AR044363A1 - Derivados de benzoxazepinona, como inhibidores de gamma secretasa para el tratamiento de la enfermedad de alzheimer - Google Patents
Derivados de benzoxazepinona, como inhibidores de gamma secretasa para el tratamiento de la enfermedad de alzheimerInfo
- Publication number
- AR044363A1 AR044363A1 ARP040101685A ARP040101685A AR044363A1 AR 044363 A1 AR044363 A1 AR 044363A1 AR P040101685 A ARP040101685 A AR P040101685A AR P040101685 A ARP040101685 A AR P040101685A AR 044363 A1 AR044363 A1 AR 044363A1
- Authority
- AR
- Argentina
- Prior art keywords
- lower alkyl
- phenyl
- halogen
- substituted
- alzheimer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/14—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La presente se refiere a derivados de benzoxazepinona de fórmula (1), en donde: R1 es hidrógeno, alcoxilo inferior, halógeno o -NR'R''; n es 1 ó 2; R', R'' son independientemente uno del otro hidrógeno o alquilo inferior; R2 es hidrógeno, alquilo inferior, -(CH2)m-cicloalquilo, -(CH2)m-fenilo o -(CH2)m-O-alquilo inferior; m es 0, 1 ó 2; R3 es alquilo inferior, -(CH2)m-C(O)O-alquilo inferior, cicloalquilo o -(CH2)m-fenilo, que está sin sustituir o sustituido por uno o dos sustituyentes, seleccionados del grupo constituido por halógeno o alquilo inferior; R4 es -(CH2)o-fenilo, que está sin sustituir o sustituido por uno o dos sustituyentes, seleccionados del grupo constituido por halógeno, trifluorometilo, -NR'R'', nitro o -SO2NH2, o es -cicloalquilo, sin sustituir o sustituido por fenilo, o es -(CR'R'')o-heterociclilo, seleccionado del grupo constituido por tetrahidropiran-4-ilo, piridin-3-ilo, indol-3-ilo, sustituido opcionalmente por halógeno o alcoxilo inferior, o tiofen-2- ilo, furan-2-ilo, -NH-piridin-2-ilo, sustituido opcionalmente por nitro, o benzoimidazol-2-ilo, 2-oxo-tetrahidrofurano, 1-bencil-piperidin-4-ilo, o benzo[1,3]dioxol-5-ilo o es tetrahidro-naftalen-1-ilo; CHR'-naftalen-2-ilo; fluoren-9-ilo; (CH2)o-S- alquilo inferior; (CH2)o-S-bencilo; (CH2)o-C(O)NH2; (CH2)oNR'R''; -H[C(O)NH2]-(CH2)o-fenilo; -(CH2)o-CF3; -(CH2)o-CR'R''-CH2-NR'R''; y o es 1 ó 2; y las sales de adición ácida farmacéuticamente aceptables de los mismos. Estos compuestos son buenos inhibidores de la g-secretasa para el tratamiento de la enfermedad de Alzheimer.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03011040 | 2003-05-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR044363A1 true AR044363A1 (es) | 2005-09-07 |
Family
ID=33442730
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040101685A AR044363A1 (es) | 2003-05-19 | 2004-05-17 | Derivados de benzoxazepinona, como inhibidores de gamma secretasa para el tratamiento de la enfermedad de alzheimer |
Country Status (19)
Country | Link |
---|---|
US (1) | US7060698B2 (es) |
EP (1) | EP1631296B1 (es) |
JP (1) | JP4510021B2 (es) |
KR (1) | KR100731368B1 (es) |
CN (1) | CN1794997B (es) |
AR (1) | AR044363A1 (es) |
AT (1) | ATE360424T1 (es) |
AU (1) | AU2004238037B2 (es) |
BR (1) | BRPI0410647A (es) |
CA (1) | CA2524640C (es) |
CL (1) | CL2004001068A1 (es) |
DE (1) | DE602004006118T2 (es) |
ES (1) | ES2285458T3 (es) |
MX (1) | MXPA05012368A (es) |
MY (1) | MY143953A (es) |
PL (1) | PL1631296T3 (es) |
RU (1) | RU2332408C2 (es) |
TW (1) | TWI290550B (es) |
WO (1) | WO2004100958A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200502221A (en) | 2002-10-03 | 2005-01-16 | Astrazeneca Ab | Novel lactams and uses thereof |
US7521481B2 (en) | 2003-02-27 | 2009-04-21 | Mclaurin Joanne | Methods of preventing, treating and diagnosing disorders of protein aggregation |
US7060698B2 (en) * | 2003-05-19 | 2006-06-13 | Hoffmann-La Roche Inc. | Benzoxazepinone derivatives |
CA2589102C (en) | 2004-11-02 | 2013-08-13 | Northwestern University | Pyridazine compounds and methods for using the compounds to treat inflammatory diseases |
US7211573B2 (en) | 2004-12-08 | 2007-05-01 | Hoffmann-La Roche Inc. | Malonamide derivatives |
WO2006065218A1 (en) * | 2004-12-14 | 2006-06-22 | Astrazeneca Ab | Novel molecular probes |
RU2318818C1 (ru) * | 2006-04-12 | 2008-03-10 | Общество С Ограниченной Ответственностью "Исследовательский Институт Химического Разнообразия" | Азагетероциклы, комбинаторная библиотека, фокусированная библиотека, фармацевтическая композиция и способ получения (варианты) |
US8855099B2 (en) | 2007-03-19 | 2014-10-07 | Qualcomm Incorporated | Selective phase connection establishment |
FR2913886B1 (fr) | 2007-03-22 | 2012-03-02 | Guerbet Sa | Utilisation de nanoparticules metalliques dans le diagnostique de la maladie d'alzheimer |
JP5275315B2 (ja) * | 2010-10-01 | 2013-08-28 | 学校法人近畿大学 | 新規化合物及びβ−セクレターゼ阻害剤 |
JP2014001142A (ja) * | 2010-10-05 | 2014-01-09 | Astellas Pharma Inc | シクロアルカン化合物 |
ES2650744T3 (es) | 2010-12-14 | 2018-01-22 | Electrophoretics Limited | Inhibidores de la caseína quinasa 1 delta (CK1delta) |
NO3175985T3 (es) * | 2011-07-01 | 2018-04-28 | ||
WO2019173761A1 (en) | 2018-03-09 | 2019-09-12 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | C-abl tyrosine kinase inhibitory compound embodiments and methods of making and using the same |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5965553A (en) * | 1996-06-20 | 1999-10-12 | Pfizer Inc. | Squalene synthetase inhibitors |
DE69732712T2 (de) * | 1996-12-06 | 2006-04-13 | Vertex Pharmaceuticals Inc., Cambridge | INHIBITOREN DES INTERLEUKIN-1beta KONVERTIERENDEN ENZYMS |
CZ20024151A3 (cs) | 2000-06-23 | 2003-05-14 | Takeda Chemical Industries, Ltd. | Benzoxazepinony, způsob jejich výroby a použití |
JP2002080468A (ja) * | 2000-06-23 | 2002-03-19 | Takeda Chem Ind Ltd | ベンゾオキサゼピン化合物 |
GB0025173D0 (en) | 2000-10-13 | 2000-11-29 | Merck Sharp & Dohme | Therapeutic agents |
US7060798B2 (en) * | 2002-05-13 | 2006-06-13 | State Of Oregon Acting By And Through The Oregon State Board Of Higher Education On Behalf Of Oregon State University | Modified protein adhesives and lignocellulosic composites made from the adhesives |
US7060698B2 (en) * | 2003-05-19 | 2006-06-13 | Hoffmann-La Roche Inc. | Benzoxazepinone derivatives |
-
2004
- 2004-05-03 US US10/838,054 patent/US7060698B2/en not_active Expired - Fee Related
- 2004-05-13 TW TW093113546A patent/TWI290550B/zh not_active IP Right Cessation
- 2004-05-14 DE DE602004006118T patent/DE602004006118T2/de not_active Expired - Lifetime
- 2004-05-14 AT AT04732944T patent/ATE360424T1/de active
- 2004-05-14 EP EP04732944A patent/EP1631296B1/en not_active Expired - Lifetime
- 2004-05-14 RU RU2005139529/04A patent/RU2332408C2/ru not_active IP Right Cessation
- 2004-05-14 BR BRPI0410647-4A patent/BRPI0410647A/pt not_active IP Right Cessation
- 2004-05-14 CA CA2524640A patent/CA2524640C/en not_active Expired - Fee Related
- 2004-05-14 JP JP2006529815A patent/JP4510021B2/ja not_active Expired - Fee Related
- 2004-05-14 AU AU2004238037A patent/AU2004238037B2/en not_active Ceased
- 2004-05-14 MX MXPA05012368A patent/MXPA05012368A/es active IP Right Grant
- 2004-05-14 KR KR1020057021910A patent/KR100731368B1/ko not_active IP Right Cessation
- 2004-05-14 ES ES04732944T patent/ES2285458T3/es not_active Expired - Lifetime
- 2004-05-14 CN CN2004800140158A patent/CN1794997B/zh not_active Expired - Fee Related
- 2004-05-14 PL PL04732944T patent/PL1631296T3/pl unknown
- 2004-05-14 WO PCT/EP2004/005177 patent/WO2004100958A1/en active IP Right Grant
- 2004-05-17 CL CL200401068A patent/CL2004001068A1/es unknown
- 2004-05-17 AR ARP040101685A patent/AR044363A1/es unknown
- 2004-05-18 MY MYPI20041936A patent/MY143953A/en unknown
Also Published As
Publication number | Publication date |
---|---|
KR20060003107A (ko) | 2006-01-09 |
KR100731368B1 (ko) | 2007-06-21 |
BRPI0410647A (pt) | 2006-07-04 |
TW200510355A (en) | 2005-03-16 |
ES2285458T3 (es) | 2007-11-16 |
US20040235819A1 (en) | 2004-11-25 |
DE602004006118T2 (de) | 2008-01-03 |
WO2004100958A1 (en) | 2004-11-25 |
MXPA05012368A (es) | 2006-02-02 |
JP2007501261A (ja) | 2007-01-25 |
ATE360424T1 (de) | 2007-05-15 |
CN1794997B (zh) | 2010-05-12 |
RU2332408C2 (ru) | 2008-08-27 |
JP4510021B2 (ja) | 2010-07-21 |
CA2524640A1 (en) | 2004-11-25 |
DE602004006118D1 (de) | 2007-06-06 |
US7060698B2 (en) | 2006-06-13 |
RU2005139529A (ru) | 2006-08-10 |
EP1631296A1 (en) | 2006-03-08 |
PL1631296T3 (pl) | 2007-08-31 |
CA2524640C (en) | 2011-10-11 |
MY143953A (en) | 2011-07-29 |
EP1631296B1 (en) | 2007-04-25 |
TWI290550B (en) | 2007-12-01 |
AU2004238037A1 (en) | 2004-11-25 |
CN1794997A (zh) | 2006-06-28 |
CL2004001068A1 (es) | 2005-04-15 |
AU2004238037B2 (en) | 2009-11-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR044363A1 (es) | Derivados de benzoxazepinona, como inhibidores de gamma secretasa para el tratamiento de la enfermedad de alzheimer | |
AR052903A1 (es) | Compuestos de bis arilo y heteroarilo sustituidos como antagonistas selectivos de 5ht2a, composiciones farmaceuticas que los contienen y su empleo en el tratamiento de trastornos del sueno. | |
AR079327A1 (es) | Derivados de 2-amino-5,5-difluor -5,6-dihidro-4h-(1,3) oxazin-4-il) fenil)-amida | |
AR078163A1 (es) | Utilizacion de aminodihidrotiazinas para el tratamiento o prevencion de la diabetes | |
AR058287A1 (es) | Derivados de isoquinolina y composicion farmaceutica | |
EA200970461A1 (ru) | ЗАМЕЩЕННЫЕ ПРОИЗВОДНЫЕ 3-ИЗОБУТИЛ-9,10-ДИМЕТОКСИ-1,3,4,6,7,11b-ГЕКСАГИДРО-2Н-ПИРИДО[2,1-a]ИЗОХИНОЛИН-2-ОЛА И СВЯЗАННЫЕ С НИМИ СПОСОБЫ | |
NO20083434L (no) | Benzamid- og heteroarenderivater | |
PE20090042A1 (es) | Analogos de ciclopamina | |
AR032436A1 (es) | Oxazolidinonas substituidas, procedimiento para su preparacion, medicamentos, el uso de las mismas para la fabricacion de medicamentos, y el metodo para impedir la coagulacion sanguinea in vitro | |
PE20091621A1 (es) | Derivados de amina como moduladores de la actividad de tlr y composiciones que los contienen | |
AR077935A1 (es) | Derivados de 3-amino-5 fenil-5,6-dihidro-2h-(1,4)oxazina | |
PE20090276A1 (es) | Compuestos derivados de imidazoquinolina como moduladores de tlr7 | |
PE20070212A1 (es) | Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen | |
UY31126A1 (es) | Derivados de quinoxalina como inhibidores de la actividad de cinasa de tirosina de las cinasas janus | |
AR054799A1 (es) | Derivados de oxindol | |
PE20070218A1 (es) | COMPUESTOS DE CICLOALQUILO AMINO-HIDANTOINA Y USO DE ESTOS PARA LA MODULACION DE ß-SECRETASA | |
ECSP088129A (es) | Derivado novedoso de heterocicliden acetamida | |
NO20075641L (no) | Kroman og kromenderivater og ders anvendelse | |
AR054560A1 (es) | Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer | |
CO5690643A2 (es) | Derivados de triaza-espiropiperidina para usarlos como inhibidores de glyt-1 en el tratamiento de desordenes neurologicos y neuropsiquiatricos | |
PE20071322A1 (es) | Derivados de 2-morfolinopirimidina como inhibidores de fosfatidinoinositol(pi) 3-quinasa | |
AR063988A1 (es) | Derivados heterociclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen | |
PE20090189A1 (es) | Derivados de aza-piridopirimidinona como agonistas de hm74a | |
AR071925A1 (es) | Malonamidas como antagonistas de orexina | |
AR035235A1 (es) | Derivados heterocicliloxi-,-tioxi- y -aminobenzazol como ligandos de 5-hidroxitriptamina-6, un procedimiento para su preparacion, composicion farmaceutica, y el uso de dichos derivados para la manufactura de un medicamento |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |