[go: up one dir, main page]

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)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (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 (36)

* 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
US8633212B2 (en) 2009-03-13 2014-01-21 Vitae Pharmaceuticals, Inc. Inhibitors of beta-secretase
UA108363C2 (uk) 2009-10-08 2015-04-27 Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
US8889703B2 (en) 2010-02-24 2014-11-18 Vitae Pharmaceuticals, Inc. Inhibitors of beta-secretase
EP2547686B1 (fr) * 2010-03-15 2014-01-22 Amgen Inc. Composés spirannique de amino-dihydrooxazine et amino-dihydrothiazine comme modulateur de bêta-sécrétase et leur utilisation médicale
MX2012010658A (es) * 2010-03-15 2012-12-05 Amgen Inc Compuestos de anillo espiro tetraciclico como moduladores de beta-secretasa.
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
JP2013536233A (ja) 2010-08-23 2013-09-19 アムジエン・インコーポレーテツド グルコキナーゼ調節タンパク質と相互作用する糖尿病治療用の化合物
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
WO2012071458A1 (fr) * 2010-11-22 2012-05-31 Array Biopharma Inc. Inhibiteurs hétérocycliques de la bêta-secrétase pour le traitement de maladies neurodégénératives
WO2012071279A1 (fr) * 2010-11-23 2012-05-31 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
US9346827B2 (en) 2011-02-07 2016-05-24 Amgen Inc. 5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use
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
KR20140041590A (ko) 2011-06-07 2014-04-04 에프. 호프만-라 로슈 아게 [1,3]옥사진
BR112014004181A2 (pt) 2011-08-22 2017-06-13 Merck Sharp & Dohme composto, composição farmacêutica, e, método de tratamento, prevenção, e / ou retardo do início de uma doença ou patologia
US9296759B2 (en) 2011-09-21 2016-03-29 Amgen Inc. Amino-oxazine and amino-dihydrothiazine compounds as beta-secretase modulators and methods of use
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
US9000183B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-indene-1′,2″-imidazol 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
US9000182B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab 2H-imidazol-4-amine compounds and their use as BACE inhibitors
US9000185B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cycloalkyl ether 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
WO2014052398A1 (fr) 2012-09-28 2014-04-03 Vitae Pharmaceuticals, Inc. Inhibiteur de beta-secrétase
WO2014078314A1 (fr) * 2012-11-15 2014-05-22 Amgen Inc. Composés d'amino-oxazine et d'amino-dihydrothiazine jouant le rôle de modulateurs de bêta-sécrétase et procédés d'utilisation
CN114057765A (zh) 2015-02-02 2022-02-18 瓦洛健康股份有限公司 作为hdac抑制剂的3-芳基-4-酰氨基-二环[4,5,0]异羟肟酸
AR103598A1 (es) 2015-02-02 2017-05-24 Forma Therapeutics Inc Ácidos bicíclicos[4,6,0]hidroxámicos como inhibidores de hdac
US10555935B2 (en) 2016-06-17 2020-02-11 Forma Therapeutics, Inc. 2-spiro-5- and 6-hydroxamic acid indanes as HDAC inhibitors
DE102023106829A1 (de) 2023-03-19 2024-09-19 List Technology Ag Verfahren und Vorrichtung zur Behandlung eines Ausgangsproduktes

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
US5942400A (en) 1995-06-07 1999-08-24 Elan Pharmaceuticals, Inc. Assays for detecting β-secretase
KR20060111905A (ko) 1998-09-24 2006-10-30 파마시아 앤드 업존 캄파니 엘엘씨 알츠하이머병 세크레타제
MY138097A (en) 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
CA2410680A1 (fr) 2000-06-30 2002-01-10 Elan Pharmaceuticals, Inc. Composes pour le traitement de la maladie d'alzheimer
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
MXPA04000140A (es) 2001-06-27 2004-06-03 Elan Pharm Inc Derivados de beta-hidroxiamina utiles en el tratamiento de enfermedad de alzheimer.
KR100713137B1 (ko) 2001-06-28 2007-05-02 동화약품공업주식회사 신규의 2,4-디플루오로벤즈아미드 유도체
WO2003006021A1 (fr) 2001-07-10 2003-01-23 Elan Pharmaceuticals, Inc. Derives de statine alpha-hydroxyamide pour le traitement de la maladie d'alzheimer
CA2453444A1 (fr) 2001-07-10 2003-01-23 Elan Pharmaceuticals, Inc. Diaminediols pour le traitement de la maladie d'alzheimer
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
MXPA04003244A (es) 2001-10-05 2004-07-08 Elan Pharm Inc Alilamidas utiles para tratamiento de enfermedad de alzheimer.
JP2005535559A (ja) 2001-10-29 2005-11-24 ファルマシア・アンド・アップジョン・カンパニー・エルエルシー アルツハイマー病を治療するためのヒドロキシ置換アミド
IL161881A0 (en) 2001-11-08 2005-11-20 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
AU2003206413A1 (en) 2002-01-04 2003-07-24 Elan Pharmaceuticals, Inc. Substituted amino carboxamides for the treatment of alzheimer's disease
CA2473796A1 (fr) 2002-01-17 2003-07-31 Neurogen Corporation Analogues de quinazoline-4-ylamine substitues
US7132568B2 (en) 2002-06-17 2006-11-07 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
US7115652B2 (en) 2002-06-17 2006-10-03 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
CN1324017C (zh) 2002-06-20 2007-07-04 法玛西和厄普约翰有限责任公司 5-(1,3-噁唑-2-基)苯甲酸衍生物的制备方法
UY27967A1 (es) 2002-09-10 2004-05-31 Pfizer Acetil 2-hindroxi-1,3-diaminoalcanos
US7109217B2 (en) 2002-11-12 2006-09-19 Merck & Co., Inc. Phenylcarboxamide beta-secretase inhibitors for the treatment of Alzheimer's disease
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
MXPA05009850A (es) 2003-03-14 2005-12-06 Merck Sharp & Dohme Metodo para tratar el deterioro cognitivo leve y para prevenir o atrasar la enfermedad de alzheimer.
GB0305918D0 (en) 2003-03-14 2003-04-23 Glaxo Group Ltd Novel compounds
CA2523232A1 (fr) 2003-04-21 2004-11-04 Elan Pharmaceuticals, Inc. Benzamide 2-hydroxy-3-diaminoalcanes
JP2006524258A (ja) 2003-04-21 2006-10-26 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 フェナシル2−ヒドロキシ−3−ジアミノアルカン
AU2004255183A1 (en) 2003-06-30 2005-01-20 Merck & Co., Inc. N-alkyl phenylcarboxamide beta-secretase inhibitors for the treatment of Alzheimer's disease
JP2007522088A (ja) 2003-07-01 2007-08-09 メルク エンド カムパニー インコーポレーテッド アルツハイマー病の治療用フェニルカルボン酸ベータセクレターゼ阻害剤
US7763609B2 (en) 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
US7700603B2 (en) 2003-12-15 2010-04-20 Schering Corporation Heterocyclic aspartyl protease inhibitors
US7592348B2 (en) 2003-12-15 2009-09-22 Schering Corporation Heterocyclic aspartyl protease inhibitors
SG163508A1 (en) 2003-12-15 2010-08-30 Schering Corp Heterocyclic aspartyl protease inhibitors
GB0402143D0 (en) 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
JP2007530696A (ja) 2004-03-30 2007-11-01 メルク エンド カムパニー インコーポレーテッド アスパラギン酸プロテアーゼ阻害剤として有用な2−アミノチアゾール化合物
JP2008503459A (ja) 2004-06-16 2008-02-07 ワイス β−セクレターゼを阻害するためのアミノ−5,5−ジフェニルイミダゾロン誘導体
WO2006041404A1 (fr) 2004-10-15 2006-04-20 Astrazeneca Ab Composes amino substitues et utilisation de ces compose
EP2264036A1 (fr) 2005-01-14 2010-12-22 Wyeth LLC (Formerly Known As Wyeth) Amino-imidazolones destinés à l' inhibition de la beta-secretase
US7759337B2 (en) 2005-03-03 2010-07-20 Amgen Inc. Phthalazine compounds and methods of use
MX2007016186A (es) 2005-06-14 2008-03-07 Schering Corp Preparacion y uso de inhibidores de proteasas.
BRPI0612545A2 (pt) 2005-06-14 2010-11-23 Schering Corp compostos inibidores de protease, composições farmacêuticas e uso dos mesmos
RU2008101667A (ru) * 2005-06-16 2009-07-27 Янссен Фармацевтика Н.В. (Be) Трициклические модуляторы опиоидов
TW200738683A (en) 2005-06-30 2007-10-16 Wyeth Corp Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation
WO2007009014A2 (fr) * 2005-07-13 2007-01-18 Raviv Laor Dispositif desinfectant topique personnel
AU2006270084B2 (en) 2005-07-18 2011-08-25 Merck Sharp & Dohme Corp. Spiropiperidine beta-secretase inhibitors for the treatment of Alzheimer's disease
TW200730523A (en) 2005-07-29 2007-08-16 Wyeth Corp Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation
BRPI0616757A2 (pt) 2005-09-26 2011-06-28 Wyeth Corp composto da fórmula i; processo para o tratamento de uma doença ou de um distúrbio associado com a atividade excessiva de bace; processo para a modulação da atividade de bace; processo para o tratamento da doença de alzheimer; e composição farmacêutica
AU2006307314C1 (en) 2005-10-25 2011-08-25 Shionogi & Co., Ltd. Aminodihydrothiazine derivative
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
JP2009532464A (ja) 2006-04-05 2009-09-10 アストラゼネカ・アクチエボラーグ 2−アミノピリミジン−4−オン及びAβ−関連の病理を治療又は予防するためのその使用
TW200808751A (en) 2006-04-13 2008-02-16 Astrazeneca Ab New compounds
CA2653650A1 (fr) 2006-06-12 2007-12-21 Schering Corporation Inhibiteurs d'aspartyl protease heterocycliques
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
EP2091328B1 (fr) 2006-10-30 2011-12-28 Merck Sharp & Dohme Corp. Composés de spiropipéridine inhibiteurs de la bêta-sécrétase pour le traitement de la maladie d'alzheimer
TW200831484A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
TW200831091A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
EP2114906B1 (fr) 2007-02-02 2014-08-06 F. Hoffmann-La Roche AG Composés de 2-aminooxazoline comme ligands du taar1 pour des troubles du snc
PE20090617A1 (es) 2007-03-23 2009-05-08 Wyeth Corp Compuestos amino-5-[-4-(difluorometoxi)fenil]-5-fenilimidazolona para la inhibicion de -secretasa
WO2008133273A1 (fr) 2007-04-24 2008-11-06 Shionogi & Co., Ltd. Composition pharmaceutique pour le traitement de la maladie d'alzheimer
EP2147914B1 (fr) 2007-04-24 2014-06-04 Shionogi&Co., Ltd. Dérivés d'aminodihydrothiazine substitués par des groupes cycliques
UY31083A1 (es) 2007-05-15 2009-01-05 Astrazeneca Ab Derivados de sulfoximinas para la inhibicion de b-secretasa
MY160690A (en) 2008-01-18 2017-03-15 Eisai R&D Man Co Ltd Condensed aminodihydrothiazine derivative
CA2712228C (fr) 2008-02-18 2013-04-16 F. Hoffmann-La Roche Ag Derives de 4,5-dihydrooxazol-2-ylamine
MX2010011563A (es) 2008-04-22 2010-11-12 Schering Corp Compuestos 2-imino-3-metil pirrolo pirimidinona fenil-sustituidos como inhibidores de enzima de escision de proteina precursora amiloide sitio beta-1, composiciones y su uso.
TWI431004B (zh) 2008-05-02 2014-03-21 Lilly Co Eli Bace抑制劑
EP2321287B1 (fr) 2008-07-24 2015-11-11 F. Hoffmann-La Roche AG Dérivés de 4,5-dihydrooxazol-2-yle
AU2009277485B2 (en) * 2008-07-28 2013-05-02 Eisai R&D Management Co., Ltd. Spiroaminodihydrothiazine derivatives

Also Published As

Publication number Publication date
TW201022280A (en) 2010-06-16
JP2012502112A (ja) 2012-01-26
BRPI0918449A2 (pt) 2019-09-24
CL2011000516A1 (es) 2011-08-26
CA2736130C (fr) 2014-01-14
IL211440A0 (en) 2011-05-31
ES2459195T3 (es) 2014-05-08
CA2736130A1 (fr) 2010-03-18
EA201100461A1 (ru) 2011-10-31
CO6362014A2 (es) 2012-01-20
CN102209721A (zh) 2011-10-05
PE20110805A1 (es) 2011-11-09
AU2009291602B2 (en) 2013-02-14
JP5579720B2 (ja) 2014-08-27
EP2328903B1 (fr) 2014-03-05
US20100087429A1 (en) 2010-04-08
ZA201102674B (en) 2011-12-28
MX2011002705A (es) 2011-09-09
US8426447B2 (en) 2013-04-23
MY148558A (en) 2013-04-30
WO2010030954A1 (fr) 2010-03-18
EP2328903A1 (fr) 2011-06-08
TWI385175B (zh) 2013-02-11
KR20110073511A (ko) 2011-06-29
AU2009291602A1 (en) 2010-03-18
CR20110134A (es) 2011-08-04

Similar Documents

Publication Publication Date Title
MA32705B1 (fr) Composes cycliques spiro-tetracycliques utiles en tant que modulateurs de la beta-secretase et leurs procedes d'utilisation
TNSN05104A1 (fr) Derives de thiazole pour le traitement de troubles neurodegeneratifs
MA29807B1 (fr) Dérives de phenyl-[1,2,4]- oxadiazol-5-one avec un groupement phényle, leurs procédés de préparation et leur utilisation comme produits pharmaceutiques.
MX2009012608A (es) Compuestos de hidroxietil amina substituidos como moduladores de beta-secretasa y metodos de uso.
MX2012010658A (es) Compuestos de anillo espiro tetraciclico como moduladores de beta-secretasa.
MA31865B1 (fr) Dérivés isoxazolo-pyridine
MA33053B1 (fr) Inhibiteurs de la poly(adp-ribose) polymerase (parp)
MA29805B1 (fr) Derives de phenyl-1.2.4-oxadiazolone, leurs procedes de preparation et leur utilisation comme produits pharmaceutiques
MX2012010657A (es) Compuestos de espiro amino-dihidrooxazina y amino-dihidrotiazina como moduladores de beta-secretasa y su uso medico.
MA34922B1 (fr) Imidazo[5,1-f][1,2,4] triazines pour le traitement de troubles neurologiques
MA30696B1 (fr) Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique
MA30981B1 (fr) Derives de sulfonyl-phenyl-2h-(1,2,4)oxadiazol-5-one, procedes de preparation associes et utilisation comme medicaments
MA27132A1 (fr) Composes de n-(3-amino-2hydroxy-propyl)alkylamide substitues
MA30089B1 (fr) (arylsulfonyl)-pyrasolopiperidines
MA47447B1 (fr) 2-hétéroaryl-3-oxo-2,3-dihydropyridazine-4-carboxamides pour le traitement du cancer
MA32655B1 (fr) Composés modulant sélectivement le récepteur cb2
MA31857B1 (fr) N-phenyl-pyrrolidinylmethylpyrrolidine-amides substitues et utilisation therapeutique de ceux -ci
MA32506B1 (fr) Nouveaux composes
MA29809B1 (fr) N-[1,3,4]-thiadiazol-2-yl-benzenesulfonamides,procedes pour leur preparation et leur utilisation en tant que produits pharmaceutiques
MA46342A (fr) Dérivés de chromane, d'isochromane et de dihydroisobenzofurane en tant que modulateurs allostériques négatifs de mglur2, compositions et leur utilisation
MA32374B1 (fr) Composes comprenant un groupe cyclobutoxy
MA29989B1 (fr) Tetrahydro-pyridoazepine-8-ones et composes apparentes, pour le traitement de la schizophrenie
MA28241A1 (fr) Derives d'indole hydroxyethylamine tricycliques et leur utilisation dans le traitement de la maladie d'alzheimer
MA52482B1 (fr) Dérivés de spiropipéridine en tant que modulateurs allostériques des récepteurs nicotiniques de l'acétylcholine
DE602004010314D1 (de) Behandlung von neurodegenerativen erkrankungen durch verwendung von degs-inhibitoren