MA38697A1 - 4-(5-(4-chlorophényl)-2-(2-cyclopropylacétyl)-1,4-diméthyl-1h-pyrrol-3-yl)benzène-sulfonamide à titre de modulateur du nachr alpha 7 - Google Patents
4-(5-(4-chlorophényl)-2-(2-cyclopropylacétyl)-1,4-diméthyl-1h-pyrrol-3-yl)benzène-sulfonamide à titre de modulateur du nachr alpha 7Info
- Publication number
- MA38697A1 MA38697A1 MA38697A MA38697A MA38697A1 MA 38697 A1 MA38697 A1 MA 38697A1 MA 38697 A MA38697 A MA 38697A MA 38697 A MA38697 A MA 38697A MA 38697 A1 MA38697 A1 MA 38697A1
- Authority
- MA
- Morocco
- Prior art keywords
- cyclopropylacetyl
- benzenesulfonamide
- pyrrol
- chlorophenyl
- dimethyl
- Prior art date
Links
- 208000024827 Alzheimer disease Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 abstract 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 abstract 1
- 208000028698 Cognitive impairment Diseases 0.000 abstract 1
- 206010012289 Dementia Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- 206010039966 Senile dementia Diseases 0.000 abstract 1
- 201000004810 Vascular dementia Diseases 0.000 abstract 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 abstract 1
- 208000010877 cognitive disease Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229940075993 receptor modulator Drugs 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—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
- C07D207/30—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 two double bonds between ring members or between ring members and non-ring members
- C07D207/32—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 two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—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 two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/335—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—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
- C07D207/30—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 two double bonds between ring members or between ring members and non-ring members
- C07D207/32—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 two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—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 two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/333—Radicals substituted by oxygen or sulfur atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Addiction (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Communicable Diseases (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Toxicology (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrrole Compounds (AREA)
Abstract
Cette invention concerne un composé modulateur du récepteur nachr alpha 7, 4-(5-(4-chlorophényl)-2-(2-cyclopropylacétyl)-1,4-diméthyl-1h-pyrrol-3-yl)benzènesulfonamide, sa forme tautomère, ses sels pharmaceutiquement acceptables, des compositions pharmaceutiques contenant ledit composé ou un de ses sels, et une méthode de traitement de diverses maladies, troubles ou affections, par exemple, la maladie d'alzheimer, la déficience cognitive modérée, la démence sénile, la démence vasculaire, la démence de la maladie de parkinson, et le trouble déficitaire de l'attention.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1937MU2013 | 2013-06-03 | ||
| PCT/IB2014/061891 WO2014195848A1 (fr) | 2013-06-03 | 2014-06-02 | 4-(5-(4-chlorophényl)-2-(2-cyclopropylacétyl)-1,4-diméthyl-1h-pyrrol-3-yl)benzène-sulfonamide à titre de modulateur du nachr alpha 7 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA38697A1 true MA38697A1 (fr) | 2017-03-31 |
Family
ID=50981599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38697A MA38697A1 (fr) | 2013-06-03 | 2014-06-02 | 4-(5-(4-chlorophényl)-2-(2-cyclopropylacétyl)-1,4-diméthyl-1h-pyrrol-3-yl)benzène-sulfonamide à titre de modulateur du nachr alpha 7 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US9447037B2 (fr) |
| EP (1) | EP3004054A1 (fr) |
| JP (1) | JP2016520642A (fr) |
| CN (1) | CN105263905A (fr) |
| AP (1) | AP2015008884A0 (fr) |
| AR (1) | AR096462A1 (fr) |
| AU (1) | AU2014276436B2 (fr) |
| BR (1) | BR112015030171A2 (fr) |
| CA (1) | CA2912841A1 (fr) |
| CL (1) | CL2015003515A1 (fr) |
| CR (1) | CR20150646A (fr) |
| CU (1) | CU20150168A7 (fr) |
| EA (1) | EA201592247A1 (fr) |
| IL (1) | IL242837A0 (fr) |
| MA (1) | MA38697A1 (fr) |
| MX (1) | MX2015016539A (fr) |
| PE (1) | PE20160009A1 (fr) |
| PH (1) | PH12015502676A1 (fr) |
| SG (1) | SG11201509442RA (fr) |
| TW (1) | TW201446243A (fr) |
| WO (1) | WO2014195848A1 (fr) |
| ZA (1) | ZA201600021B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3233087B1 (fr) | 2014-12-16 | 2019-10-02 | Axovant Sciences GmbH | Composés amide de quinuclidine à substituants géminal, en tant qu'agonistes des récepteurs nicotiniques de l'acétylcholine 7 |
| JP2018516973A (ja) | 2015-06-10 | 2018-06-28 | フォーラム・ファーマシューティカルズ・インコーポレイテッドForum Pharmaceuticals Inc. | α7−ニコチン性アセチルコリン受容体のアゴニストとしてのアミノベンゾイソオキサゾール化合物 |
| WO2017027600A1 (fr) | 2015-08-12 | 2017-02-16 | Forum Pharmaceuticals, Inc. | Composés d'aminobenzisoxazole à substitution géminale utilisés en tant qu'agonistes de récepteurs de l'acétylcholine α7-nicotinique |
| CR20180452A (es) | 2016-03-22 | 2019-02-06 | Merck Sharp & Dohme | Moduladores alostéricos de receptores de acetilcolina nicotícos |
| WO2018187606A1 (fr) * | 2017-04-07 | 2018-10-11 | Los Angeles Biomedical Research Institute At Harbor-Ucla Medical Center | PROCÉDÉS ET COMPOSITIONS POUR MODULER LES INTERACTIONS β-AMYLOÏDE/α7-NACHR |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| US4501728A (en) | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
| US5019369A (en) | 1984-10-22 | 1991-05-28 | Vestar, Inc. | Method of targeting tumors in humans |
| US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| BRPI0507296A (pt) | 2004-03-29 | 2007-07-03 | Neurosearch As | derivado de uréia, composição farmacêutica, uso de um derivado de uréia, e, método de tratamento, prevenção ou alìvio de uma doença ou um distúrbio ou uma condição de um corpo de animal vivo |
| US20060142349A1 (en) | 2004-12-23 | 2006-06-29 | Pfizer Inc | Methods of modulating the activities of alpha-7 nicotinic acetylcholine receptor |
| WO2006087305A1 (fr) | 2005-02-16 | 2006-08-24 | Neurosearch A/S | Derives aryle diazabicycliques et utilisation medicale |
| EA015034B1 (ru) | 2005-09-13 | 2011-04-29 | Янссен Фармацевтика Н.В. | 2-анилин-4-арилзамещенные тиазольные производные |
| US20100227869A1 (en) | 2006-02-16 | 2010-09-09 | Dan Peters | Enantiopure quinuclidinyloxy pyridazines and their use as nicotinic acetylcholine receptor ligands |
| JO3019B1 (ar) | 2006-04-19 | 2016-09-05 | Janssen Pharmaceutica Nv | ثلاثي مستبدل 4،2،1-ثلاثي زولات |
| MX2008016338A (es) | 2006-06-27 | 2009-01-16 | Abbott Lab | Derivados de pirrol y sus metodos de uso. |
| US7683084B2 (en) | 2006-06-27 | 2010-03-23 | Abbott Laboratories | Thiazoline and oxazoline derivatives and their methods of use |
| JP2010535738A (ja) | 2007-08-08 | 2010-11-25 | ノイロサーチ アクティーゼルスカブ | ニコチン性アセチルコリン受容体の調節物質として有用な新規1,2,3−トリアゾール誘導体 |
| MX2010003156A (es) | 2007-10-04 | 2010-04-01 | Hoffmann La Roche | Derivados de aril amida substituida con tetrazol y usos de los mismos. |
| CN101815512B (zh) | 2007-10-04 | 2013-04-24 | 弗·哈夫曼-拉罗切有限公司 | 环丙基芳基酰胺衍生物和其用途 |
| JO2784B1 (en) | 2007-10-18 | 2014-03-15 | شركة جانسين فارماسوتيكا ان. في | 5,3,1 - Triazole substitute derivative |
| CA2714662C (fr) | 2008-03-19 | 2016-05-10 | Janssen Pharmaceutica Nv | 1,2,4-triazoles trisubstitues comme modulateurs des recepteurs nicotiniques a l'acetylcholine |
| US7786171B2 (en) | 2008-04-04 | 2010-08-31 | Abbott Laboratories | Amide derivatives as positive allosteric modulators and methods of use thereof |
| KR20100135911A (ko) | 2008-04-17 | 2010-12-27 | 글락소 그룹 리미티드 | 니코틴성 아세틸콜린 수용체 아형 알파-7의 조절인자로서의 인돌 |
| CL2009001125A1 (es) | 2008-05-09 | 2011-02-11 | Janssen Pharmaceutica Nv | Compuestos derivados de pirazol trisustituido, moduladores alostericos positivos de los receptores ach nicotinicos; composicion farmaceutica que los comprende; proceso de preparacion de la composicion; y su uso en el tratamiento de enfermedades de snc o inflamatorias. |
| EP2387575B1 (fr) | 2009-01-15 | 2013-09-04 | Anvyl, LLC | Modulateurs allostériques des récepteurs nicotiniques de l'acétylcholine de type alpha7, leurs dérivés et leurs utilisations |
| WO2010130768A1 (fr) | 2009-05-14 | 2010-11-18 | Neurosearch A/S | Nouveaux dérivés de 1,4-diazabicyclo[3.2.1]octane utiles comme modulateurs du récepteur nicotinique à l'acétylcholine |
| JO3250B1 (ar) | 2009-09-22 | 2018-09-16 | Novartis Ag | إستعمال منشطات مستقبل نيكوتينيك أسيتيل كولين ألفا 7 |
| JO3078B1 (ar) | 2009-11-27 | 2017-03-15 | Janssen Pharmaceutica Nv | مورفولينوثيازولات بصفتها منظمات الوستيرية نوع الفا 7 موجبة |
| MX344701B (es) | 2011-02-03 | 2017-01-03 | Lupin Ltd | Derivados de pirrol como moduladores de nachr alfa 7. |
| AP3649A (en) | 2011-02-23 | 2016-03-18 | Lupin Ltd | Heteroaryl derivatives as alpha7 nachr modulators |
| CA2829860A1 (fr) | 2011-03-31 | 2012-10-04 | Lupin Limited | Derives de pyrrole en tant que modulateurs des recepteurs nicotiniques d'acetylcholine pour l'utilisation dans le traitement de troubles neurodegeneratifs comme la maladie d'alzheimer et la maladie de parkinson |
| EP2729455B1 (fr) * | 2011-07-05 | 2016-09-14 | Lupin Limited | Dérivés de biaryle en tant que modulateurs de nachr |
| IN2014MN01756A (fr) | 2012-03-06 | 2015-07-03 | Lupin Ltd | |
| WO2014072957A1 (fr) | 2012-11-12 | 2014-05-15 | Lupin Limited | Dérivés de thiazole en tant que modulateurs de nachr alpha-7 |
| WO2014111839A1 (fr) | 2013-01-16 | 2014-07-24 | Lupin Limited | Dérivés de pyrrole en tant que modulateurs d'alpha-7-nachr |
| JP2016512225A (ja) | 2013-03-13 | 2016-04-25 | ルピン・リミテッドLupin Limited | アルファー7nachrモジュレータとしてのピロール誘導体 |
-
2014
- 2014-05-30 TW TW103118995A patent/TW201446243A/zh unknown
- 2014-06-02 AP AP2015008884A patent/AP2015008884A0/xx unknown
- 2014-06-02 US US14/894,803 patent/US9447037B2/en not_active Expired - Fee Related
- 2014-06-02 WO PCT/IB2014/061891 patent/WO2014195848A1/fr not_active Ceased
- 2014-06-02 EA EA201592247A patent/EA201592247A1/ru unknown
- 2014-06-02 PE PE2015002547A patent/PE20160009A1/es not_active Application Discontinuation
- 2014-06-02 EP EP14732406.5A patent/EP3004054A1/fr not_active Withdrawn
- 2014-06-02 MX MX2015016539A patent/MX2015016539A/es unknown
- 2014-06-02 MA MA38697A patent/MA38697A1/fr unknown
- 2014-06-02 JP JP2016517710A patent/JP2016520642A/ja not_active Withdrawn
- 2014-06-02 BR BR112015030171A patent/BR112015030171A2/pt not_active IP Right Cessation
- 2014-06-02 CN CN201480031584.7A patent/CN105263905A/zh active Pending
- 2014-06-02 AU AU2014276436A patent/AU2014276436B2/en not_active Ceased
- 2014-06-02 CA CA2912841A patent/CA2912841A1/fr not_active Abandoned
- 2014-06-02 SG SG11201509442RA patent/SG11201509442RA/en unknown
- 2014-06-03 AR ARP140102165A patent/AR096462A1/es unknown
-
2015
- 2015-11-27 PH PH12015502676A patent/PH12015502676A1/en unknown
- 2015-11-30 IL IL242837A patent/IL242837A0/en unknown
- 2015-12-01 CL CL2015003515A patent/CL2015003515A1/es unknown
- 2015-12-03 CU CUP2015000168A patent/CU20150168A7/es unknown
- 2015-12-08 CR CR20150646A patent/CR20150646A/es unknown
-
2016
- 2016-01-04 ZA ZA2016/00021A patent/ZA201600021B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL242837A0 (en) | 2016-02-01 |
| AR096462A1 (es) | 2015-12-30 |
| AP2015008884A0 (en) | 2015-11-30 |
| MX2015016539A (es) | 2016-04-15 |
| US20160107990A1 (en) | 2016-04-21 |
| EP3004054A1 (fr) | 2016-04-13 |
| CR20150646A (es) | 2016-04-07 |
| CL2015003515A1 (es) | 2016-07-01 |
| AU2014276436A1 (en) | 2015-12-17 |
| BR112015030171A2 (pt) | 2017-07-25 |
| TW201446243A (zh) | 2014-12-16 |
| SG11201509442RA (en) | 2015-12-30 |
| WO2014195848A1 (fr) | 2014-12-11 |
| CN105263905A (zh) | 2016-01-20 |
| AU2014276436B2 (en) | 2017-03-02 |
| PE20160009A1 (es) | 2016-02-14 |
| PH12015502676A1 (en) | 2016-03-07 |
| ZA201600021B (en) | 2017-05-31 |
| EA201592247A1 (ru) | 2016-04-29 |
| JP2016520642A (ja) | 2016-07-14 |
| CU20150168A7 (es) | 2016-06-29 |
| CA2912841A1 (fr) | 2014-12-11 |
| US9447037B2 (en) | 2016-09-20 |
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