이의 사용 방법 |
| US20130109758A1 (en) * | 2010-01-06 | 2013-05-02 | The University Of British Columbia | Bisphenol derivative therapeutics and methods for their use |
| WO2011082487A1 (fr) | 2010-01-06 | 2011-07-14 | British Columbia Cancer Agency Branch | Dérivés du bisphénol et leur utilisation en tant que modulateurs de l'activité du récepteur des androgènes |
| TW201206939A (en) * | 2010-05-11 | 2012-02-16 | Sanofi Aventis | Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof |
| BR112014013461A2 (pt) | 2011-12-08 | 2017-06-13 | Taisho Pharmaceutical Co Ltd | derivado de fenilpirrol |
| WO2013100054A1 (fr) * | 2011-12-27 | 2013-07-04 | 大正製薬株式会社 | Dérivé de phényltriazole |
| US9365510B2 (en) | 2012-04-16 | 2016-06-14 | British Columbia Cancer Agency Branch | Aziridine bisphenol ethers and related compounds and methods for their use |
| JP6062077B2 (ja) * | 2013-03-12 | 2017-01-18 | バイオ−ファーム ソリューションズ カンパニー リミテッド | 小児てんかん及びてんかん関連症侯群の予防又は治療用フェニルカルバメート化合物{phenylcarbamatecompoundsforuseinpreventingortreatingpediatricepilesyandepilesy−relatedsyndromes} |
| SG10201607177XA (en) | 2013-05-10 | 2016-10-28 | British Columbia Cancer Agency | Ester derivatives of androgen receptor modulators and methods for their use |
| WO2015031984A1 (fr) | 2013-09-09 | 2015-03-12 | British Columbia Cancer Agency Branch | Composés halogénés pour imagerie et traitement du cancer, et procédés pour leur utilisation |
| FI3988541T3 (fi) | 2015-01-13 | 2024-09-17 | British Columbia Cancer Agency Branch | Heterosyklisiä yhdisteitä syövän kuvantamiseksi ja hoitamiseksi ja menetelmiä niiden käyttämiseksi |
| US10471023B2 (en) | 2015-03-12 | 2019-11-12 | British Columbia Cancer Agency Branch | Bisphenol ether derivatives and methods for using the same |
| US20170298033A1 (en) | 2016-04-15 | 2017-10-19 | The University Of British Columbia | Bisphenol derivatives and their use as androgen receptor activity modulators |
| US10144706B2 (en) * | 2016-09-01 | 2018-12-04 | Bristol-Myers Squibb Company | Compounds useful as immunomodulators |
| EP3378858A1 (fr) * | 2017-03-21 | 2018-09-26 | Bioprojet | Tétrahydrate de ligand h3, son procédé de préparation et compositions pharmaceutiques le comprenant |
| EP3378477A1 (fr) * | 2017-03-21 | 2018-09-26 | BIOPROJET Pharma | Nouvelles utilisations thérapeutiques de ligands h3 |
| WO2019226991A1 (fr) | 2018-05-25 | 2019-11-28 | Essa Pharma, Inc. | Modulateurs du récepteur des androgènes et leurs procédés d'utilisation |
| LT3806859T (lt) * | 2018-05-31 | 2025-03-25 | Suven Life Sciences Limited | Gydymo histamino-3 receptorių atvirkštiniu agonistu būdas |
| PT3598975T (pt) | 2018-07-27 | 2020-12-21 | Bioprojet Soc Civ | Novas combinações de um antagonista h3 e um inibidor da re-assimilação da noradrenalina, e suas utilizações terapêuticas |
| AU2019362061B2 (en) | 2018-10-18 | 2024-09-26 | Essa Pharma Inc | Androgen receptor modulators and methods for their use |
| US12109179B2 (en) | 2019-03-28 | 2024-10-08 | Essa Pharma Inc. | Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof |
| EP4135675A4 (fr) | 2020-04-17 | 2024-04-10 | Essa Pharma, Inc. | Formes solides d'un inhibiteur de récepteur des androgènes de domaine n-terminal et leurs utilisations |
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| US2914529A (en) * | 1957-09-05 | 1959-11-24 | Wm S Merrell Co | Mono aminoethers of triphenyl ethylenes |
| BE788032A (fr) * | 1971-08-25 | 1973-02-26 | Hoechst Ag | Isoindolines substituees leur procede de preparation et leurs applications |
| HU186655B (en) * | 1982-12-28 | 1985-09-30 | Richter Gedeon Vegyeszet | Process for producing new piperidine derivatives, acid additional salts and quaternary salts and pharmaceutical compositions containing them |
| FR2579596B1 (fr) | 1985-03-26 | 1987-11-20 | Inst Nat Sante Rech Med | (imidazolyl-4) piperidines, leur preparation et leur application en therapeutique |
| US4810713A (en) * | 1985-12-20 | 1989-03-07 | A. H. Robins Company, Incorporated | Arylalkyl-heterocyclic amines, n-substituted by aryloxyalkyl groups used in a method for allergy treatment |
| DK0382185T3 (da) * | 1989-02-10 | 1994-07-04 | Otsuka Pharma Co Ltd | Carbostyrilderivater |
| FR2671083B1 (fr) | 1990-12-31 | 1994-12-23 | Inst Nat Sante Rech Med | Nouvelles 4-(4-imidazolyl) piperidines substituees en 1, leur preparation ainsi que leurs applications therapeutiques. |
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| US5639775A (en) | 1992-04-01 | 1997-06-17 | The University Of Toledo | 4-[4'-piperodinyl or 3'-pirrolidinyl] substituted imidazoles as H3 -receptor antagonists and therapeutic uses thereof |
| US5380858A (en) | 1992-04-01 | 1995-01-10 | The University Of Toledo | Process for the preparation of intermediates useful for the synthesis of histamine receptor antagonists |
| US5486526A (en) | 1992-04-01 | 1996-01-23 | The University Of Toledo | Histamine H3 -receptor antagonists and therapeutic uses thereof |
| KR960701858A (ko) | 1993-01-25 | 1996-03-28 | 가와노 다케히코 | 이미다졸계 화합물(Imidazole-series compound) |
| AU7823894A (en) | 1993-08-27 | 1995-03-21 | Vrije Universiteit | New imidazole derivatives having agonistic or antagonistic activity on the histamine h3 receptor |
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| FR2732017B1 (fr) | 1995-03-21 | 2000-09-22 | Inst Nat Sante Rech Med | Nouveaux derives de l'imidazole antagonistes et/ou agonistes du recepteur h3 de l'histamine, leur preparation et leurs applications therapeutiques |
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| PL195384B1 (pl) * | 2003-09-16 | 2007-09-28 | Univ Adama Mickiewicza | Nowe związki N-[(E)-4-stilbenylooksyalkilo] piperydyny oraz sposób ich otrzymywania |
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| WO2006059778A1 (fr) * | 2004-12-01 | 2006-06-08 | Banyu Pharmaceutical Co., Ltd. | Dérivé substitué de pyridone |
-
2005
- 2005-08-26 EP EP05291793A patent/EP1717235A3/fr not_active Withdrawn
-
2006
- 2006-04-25 ES ES06744550.2T patent/ES2563065T3/es not_active Expired - Lifetime
- 2006-04-25 CA CA2606262A patent/CA2606262C/fr not_active Expired - Lifetime
- 2006-04-25 SG SG201003753-9A patent/SG162732A1/en unknown
- 2006-04-25 EA EA200702363A patent/EA019594B1/ru not_active IP Right Cessation
- 2006-04-25 KR KR1020077027780A patent/KR101291575B1/ko not_active Expired - Lifetime
- 2006-04-25 JP JP2008508317A patent/JP5693814B2/ja not_active Expired - Lifetime
- 2006-04-25 NZ NZ562873A patent/NZ562873A/en unknown
- 2006-04-25 SI SI200632024T patent/SI1874746T1/sl unknown
- 2006-04-25 CN CN2006800228844A patent/CN101258138B/zh not_active Expired - Lifetime
- 2006-04-25 PT PT67445502T patent/PT1874746E/pt unknown
- 2006-04-25 HU HUE06744550A patent/HUE026549T2/hu unknown
- 2006-04-25 US US11/912,816 patent/US8076329B2/en not_active Expired - Lifetime
- 2006-04-25 EP EP06744550.2A patent/EP1874746B1/fr not_active Expired - Lifetime
- 2006-04-25 WO PCT/IB2006/000991 patent/WO2006117609A2/fr not_active Ceased
- 2006-04-25 BR BRPI0612957A patent/BRPI0612957B8/pt active IP Right Grant
- 2006-04-25 AU AU2006242950A patent/AU2006242950B2/en not_active Expired
- 2006-04-25 PL PL06744550T patent/PL1874746T3/pl unknown
- 2006-04-25 DK DK06744550.2T patent/DK1874746T3/en active
- 2006-04-25 MX MX2007013384A patent/MX2007013384A/es active IP Right Grant
-
2007
- 2007-10-23 MA MA30309A patent/MA29399B1/fr unknown
- 2007-10-24 TN TNP2007000393A patent/TNSN07393A1/fr unknown
- 2007-11-06 NO NO20075624A patent/NO340728B1/no unknown
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