BRPI0606902A2 - composto; método para o tratamento de uma doença ou distúrbio associado a atividade excessiva de bace em um paciente que dele necessite; método para modular a atividade de bace; composição farmacêutica - Google Patents

composto; método para o tratamento de uma doença ou distúrbio associado a atividade excessiva de bace em um paciente que dele necessite; método para modular a atividade de bace; composição farmacêutica

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Publication number
BRPI0606902A2
BRPI0606902A2 BRPI0606902-9A BRPI0606902A BRPI0606902A2 BR PI0606902 A2 BRPI0606902 A2 BR PI0606902A2 BR PI0606902 A BRPI0606902 A BR PI0606902A BR PI0606902 A2 BRPI0606902 A2 BR PI0606902A2
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BR
Brazil
Prior art keywords
activity
compound
disease
excessive
pharmaceutical composition
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Application number
BRPI0606902-9A
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English (en)
Inventor
Derek Cecil Cole
Eric Steven Manas
Lee Dalton Jennings
Joseph Raymond Stock
William Jay Moore
John Watson Ellingboe
Mohani Nirmala Sukhdeo
Ping Zhou
Koi Michele Morris
Frank Eldridge Lovering
Jeffrey Scott Condon
Junjun Wu
Original Assignee
Wyeth Corp
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Publication date
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of BRPI0606902A2 publication Critical patent/BRPI0606902A2/pt

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    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/32Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D207/325Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
    • C07D207/327Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Abstract

COMPOSTO; MéTODO PARA O TRATAMENTO DE UMA DOENçA OU DISTúRBIO ASSOCIADO A ATIVIDADE EXCESSIVA DE BACE EM UM PACIENTE QUE DELE NECESSITE; MéTODO PARA MODULAR A ATIVIDADE DE BACE; COMPOSIçãO FARMACêUTICA. A presente invenção proporciona um composto de azolilacilguanidina de fórmula I A presente invenção também proporciona métodos para o seu uso para inibir a <225>-secretase (BACE) e tratar depósitos de <225>-amilóide e entrelaçamentos neurofibrilares.
BRPI0606902-9A 2005-02-14 2006-02-06 composto; método para o tratamento de uma doença ou distúrbio associado a atividade excessiva de bace em um paciente que dele necessite; método para modular a atividade de bace; composição farmacêutica BRPI0606902A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US65269605P 2005-02-14 2005-02-14
PCT/US2006/004471 WO2006088711A1 (en) 2005-02-14 2006-02-06 AZOLYLACYLGUANIDINES AS β-SECRETASE INHIBITORS

Publications (1)

Publication Number Publication Date
BRPI0606902A2 true BRPI0606902A2 (pt) 2009-07-28

Family

ID=36586172

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0606902-9A BRPI0606902A2 (pt) 2005-02-14 2006-02-06 composto; método para o tratamento de uma doença ou distúrbio associado a atividade excessiva de bace em um paciente que dele necessite; método para modular a atividade de bace; composição farmacêutica

Country Status (14)

Country Link
US (2) US7488832B2 (pt)
EP (1) EP1848692A1 (pt)
JP (1) JP2008530103A (pt)
KR (1) KR20070102751A (pt)
CN (1) CN101146769A (pt)
AU (1) AU2006214627A1 (pt)
BR (1) BRPI0606902A2 (pt)
CA (1) CA2597594A1 (pt)
IL (1) IL185185A0 (pt)
MX (1) MX2007009864A (pt)
NO (1) NO20074148L (pt)
RU (1) RU2007131043A (pt)
WO (1) WO2006088711A1 (pt)
ZA (1) ZA200707650B (pt)

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RU2006144075A (ru) 2004-06-16 2008-07-27 Вайет (Us) ДИФЕНИЛИМИДАЗОПИРИМИДИН И -ИМИДАЗОЛАМИНЫ КАК ИНГИБИТОРЫ β-СЕКРЕТАЗЫ
CA2593515A1 (en) * 2005-01-14 2006-07-20 Wyeth Amino-imidazolones for the inhibition of beta-secretase
CN101111489A (zh) * 2005-02-01 2008-01-23 惠氏公司 作为β-分泌酶的抑制剂的氨基-吡啶
US7273882B2 (en) * 2005-06-21 2007-09-25 Bristol-Myers Squibb Company Aminoacetamide acyl guanidines as β-secretase inhibitors
WO2007002214A2 (en) * 2005-06-21 2007-01-04 Bristol-Myers Squibb Company Acyl guanidines as beta-secretase inhibitors
TW200738683A (en) * 2005-06-30 2007-10-16 Wyeth Corp Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation
AU2006266167A1 (en) * 2005-06-30 2007-01-11 Wyeth Amino-5-(6-membered)heteroarylimidazolone compounds and the use thereof for beta-secretase modulation
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
CA2628074C (en) 2005-10-25 2014-01-14 Shionogi & Co., Ltd. Aminodihydrothiazine derivative
AU2006333049A1 (en) * 2005-12-19 2007-07-12 Wyeth 2-amino-5-piperidinylimidazolone compounds and use thereof for beta-secretase modulation
WO2007100536A1 (en) * 2006-02-24 2007-09-07 Wyeth DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] COMPOUNDS FOR THE INHIBITION OF β-SECRETASE
US7700606B2 (en) * 2006-08-17 2010-04-20 Wyeth Llc Imidazole amines as inhibitors of β-secretase
WO2008036196A2 (en) * 2006-09-21 2008-03-27 Wyeth Indolylalkylpyridin-2-amines for the inhibition of beta-secretase
CL2008000784A1 (es) * 2007-03-20 2008-05-30 Wyeth Corp Compuestos amino-5-[-4-(diflourometoxi) fenil sustituido]-5-fenilmidazolona, inhibidores de b-secretasa; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar alzheimer, deterioro cognitivo, sindrome de down, disminucion co
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
JP5383484B2 (ja) * 2007-04-24 2014-01-08 塩野義製薬株式会社 環式基で置換されたアミノジヒドロチアジン誘導体
US8653067B2 (en) * 2007-04-24 2014-02-18 Shionogi & Co., Ltd. Pharmaceutical composition for treating Alzheimer's disease
EP2687513B1 (en) 2008-06-09 2020-12-02 Ludwig-Maximilians-Universität München Drugs for inhibiting aggregation of proteins involved in diseases linked to protein aggregation and/or neurodegenerative diseases
KR101324426B1 (ko) * 2008-06-13 2013-10-31 시오노기세야쿠 가부시키가이샤 β 세크레타제 저해 작용을 갖는 황 함유 복소환 유도체
CN102186841A (zh) * 2008-10-22 2011-09-14 盐野义制药株式会社 具有bace1抑制活性的2-氨基嘧啶-4-酮及2-氨基吡啶衍生物
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EP1848692A1 (en) 2007-10-31
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MX2007009864A (es) 2007-09-04
WO2006088711A1 (en) 2006-08-24
KR20070102751A (ko) 2007-10-19
RU2007131043A (ru) 2009-03-20
US20080287424A1 (en) 2008-11-20
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