MA37886A1 - Nouvelles pyridinones bicycliques - Google Patents

Nouvelles pyridinones bicycliques

Info

Publication number
MA37886A1
MA37886A1 MA37886A MA37886A MA37886A1 MA 37886 A1 MA37886 A1 MA 37886A1 MA 37886 A MA37886 A MA 37886A MA 37886 A MA37886 A MA 37886A MA 37886 A1 MA37886 A1 MA 37886A1
Authority
MA
Morocco
Prior art keywords
new bicyclic
compounds
pyridinones
bicyclic pyridinones
methods
Prior art date
Application number
MA37886A
Other languages
English (en)
Other versions
MA37886B1 (fr
Inventor
Antonia Friederike Stepan
Patrick Robert Verhoest
Ende Christopher William Am
Michael Eric Green
Douglas Scott Johnson
Gregory Wayne Kauffman
Christopher John O'donnell
Nandini Chaturbhai Patel
Martin Youngjin Pettersson
Cory Michael Stiff
Chakrapani Subramanyam
Tuan Phong Tran
Original Assignee
Pfizer
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
Application filed by Pfizer filed Critical Pfizer
Publication of MA37886A1 publication Critical patent/MA37886A1/fr
Publication of MA37886B1 publication Critical patent/MA37886B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Epidemiology (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention concerne des composés et des sels pharmaceutiquement acceptables desdits composés, lesdits composés présentant une structure répondant à la formule (i) telle que définie dans la description. L'invention concerne également des compositions pharmaceutiques correspondantes, des méthodes de traitement, des procédés de synthèse et des intermédiaires.
MA37886A 2012-09-21 2013-09-05 Nouvelles pyridinones bicycliques MA37886B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261703969P 2012-09-21 2012-09-21
PCT/IB2013/058347 WO2014045156A1 (fr) 2012-09-21 2013-09-06 Nouvelles pyridinones bicycliques

Publications (2)

Publication Number Publication Date
MA37886A1 true MA37886A1 (fr) 2016-02-29
MA37886B1 MA37886B1 (fr) 2016-09-30

Family

ID=49585452

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37886A MA37886B1 (fr) 2012-09-21 2013-09-05 Nouvelles pyridinones bicycliques

Country Status (47)

Country Link
US (3) US8916564B2 (fr)
EP (1) EP2897956B1 (fr)
JP (1) JP5844018B2 (fr)
KR (1) KR101725696B1 (fr)
CN (1) CN104662021B (fr)
AP (1) AP2015008277A0 (fr)
AR (1) AR092628A1 (fr)
AU (1) AU2013319845B2 (fr)
BR (1) BR112015006436A2 (fr)
CA (1) CA2882386C (fr)
CL (1) CL2015000717A1 (fr)
CR (1) CR20150053A (fr)
CU (1) CU20150021A7 (fr)
CY (1) CY1118662T1 (fr)
DK (1) DK2897956T3 (fr)
DO (1) DOP2015000069A (fr)
EA (1) EA026668B1 (fr)
EC (1) ECSP15015594A (fr)
ES (1) ES2609987T3 (fr)
GE (1) GEP201706659B (fr)
GT (1) GT201500069A (fr)
HK (1) HK1206013A1 (fr)
HR (1) HRP20161558T1 (fr)
HU (1) HUE031248T2 (fr)
IL (1) IL237163A (fr)
IN (1) IN2015DN01119A (fr)
LT (1) LT2897956T (fr)
MA (1) MA37886B1 (fr)
MD (1) MD4583B1 (fr)
ME (1) ME02571B (fr)
MX (1) MX360599B (fr)
MY (1) MY181891A (fr)
NI (1) NI201500038A (fr)
NZ (1) NZ704863A (fr)
PE (1) PE20150686A1 (fr)
PH (1) PH12015500376B1 (fr)
PL (1) PL2897956T3 (fr)
PT (1) PT2897956T (fr)
RS (1) RS55426B1 (fr)
SG (1) SG11201501074WA (fr)
SI (1) SI2897956T1 (fr)
TN (1) TN2015000084A1 (fr)
TW (1) TWI500616B (fr)
UA (1) UA110688C2 (fr)
UY (1) UY35039A (fr)
WO (1) WO2014045156A1 (fr)
ZA (1) ZA201501195B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA110688C2 (uk) 2012-09-21 2016-01-25 Пфайзер Інк. Біциклічні піридинони
CN104918938B (zh) 2012-12-20 2017-08-15 詹森药业有限公司 新颖的作为γ分泌酶调节剂的三环3，4‑二氢‑2H‑吡啶并[1，2‑a]吡嗪‑1，6‑二酮衍生物
EP2945944B1 (fr) 2013-01-17 2016-11-09 Janssen Pharmaceutica, N.V. Nouveaux dérivés de pyrido-pipérazinone substitués en tant que modulateurs de la gamma sécrétase
ES2742078T3 (es) * 2013-10-04 2020-02-13 Pfizer Piridonas bicíclicas novedosas como moduladores de gamma-secretasa
US10562897B2 (en) 2014-01-16 2020-02-18 Janssen Pharmaceutica Nv Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators
ES2759277T3 (es) * 2014-04-01 2020-05-08 Pfizer Cromeno y 1,1a,2,7b-tetrahidrociclopropa[c]cromeno piridopiracinadionionas como moduladores de gamma-secretasa
EP3253755B1 (fr) 2015-02-03 2020-08-26 Pfizer Inc Nouveaux pyridopyrazinediones cyclopropabenzofuranyl
US9802927B2 (en) 2015-06-10 2017-10-31 Denali Therapeutics, Inc. Oxadiazine compounds and methods of use thereof
WO2017216279A1 (fr) 2016-06-16 2017-12-21 F. Hoffmann-La Roche Ag Modulateurs des récepteurs des œstrogènes hétéroaryles et leurs utilisations
IL267253B2 (en) 2016-12-16 2023-04-01 Pipeline Therapeutics Inc Methods for treating cochlear synaptopathy
MX2021003773A (es) 2018-10-02 2021-07-16 Frequency Therapeutics Inc Composiciones farmacéuticas y métodos relacionados con los agentes terapéuticos óticos.
MA55611A (fr) 2019-04-08 2022-02-16 Frequency Therapeutics Inc Association de chir99021 et d'acide valproïque pour traiter une perte auditive
TW202128675A (zh) 2019-12-06 2021-08-01 美商維泰克斯製藥公司 作為鈉通道調節劑之經取代四氫呋喃
CN113402490B (zh) * 2021-03-29 2023-01-03 白银京宇新药业有限公司 一种1，2，6，7-四氢-8H-茚并[5，4-b]呋喃-8-酮的制备方法
PE20241335A1 (es) 2021-06-04 2024-07-03 Vertex Pharma N-(hidroxialquil (hetero)aril) tetrahidrofurano carboxamidas como moduladores de canales de sodio
CN114034792B (zh) * 2021-11-09 2024-06-25 山东新华制药股份有限公司 检测氯酮含量的液相色谱分析方法

Family Cites Families (134)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1419788A (en) 1972-08-02 1975-12-31 Pfizer Herbicidal method using 2-trifuluromethyl-4-quinolinols
WO1992000075A1 (fr) 1990-06-29 1992-01-09 Pfizer Inc. Derives de pyridopyrazine utilises dans le traitement de l'abus et de la dependance de substances
US5482967A (en) 1992-09-04 1996-01-09 Takeda Chemical Industries, Ltd. Condensed heterocyclic compounds, their production and use
US5750349A (en) 1993-01-25 1998-05-12 Takeda Chemical Industries Ltd. Antibodies to β-amyloids or their derivatives and use thereof
DE69628484T2 (de) 1995-03-24 2004-05-19 Takeda Chemical Industries, Ltd. Zyklische Verbindungen, ihre Herstellung und ihre Verwendung als Tachykininrezeptorantagonisten
DE19709877A1 (de) 1997-03-11 1998-09-17 Bayer Ag 1,5-Dihydro-pyrazolo[3,4-d]-pyrimidinon-derivate
ATE402717T1 (de) 1997-04-09 2008-08-15 Intellect Neurosciences Inc Für die termini des beta-amyloids spezifische, rekombinante antikörper, dafür kodierende dna und verfahren zu ihrer verwendung
US8173127B2 (en) 1997-04-09 2012-05-08 Intellect Neurosciences, Inc. Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof
GB9722520D0 (en) 1997-10-24 1997-12-24 Pfizer Ltd Compounds
TWI239847B (en) 1997-12-02 2005-09-21 Elan Pharm Inc N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease
US6743427B1 (en) 1997-12-02 2004-06-01 Neuralab Limited Prevention and treatment of amyloidogenic disease
AU2787299A (en) 1998-03-03 1999-09-20 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US20020132817A1 (en) 1998-03-19 2002-09-19 Hideaki Natsugari Heterocyclic compounds, their production and use
EP1145714A4 (fr) 1998-11-27 2004-12-15 Takeda Chemical Industries Ltd Medicaments
SK288711B6 (sk) 2000-02-24 2019-11-05 Univ Washington Humanizovaná protilátka, jej fragment a ich použitie, polynukleová kyselina, expresný vektor, bunka a farmaceutický prostriedok
DE10045112A1 (de) 2000-09-11 2002-03-21 Merck Patent Gmbh Verwendung von Indolderivaten zur Behandlung von Erkrankungen des zentralen Nervensystems
EP1335738A4 (fr) 2000-11-03 2004-09-08 Proteotech Inc Procedes d'isolement de composes inhibiteurs d'amyloide, et utilisation de composes utilises a partir d'uncaria tomentosa et de plantes parentes
WO2003016466A2 (fr) 2001-08-17 2003-02-27 Eli Lilly And Company Anticorps anti-$g(a)$g(b)
US20030195205A1 (en) 2001-11-02 2003-10-16 Pfizer Inc. PDE9 inhibitors for treating cardiovascular disorders
DE10238723A1 (de) 2002-08-23 2004-03-11 Bayer Ag Phenyl-substituierte Pyrazolyprimidine
DE10238724A1 (de) 2002-08-23 2004-03-04 Bayer Ag Alkyl-substituierte Pyrazolpyrimidine
CA2498111A1 (fr) 2002-09-11 2004-03-25 Merck & Co., Inc. Composes de dihydroxypyridopyrazine-1,6-diones utiles en tant qu'inhibiteurs de l'integrase du vih
BR0315157A (pt) 2002-10-09 2005-08-09 Rinat Neuroscience Corp Métodos de tratar doença de alzheimer empregando-se anticorpos direcionados contra peptìdeo beta amilóide e composições deste
BR0315158A (pt) 2002-10-09 2005-08-16 Pfizer Prod Inc Compostos de pirazol para o tratamento de distúrbios neurodegenarativos
AU2003301439A1 (en) 2002-10-16 2004-05-04 Gilead Sciences, Inc. Pre-organized tricyclic integrase inhibitor compounds
US20040220186A1 (en) 2003-04-30 2004-11-04 Pfizer Inc. PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease
EP1638935A1 (fr) 2003-06-19 2006-03-29 Pfizer Products Inc. Antagoniste de nk1
WO2005020991A1 (fr) 2003-08-21 2005-03-10 Pfizer Products, Inc. Composes pour le traitement de maladies neurodegeneratives
CA2538220A1 (fr) 2003-09-09 2005-03-24 Takeda Pharmaceutical Company Limited Utilisation d'un anticorps
GB0327319D0 (en) 2003-11-24 2003-12-24 Pfizer Ltd Novel pharmaceuticals
US7572799B2 (en) 2003-11-24 2009-08-11 Pfizer Inc Pyrazolo[4,3-d]pyrimidines as Phosphodiesterase Inhibitors
US20070155731A1 (en) 2004-01-28 2007-07-05 Gabor Butora Aminocyclopentyl pyridopyrazinone modulators of chemokine receptor activity
WO2005080361A1 (fr) 2004-02-02 2005-09-01 Pfizer Products Inc. Modulateurs du recepteur de l'histamine-3
CA2557785A1 (fr) 2004-03-09 2005-10-06 Merck & Co. Inc. Inhibiteurs de l'integrase du vih
BRPI0509069B8 (pt) 2004-03-23 2021-05-25 Pfizer Prod Inc compostos de imidazol e composição farmacêutica que os compreende para o tratamento de distúrbios neurodegenerativos
AU2005249363A1 (en) 2004-04-14 2005-12-15 Zhenhong R. Cai Phosphonate analogs of HIV integrase inhibitor compounds
US7456164B2 (en) 2004-05-07 2008-11-25 Pfizer, Inc 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands
EP1595881A1 (fr) 2004-05-12 2005-11-16 Pfizer Limited Dérivés de tetrahydronaphthyridine en tant que ligands de récepteur H3 d'histamine
GEP20115195B (en) 2004-07-30 2011-04-11 Rinat Neuroscience Corp Antibodies directed against amyloid-beta peptide and use thereof
GB0423356D0 (en) 2004-10-21 2004-11-24 Merck Sharp & Dohme Therapeutic agents
FR2877015B1 (fr) 2004-10-21 2007-10-26 Commissariat Energie Atomique Revetement nanostructure et procede de revetement.
US20090074775A1 (en) 2004-12-22 2009-03-19 David Michael Holtzman Use Of Anti-AB Antibody To Treat Traumatic Brain Injury
PE20061323A1 (es) 2005-04-29 2007-02-09 Rinat Neuroscience Corp Anticuerpos dirigidos contra el peptido amiloide beta y metodos que utilizan los mismos
JP4982482B2 (ja) 2005-05-10 2012-07-25 メルク・シャープ・エンド・ドーム・コーポレイション Ｈｉｖインテグラ−ゼ阻害剤
WO2006120552A2 (fr) 2005-05-12 2006-11-16 Pfizer Inc. Formes cristallines anhydres de n-[1-(2-ethoxyethyl)-5-(n-ethyl-n-methylamino)-7-(4-methylpyridin-2-yl-amino)-1h-pyrazolo[4,3-d]pyrimidine-3-carbonyl]methanesulfonamide
WO2006126081A2 (fr) 2005-05-24 2006-11-30 Pharmacia & Upjohn Company Llc Pyridine [2,3-b] pyrazinones
WO2006126083A1 (fr) 2005-05-24 2006-11-30 Pharmacia & Upjohn Company Llc Composes de pyridine [3 , 4-b] pyrazinones utilises comme inhibiteurs de pde-5
CA2608672A1 (fr) 2005-05-24 2006-11-30 Pharmacia & Upjohn Company Llc Pyridine [3,4-b] pyrazinones
JP2008543923A (ja) 2005-06-22 2008-12-04 ファイザー・プロダクツ・インク ヒスタミン−３受容体アンタゴニスト
US20070060534A1 (en) 2005-06-30 2007-03-15 Threshold Pharmaceuticals, Inc. Anthracycline analogs
US8158673B2 (en) 2005-10-27 2012-04-17 Pfizer Inc. Histamine-3 receptor antagonists
EP1945639A1 (fr) 2005-11-04 2008-07-23 Pfizer Limited Dérivé de tétrahydronaphtyridine
EP1948614A2 (fr) 2005-11-18 2008-07-30 Takeda San Diego, Inc. Activateurs de la glucokinase
JP2009516703A (ja) 2005-11-18 2009-04-23 グラクソ グループ リミテッド 新規中間体およびその使用
JP5221144B2 (ja) 2005-11-24 2013-06-26 エーザイ・アール・アンド・ディー・マネジメント株式会社 モルホリンタイプ・シンナミド化合物
US20070117839A1 (en) 2005-11-24 2007-05-24 Eisai R&D Management Co., Ltd. Two cyclic cinnamide compound
WO2007063385A2 (fr) 2005-12-01 2007-06-07 Pfizer Products Inc. Antagonistes des recepteurs de l'histamine 3 pour des amines spirocycliques
WO2007069053A1 (fr) 2005-12-14 2007-06-21 Pfizer Products Inc. Antagonistes benzimidazoliques du récepteur h-3
WO2007084595A2 (fr) * 2006-01-20 2007-07-26 Schering Corporation Benzènesulfonyle-chromane, thiochromane, tétrahydronaphthalène et inhibiteurs de la gamma secrétase associés
WO2007088462A1 (fr) 2006-02-01 2007-08-09 Pfizer Products Inc. Antagonistes du récepteur du h-3 à base de spirochromane
WO2007088450A2 (fr) 2006-02-01 2007-08-09 Pfizer Products Inc. Chromane antagoniste du récepteur h-3
WO2007099423A1 (fr) 2006-03-02 2007-09-07 Pfizer Products Inc. Dérivés de 1-pyrrolidine indane en tant qu'antagonistes du récepteur d'histamine 3
TWI378091B (en) 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
WO2007105053A2 (fr) 2006-03-13 2007-09-20 Pfizer Products Inc. Tétralines en tant qu'antagonistes du récepteur h-3
BRPI0710658A2 (pt) 2006-04-21 2011-08-16 Pfizer Prod Inc compostos de piridina[3,4-b] pirazinonas, seus usos na preparação de composições farmacêuticas e composições farmacêuticas compreendendo os mesmos
JP5271895B2 (ja) 2006-05-15 2013-08-21 メルク・シャープ・アンド・ドーム・コーポレーション 抗糖尿病性の二環式化合物
WO2007136714A2 (fr) 2006-05-16 2007-11-29 Gilead Sciences, Inc. Inhibiteurs d'intégrase
AU2007252643A1 (en) 2006-05-19 2007-11-29 Eisai R & D Management Co., Ltd. Urea type cinnamide derivative
WO2007138431A2 (fr) 2006-05-30 2007-12-06 Pfizer Products Inc. Antagonistes de l'éther histamine-3 azabicyclique
SI2124933T1 (sl) 2007-01-22 2012-12-31 Pfizer Products Inc. Tosilatna sol terapevtske spojine in farmacevtski sestavi tega
EP2121633A2 (fr) 2007-02-12 2009-11-25 Merck & Co., Inc. Dérivés de pipérazine pour le traitement de la maladie d'alzheimer et des conditions apparentées
CA2676920A1 (fr) 2007-02-12 2008-08-21 Merck & Co., Inc. Derives de la piperidine
US20080207900A1 (en) 2007-02-28 2008-08-28 Teiji Kimura Two cyclic oxomorphorin derivatives
WO2008137102A2 (fr) 2007-05-04 2008-11-13 Torreypines Therapeutics, Inc. Procédés de modulation de la bêta-amyloïde et composés utiles pour cette modulation
JP5209043B2 (ja) 2007-05-07 2013-06-12 メルク・シャープ・アンド・ドーム・コーポレーション ガンマセクレターゼ調節剤
ES2358863T3 (es) 2007-05-11 2011-05-16 F. Hoffmann-La Roche Ag Hetarilanilinas como moduladores de beta-amiloide.
CL2008001540A1 (es) 2007-05-29 2009-05-22 Sgx Pharmaceuticals Inc Compuestos derivados de pirrolopiridinas y pirazolopiridinas; composicion farmaceutica; y uso en el tratamiento del cancer.
KR20100037053A (ko) 2007-06-01 2010-04-08 쉐링 코포레이션 감마 세크레타제 조절인자
AU2008263206A1 (en) 2007-06-01 2008-12-18 Schering Corporation Gamma secretase modulators
EP2166854A4 (fr) 2007-06-13 2012-05-16 Merck Sharp & Dohme Dérivés du triazole destinés au traitement de la maladie d'alzheimer et d'états associés
CA2692253A1 (fr) 2007-06-29 2009-01-08 Schering Corporation Modulateurs de la gamma-secretase
EP2185522A1 (fr) 2007-08-06 2010-05-19 Schering Corporation Modulateurs de la gamma-sécrétase
CA2694401C (fr) 2007-08-31 2012-12-04 Eisai R&D Management Co., Ltd. Compose polycyclique
US7935815B2 (en) 2007-08-31 2011-05-03 Eisai R&D Management Co., Ltd. Imidazoyl pyridine compounds and salts thereof
WO2009032277A1 (fr) 2007-09-06 2009-03-12 Schering Corporation Modulateurs de la gamma sécrétase
US20100298381A1 (en) 2007-09-28 2010-11-25 Schering Corporation Gamma secretase modulators
GB0720444D0 (en) 2007-10-18 2007-11-28 Glaxo Group Ltd Novel compounds
US8487099B2 (en) 2007-11-05 2013-07-16 Merck Sharp & Dohme Corp. Gamma secretase modulators
MX2010006244A (es) * 2007-12-06 2010-12-02 Schering Corp Moduladores de gamma secretasa.
CA2708151A1 (fr) 2007-12-11 2009-06-18 Schering Corporation Modulateurs de la gamma secretase
MX2010006378A (es) 2007-12-11 2010-09-07 Schering Corp Moduladores de gamma secretasa.
AU2008335709A1 (en) 2007-12-13 2009-06-18 Amgen Inc. Gamma secretase modulators
KR101244517B1 (ko) 2008-01-11 2013-03-18 에프. 호프만-라 로슈 아게 아밀로이드 베타에 대한 조절제
MX2010008700A (es) 2008-02-22 2010-08-30 Hoffmann La Roche Moduladores de beta-amiloide.
US20100137320A1 (en) 2008-02-29 2010-06-03 Schering Corporation Gamma secretase modulators
WO2009108766A1 (fr) 2008-02-29 2009-09-03 Schering Corporation Modulateurs de l’activité gamma-secrétase pour le traitement de la maladie d'alzheimer
CN102083794A (zh) 2008-05-05 2011-06-01 安姆根有限公司 作为γ分泌酶调节剂的脲化合物
FR2933700B1 (fr) * 2008-07-08 2010-07-30 Sanofi Aventis Derives de pyridino-pyridinones, leur preparation et leur application en therapeutique
TW201006801A (en) 2008-07-18 2010-02-16 Lilly Co Eli Imidazole carboxamides
WO2010019393A1 (fr) 2008-08-13 2010-02-18 Merck Sharp & Dohme Corp. Dérivés de pyrimidine pour le traitement de la maladie d’alzheimer
WO2010019392A1 (fr) 2008-08-13 2010-02-18 Merck Sharp & Dohme Corp. Dérivés de purine pour le traitement de la maladie d’alzheimer
EP2324009A1 (fr) 2008-08-27 2011-05-25 Eisai R&D Management Co., Ltd. Procédé de préparation de certains composés de cinnamide
AU2009301210B2 (en) 2008-10-09 2014-05-15 F. Hoffmann-La Roche Ag Modulators for amyloid beta
WO2010054064A1 (fr) 2008-11-06 2010-05-14 Schering Corporation Modulateurs de sécrétase gamma
JP2012508182A (ja) 2008-11-06 2012-04-05 シェーリング コーポレイション γ−セクレターゼ調節剤
CN102272133A (zh) 2008-11-06 2011-12-07 阿斯利康(瑞典)有限公司 淀粉样β的调节剂
MX2011004954A (es) 2008-11-10 2011-05-30 Hoffmann La Roche Moduladores heterociclicos de gamma-secretasa.
US20110313001A1 (en) 2008-12-16 2011-12-22 Christian Fischer Triazole derivatives for treatment of alzheimer's disease
WO2010071741A1 (fr) 2008-12-16 2010-06-24 Merck Sharp & Dohme Corp. Dérivés du triazole pour traitement de la maladie d'alzheimer
PA8854101A1 (es) 2008-12-18 2010-07-27 Ortho Mcneil Janssen Pharm Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa
EA020548B1 (ru) 2008-12-19 2014-12-30 Бёрингер Ингельхайм Интернациональ Гмбх Циклические пиримидин-4-карбоксамиды в качестве антагонистов рецептора ccr2, предназначенные для лечения воспаления, астмы и хозл
CA2747750A1 (fr) 2008-12-22 2010-07-01 Theodros Asberom Modulateurs de gamma secretase
TW201034666A (en) 2008-12-22 2010-10-01 Schering Corp Gamma secretase modulators
TW201030002A (en) 2009-01-16 2010-08-16 Bristol Myers Squibb Co Bicyclic compounds for the reduction of beta-amyloid production
EP2393804B1 (fr) 2009-02-06 2014-04-16 Janssen Pharmaceuticals, Inc. Nouveaux composés hétérocycliques bicycliques substitués en tant que modulateurs de la secrétase gamma
TWI461425B (zh) * 2009-02-19 2014-11-21 Janssen Pharmaceuticals Inc 作為伽瑪分泌酶調節劑之新穎經取代的苯并唑、苯并咪唑、唑并吡啶及咪唑并吡啶衍生物類
JP2012051805A (ja) 2009-02-26 2012-03-15 Eisai R & D Management Co Ltd テトラヒドロトリアゾロピリジン誘導体の製造方法
JP2012051807A (ja) 2009-02-26 2012-03-15 Eisai R & D Management Co Ltd アリールイミダゾール化合物
JP2012051806A (ja) 2009-02-26 2012-03-15 Eisai R & D Management Co Ltd イミダゾリルピラジン誘導体
MX2011006782A (es) 2009-02-26 2011-07-20 Eisai R&D Man Co Ltd Sal de derivado de tetrahidrotriazolopiridina y un cristal de la misma.
JP2012121809A (ja) 2009-02-26 2012-06-28 Eisai R & D Management Co Ltd 多環式化合物の製造法およびその中間体
US20120053165A1 (en) 2009-03-03 2012-03-01 Pfizer Inc. Novel Phenyl Imidazoles and Phenyl Triazoles As Gamma-Secretase Modulators
MX2012001621A (es) 2009-08-07 2012-04-11 Dow Agrosciences Llc Composiciones plaguicidas.
WO2011048525A1 (fr) * 2009-10-20 2011-04-28 Pfizer Inc. Nouveaux hétéroaryl-imidazoles et hétéroaryl-triazoles à titre de modulateurs de gamma-sécrétase
AU2010341573B2 (en) * 2009-12-22 2016-10-13 Vertex Pharmaceuticals Incorporated Isoindolinone inhibitors of phosphatidylinositol 3-kinase
CA2830027C (fr) 2011-03-31 2016-04-26 Pfizer Inc. Nouvelles pyridones bicycliques
JP6106745B2 (ja) * 2012-05-16 2017-04-05 ヤンセン ファーマシューティカルズ，インコーポレーテッド （特に）アルツハイマー病の治療に有用な置換３，４−ジヒドロ−２Ｈ−ピリド［１，２−ａ］ピラジン−１，６−ジオン誘導体
UA110688C2 (uk) 2012-09-21 2016-01-25 Пфайзер Інк. Біциклічні піридинони
TWI614238B (zh) 2012-09-21 2018-02-11 必治妥美雅史谷比公司 雙（氟烷基）－１，４－苯并二氮呯酮化合物及其前藥
CN104918938B (zh) 2012-12-20 2017-08-15 詹森药业有限公司 新颖的作为γ分泌酶调节剂的三环3，4‑二氢‑2H‑吡啶并[1，2‑a]吡嗪‑1，6‑二酮衍生物
EP2945944B1 (fr) 2013-01-17 2016-11-09 Janssen Pharmaceutica, N.V. Nouveaux dérivés de pyrido-pipérazinone substitués en tant que modulateurs de la gamma sécrétase
ES2742078T3 (es) 2013-10-04 2020-02-13 Pfizer Piridonas bicíclicas novedosas como moduladores de gamma-secretasa
CN115068134A (zh) 2014-03-21 2022-09-20 阿莱恩技术有限公司 具有弹性体的分段的正畸矫正器
ES2759277T3 (es) 2014-04-01 2020-05-08 Pfizer Cromeno y 1,1a,2,7b-tetrahidrociclopropa[c]cromeno piridopiracinadionionas como moduladores de gamma-secretasa

Also Published As

Publication number Publication date
DOP2015000069A (es) 2015-05-15
NI201500038A (es) 2015-06-05
EP2897956A1 (fr) 2015-07-29
HUE031248T2 (en) 2017-06-28
DK2897956T3 (en) 2017-01-16
AP2015008277A0 (en) 2015-02-28
TN2015000084A1 (fr) 2016-06-29
CA2882386C (fr) 2017-11-28
SG11201501074WA (en) 2015-05-28
GEP201706659B (en) 2017-04-25
UA110688C2 (uk) 2016-01-25
MY181891A (en) 2021-01-12
US9193726B2 (en) 2015-11-24
MX2015003637A (es) 2015-06-05
MD20150023A2 (ro) 2015-07-31
KR101725696B1 (ko) 2017-04-10
LT2897956T (lt) 2017-01-10
AU2013319845A1 (en) 2015-02-26
JP2015529238A (ja) 2015-10-05
GT201500069A (es) 2016-03-01
NZ704863A (en) 2017-03-31
US20140088111A1 (en) 2014-03-27
CY1118662T1 (el) 2017-07-12
HK1206013A1 (zh) 2015-12-31
CA2882386A1 (fr) 2014-03-27
US20160024088A1 (en) 2016-01-28
ZA201501195B (en) 2016-01-27
UY35039A (es) 2014-04-30
BR112015006436A2 (pt) 2017-07-04
CN104662021A (zh) 2015-05-27
ECSP15015594A (es) 2017-08-31
JP5844018B2 (ja) 2016-01-13
AR092628A1 (es) 2015-04-29
CU20150021A7 (es) 2015-08-27
PL2897956T3 (pl) 2017-05-31
TW201425311A (zh) 2014-07-01
MX360599B (es) 2018-11-08
AU2013319845B2 (en) 2017-09-14
PT2897956T (pt) 2017-01-13
CL2015000717A1 (es) 2015-06-19
KR20150044948A (ko) 2015-04-27
IL237163A0 (en) 2015-04-30
WO2014045156A1 (fr) 2014-03-27
ME02571B (me) 2017-06-20
MD4583B1 (ro) 2018-07-31
US9751877B2 (en) 2017-09-05
PH12015500376A1 (en) 2015-04-20
EA201590319A1 (ru) 2015-09-30
EA026668B1 (ru) 2017-05-31
CN104662021B (zh) 2016-08-24
RS55426B1 (sr) 2017-04-28
ES2609987T3 (es) 2017-04-25
EP2897956B1 (fr) 2016-11-09
SI2897956T1 (sl) 2017-02-28
PH12015500376B1 (en) 2015-04-20
TWI500616B (zh) 2015-09-21
US8916564B2 (en) 2014-12-23
IL237163A (en) 2016-12-29
PE20150686A1 (es) 2015-05-23
CR20150053A (es) 2015-03-25
IN2015DN01119A (fr) 2015-06-26
MA37886B1 (fr) 2016-09-30
HRP20161558T1 (hr) 2016-12-30
US20150072990A1 (en) 2015-03-12

Similar Documents

Publication Publication Date Title
MA37886B1 (fr) Nouvelles pyridinones bicycliques
ECSP099755A (es) Derivados de pirrolopiridina y su uso como inhibidores de bace
MA37405A1 (fr) Composés hétérocyclyle
GEP20146146B (en) Pyrrolopyrimidine compounds as inhibitors of cdk4/6
MA39995B1 (fr) Composés destinés à traiter l'amyotrophie spinale
AR080197A1 (es) Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk 4/6
UY30498A1 (es) Nueva clase de compuestos de benzimidazolilo, sus sales, composiciones farmacéuticas conteniéndolos y aplicaciones
HRP20090235B1 (hr) Karbonilirani (aza) cikloheksani kao ligandi dopaminskog receptora d
MA35749B1 (fr) Dérivés nucléosidiques 4'-azido, 3'-fluoro substitués en tant qu'inhibiteurs de la réplication de l'arn du vhc
MA35285B1 (fr) Indazoles
MA32929B1 (fr) Lactames en tant qu'inhibiteurs de bêta-sécrétase
MA34819B1 (fr) Dérivés bicyclo[3.2.1]octylamide et leurs utilisations
SV2011003903A (es) Aminotetrahidropiranos como inhibidores de dipeptidil peptidasa iv para el tratamiento o prevencion de diabetes
EA201070988A1 (ru) Противовирусные терапевтические средства
TN2011000654A1 (fr) Sulfonamides heterocycliques leurs utilisations et compositions pharmaceutiques les contenant
MA38039A1 (fr) Composés de céphem substitués en position 2
BR112014007163A2 (pt) composições farmacêuticas de n-metil-2 [3 ((e)-2 piridin-2 il-vinil)-1h-indazol-6 ilsulfanil]-benzamida
MA35342B1 (fr) Composés de-pipéridinyle utiles comme inhibiteurs de la tankyrase
MA35184B1 (fr) Antagonistes de trpv4
MA35032B1 (fr) Derives de glycoside et leurs utilisations dans le traitement du diabete
MA39165A1 (fr) Dérivés de benzimidazole-proline pour leurs utilisations dans le traitement du syndrome des etats crepusculaires
MA39152B1 (fr) Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine
MA32290B1 (fr) Nouvelle classe de spiro pipéridines pour le traitement de maladies neurodégénératives
MA35188B1 (fr) Tétrahydroquinolines à fusion cycloalkyle en tant que modulateurs de l'activité du récepteur crth2
UA103329C2 (ru) Соли соединений-ингибиторов вич