MA32705B1 - Composes cycliques spiro-tetracycliques utiles en tant que modulateurs de la beta-secretase et leurs procedes d'utilisation - Google Patents

Composes cycliques spiro-tetracycliques utiles en tant que modulateurs de la beta-secretase et leurs procedes d'utilisation

Info

Publication number
MA32705B1
MA32705B1 MA33762A MA33762A MA32705B1 MA 32705 B1 MA32705 B1 MA 32705B1 MA 33762 A MA33762 A MA 33762A MA 33762 A MA33762 A MA 33762A MA 32705 B1 MA32705 B1 MA 32705B1
Authority
MA
Morocco
Prior art keywords
beta
compounds
secretase
disorders
useful
Prior art date
Application number
MA33762A
Other languages
Arabic (ar)
English (en)
Inventor
Marian C Bryan
Ryan White
Albert Amegadzie
Jian J Chen
Alan C Cheng
Thomas Dineen
Oleg Epstein
Vijay Keshav Gore
Zihao Hua
Jason B Human
Hongbing Huang
Charles Kreiman
Daniel La
Qingyian Liu
Vu Van Ma
Isaac Marx
Vinod F Patel
Wenyuan Qian
Matthew Weiss
Chester C Yuan
Original Assignee
Amgen Inc
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 Amgen Inc filed Critical Amgen Inc
Publication of MA32705B1 publication Critical patent/MA32705B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/424Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/10Spiro-condensed systems

Landscapes

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

Abstract

LA PRÉSENTE INVENTION PORTE SUR UNE NOUVELLE CLASSE DE COMPOSÉS UTILES POUR LA MODULATION DE L'ACTIVITÉ DE L'ENZYME BÊTA-SÉCRÉTASE ET POUR LE TRAITEMENT DE MALADIES À MÉDIATION PAR LA BÊTA-SÉCRÉTASE, DONT LA MALADIE D'ALZHEIMER (MA) ET LES AFFECTIONS APPARENTÉES. DANS UN MODE DE RÉALISATION, LES COMPOSÉS SONT REPRÉSENTÉS PAR UNE FORMULE GÉNÉRALE (I); DANS LAQUELLE A1, A2, A3, A4, A5, A6, T1, T2, W, X, Y ET Z SONT TELS QUE DÉFINIS DANS LA DESCRIPTION. L'INVENTION PORTE ÉGALEMENT SUR L'UTILISATION DE CES COMPOSÉS DANS DES COMPOSITIONS PHARMACEUTIQUES POUR LE TRAITEMENT, PROPHYLACTIQUE OU THÉRAPEUTIQUE, DE TROUBLES ET D'AFFECTIONS LIÉS À L'ACTIVITÉ DE LA PROTÉINE BÊTA-SÉCRÉTASE. DE TELS TROUBLES COMPRENNENT, PAR EXEMPLE, LA MALADIE D'ALZHEIMER, DES DÉFICITS INTELLECTUELS, UNE DÉFICIENCE COGNITIVE, LA SCHIZOPHRÉNIE ET D'AUTRES MALADIES DU SYSTÈME NERVEUX CENTRAL LIÉES À LA FORMATION ET/OU AU DÉPÔT DE PLAQUES AU NIVEAU DU CERVEAU ET/OU PROVOQUÉES PAR LA FORMATION ET/OU LE DÉPÔT DE PLAQUES AU NIVEAU DU CERVEAU. L'INVENTION PORTE ÉGALEMENT SUR D'AUTRES MODES DE RÉALISATION DE LA FORMULE (I), SUR DES INTERMÉDIAIRES ET DES PROCÉDÉS UTILES POUR LA PRÉPARATION DE COMPOSÉS DE FORMULE (I).
MA33762A 2008-09-11 2011-04-11 Composes cycliques spiro-tetracycliques utiles en tant que modulateurs de la beta-secretase et leurs procedes d'utilisation MA32705B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9608208P 2008-09-11 2008-09-11
PCT/US2009/056748 WO2010030954A1 (fr) 2008-09-11 2009-09-11 Composés cycliques spiro-tétracycliques utiles en tant que modulateurs de la bêta-sécrétase et leurs procédés d'utilisation

Publications (1)

Publication Number Publication Date
MA32705B1 true MA32705B1 (fr) 2011-10-02

Family

ID=41319591

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33762A MA32705B1 (fr) 2008-09-11 2011-04-11 Composes cycliques spiro-tetracycliques utiles en tant que modulateurs de la beta-secretase et leurs procedes d'utilisation

Country Status (21)

Country Link
US (1) US8426447B2 (fr)
EP (1) EP2328903B1 (fr)
JP (1) JP5579720B2 (fr)
KR (1) KR20110073511A (fr)
CN (1) CN102209721A (fr)
AU (1) AU2009291602B2 (fr)
BR (1) BRPI0918449A2 (fr)
CA (1) CA2736130C (fr)
CL (1) CL2011000516A1 (fr)
CO (1) CO6362014A2 (fr)
CR (1) CR20110134A (fr)
EA (1) EA201100461A1 (fr)
ES (1) ES2459195T3 (fr)
IL (1) IL211440A0 (fr)
MA (1) MA32705B1 (fr)
MX (1) MX2011002705A (fr)
MY (1) MY148558A (fr)
PE (1) PE20110805A1 (fr)
TW (1) TWI385175B (fr)
WO (1) WO2010030954A1 (fr)
ZA (1) ZA201102674B (fr)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7763609B2 (en) 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
EP2406240B1 (fr) 2009-03-13 2015-12-23 Vitae Pharmaceuticals, Inc. Inhibiteurs de la beta-secretase
UA108363C2 (uk) 2009-10-08 2015-04-27 Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
EP2539322B1 (fr) 2010-02-24 2014-01-01 Vitae Pharmaceuticals, Inc. Inhibiteurs de la bêta-secrétase
EP2547685A1 (fr) * 2010-03-15 2013-01-23 Amgen Inc. Composés spiro tétracycliques en tant que modulateurs de la béta-sécrétase
MX2012010657A (es) * 2010-03-15 2013-02-07 Amgen Inc Compuestos de espiro amino-dihidrooxazina y amino-dihidrotiazina como moduladores de beta-secretasa y su uso medico.
WO2011130741A1 (fr) * 2010-04-16 2011-10-20 Array Biopharma Inc. Composés pour le traitement de maladies neurodégénératives
US8921363B2 (en) * 2010-08-05 2014-12-30 Amgen Inc. Derivatives of 1 H-isoindol-3-amine, 1 H-iso-aza-indol-3amine, 3,4-dihydroisoquinolin-1-amine, and 1,4-dihydroisoquinolin-3-amine as beta-secretase inhibitors
EP2609081A1 (fr) 2010-08-23 2013-07-03 Amgen Inc. Dérivés de sulfonylpipérazine qui interagissent avec la protéine régulatrice de la glucokinase pour le traitement du diabète
CN103221407A (zh) * 2010-11-22 2013-07-24 出光兴产株式会社 含氧稠环衍生物和含有其而成的有机电致发光元件
TW201307357A (zh) * 2010-11-22 2013-02-16 Array Biopharma Inc 治療神經退化性疾病之化合物
EP2643325A1 (fr) 2010-11-23 2013-10-02 Amgen Inc. Spiro-amino-imidazolones et spiro-amino-dihydro-pyrimidinones en tant que modulateurs de bêta-sécrétase et leurs méthodes d'utilisation
US8415483B2 (en) 2010-12-22 2013-04-09 Astrazeneca Ab Compounds and their use as BACE inhibitors
EP2673279A1 (fr) 2011-02-07 2013-12-18 Amgen Inc. Composés de 5-amino-oxazépine et 5-amino-thiazépane en tant qu'antagonistes de la bêta-sécrétase et leurs procédés d'utilisation
US8962859B2 (en) 2011-02-15 2015-02-24 Amgen Inc. Spiro-amino-imidazo-fused heterocyclic compounds as beta-secretase modulators and methods of use
US9145426B2 (en) 2011-04-07 2015-09-29 Merck Sharp & Dohme Corp. Pyrrolidine-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use
US9221839B2 (en) 2011-04-07 2015-12-29 Merck Sharp & Dohme Corp. C5-C6 oxacyclic-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use
WO2012168175A1 (fr) 2011-06-07 2012-12-13 F. Hoffmann-La Roche Ag [1,3]oxazines
KR20140054295A (ko) 2011-08-22 2014-05-08 머크 샤프 앤드 돔 코포레이션 Bace 억제제로서의 2-스피로-치환된 이미노티아진 및 그의 모노- 및 디옥시드, 조성물 및 그의 용도
WO2013044092A1 (fr) * 2011-09-21 2013-03-28 Amgen Inc. Composés d'amino-oxazines et d'amino-dihydrothiazine comme modulateurs de sécrétase bêta et procédés d'utilisation
ES2566373T3 (es) * 2011-10-10 2016-04-12 Astrazeneca Ab Inhibidores monofluoro beta-secretasa
TWI557112B (zh) 2012-03-05 2016-11-11 百靈佳殷格翰國際股份有限公司 β-分泌酶抑制劑
EP2650284A1 (fr) * 2012-04-10 2013-10-16 Merz Pharma GmbH & Co. KGaA Dérivés hétérocycliques comme modulateurs de récepteurs du glutamate métabotropique
JP2015518048A (ja) * 2012-05-30 2015-06-25 コメンティス, インコーポレイテッド クロマン化合物
US9000185B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cycloalkyl ether compounds and their use as BACE inhibitors
US9000183B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-indene-1′,2″-imidazol compounds and their use as BACE inhibitors
US9000182B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab 2H-imidazol-4-amine compounds and their use as BACE inhibitors
US9000184B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-naphthalene-1′,2″-imidazol compounds and their use as BACE inhibitors
US10548882B2 (en) 2012-06-21 2020-02-04 Astrazeneca Ab Camsylate salt
TW201422592A (zh) 2012-08-27 2014-06-16 Boehringer Ingelheim Int β-分泌酶抑制劑
JP2015532282A (ja) 2012-09-28 2015-11-09 ヴァイティー ファーマシューティカルズ,インコーポレイテッド β−セクレターゼの阻害剤
US9725469B2 (en) 2012-11-15 2017-08-08 Amgen, Inc. Amino-oxazine and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use
AR103598A1 (es) 2015-02-02 2017-05-24 Forma Therapeutics Inc Ácidos bicíclicos[4,6,0]hidroxámicos como inhibidores de hdac
AU2016215432B2 (en) 2015-02-02 2020-07-30 Valo Early Discovery, Inc. 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as HDAC inhibitors
US10555935B2 (en) 2016-06-17 2020-02-11 Forma Therapeutics, Inc. 2-spiro-5- and 6-hydroxamic acid indanes as HDAC inhibitors

Family Cites Families (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2683718A (en) * 1952-01-11 1954-07-13 Searle & Co Spiro-[xanthene-9, 4'-imidazolidine]-2, 5-dione
US3185696A (en) * 1959-03-12 1965-05-25 Jack M Tien 3', 6'-diaminofluoran derivatives of gamma-lactam
FR2576178B1 (fr) 1985-01-24 1987-04-17 Furodet Philippe Procede de fabrication pour un enfumoir a chargement par-dessous
DE3601492A1 (de) 1986-01-20 1987-07-23 Vacuumschmelze Gmbh Verfahren zur herstellung eines stabilisierten filament-supraleiters mit hohem anteil an stabilisierungsmaterial
US5441870A (en) 1992-04-15 1995-08-15 Athena Neurosciences, Inc. Methods for monitoring cellular processing of β-amyloid precursor protein
SI9300303A (en) 1993-06-08 1994-12-31 Krka Tovarna Zdravil Process for isolation of hypolipemic effective substance
WO1996040885A2 (fr) 1995-06-07 1996-12-19 Athena Neurosciences, Inc. β-SECRETASE, ANTICORPS DIRIGES CONTRE LA β-SECRETASE ET DOSAGES PERMETTANT DE DETECTER L'INHIBITION DE LA β-SECRETASE
KR100866676B1 (ko) 1998-09-24 2008-11-11 파마시아 앤드 업존 캄파니 엘엘씨 알츠하이머병 세크레타제
MY138097A (en) 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
DE60116313T2 (de) 2000-06-30 2006-08-31 Elan Pharmaceuticals, Inc., San Francisco Verbindungen zur behandlung der alzheimerischen krankheit
US7196163B2 (en) 2001-05-22 2007-03-27 Merk & Co., Inc. Assays using amyloid precursor proteins with modified β-secretase cleavage sites to monitor β-secretase activity
CA2452039A1 (fr) 2001-06-27 2003-01-09 Elan Pharmaceuticals, Inc. Derives de beta-hydroxyamine utiles dans le traitement de la maladie d'alzheimer
KR100713137B1 (ko) 2001-06-28 2007-05-02 동화약품공업주식회사 신규의 2,4-디플루오로벤즈아미드 유도체
WO2003006013A1 (fr) 2001-07-10 2003-01-23 Elan Pharmaceuticals, Inc. Diaminediols pour le traitement de la maladie d'alzheimer
BR0211122A (pt) 2001-07-10 2004-10-26 Elan Pharm Inc Composto, métodos para o tratamento ou prevenção de doenças e para fabricar um composto, intermediário, e, uso de um composto ou sal
US20030109559A1 (en) 2001-07-11 2003-06-12 Andrea Gailunas N-(3-amino-2-hydroxy-propyl)substituted alkylamide compounds
BR0213139A (pt) 2001-10-04 2004-08-10 Elan Pharm Inc Composto, método de tratamento ou prevenção de doenças e de preparação de um composto, uso de um composto e composição farmacêutica
JP2005508940A (ja) 2001-10-05 2005-04-07 イーラン ファーマスーティカルズ、インコーポレイテッド アルツハイマー病の治療に有用なアリルアミド
CA2465316A1 (fr) 2001-10-29 2003-05-08 James P. Beck Amides a substitution hydroxy pour le traitement de la maladie d'alzheimer
NZ533107A (en) 2001-11-08 2007-04-27 Upjohn Co N, N'-substituted-1,3-diamino-2-hydroxypropane derivatives
AR037460A1 (es) 2001-11-30 2004-11-10 Smithkline Beecham Plc Compuesto de hidroxietileno, composicion farmaceutica que lo comprende, uso del mismo para la fabricacion de un medicamento y procedimiento para su preparacion
BR0214736A (pt) 2001-12-06 2004-11-23 Elan Pharm Inc Composto e seus sais farmaceuticamente aceitáveis, composição farmacêutica e método de tratar seres humanos ou animais que sofrem de doenças ou condições
WO2003057721A2 (fr) 2002-01-04 2003-07-17 Elan Pharmaceuticals, Inc. Amino carboxamides substitues destines au traitement de la maladie d'alzheimer
BR0306982A (pt) 2002-01-17 2004-10-26 Neurogen Corp Composto ou um sal deste farmaceuticamente aceitável, composição farmacêutica, métodos para reduzir a condutância de cálcio de um receptor da capsaicina celular, para inibir a ligação de ligando vanilóide a um receptor da capsaicina in vitro e em um paciente, para tratar uma condição responsiva à modulação do receptor da capsaicina em um paciente, para tratar a dor em um paciente, para tratar coceira em um paciente, para tratar tosse ou soluço em um paciente, promover a perda de peso em um paciente obeso, e para determinar a presença ou ausência de receptor da capsaicina em uma amostra, preparação farmacêutica embalada, e, uso de um composto
US7115652B2 (en) 2002-06-17 2006-10-03 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
AU2003276047A1 (en) 2002-06-17 2003-12-31 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
DE60315664D1 (de) 2002-06-20 2007-09-27 Pharmacia & Upjohn Co Llc Verfahren zur herstellung von 5-(1,3-oxazol-2-yl)benzoesäurederivaten
UY27967A1 (es) 2002-09-10 2004-05-31 Pfizer Acetil 2-hindroxi-1,3-diaminoalcanos
EP1562897B1 (fr) 2002-11-12 2009-09-16 Merck & Co., Inc. Inhibiteurs de beta-secretase phenylcarboxamide utilises dans le traitement de la maladie d'alzheimer
GB0228410D0 (en) 2002-12-05 2003-01-08 Glaxo Group Ltd Novel Compounds
EP1583750B1 (fr) 2003-01-07 2013-02-27 Merck Sharp & Dohme Corp. Inhibiteurs de bêta-sécrétase macrocyclique pour traiter la maladie d'Alzheimer
GB0305918D0 (en) 2003-03-14 2003-04-23 Glaxo Group Ltd Novel compounds
JP2006520371A (ja) 2003-03-14 2006-09-07 メルク シャープ エンド ドーム リミテッド 軽症の認識損傷の治療方法及びアルツハイマー病の予防又は遅延方法
AR044043A1 (es) 2003-04-21 2005-08-24 Elan Pharm Inc Fenacilo 2-hidroxi-3-diaminoalcanos
CA2523232A1 (fr) 2003-04-21 2004-11-04 Elan Pharmaceuticals, Inc. Benzamide 2-hydroxy-3-diaminoalcanes
EP1641748B1 (fr) 2003-06-30 2013-08-28 Merck Sharp & Dohme Corp. Inhibiteurs de la beta-secretase a base de n-alkyle phenylcarboxamide pour le traitement de la maladie d'alzheimer
CA2530006A1 (fr) 2003-07-01 2005-01-20 Merck & Co., Inc. Inhibiteurs de la beta-secretase de phenylcarboxylate destines au traitement de la maladie d'alzheimer
US7763609B2 (en) 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
US7592348B2 (en) 2003-12-15 2009-09-22 Schering Corporation Heterocyclic aspartyl protease inhibitors
US7700603B2 (en) 2003-12-15 2010-04-20 Schering Corporation Heterocyclic aspartyl protease inhibitors
MY149978A (en) 2003-12-15 2013-11-15 Merck Sharp & Dohme Heterocyclic aspartyl protease inhibitors
GB0402143D0 (en) 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
WO2005097767A1 (fr) 2004-03-30 2005-10-20 Merck & Co., Inc. Composes de 2-aminothiazole utiles en tant qu'inhibiteurs de l'aspartyle-protease
BRPI0512213A (pt) 2004-06-16 2008-02-19 Wyeth Corp método para tratamento, prevenção ou melhora de uma doença ou distúrbio; composição farmacêutica; processo para a preparação de um composto; e uso de um composto
WO2006041404A1 (fr) 2004-10-15 2006-04-20 Astrazeneca Ab Composes amino substitues et utilisation de ces compose
AU2006205127A1 (en) 2005-01-14 2006-07-20 Wyeth Amino-imidazolones for the inhibition of beta-secretase
US7759337B2 (en) 2005-03-03 2010-07-20 Amgen Inc. Phthalazine compounds and methods of use
JP2008543846A (ja) 2005-06-14 2008-12-04 シェーリング コーポレイション プロテアーゼ阻害剤として化合物の調製およびその使用
MX2007016183A (es) 2005-06-14 2008-03-10 Schering Corp Preparacion y uso de compuestos como inhibidores de proteasas.
TW200716134A (en) * 2005-06-16 2007-05-01 Janssen Pharmaceutica Nv Tricyclic opioid modulators
TW200738683A (en) 2005-06-30 2007-10-16 Wyeth Corp Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation
US20070020316A1 (en) * 2005-07-13 2007-01-25 Raviv Laor Personal topical disinfectant device
WO2007011810A1 (fr) 2005-07-18 2007-01-25 Merck & Co., Inc. Inhibiteurs de beta-secretase de spiropiperidine destines au traitement de la maladie d'alzheimer
TW200730523A (en) 2005-07-29 2007-08-16 Wyeth Corp Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation
WO2007038271A1 (fr) 2005-09-26 2007-04-05 Wyeth Composes d'amino-5-[4-(difluoromethoxy) phenyl]-5-phenylimidazolone utilises comme inhibiteurs de la beta-secretase (bace)
US8173642B2 (en) 2005-10-25 2012-05-08 Shionogi & Co., Ltd. Aminodihydrothiazine derivatives
WO2007100536A1 (fr) 2006-02-24 2007-09-07 Wyeth COMPOSES DE DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] POUR L'INHIBITION DE LA β-SECRETASE
US20090099217A1 (en) 2006-04-05 2009-04-16 Astex Therapeutics Ltd. 2-Aminopyrimidin-4-Ones And Their Use For Treating Or Preventing Alpha Beta-Related Pathologies
TW200808751A (en) 2006-04-13 2008-02-16 Astrazeneca Ab New compounds
WO2007146225A2 (fr) 2006-06-12 2007-12-21 Schering Corporation Inhibiteurs d'aspartyl protéase hétérocycliques
TW200815447A (en) 2006-06-14 2008-04-01 Astrazeneca Ab Novel compounds IV
TW200815349A (en) 2006-06-22 2008-04-01 Astrazeneca Ab New compounds
CA2668065A1 (fr) 2006-10-30 2008-05-08 Merck & Co., Inc. Composes de spiropiperidine inhibiteurs de la beta-secretase pour le traitement de la maladie d'alzheimer
TW200831091A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
TW200831484A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
KR101174191B1 (ko) 2007-02-02 2012-08-14 에프. 호프만-라 로슈 아게 중추 신경계 장애의 치료용 taar1 리간드로서 2-아미노옥사졸린
CL2008000791A1 (es) 2007-03-23 2008-05-30 Wyeth Corp Compuestos derivados de 2-amino-5-(4-difluorometoxi-fenil)-5-fenil-imidazolidin-4-ona; composicion farmaceutica que comprende a dichos compuestos; y su uso en el tratamiento de una enfermedad asociada con la actividad bace excesiva, tales como enferm
AU2008245082B8 (en) 2007-04-24 2012-09-13 Shionogi & Co., Ltd. Aminodihydrothiazine derivatives substituted with a cyclic group
JP5383483B2 (ja) 2007-04-24 2014-01-08 塩野義製薬株式会社 アルツハイマー症治療用医薬組成物
TW200902503A (en) 2007-05-15 2009-01-16 Astrazeneca Ab New compounds
UA101352C2 (uk) 2008-01-18 2013-03-25 Ейсей Р Енд Д Менеджмент Ко., Лтд. Конденсоване похідне амінодигідротіазину
CN101952260B (zh) 2008-02-18 2013-02-13 弗·哈夫曼-拉罗切有限公司 4,5-二氢-*唑-2-基胺衍生物
JP2011518224A (ja) 2008-04-22 2011-06-23 シェーリング コーポレイション Bace−1阻害剤としてのチオフェニル置換2−イミノ−3−メチルピロロピリミジノン化合物、組成物、およびそれらの使用
TWI431004B (zh) 2008-05-02 2014-03-21 Lilly Co Eli Bace抑制劑
KR101307007B1 (ko) 2008-07-24 2013-09-11 에프. 호프만-라 로슈 아게 4,5-다이하이드로-옥사졸-2-일 유도체
CA2731209A1 (fr) * 2008-07-28 2010-02-04 Eisai R&D Management Co., Ltd. Derives de spiroaminodihydrothiazine

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CL2011000516A1 (es) 2011-08-26
CN102209721A (zh) 2011-10-05
PE20110805A1 (es) 2011-11-09
ZA201102674B (en) 2011-12-28
TW201022280A (en) 2010-06-16
IL211440A0 (en) 2011-05-31
ES2459195T3 (es) 2014-05-08
CR20110134A (es) 2011-08-04
EA201100461A1 (ru) 2011-10-31
MX2011002705A (es) 2011-09-09
KR20110073511A (ko) 2011-06-29
US8426447B2 (en) 2013-04-23
BRPI0918449A2 (pt) 2019-09-24
EP2328903A1 (fr) 2011-06-08
MY148558A (en) 2013-04-30
AU2009291602B2 (en) 2013-02-14
CA2736130A1 (fr) 2010-03-18
CA2736130C (fr) 2014-01-14
JP5579720B2 (ja) 2014-08-27
JP2012502112A (ja) 2012-01-26
AU2009291602A1 (en) 2010-03-18
WO2010030954A1 (fr) 2010-03-18
TWI385175B (zh) 2013-02-11
CO6362014A2 (es) 2012-01-20
US20100087429A1 (en) 2010-04-08

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