MA35945B1 - Inhibiteurs de la bêta-sécrétase - Google Patents

Inhibiteurs de la bêta-sécrétase

Info

Publication number
MA35945B1
MA35945B1 MA37375A MA37375A MA35945B1 MA 35945 B1 MA35945 B1 MA 35945B1 MA 37375 A MA37375 A MA 37375A MA 37375 A MA37375 A MA 37375A MA 35945 B1 MA35945 B1 MA 35945B1
Authority
MA
Morocco
Prior art keywords
beta
secretase
inhibitors
disorders
bacei
Prior art date
Application number
MA37375A
Other languages
English (en)
Inventor
Zhenrong Xu
Cornelia Dorner-Ciossek
Lanqi Jia
Salvacion Cacatian
Shankar Venkatraman
Georg Rast
Angel Morales-Ramos
Jing Yuan
Klaus Fuchs
Yajun Zheng
Yuri Bukhtiyarov
Lawrence Wayne Dillard
Deepak S Lala
Jonathan Reeves
Suresh B Singh
Yi Zhao
Original Assignee
Vitae Pharmaceuticals 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 Vitae Pharmaceuticals Inc filed Critical Vitae Pharmaceuticals Inc
Publication of MA35945B1 publication Critical patent/MA35945B1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/46—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C229/50—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms being part of the same condensed ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/45—Carboxylic acid nitriles having cyano groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C255/47—Carboxylic acid nitriles having cyano groups bound to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of rings being part of condensed ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/02—Sulfinic acids; Derivatives thereof
    • C07C313/06—Sulfinamides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
    • C07C331/02—Thiocyanates
    • C07C331/14—Thiocyanates having sulfur atoms of thiocyanate groups bound to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
    • C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
    • C07C49/747—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
    • C07C49/755—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups a keto group being part of a condensed ring system with two or three rings, at least one ring being a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/93—Spiro compounds
    • C07C2603/94—Spiro compounds containing "free" spiro atoms

Abstract

La présente invention a trait à des acylguanidines spirocycliques et leur utilisation en tant qu'inhibiteurs de l'activité de l'enzyme bêta-sécrétase (bacei), des compositions pharmaceutiques les contenant, et des procédés pour les utiliser en tant qu'agents thérapeutiques dans le traitement de troubles neurodégénératifs, des troubles caractérisés par un déclin cognitif, une déficience cognitive, la démence et des maladies caractérisées par la production d'agrégats de bêta-amyloïde.
MA37375A 2012-03-05 2014-09-26 Inhibiteurs de la bêta-sécrétase MA35945B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261606786P 2012-03-05 2012-03-05
PCT/US2013/028796 WO2013134085A1 (fr) 2012-03-05 2013-03-04 Inhibiteurs de la bêta-sécrétase

Publications (1)

Publication Number Publication Date
MA35945B1 true MA35945B1 (fr) 2014-12-01

Family

ID=47902355

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37375A MA35945B1 (fr) 2012-03-05 2014-09-26 Inhibiteurs de la bêta-sécrétase

Country Status (40)

Country Link
US (4) US8981112B2 (fr)
EP (1) EP2822930B1 (fr)
JP (1) JP6161643B2 (fr)
KR (1) KR20140138774A (fr)
CN (1) CN104271558B (fr)
AP (1) AP4029A (fr)
AR (1) AR090241A1 (fr)
AU (2) AU2013230523B2 (fr)
BR (1) BR112014021269A2 (fr)
CA (1) CA2864143C (fr)
CL (1) CL2014002334A1 (fr)
CO (1) CO7091177A2 (fr)
CY (1) CY1117543T1 (fr)
DK (1) DK2822930T3 (fr)
EA (1) EA024995B1 (fr)
EC (1) ECSP14020640A (fr)
ES (1) ES2568928T3 (fr)
HK (1) HK1205739A1 (fr)
HR (1) HRP20160415T1 (fr)
HU (1) HUE027289T2 (fr)
IL (1) IL233887A (fr)
IN (1) IN2014DN06710A (fr)
MA (1) MA35945B1 (fr)
ME (1) ME02390B (fr)
MX (1) MX353432B (fr)
MY (1) MY171091A (fr)
NZ (1) NZ629239A (fr)
PE (1) PE20141972A1 (fr)
PH (1) PH12014501963A1 (fr)
PL (1) PL2822930T3 (fr)
RS (1) RS54730B1 (fr)
SG (1) SG11201404600VA (fr)
SI (1) SI2822930T1 (fr)
SM (1) SMT201600114B (fr)
TN (1) TN2014000326A1 (fr)
TW (1) TWI557112B (fr)
UA (1) UA113641C2 (fr)
UY (1) UY34654A (fr)
WO (1) WO2013134085A1 (fr)
ZA (1) ZA201405846B (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2789684B1 (fr) 2008-05-23 2016-12-21 Siwa Corporation Procédés et compositions pour faciliter la régénération
AR075854A1 (es) 2009-03-13 2011-05-04 Vitae Pharmaceuticals Inc Inhibidores de beta- secretasa
CN102812005B (zh) 2010-02-24 2014-12-10 生命医药公司 β-分泌酶抑制剂
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
JP6030752B2 (ja) 2012-05-09 2016-11-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング オキセタン−３−イルメタンアミンの製造方法
TW201422592A (zh) 2012-08-27 2014-06-16 Boehringer Ingelheim Int β－分泌酶抑制劑
EP2900650A1 (fr) 2012-09-28 2015-08-05 Vitae Pharmaceuticals, Inc. Inhibiteurs de beta-secrétase
US9079832B2 (en) 2012-11-21 2015-07-14 Boehringer Ingelheim International Gmbh Process for making N-sulfinyl α-amino amides
US10053453B2 (en) 2014-10-07 2018-08-21 Astrazeneca Ab Compounds and their use as BACE inhibitors
US9993535B2 (en) 2014-12-18 2018-06-12 Siwa Corporation Method and composition for treating sarcopenia
US10358502B2 (en) 2014-12-18 2019-07-23 Siwa Corporation Product and method for treating sarcopenia
JP6722293B2 (ja) 2016-02-19 2020-07-15 シワ コーポレーション 終末糖化産物（ａｇｅ）に対する抗体を使用して、がんを治療、転移性がん細胞を殺傷、及びがん転移を予防するための方法及び組成物
CA3057829A1 (fr) 2016-04-15 2017-10-19 Siwa Corporation Anticorps anti-age pour le traitement de troubles neurodegeneratifs
WO2017222535A1 (fr) 2016-06-23 2017-12-28 Siwa Corporation Vaccins pour l'utilisation dans le traitement de diverses maladies et troubles
CA3039026A1 (fr) * 2016-09-07 2018-03-15 The Regents Of The University Of California Antagonistes allosteriques du recepteur 1 du facteur de liberation de la corticotropine (crfr1) qui diminuent la p-tau et ameliorent la cognition
JP2020516648A (ja) 2017-04-13 2020-06-11 シワ コーポレーション ヒト化モノクローナル終末糖化産物抗体
US11518801B1 (en) 2017-12-22 2022-12-06 Siwa Corporation Methods and compositions for treating diabetes and diabetic complications
CN113082209A (zh) * 2021-03-31 2021-07-09 中国科学技术大学 Cd4+t细胞源性bace1、ep2、ep4作为阿尔茨海默病治疗靶点的应用

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5745185A (en) 1980-07-21 1982-03-13 Eisai Co Ltd Hydantoin derivative and its preparation
EP0602060A1 (fr) 1991-08-28 1994-06-22 PHARMACIA & UPJOHN COMPANY Imidazolines de benzopyranne spirocycliques, leur préparation et leur utilisation comme activateurs des canaux de potassium
EP0758313A4 (fr) 1994-05-06 1999-09-15 Pharmacopeia Inc Bibliotheque combinatoire de dihydrobenzopyranes
US7700603B2 (en) 2003-12-15 2010-04-20 Schering Corporation Heterocyclic aspartyl protease inhibitors
US7763609B2 (en) 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
EP1699455B1 (fr) 2003-12-15 2013-05-08 Merck Sharp & Dohme Corp. Inhibiteurs de protéase aspartyle hétérocyclique
US7592348B2 (en) 2003-12-15 2009-09-22 Schering Corporation Heterocyclic aspartyl protease inhibitors
EP1756087B1 (fr) 2004-06-16 2009-10-07 Wyeth Dérivés d'amino-5,5-diphénylimidazolone servant à inhiber la bêta-secrétase
KR20070026811A (ko) 2004-06-16 2007-03-08 와이어쓰 베타-세크리타제 억제제로서의 디페닐이미다조피리미딘 및디페닐이미다졸 아민
CA2583342A1 (fr) 2004-10-13 2006-04-27 Merck And Co., Inc. Composes de spiropiperidine utilises comme inhibiteurs de beta-secretase en vue du traitement de la maladie d'alzheimer
WO2006138217A1 (fr) 2005-06-14 2006-12-28 Schering Corporation Inhibiteurs d'aspartyl protease
KR20080031189A (ko) 2005-06-14 2008-04-08 쉐링 코포레이션 아스파르틸 프로테아제 억제제
AU2006266167A1 (en) 2005-06-30 2007-01-11 Wyeth Amino-5-(6-membered)heteroarylimidazolone compounds and the use thereof for beta-secretase modulation
TW200738683A (en) 2005-06-30 2007-10-16 Wyeth Corp Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation
EP1913193B1 (fr) 2005-07-29 2018-12-05 Koninklijke Philips N.V. Dispositif de repassage à vapeur de generation d'une rafale de vapeur
TW200730523A (en) 2005-07-29 2007-08-16 Wyeth Corp Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation
JP2009509957A (ja) 2005-09-26 2009-03-12 ワイス β−セクレターゼ阻害剤としてのアミノ−５−［４−（ジフルオロメトキシ）フェニル］−５−フェニルイミダゾロン化合物
CN103936690B (zh) 2005-10-25 2016-06-08 盐野义制药株式会社 氨基二氢噻嗪衍生物
US7872009B2 (en) 2005-11-21 2011-01-18 Amgen Inc. Beta-Secretase modulators and methods of use
DE102005057688A1 (de) 2005-12-01 2007-06-14 Endress + Hauser Flowtec Ag Vorrichtung zur Bestimmung und/oder Überwachung des Massedurchflusses eines gasförmigen Mediums
JP2009520027A (ja) 2005-12-19 2009-05-21 ワイス ２−アミノ−５−ピペリジニルイミダゾロン化合物およびβ−セクレターゼ調節におけるその使用
WO2007076284A2 (fr) 2005-12-20 2007-07-05 Fieldbus Foundation Systeme et procede pour mettre en oeuvre des systemes instrumentes de securite
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
AR061264A1 (es) 2006-06-12 2008-08-13 Schering Corp Inhibidores de aspartil-proteasas derivados de pirimidina, composiciones farmaceuticas que los contienen y usos para tratar enfermedades cognitivas o neurodegenerativas, y como inhibidores del virus vih.
CN101489984B (zh) 2006-07-18 2013-04-03 安斯泰来制药株式会社 氨基茚满衍生物或其盐
AU2007293416A1 (en) 2006-09-07 2008-03-13 Merck & Co., Inc. Spiropiperidine beta-secretase inhibitors for the treatment of Alzheimer's disease
TW200831091A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
WO2008076043A1 (fr) 2006-12-20 2008-06-26 Astrazeneca Ab Nouveaux 2-amino-5,5-diaryl-imidazol-4-ones
TW200831484A (en) 2006-12-20 2008-08-01 Astrazeneca Ab New compounds
PE20090160A1 (es) 2007-03-20 2009-02-11 Wyeth Corp COMPUESTOS AMINO-5-[4-(DIFLUOROMETOXI)FENIL SUSTITUIDO]-5-FENILIMIDAZOLONA COMO INHIBIDORES DE ß-SECRETASA
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
EP2151435A4 (fr) 2007-04-24 2011-09-14 Shionogi & Co Composition pharmaceutique pour le traitement de la maladie d'alzheimer
MX2009011498A (es) 2007-04-24 2009-11-10 Shionogi & Co Derivados de aminodihidrotiazina sustituida con un grupo ciclico.
UY31083A1 (es) 2007-05-15 2009-01-05 Astrazeneca Ab Derivados de sulfoximinas para la inhibicion de b-secretasa
EP2077637B1 (fr) 2007-12-12 2020-03-11 Alcatel Lucent Système et procédé de protection d'informations de données utiles dans une transmission radio
BRPI0907563A2 (pt) 2008-02-18 2015-08-04 Hoffmann La Roche Derivados de 4,5-di-hidro-xazol-2-il amina
TWI431004B (zh) 2008-05-02 2014-03-21 Lilly Co Eli Ｂａｃｅ抑制劑
WO2010013302A1 (fr) 2008-07-28 2010-02-04 エーザイ・アール・アンド・ディー・マネジメント株式会社 Dérivé de spiroaminodihydrothiazine
AU2009277485B2 (en) 2008-07-28 2013-05-02 Eisai R&D Management Co., Ltd. Spiroaminodihydrothiazine derivatives
WO2010021680A2 (fr) 2008-08-19 2010-02-25 Vitae Pharmaceuticals, Inc. Inhibiteurs de la bêta-sécrétase
US8426447B2 (en) 2008-09-11 2013-04-23 Amgen Inc. Spiro-tricyclic ring compounds as beta-secretase modulators and methods of use
PE20110777A1 (es) * 2008-11-23 2011-10-29 Pfizer Nuevas lactamas como inhibidores de beta secretasa
AR075854A1 (es) * 2009-03-13 2011-05-04 Vitae Pharmaceuticals Inc Inhibidores de beta- secretasa
WO2011072064A1 (fr) 2009-12-08 2011-06-16 Array Biopharma Inc. Spiro[chromane-4,4'-imidazol]ones en tant qu'inhibiteurs de bêta-sécrétase
CN102812005B (zh) * 2010-02-24 2014-12-10 生命医药公司 β-分泌酶抑制剂
US20120065195A1 (en) 2010-03-31 2012-03-15 Clark Christopher T Compounds for treating neurodegenerative diseases
US8415483B2 (en) * 2010-12-22 2013-04-09 Astrazeneca Ab Compounds and their use as BACE inhibitors
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

Also Published As

Publication number Publication date
AU2017236042A1 (en) 2017-10-26
SI2822930T1 (sl) 2016-09-30
ES2568928T3 (es) 2016-05-05
IL233887A (en) 2017-09-28
PH12014501963B1 (en) 2014-11-17
TW201339139A (zh) 2013-10-01
AP4029A (en) 2017-02-05
TWI557112B (zh) 2016-11-11
CN104271558B (zh) 2016-08-24
AU2013230523B2 (en) 2017-10-05
IN2014DN06710A (fr) 2015-05-22
ME02390B (fr) 2016-09-20
PE20141972A1 (es) 2014-12-28
AU2017236042B2 (en) 2019-01-03
CL2014002334A1 (es) 2015-04-17
CA2864143C (fr) 2020-04-14
PH12014501963A1 (en) 2014-11-17
MX353432B (es) 2018-01-11
IL233887A0 (en) 2014-09-30
AU2013230523A1 (en) 2014-09-18
EP2822930B1 (fr) 2016-01-20
ZA201405846B (en) 2017-08-30
MX2014010625A (es) 2015-04-08
SG11201404600VA (en) 2014-10-30
BR112014021269A2 (pt) 2017-07-04
SMT201600114B (it) 2016-08-31
US9949975B2 (en) 2018-04-24
NZ629239A (en) 2016-04-29
US8981112B2 (en) 2015-03-17
RS54730B1 (sr) 2016-10-31
EP2822930A1 (fr) 2015-01-14
MY171091A (en) 2019-09-25
HRP20160415T1 (hr) 2016-06-03
US20150150872A1 (en) 2015-06-04
WO2013134085A1 (fr) 2013-09-12
CA2864143A1 (fr) 2013-09-12
PL2822930T3 (pl) 2016-09-30
JP2015511958A (ja) 2015-04-23
CO7091177A2 (es) 2014-10-21
JP6161643B2 (ja) 2017-07-12
US9526727B2 (en) 2016-12-27
HK1205739A1 (zh) 2015-12-24
US20170196867A1 (en) 2017-07-13
EA201491534A1 (ru) 2014-12-30
KR20140138774A (ko) 2014-12-04
HUE027289T2 (en) 2016-09-28
UA113641C2 (xx) 2017-02-27
US20180344734A1 (en) 2018-12-06
DK2822930T3 (en) 2016-04-25
AR090241A1 (es) 2014-10-29
AP2014007900A0 (en) 2014-08-31
US20130289050A1 (en) 2013-10-31
CY1117543T1 (el) 2017-04-26
ECSP14020640A (es) 2015-06-30
EA024995B1 (ru) 2016-11-30
CN104271558A (zh) 2015-01-07
TN2014000326A1 (en) 2015-12-21
UY34654A (es) 2013-09-30
WO2013134085A8 (fr) 2014-09-04

Similar Documents

Publication Publication Date Title
MA35945B1 (fr) Inhibiteurs de la bêta-sécrétase
MA46018A (fr) Activateurs d'édition du génome
MA35191B1 (fr) Spiro-[1,3]-oxazines et spiro-[1,4]-oxazepines en tant qu'inhibiteurs de baec1 et/ou bace2
MA34969B1 (fr) Composes et compositions en tant qu inibiteurs de trk
MA38837A1 (fr) Inhibiteurs de l'autotaxine contenant un noyau à cycle benzyle-amide cyclique hétéroaromatique
MA35246B1 (fr) 1,3-oxazines en tant qu'inhibiteurs de bace1 et/ou de bace2
MA35455B1 (fr) (wo2013045407) dérivés d'estra-1,3,5(10),16-tétraène-3-carboxamide, procédé pour leur fabrication, préparations pharmaceutiques contenant ces substances ainsi que leur utilisation dans la fabrication de médicaments
MA35096B1 (fr) Cyclopropylamines en tant qu'inhibiteurs de lsd1
MA35193B1 (fr) Halogeno-alkyl-1,3 oxazines en tant qu'inhibiteurs de bace1 et/ou bace2
PH12015500420A1 (en) Inhibitors of beta-secretase
MA42397B1 (fr) 4-azaindoles substituées et leur utilisation comme modulatoeurs de la récepteur glun2b
MA38190A2 (fr) Inhibiteurs d'autotaxine
MA38349A1 (fr) Œstra-1,3,5(10),16-tétraéno-3-carboxamide pour inhiber la 17-bêta-hydroxystéroïde déshydrogénase (akr1c3)
MA37763A1 (fr) Difluoro-hexahydro-cyclopentaoxazinyles et difluoro-hexahydro-benzooxazinyles en tant qu'inhibiteurs de bace1
MA37742B1 (fr) Dérivés d'oestra-1,3,5 (10), 16-tétraène substitués en position 3, leurs procédés de préparation, préparations pharmaceutiques les contenant, et leur utilisation pour la fabrication de médicaments
MA34545B1 (fr) Co-cristaux et sels d'inhibiteurs de ccr3
MA38253A1 (fr) Compositions comprenant de la vortioxétine et du donépézil
MA37955A1 (fr) Inhibiteurs de bêta-secrétase
WO2014052398A8 (fr) Inhibiteur de beta-secrétase
MA38473B1 (fr) (benzyl-cyano-méthyl)-amides substitués de l'acide 2-aza-bicyclo[2.2.1]heptane-3-carboxylique utilisés comme inhibiteurs de la cathépsine c
MA39260A1 (fr) (benzyl-cyano-méthyl)-amides substitués de l'acide 2-aza-bicyclo[2.2.1]heptane-3-carboxylique utilisés comme inhibiteurs de la cathépsine c
MA38451A1 (fr) Benzoimidazol-2-ylpyrimidines modulatrices du récepteur de l'histamine h4