ATE504580T1 - Malonsäureamidderivate als inhibitoren von g- sekretase zur behandlung von alzheimer-krankheit - Google Patents

Malonsäureamidderivate als inhibitoren von g- sekretase zur behandlung von alzheimer-krankheit

Info

Publication number
ATE504580T1
ATE504580T1 AT05811672T AT05811672T ATE504580T1 AT E504580 T1 ATE504580 T1 AT E504580T1 AT 05811672 T AT05811672 T AT 05811672T AT 05811672 T AT05811672 T AT 05811672T AT E504580 T1 ATE504580 T1 AT E504580T1
Authority
AT
Austria
Prior art keywords
secretase
alzheimer
inhibitors
disease
treatment
Prior art date
Application number
AT05811672T
Other languages
English (en)
Inventor
Alexander Flohr
Roland Jakob-Roetne
Wolfgang Wostl
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of ATE504580T1 publication Critical patent/ATE504580T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/14Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
AT05811672T 2004-12-08 2005-12-01 Malonsäureamidderivate als inhibitoren von g- sekretase zur behandlung von alzheimer-krankheit ATE504580T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04106395 2004-12-08
EP05100816 2005-02-07
PCT/EP2005/012834 WO2006061136A2 (en) 2004-12-08 2005-12-01 Malonamide derivatives as inhibitors of gamma-secretase for the treatment of alzheimer’s disease

Publications (1)

Publication Number Publication Date
ATE504580T1 true ATE504580T1 (de) 2011-04-15

Family

ID=36293585

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05811672T ATE504580T1 (de) 2004-12-08 2005-12-01 Malonsäureamidderivate als inhibitoren von g- sekretase zur behandlung von alzheimer-krankheit

Country Status (22)

Country Link
US (1) US7211573B2 (de)
EP (1) EP1828151B1 (de)
JP (1) JP4979590B2 (de)
KR (1) KR100890678B1 (de)
CN (1) CN101072760B (de)
AR (1) AR053987A1 (de)
AT (1) ATE504580T1 (de)
AU (1) AU2005313582B8 (de)
BR (1) BRPI0518615A2 (de)
CA (1) CA2589196A1 (de)
DE (1) DE602005027388D1 (de)
DK (1) DK1828151T3 (de)
IL (1) IL183293A0 (de)
MX (1) MX2007006504A (de)
NO (1) NO20072609L (de)
NZ (1) NZ555184A (de)
PL (1) PL1828151T3 (de)
PT (1) PT1828151E (de)
RU (1) RU2402538C2 (de)
TW (1) TWI349005B (de)
WO (1) WO2006061136A2 (de)
ZA (1) ZA200705018B (de)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007299129A1 (en) * 2006-09-20 2008-03-27 F. Hoffmann-La Roche Ag 4-oxo-2,3,4,5-tetrahydro-benzo[b][1,4]diazepine derivatives
JP2010517954A (ja) * 2007-02-02 2010-05-27 エフ.ホフマン−ラ ロシュ アーゲー 6−オキソ−6,7−ジヒドロ−5H−ジベンゾ[b,d]アゼピン−7−イル誘導体
KR20140007979A (ko) * 2008-01-11 2014-01-20 에프. 호프만-라 로슈 아게 암 치료를 위한 감마-세크레타제 저해제의 용도
US8741889B2 (en) * 2008-01-11 2014-06-03 Hoffmann-La Roche Inc Method of treating non-small cell lung cancer and colon cancer with gamma-secretase inhibitor
WO2016198366A1 (en) 2015-06-11 2016-12-15 F. Hoffmann-La Roche Ag Targeted notch pathway inhibitors
CA3079786A1 (en) 2017-10-24 2019-05-02 The Broad Institute, Inc. 4h-pyrrolo[3,2-c]pyridin-4-one derivatives
JP7279073B2 (ja) * 2018-11-07 2023-05-22 中外製薬株式会社 O-置換セリン誘導体の製造方法
US12403135B2 (en) 2019-04-24 2025-09-02 Bayer Aktiengesellschaft 4H-pyrrolo[3,2-c]pyridin-4-one derivatives
US20240307362A1 (en) 2019-04-24 2024-09-19 Bayer Aktiengesellschaft 4H-PYRROLO[3,2-c]PYRIDIN-4-ONE COMPOUNDS
CN114127064B (zh) 2019-04-24 2023-12-26 拜耳股份有限公司 4H-吡咯并[3,2-c]吡啶-4-酮化合物
CN112300019A (zh) * 2019-07-31 2021-02-02 华东师范大学 一种邻乙酰氨基苯丁酸类化合物的制备方法
EP4126861B1 (de) 2020-03-31 2025-06-18 Bayer Aktiengesellschaft 3-(anilino)-2-[3-(3-alkoxy-pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-on-derivate als egfr inhibitoren zur behandlung von krebs
CR20230440A (es) 2021-03-09 2023-10-26 Basf Se Malonamidas y su uso como herbicidas
WO2023025855A1 (en) * 2021-08-25 2023-03-02 Basf Se Herbicidal malonamides
EP4396173A1 (de) * 2021-08-31 2024-07-10 Basf Se Herbizide malonamide mit einem kondensierten ringsystem

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL72523A (en) * 1983-08-12 1988-06-30 Takeda Chemical Industries Ltd 3-amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine derivatives,their production and pharmaceutical compositions containing them
JP2002241368A (ja) * 1997-02-18 2002-08-28 Shionogi & Co Ltd 新規ベンゾラクタム誘導体およびそれを含有する医薬組成物
WO1999067219A1 (en) * 1998-06-22 1999-12-29 Elan Pharmaceuticals, Inc. Compounds for inhibiting beta-amyloid peptide release and/or its synthesis
GB0012671D0 (en) 2000-05-24 2000-07-19 Merck Sharp & Dohme Therapeutic agents
PT1511718E (pt) * 2002-05-29 2009-06-12 Hoffmann La Roche Derivados de n-acilaminobenzeno como inibidores selectivos de monoamina-oxidase b
TW200502221A (en) * 2002-10-03 2005-01-16 Astrazeneca Ab Novel lactams and uses thereof
KR100810810B1 (ko) 2003-02-04 2008-03-06 에프. 호프만-라 로슈 아게 감마-세크레타제 억제제로서 말론아마이드 유도체
US7060698B2 (en) 2003-05-19 2006-06-13 Hoffmann-La Roche Inc. Benzoxazepinone derivatives
EA009940B1 (ru) 2003-09-09 2008-04-28 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ МАЛОНАМИДА, БЛОКИРУЮЩИЕ АКТИВНОСТЬ γ-СЕКРЕТАЗЫ
CN1894217B (zh) 2003-10-06 2011-09-21 弗·哈夫曼-拉罗切有限公司 用作γ-分泌酶抑制剂的取代的二苯并氮杂*和苯并二氮杂*

Also Published As

Publication number Publication date
JP2008522994A (ja) 2008-07-03
US7211573B2 (en) 2007-05-01
PT1828151E (pt) 2011-06-16
CA2589196A1 (en) 2006-06-15
TWI349005B (en) 2011-09-21
EP1828151A2 (de) 2007-09-05
BRPI0518615A2 (pt) 2008-11-25
NO20072609L (no) 2007-06-19
KR100890678B1 (ko) 2009-03-26
WO2006061136A3 (en) 2006-08-03
CN101072760A (zh) 2007-11-14
HK1114840A1 (en) 2008-11-14
PL1828151T3 (pl) 2011-09-30
AU2005313582B8 (en) 2011-06-16
RU2007120211A (ru) 2009-01-20
AU2005313582B2 (en) 2011-06-02
NZ555184A (en) 2010-01-29
CN101072760B (zh) 2011-12-28
US20060122168A1 (en) 2006-06-08
JP4979590B2 (ja) 2012-07-18
MX2007006504A (es) 2007-06-22
RU2402538C2 (ru) 2010-10-27
DK1828151T3 (da) 2011-05-16
IL183293A0 (en) 2007-09-20
KR20070086979A (ko) 2007-08-27
TW200626568A (en) 2006-08-01
AU2005313582A8 (en) 2011-06-16
WO2006061136A2 (en) 2006-06-15
ZA200705018B (en) 2010-04-28
EP1828151B1 (de) 2011-04-06
DE602005027388D1 (de) 2011-05-19
AR053987A1 (es) 2007-05-30
AU2005313582A1 (en) 2006-06-15

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