MA34957B1 - Derives heteroaryle a titre modulateurs des nachr alpha 7 - Google Patents

Derives heteroaryle a titre modulateurs des nachr alpha 7

Info

Publication number
MA34957B1
MA34957B1 MA36224A MA36224A MA34957B1 MA 34957 B1 MA34957 B1 MA 34957B1 MA 36224 A MA36224 A MA 36224A MA 36224 A MA36224 A MA 36224A MA 34957 B1 MA34957 B1 MA 34957B1
Authority
MA
Morocco
Prior art keywords
analogues
modulators
formula
heteroaryl derivatives
nachr alpha
Prior art date
Application number
MA36224A
Other languages
English (en)
Inventor
Neelima Sinha
Gourhari Jana
Sachchidanand Sachchidanand
Sanjay Pralhad Kurhade
Navnath Popat Karche
Anil Kashiram Hajare
Ajay Ramchandra Tilekar
Venkata P Palle
Rajender Kumar Kamboj
Original Assignee
Lupin Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=45873193&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA34957(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lupin Ltd filed Critical Lupin Ltd
Publication of MA34957B1 publication Critical patent/MA34957B1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • A—HUMAN NECESSITIES
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    • 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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    • 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
    • A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4535—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom, e.g. pizotifen
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    • 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
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • 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
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    • 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
    • C07D207/337—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Furan Compounds (AREA)

Abstract

CETTE INVENTION CONCERNE UN COMPOSÉ DE FORMULE (I), Z, M ET R1 -R6 DANS LA FORMULE ÉTANT TELS QUE DÉFINIS DANS LA DESCRIPTION, À TITRE DE MODULATEUR DES RÉCEPTEURS NICOTINIQUES D'ACÉTYLCHOLINE, EN PARTICULIER, DU SOUS-TYPE A7, CHEZ UN SUJET EN AYANT BESOIN, AINSI QUE LES ANALOGUES, PROMÉDICAMENTS, ANALOGUES ISOTOPIQUEMENT SUBSTITUÉS, MÉTABOLITES, SELS DE QUALITÉ PHARMACEUTIQUE, POLYMORPHES, SOLVATES, ISOMÈRES, CLATHRATES, ET CO-CRISTAUX DE CELUI-CI, À UTILISER SOIT SEULS, SOIT EN ASSOCIATION AVEC D'AUTRES MÉDICAMENTS APPROPRIÉS, ET DES COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSÉS ET LEURS ANALOGUES. UN PROCÉDÉ DE PRÉPARATION DES COMPOSÉS SELON L'INVENTION ET LEURS UTILISATIONS EN THÉRAPIE, EN PARTICULIER, POUR PRÉVENIR ET TRAITER LES TROUBLES TELS QUE LA MALADIE D'ALZHEIMER, LE DÉFICIT COGNITIF MODÉRÉ, LA DÉMENCE SÉNILE, ET AUTRES, SONT ÉGALEMENT DÉCRITS.
MA36224A 2011-02-23 2012-02-22 Derives heteroaryle a titre modulateurs des nachr alpha 7 MA34957B1 (fr)

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Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS55433B1 (sr) 2011-02-23 2017-04-28 Lupin Ltd Derivati heteroarila kao modulatori nachr alfa7
NZ629453A (en) 2012-03-06 2016-04-29 Lupin Ltd Thiazole derivatives as alpha 7 nachr modulators
PT3415517T (pt) * 2012-09-28 2022-05-13 Takeda Pharmaceuticals Co Forma cristalina de 1-(4-1-(2,6-difluorobenzil)-5- dimetilaminometil-3-(6-metoxipiridazin-3-il)-2,4-dioxo- 1,2,3,4-tetrahidrotieno(2,3-d)-pirimidin-6-il)fenil)-3- metoxiureia
EP2945936A1 (fr) 2012-11-12 2015-11-25 Lupin Limited Dérivés de thiazole en tant que modulateurs de nachr alpha-7
EP2945941B1 (fr) 2013-01-16 2016-12-07 Lupin Limited Dérivés de pyrrole en tant que modulateurs d'alpha-7-nachr
US9617210B2 (en) 2013-03-13 2017-04-11 Lupin Limited Pyrrole derivatives as alpha 7 NACHR modulators
TW201446243A (zh) 2013-06-03 2014-12-16 Lupin Ltd 4-(5-(4-氯苯基)-2-(2-環丙基乙醯基)-1,4-二甲基-1氫-吡咯-3-基)苯磺醯胺作為α7尼古丁乙醯膽鹼受體調節劑
WO2014203150A1 (fr) 2013-06-17 2014-12-24 Lupin Limited Dérivés de pyrrole utilisés comme modulateurs d'alpha-7-nachr
EP3623371A1 (fr) 2014-12-16 2020-03-18 Axovant Sciences GmbH Composés amide de quinuclidine à substituants géminal en tant qu'agonistes des récepteurs nicotiniques de l'acétylcholine 7
CA2988968A1 (fr) 2015-06-10 2016-12-15 Forum Pharmaceuticals, Inc. Composes d'aminobenzisoxazole en tant qu'agonistes des recepteurs de l'acetylcholine ?7-nicotinique
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
GEAP202014908A (en) * 2016-03-22 2020-03-10 Merck Sharp & Dohme Allosteric modulators of nicotinic acetylcholine receptors
EP4155293B1 (fr) * 2018-06-07 2025-07-30 The Regents of The University of Michigan Inhibiteurs de prc1 et méthodes de traitement comprenant ces derniers
MA53085B1 (fr) * 2018-07-05 2022-12-30 Bayer Ag Thiophènecarboxamides substitués et analogues comme agents antibactériens
MA56441B1 (fr) 2019-07-03 2024-10-31 Bayer Aktiengesellschaft Carboxamides de thiophène substitués et leurs dérivés comme microbicides
CN118496197A (zh) 2019-12-20 2024-08-16 拜耳公司 取代的噻吩甲酰胺、噻吩甲酸及其衍生物

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3953596A (en) 1973-06-14 1976-04-27 Ici United States Inc. 8-Oxa-3-azabicyclo(3.2.1)octane analgesic compositions and method of alleviating pain in animals
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
US5608082A (en) 1994-07-28 1997-03-04 Agouron Pharmaceuticals, Inc. Compounds useful as antiproliferative agents and GARFT inhibitors
WO1999014194A1 (fr) 1997-09-12 1999-03-25 Merck Frosst Canada & Co. Pyridines 2,3,5-trisubstituees utilisees comme inhibiteurs de la cyclo-oxygenase 2
EP1311505A2 (fr) * 2000-08-21 2003-05-21 PHARMACIA & UPJOHN COMPANY Fragments heteroaryle a substitution quinuclidine destines au traitement de maladies
BR0307409A (pt) 2002-02-01 2004-12-28 Dainippon Pharmaceutical Co Compostos de hidrazida de ácido 2-furanocarboxìlico, composições farmacêuticas contendo os mesmos e uso dos mesmos para preparação de um agente preventivo ou terapêutico
FR2840303B1 (fr) 2002-05-31 2005-07-15 Rhodia Chimie Sa Procede d'arylation ou de vinylation ou d'alcylynation d'un compose nucleophile
SE0201938D0 (sv) 2002-06-20 2002-06-20 Astrazeneca Ab New process
DE10244810A1 (de) 2002-09-26 2004-04-08 Bayer Ag Neue Morpholin-überbrückte Indazolderivate
US7129235B2 (en) 2003-07-11 2006-10-31 Abbott Laboratories Amides useful for treating pain
US7442805B2 (en) 2003-09-25 2008-10-28 Wyeth Substituted sulfonamide-indoles
GB0403038D0 (en) 2004-02-11 2004-03-17 Novartis Ag Organic compounds
CA2561639A1 (fr) 2004-03-29 2005-10-06 Neurosearch A/S Nouveaux derives d'uree et leur utilisation medicale
ITTO20040264A1 (it) 2004-04-28 2004-07-28 Rotta Res Lab Spa Nuovi derivati pirrolici ad attivita' angiotensina-ii antagonista
KR20070106969A (ko) 2004-09-09 2007-11-06 추가이 세이야쿠 가부시키가이샤 신규 이미다졸리딘 유도체 및 그 용도
US20060142349A1 (en) 2004-12-23 2006-06-29 Pfizer Inc Methods of modulating the activities of alpha-7 nicotinic acetylcholine receptor
EP1866314B1 (fr) 2005-02-16 2010-09-15 NeuroSearch A/S Derives aryle diazabicycliques et utilisation medicale
FR2885616B1 (fr) 2005-05-12 2007-06-22 Servier Lab Nouveaux derives de phenylpyridinylpiperazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
EP1910328A1 (fr) * 2005-06-29 2008-04-16 AstraZeneca AB Derives de thiophene-2-carboxamide utilises comme modulateurs du recepteur nicotinique alpha7.
CA2617788A1 (fr) 2005-08-04 2007-02-15 Apogee Biotechnology Corporation Inhibiteurs de la sphingosine kinase et leurs methodes d'utilisation
NZ566036A (en) 2005-09-13 2010-06-25 Janssen Pharmaceutica Nv 2-Aniline-4-aryl substituted thiazole derivatives that modulate the alpha7 nicotinic receptor
JP5301286B2 (ja) 2006-02-03 2013-09-25 イーライ リリー アンド カンパニー Ｆｘ受容体を調節するための化合物及び方法
WO2007093602A1 (fr) 2006-02-16 2007-08-23 Neurosearch A/S Quinuclidinyloxy pyridazines énantiopures et leurs utilisations en tant que ligands du récepteur nicotinique de l'acétylcholine
JO3019B1 (ar) 2006-04-19 2016-09-05 Janssen Pharmaceutica Nv ثلاثي مستبدل 4،2،1-ثلاثي زولات
US7741364B2 (en) 2006-06-27 2010-06-22 Abbott Laboratories Pyrrole derivatives and their methods of use
EP2038278A2 (fr) 2006-06-27 2009-03-25 Abbott Laboratories Dérivés de thiazoline et d'oxazoline et leurs procédés d'utilisation
AU2007318058A1 (en) 2006-11-02 2008-05-15 Merck Sharp & Dohme Corp. Heterocyclyl-substituted anti-hypercholesterolemic compounds
US20080287479A1 (en) 2006-12-20 2008-11-20 Pfizer Inc Inhibitors of serine palmitoyltransferase
AU2008285644A1 (en) 2007-08-08 2009-02-12 Neurosearch A/S Novel 1,2,3-triazole derivatives useful as modulators of nicotinic acetylcholine receptors
GB0718735D0 (en) 2007-09-25 2007-11-07 Prolysis Ltd Antibacterial agents
WO2009043784A1 (fr) 2007-10-04 2009-04-09 F. Hoffmann-La Roche Ag Dérivés de cyclopropyl aryl amides et leurs utilisations
ES2443290T3 (es) 2007-10-04 2014-02-18 F. Hoffmann-La Roche Ag Derivados arilamida sustituidos con tetrazol y usos de los mismos
JO2784B1 (en) 2007-10-18 2014-03-15 شركة جانسين فارماسوتيكا ان. في 5,3,1 - Triazole substitute derivative
MY152486A (en) 2008-03-19 2014-10-15 Janssen Pharmaceutica Nv Trisubstituted 1,2,4 - triazoles as nicotinic acetylcholine receptor modulators
US7786171B2 (en) 2008-04-04 2010-08-31 Abbott Laboratories Amide derivatives as positive allosteric modulators and methods of use thereof
CL2009000916A1 (es) 2008-04-17 2010-12-31 Glaxo Group Ltd Compuestos derivados de 2-trifluorometil-1h-indol-5-metilcarboxamida, moduladores del receptor nicotinico de acetilcolina alfa7 (nachr); composicon farmaceutica; y uso para el tratamiento del deterioro cognitivo y de un trastorno psicotico como esquizofrenia.
WO2009135944A1 (fr) 2008-05-09 2009-11-12 Janssen Pharmaceutica Nv Pyrazoles trisubstitués en tant que modulateurs des récepteurs de l'acétylcholine
WO2010083444A1 (fr) 2009-01-15 2010-07-22 Anvyl, Llc Modulateurs allostériques des récepteurs nicotiniques de l'acétylcholine de type alpha7, leurs dérivés et leurs utilisations
WO2010120854A1 (fr) 2009-04-15 2010-10-21 Glaxosmithkline Llc Composés chimiques
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
CA2825519A1 (fr) 2011-02-03 2012-09-08 Lupin Limited Derives de pyrazole utilises comme modulateurs de nachr alpha-7
RS55433B1 (sr) 2011-02-23 2017-04-28 Lupin Ltd Derivati heteroarila kao modulatori nachr alfa7
AU2012235779B2 (en) 2011-03-31 2017-03-02 Lupin Limited Pyrrole derivatives as nicotinic acetylcholine receptor modulators for use in the treatment of neurodegenerative disorders such as Alzheimer's and Parkinson's disease
US8946432B2 (en) 2011-07-05 2015-02-03 Lupin Limited Biaryl derivatives as nAChR modulators

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US20130331387A1 (en) 2013-12-12
DK2678327T3 (en) 2016-12-12
WO2012114285A9 (fr) 2012-10-18
SMT201600409B (fr) 2017-01-10
GEP20156318B (en) 2015-07-10
SG192625A1 (en) 2013-09-30
CN103402994B (zh) 2017-05-31
AP3649A (en) 2016-03-18
SI2678327T1 (sl) 2017-01-31
EA024170B1 (ru) 2016-08-31
MX2013009709A (es) 2014-05-13
ES2594409T9 (es) 2017-02-09
WO2012114285A1 (fr) 2012-08-30
AP2013007121A0 (en) 2013-09-30
EP2678327B1 (fr) 2016-08-17
CY1118107T1 (el) 2017-06-28
CR20130415A (es) 2014-04-15
US20150231143A1 (en) 2015-08-20
JP2014506590A (ja) 2014-03-17
PE20140703A1 (es) 2014-06-13
JP6118270B2 (ja) 2017-04-19
IL228052A0 (en) 2013-09-30
EP2678327B9 (fr) 2016-12-28
LT2678327T (lt) 2016-11-25
CU24177B1 (es) 2016-04-25
CU20130116A7 (es) 2014-03-26
CL2013002449A1 (es) 2014-04-11
NI201300072A (es) 2013-12-17
EP2678327A1 (fr) 2014-01-01
RS55433B1 (sr) 2017-04-28
EA201370184A1 (ru) 2013-12-30
DOP2013000191A (es) 2014-04-15
ECSP13012891A (es) 2013-10-31
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AU2012221800A1 (en) 2013-10-03
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CN103402994A (zh) 2013-11-20
US9393247B2 (en) 2016-07-19
MX343788B (es) 2016-11-23
CO6761374A2 (es) 2013-09-30
ES2594409T3 (es) 2016-12-20
AU2012221800B2 (en) 2016-10-27
GT201300207A (es) 2014-11-13
IL228052A (en) 2016-11-30
HRP20161481T1 (hr) 2016-12-30
ZA201306223B (en) 2014-10-29
US9072731B2 (en) 2015-07-07
EP2678327B8 (fr) 2016-09-28
PL2678327T3 (pl) 2017-02-28
PH12013501727A1 (en) 2013-10-07
KR20140026378A (ko) 2014-03-05
CA2826792A1 (fr) 2012-08-30

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