NO20061047L - Malonamid-derivater som blokkerer aktiviteten til gama-sekretase - Google Patents

Malonamid-derivater som blokkerer aktiviteten til gama-sekretase

Info

Publication number
NO20061047L
NO20061047L NO20061047A NO20061047A NO20061047L NO 20061047 L NO20061047 L NO 20061047L NO 20061047 A NO20061047 A NO 20061047A NO 20061047 A NO20061047 A NO 20061047A NO 20061047 L NO20061047 L NO 20061047L
Authority
NO
Norway
Prior art keywords
lower alkyl
activity
block
halogen
hydrogen
Prior art date
Application number
NO20061047A
Other languages
English (en)
Norwegian (no)
Inventor
Roland Jakob-Roetne
Wolfgang Wostl
Alexander Flohr
Guido Galley
Eric Argirios Kitas
Jens-Uwe Peters
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
Publication of NO20061047L publication Critical patent/NO20061047L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16—Benzazepines; Hydrogenated benzazepines
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • 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
    • 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
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
    • 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
    • A61K31/557—Eicosanoids, e.g. leukotrienes or prostaglandins
    • A61K31/558—Eicosanoids, e.g. leukotrienes or prostaglandins having heterocyclic rings containing oxygen as the only ring hetero atom, e.g. thromboxanes
    • 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
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/18—Dibenzazepines; Hydrogenated dibenzazepines
    • C07D223/20—Dibenz [b, e] azepines; Hydrogenated dibenz [b, e] azepines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
    • C07D313/02—Seven-membered rings
    • C07D313/06—Seven-membered rings condensed with carbocyclic rings or ring systems
    • C07D313/10—Seven-membered rings condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D313/14—[b,f]-condensed

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)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
NO20061047A 2003-09-09 2006-03-03 Malonamid-derivater som blokkerer aktiviteten til gama-sekretase NO20061047L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP03019683 2003-09-09
PCT/EP2004/009700 WO2005023772A1 (en) 2003-09-09 2004-08-31 Malonamide derivatives blocking the activity of gama-secretase

Publications (1)

Publication Number Publication Date
NO20061047L true NO20061047L (no) 2006-04-04

Family

ID=34224068

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20061047A NO20061047L (no) 2003-09-09 2006-03-03 Malonamid-derivater som blokkerer aktiviteten til gama-sekretase

Country Status (34)

Country Link
US (1) US7160875B2 (de)
EP (1) EP1711470B1 (de)
JP (2) JP4571639B2 (de)
KR (3) KR100834177B1 (de)
CN (1) CN100593539C (de)
AR (1) AR045609A1 (de)
AT (1) ATE428698T1 (de)
AU (1) AU2004270361B2 (de)
BR (1) BRPI0413533A (de)
CA (1) CA2537440C (de)
CO (1) CO5660268A2 (de)
CR (1) CR8264A (de)
CY (1) CY1109225T1 (de)
DE (1) DE602004020680D1 (de)
DK (1) DK1711470T3 (de)
EA (1) EA009940B1 (de)
EC (1) ECSP066414A (de)
ES (1) ES2322652T3 (de)
HR (1) HRP20090266T1 (de)
IL (1) IL173905A (de)
MA (1) MA28034A1 (de)
MX (1) MXPA06002562A (de)
MY (1) MY141308A (de)
NO (1) NO20061047L (de)
NZ (1) NZ545538A (de)
PL (1) PL1711470T3 (de)
PT (1) PT1711470E (de)
RS (1) RS20060146A (de)
SI (1) SI1711470T1 (de)
TN (1) TNSN06077A1 (de)
TW (1) TW200519092A (de)
UA (1) UA83501C2 (de)
WO (1) WO2005023772A1 (de)
ZA (1) ZA200601989B (de)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100480248C (zh) * 2003-02-04 2009-04-22 弗·哈夫曼-拉罗切有限公司 用作γ-分泌酶抑制剂的丙二酰胺衍生物
BRPI0413533A (pt) * 2003-09-09 2006-10-10 Hoffmann La Roche derivados de malonamida que bloqueiam a atividade de gama-secretase
SI1673347T1 (sl) * 2003-10-06 2015-10-30 F. Hoffmann - La Roche Ag Substituirani derivati dibenzo-azepina in benzo-diazepina, ki so uporabni kot inhibitorji gama-sekretaze
US7211573B2 (en) * 2004-12-08 2007-05-01 Hoffmann-La Roche Inc. Malonamide derivatives
WO2007110335A1 (en) * 2006-03-27 2007-10-04 F. Hoffmann-La Roche Ag Malonamide derivatives as gamma secretase inhibitors
WO2008034735A2 (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
KR101150574B1 (ko) * 2007-02-02 2012-05-30 에프. 호프만-라 로슈 아게 6-옥소-6,7-다이하이드로-5h-다이벤조[b,d]아제핀-7-일 유도체
AU2008225922B2 (en) * 2007-03-15 2012-04-26 F. Hoffmann-La Roche Ag Malonamides as orexin antagonists
US7579464B2 (en) * 2007-05-25 2009-08-25 Hoffmann-La Roche Inc. Process for preparation of enantiomerically pure compounds
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
US20090181944A1 (en) * 2008-01-11 2009-07-16 John Frederick Boylan Method for cancer therapy
US8309299B2 (en) 2010-05-19 2012-11-13 Hoffmann-La Roche Inc. Combination therapy and method for assessing resistance to treatment
WO2012040444A2 (en) * 2010-09-24 2012-03-29 Bristol-Myers Squibb Company Treatment of patients with incipient alzheimer's disease
KR101330184B1 (ko) 2010-10-15 2013-11-15 성균관대학교산학협력단 감마-세크레타제 저해제를 유효성분으로 함유하는 류마티스성 관절염의 예방 또는 치료용 조성물
WO2012050370A2 (ko) * 2010-10-15 2012-04-19 성균관대학교산학협력단 감마-세크레타제 저해제를 유효성분으로 함유하는 류마티스성 관절염의 예방 또는 치료용 조성물
US20120114638A1 (en) 2010-11-08 2012-05-10 John Boylan Combination therapy
US20120184529A1 (en) 2011-01-14 2012-07-19 Demario Mark D Combination therapy
US20120225860A1 (en) 2011-03-02 2012-09-06 John Frederick Boylan Method for administration of a gamma secretase inhibitor
TWI530489B (zh) 2011-03-22 2016-04-21 必治妥美雅史谷比公司 雙(氟烷基)-1,4-苯二氮呯酮化合物
AR087107A1 (es) 2011-07-27 2014-02-12 Lilly Co Eli Compuesto inhibidor de la señalizacion de la trayectoria notch
JP2015531792A (ja) 2012-09-21 2015-11-05 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 1,4−ベンゾジアゼピノン化合物のプロドラッグ
EP2897954B1 (de) 2012-09-21 2016-10-26 Bristol-Myers Squibb Company Fluoralkyl-1,4-benzodiazepinon-verbindungen
US9187434B2 (en) 2012-09-21 2015-11-17 Bristol-Myers Squibb Company Substituted 1,5-benzodiazepinones compounds
WO2014047374A1 (en) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Alkyl, fluoroalkyl-1,4-benzodiazepinone compounds
US9133126B2 (en) 2012-09-21 2015-09-15 Bristol-Myers Squibb Company Fluoroalkyl dibenzoazepinone compounds
CN104822665A (zh) 2012-09-21 2015-08-05 百时美施贵宝公司 用作Notch抑制剂的氟烷基和氟环烷基1,4-苯并二氮杂*酮化合物
CN104797584A (zh) 2012-09-21 2015-07-22 百时美施贵宝公司 作为notch抑制剂的三环杂环化合物
TWI614238B (zh) 2012-09-21 2018-02-11 必治妥美雅史谷比公司 雙(氟烷基)-1,4-苯并二氮呯酮化合物及其前藥
WO2014047393A1 (en) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company N-substituted bis(fluoroalkyl)-1,4-benzodiazepinone compounds as notch inhibitors
CN105101968A (zh) 2013-04-04 2015-11-25 百时美施贵宝公司 治疗增殖性疾病的组合疗法
EP2932966A1 (de) 2014-04-16 2015-10-21 Novartis AG Gammasekretasehemmer zur Behandlung von Atemwegserkrankungen
ES2751082T3 (es) * 2015-10-30 2020-03-30 Pipeline Therapeutics Inc Compuestos de dibenzo azepina y su uso en el tratamiento de enfermedades y trastornos óticos
EP3554502A4 (de) 2016-12-16 2021-01-06 Pipeline Therapeutics, Inc. Verfahren zur behandlung von cochlea-synaptopathie
EP3615055A1 (de) 2017-04-28 2020-03-04 Novartis AG Zellen, die einen auf bcma abzielenden chimären antigenrezeptor exprimieren, und kombinationsbehandlung mit einem gamma-sekretase-inhibitor
EP3615068A1 (de) 2017-04-28 2020-03-04 Novartis AG Auf bcma abzielender wirkstoff und kombinationstherapie mit einem gamma-sekretase-inhibitor
EP3668844A1 (de) * 2017-08-15 2020-06-24 Bayer Aktiengesellschaft 4-oxo-2,3,4,5-tetrahydro-1h-1,5-benzodiazepin-7-carboxamide
PE20210320A1 (es) 2018-06-01 2021-02-16 Novartis Ag Moleculas de union contra bcma y usos de las mismas
KR20210099614A (ko) 2018-12-04 2021-08-12 노파르티스 아게 Cd3에 대한 결합 분자 및 이의 용도
AU2020307471A1 (en) 2019-06-24 2022-01-27 Novartis Ag Dosing regimen and combination therapies for multispecific antibodies targeting B-cell maturation antigen
WO2022020658A1 (en) * 2020-07-23 2022-01-27 Purdue Research Foundation Notch signaling inhibitors for treating obesity and metabolic disorders
KR20240054320A (ko) * 2021-08-31 2024-04-25 바스프 에스이 축합된 고리계를 함유하는 제초성 말론아미드
US12473382B2 (en) 2022-11-04 2025-11-18 Lg Chem, Ltd. Hologram recording medium and optical element comprising the same
CN116621721B (zh) * 2023-04-12 2025-03-18 珠海市柏瑞医药科技有限公司 一种壬二酰胺的制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2147759T3 (es) * 1992-12-10 2000-10-01 Pfizer Heterociclos no aromaticos sustituidos con aminometileno y uso como antagonistas de la sustancia p.
US5672598A (en) * 1995-03-21 1997-09-30 The Procter & Gamble Company Lactam-containing hydroxamic acids
WO2001077086A1 (en) * 2000-04-11 2001-10-18 Dupont Pharmaceuticals Company SUBSTITUTED LACTAMS AS INHIBITORS OF Aβ PROTEIN PRODUCTION
GB0012671D0 (en) * 2000-05-24 2000-07-19 Merck Sharp & Dohme Therapeutic agents
CN100480248C (zh) * 2003-02-04 2009-04-22 弗·哈夫曼-拉罗切有限公司 用作γ-分泌酶抑制剂的丙二酰胺衍生物
BRPI0413533A (pt) * 2003-09-09 2006-10-10 Hoffmann La Roche derivados de malonamida que bloqueiam a atividade de gama-secretase

Also Published As

Publication number Publication date
IL173905A0 (en) 2006-07-05
RS20060146A (sr) 2008-06-05
HRP20090266T1 (en) 2009-06-30
MY141308A (en) 2010-04-16
AR045609A1 (es) 2005-11-02
JP2007505063A (ja) 2007-03-08
PT1711470E (pt) 2009-05-21
DE602004020680D1 (de) 2009-05-28
US7160875B2 (en) 2007-01-09
MA28034A1 (fr) 2006-07-03
EP1711470A1 (de) 2006-10-18
KR20060054455A (ko) 2006-05-22
AU2004270361B2 (en) 2009-06-25
JP4571639B2 (ja) 2010-10-27
NZ545538A (en) 2008-12-24
JP2010229153A (ja) 2010-10-14
CN100593539C (zh) 2010-03-10
SI1711470T1 (sl) 2009-08-31
TW200519092A (en) 2005-06-16
AU2004270361A1 (en) 2005-03-17
KR20070087233A (ko) 2007-08-27
WO2005023772A1 (en) 2005-03-17
CA2537440A1 (en) 2005-03-17
CO5660268A2 (es) 2006-07-31
MXPA06002562A (es) 2006-06-20
KR20070087690A (ko) 2007-08-28
HK1099014A1 (zh) 2007-08-03
KR100838852B1 (ko) 2008-06-16
CY1109225T1 (el) 2014-07-02
CR8264A (es) 2008-09-22
US20050054633A1 (en) 2005-03-10
TNSN06077A1 (fr) 2007-10-03
BRPI0413533A (pt) 2006-10-10
CN1875005A (zh) 2006-12-06
IL173905A (en) 2011-05-31
DK1711470T3 (da) 2009-06-08
ZA200601989B (en) 2007-05-30
EA009940B1 (ru) 2008-04-28
KR100834177B1 (ko) 2008-05-30
EA200600503A1 (ru) 2006-08-25
ECSP066414A (es) 2006-09-18
ATE428698T1 (de) 2009-05-15
CA2537440C (en) 2012-07-10
ES2322652T3 (es) 2009-06-24
UA83501C2 (uk) 2008-07-25
EP1711470B1 (de) 2009-04-15
PL1711470T3 (pl) 2009-09-30

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