UY30411A1 - Derivados sustituidos del acetato de 2,3,4,-tetrahidroimidazo-[1,5-a]-pirimidin-6-amina, composiciones farmacéuticas y aplicaciones - Google Patents

Derivados sustituidos del acetato de 2,3,4,-tetrahidroimidazo-[1,5-a]-pirimidin-6-amina, composiciones farmacéuticas y aplicaciones

Info

Publication number
UY30411A1
UY30411A1 UY30411A UY30411A UY30411A1 UY 30411 A1 UY30411 A1 UY 30411A1 UY 30411 A UY30411 A UY 30411A UY 30411 A UY30411 A UY 30411A UY 30411 A1 UY30411 A1 UY 30411A1
Authority
UY
Uruguay
Prior art keywords
pirimidin
amina
tetrahydroimidazo
acetate
applications
Prior art date
Application number
UY30411A
Other languages
English (en)
Inventor
Jorg Holenz
Karin Kolmodin
Katharina Hogdin
Niklas Plobeck
Stefan Berg
Original Assignee
Astex Therapeutics Ltd
Astrazeneca Ab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38831994&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UY30411(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astex Therapeutics Ltd, Astrazeneca Ab filed Critical Astex Therapeutics Ltd
Publication of UY30411A1 publication Critical patent/UY30411A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

La presente invencion se refiere a nuevos compuestos que tienen la formula estructural I que figura a continuacion: y su sal farmacéuticamente aceptable, composiciones y métodos de uso. Estos compuestosproporcionan un tratamiento o profilaxis del impedimento cognitivo, el mal de Alzheimer, degeneracion neurologica y demencia.
UY30411A 2006-06-14 2007-06-13 Derivados sustituidos del acetato de 2,3,4,-tetrahidroimidazo-[1,5-a]-pirimidin-6-amina, composiciones farmacéuticas y aplicaciones UY30411A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US81354906P 2006-06-14 2006-06-14
US86645106P 2006-11-20 2006-11-20
US89698607P 2007-03-26 2007-03-26

Publications (1)

Publication Number Publication Date
UY30411A1 true UY30411A1 (es) 2008-01-31

Family

ID=38831994

Family Applications (1)

Application Number Title Priority Date Filing Date
UY30411A UY30411A1 (es) 2006-06-14 2007-06-13 Derivados sustituidos del acetato de 2,3,4,-tetrahidroimidazo-[1,5-a]-pirimidin-6-amina, composiciones farmacéuticas y aplicaciones

Country Status (16)

Country Link
US (1) US20070299087A1 (es)
EP (1) EP2035425A1 (es)
JP (1) JP2009539975A (es)
KR (1) KR20090031564A (es)
AR (1) AR061371A1 (es)
AU (1) AU2007259432A1 (es)
BR (1) BRPI0712731A2 (es)
CA (1) CA2654403A1 (es)
CL (1) CL2007001732A1 (es)
EC (1) ECSP088969A (es)
IL (1) IL195574A0 (es)
MX (1) MX2008015587A (es)
NO (1) NO20090166L (es)
TW (1) TW200808796A (es)
UY (1) UY30411A1 (es)
WO (1) WO2007145570A1 (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US7592348B2 (en) 2003-12-15 2009-09-22 Schering Corporation Heterocyclic aspartyl protease inhibitors
AR050184A1 (es) * 2004-07-28 2006-10-04 Schering Corp Inhibidores macrociclicos de beta-secretasa
TWI332005B (en) * 2005-06-14 2010-10-21 Schering Corp Aspartyl protease inhibitors
US8722708B2 (en) * 2005-06-14 2014-05-13 Merck Sharp & Dohme Inc. Substituted isoindolines as aspartyl protease inhibitors
TW200815349A (en) 2006-06-22 2008-04-01 Astrazeneca Ab New compounds
CA2672295A1 (en) * 2006-12-12 2008-06-19 Schering Corporation Aspartyl protease inhibitors containing a tricyclic ring system
WO2008073365A1 (en) 2006-12-12 2008-06-19 Schering Corporation Aspartyl protease inhibitors
AU2009239535A1 (en) * 2008-04-22 2009-10-29 Schering Corporation Thiophenyl-substituted 2-imino-3-methyl pyrrolo pyrimidinone compounds as BACE-1 inhibitors, compositions, and their use
WO2010056195A1 (en) * 2008-11-14 2010-05-20 Astrazeneca Ab New compounds 575
US20100125081A1 (en) * 2008-11-14 2010-05-20 Astrazeneca Ab New compounds 574
TW201020244A (en) 2008-11-14 2010-06-01 Astrazeneca Ab New compounds
KR20110136826A (ko) * 2009-03-26 2011-12-21 다이닛본 스미토모 세이야꾸 가부시끼가이샤 신규의 인지기능장해 치료제
EP2485590B1 (en) 2009-10-08 2015-01-07 Merck Sharp & Dohme Corp. Pentafluorosulfur imino heterocyclic compounds as bace-1 inhibitors, compositions, and their use
US8569310B2 (en) 2009-10-08 2013-10-29 Merck Sharp & Dohme Corp. Pentafluorosulfur imino heterocyclic compounds as BACE-1 inhibitors, compositions and their use
UA108363C2 (uk) 2009-10-08 2015-04-27 Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
US8563543B2 (en) 2009-10-08 2013-10-22 Merck Sharp & Dohme Corp. Iminothiadiazine dioxide compounds as bace inhibitors, compositions, and their use
WO2012138734A1 (en) 2011-04-07 2012-10-11 Merck Sharp & Dohme Corp. C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
WO2012138590A1 (en) 2011-04-07 2012-10-11 Merck Sharp & Dohme Corp. Pyrrolidine-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
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
AU2013235422B2 (en) 2012-03-19 2016-12-15 Buck Institute For Research On Aging APP specific BACE inhibitors (ASBIs) and uses thereof
EP2908824B1 (en) 2012-10-17 2018-05-02 Merck Sharp & Dohme Corp. Tricyclic substituted thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
WO2014062549A1 (en) 2012-10-17 2014-04-24 Merck Sharp & Dohme Corp. Tricyclic substituted thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
EP2956443B1 (en) 2013-02-12 2019-09-25 Buck Institute For Research On Aging Hydantoins that modulate bace-mediated app processing

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008503460A (ja) * 2004-06-16 2008-02-07 ワイス β−セクレターゼのインヒビターとしてのジフェニルイミダゾピリミジンおよびイミダゾールアミン
JP2008526966A (ja) * 2005-01-14 2008-07-24 ワイス β−セクレターゼの阻害のためのアミノ−イミダゾロン

Also Published As

Publication number Publication date
AR061371A1 (es) 2008-08-20
CL2007001732A1 (es) 2008-01-25
US20070299087A1 (en) 2007-12-27
IL195574A0 (en) 2009-09-01
WO2007145570A9 (en) 2008-12-11
KR20090031564A (ko) 2009-03-26
MX2008015587A (es) 2009-01-09
TW200808796A (en) 2008-02-16
EP2035425A1 (en) 2009-03-18
ECSP088969A (es) 2009-01-30
BRPI0712731A2 (pt) 2012-10-02
WO2007145570A1 (en) 2007-12-21
NO20090166L (no) 2009-03-12
CA2654403A1 (en) 2007-12-21
JP2009539975A (ja) 2009-11-19
AU2007259432A1 (en) 2007-12-21

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Legal Events

Date Code Title Description
109 Application deemed to be withdrawn

Effective date: 20170711