NO20081944L - Nye benzimidazol- og benzothiazolderivater, fremgangsmate for fremstilling, anvendelse derav som legemiddel, samt farmasoytiske sammensetninger og ny anvendelse spesielt som C-Met inhibitorer - Google Patents

Nye benzimidazol- og benzothiazolderivater, fremgangsmate for fremstilling, anvendelse derav som legemiddel, samt farmasoytiske sammensetninger og ny anvendelse spesielt som C-Met inhibitorer

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Publication number
NO20081944L
NO20081944L NO20081944A NO20081944A NO20081944L NO 20081944 L NO20081944 L NO 20081944L NO 20081944 A NO20081944 A NO 20081944A NO 20081944 A NO20081944 A NO 20081944A NO 20081944 L NO20081944 L NO 20081944L
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new
drug
manufacture
well
pharmaceutical compositions
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NO20081944A
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Conception Nemecek
Francois Clerc
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Aventis Pharma Sa
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Publication of NO20081944L publication Critical patent/NO20081944L/no

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C07D235/30Nitrogen atoms not forming part of a nitro radical
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    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C07D235/30Nitrogen atoms not forming part of a nitro radical
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    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Endocrinology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Rheumatology (AREA)
  • Obesity (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Dermatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Reproductive Health (AREA)
  • Neurosurgery (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Oncology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Foreliggende oppfinnelse angår nye produkter med fonnel (1), hvori: A representerer NH eller S; RI, R2 og R3 representerer H, NM, Hal eller Alk, hvor minst en av RI, R2 og R3 er forskjellig fra hydrogen; R representerer særlig: cykloalkyl, alkyl, alkoksy eller NR4R5, R4 representerer H eller Alk og R5 representerer cykloalkyl eller alkyl eventuelt substituert med hydroksyl, alkoksy, heteroaryl, heterocykloalkyl, NR6R7, fenyl, fényl-NR6R7 og CONR6R7, R6 og R7 representerer H eller Alk eller fenyl og R6 og R7 kan danne, sanimen med H, et cyklisk radikal; R4 og R5 kan også danne, sammen med N, et cyklisk radikal; alle de ovenfor nevnte heterocykloalkyl, heteroaryl og fenyl radikalene er eventuelt substituerte, nevnte produkter er i alle de isomere formene og deres salter, som medikamenter, særlig som Met inhibitorer.
NO20081944A 2005-09-27 2008-04-23 Nye benzimidazol- og benzothiazolderivater, fremgangsmate for fremstilling, anvendelse derav som legemiddel, samt farmasoytiske sammensetninger og ny anvendelse spesielt som C-Met inhibitorer NO20081944L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0509850A FR2891273B1 (fr) 2005-09-27 2005-09-27 NOUVEAUX DERIVES BENZIMIDAZOLES ET BENZOTHIAZOLES, LEUR PREPARATION ET LEUR UTILISATION PHARMACEUTIQUE NOTAMMENT COMME INHIBITEURS DE CMet
PCT/FR2006/002183 WO2007036630A1 (fr) 2005-09-27 2006-09-25 Derives de benzimidazoles et benzothiazoles et leur utilisation en tant qu'inhibiteurs de kinases notamment de met

Publications (1)

Publication Number Publication Date
NO20081944L true NO20081944L (no) 2008-06-19

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NO20081944A NO20081944L (no) 2005-09-27 2008-04-23 Nye benzimidazol- og benzothiazolderivater, fremgangsmate for fremstilling, anvendelse derav som legemiddel, samt farmasoytiske sammensetninger og ny anvendelse spesielt som C-Met inhibitorer

Country Status (20)

Country Link
US (1) US8110571B2 (no)
EP (1) EP1934187A1 (no)
JP (1) JP2009510033A (no)
KR (1) KR20080050438A (no)
CN (1) CN101273019A (no)
AR (1) AR056528A1 (no)
AU (1) AU2006296468B2 (no)
BR (1) BRPI0616754A2 (no)
CA (1) CA2620857A1 (no)
EA (1) EA014315B1 (no)
FR (1) FR2891273B1 (no)
IL (1) IL189961A0 (no)
MA (1) MA29922B1 (no)
NO (1) NO20081944L (no)
NZ (1) NZ566568A (no)
SG (1) SG165381A1 (no)
TW (1) TW200745048A (no)
UY (1) UY29814A1 (no)
WO (1) WO2007036630A1 (no)
ZA (1) ZA200802447B (no)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2868421B1 (fr) 2004-04-01 2008-08-01 Aventis Pharma Sa Nouveaux benzothiazoles et leur utilisation comme medicaments
FR2922550B1 (fr) 2007-10-19 2009-11-27 Sanofi Aventis Nouveaux derives de 6-aryl/heteroalkyloxy benzothiazole et benzimidazole, application comme medicaments, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de cmet
BR112012007137A2 (pt) 2009-09-30 2015-09-15 Harvard College metodos para modulacao da autofagia por meio da modulacao de produtos genicos inibidores da autofagia
KR20160024639A (ko) 2014-08-26 2016-03-07 삼성전자주식회사 c-Met 표적 치료제의 저항성 또는 효능 예측을 위한 바이오마커 PDGF
EA202192575A1 (ru) 2019-03-21 2022-01-14 Онксео Соединения dbait в сочетании с ингибиторами киназ для лечения рака
US20220401436A1 (en) 2019-11-08 2022-12-22 INSERM (Institute National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use

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Publication number Priority date Publication date Assignee Title
DE2541752A1 (de) * 1975-09-19 1977-03-24 Hoechst Ag Anthelminthisch wirksame 2-carbalkoxyamino-5(6)-phenyl-sulfonyloxy- benzimidazole und verfahren zu ihrer herstellung
JPS5914027B2 (ja) * 1976-02-27 1984-04-02 ヘキスト・アクチ−エンゲゼルシヤフト 2−カルボアルコキシアミノ−5(6)−フエニルスルホニルオキシ−ベンズイミダゾ−ル化合物
DE3247615A1 (de) * 1982-12-23 1984-07-05 Hoechst Ag, 6230 Frankfurt Substituierte phenylsulfonyloxybenzimidazolcarbaminate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
FR2751649B1 (fr) * 1996-07-26 1998-08-28 Adir Nouveaux derives de benzimidazole, de benzoxazole et de benzothiazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
GB9900752D0 (en) * 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
KR20020084116A (ko) * 2000-02-07 2002-11-04 애보트 게엠베하 운트 콤파니 카게 2-벤조티아졸릴 우레아 유도체 및 이의 단백질 키나제억제제로서의 용도
US6693125B2 (en) * 2001-01-24 2004-02-17 Combinatorx Incorporated Combinations of drugs (e.g., a benzimidazole and pentamidine) for the treatment of neoplastic disorders
JP2004525140A (ja) * 2001-03-26 2004-08-19 ユニサーチ リミテッド ガンの治療方法及び該治療方法に使用する組成物
EP1298125A1 (en) * 2001-09-26 2003-04-02 Aventis Pharma S.A. Substituted benzimidazole compounds and their use for the treatment of cancer
FR2868421B1 (fr) * 2004-04-01 2008-08-01 Aventis Pharma Sa Nouveaux benzothiazoles et leur utilisation comme medicaments

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AU2006296468A1 (en) 2007-04-05
ZA200802447B (en) 2009-08-26
US20080194555A1 (en) 2008-08-14
UY29814A1 (es) 2007-04-30
US8110571B2 (en) 2012-02-07
MA29922B1 (fr) 2008-11-03
EA014315B1 (ru) 2010-10-29
KR20080050438A (ko) 2008-06-05
EA200800947A1 (ru) 2009-02-27
JP2009510033A (ja) 2009-03-12
SG165381A1 (en) 2010-10-28
FR2891273A1 (fr) 2007-03-30
AU2006296468B2 (en) 2012-10-18
AR056528A1 (es) 2007-10-10
BRPI0616754A2 (pt) 2011-06-28
FR2891273B1 (fr) 2007-11-23
WO2007036630A1 (fr) 2007-04-05
EP1934187A1 (fr) 2008-06-25
TW200745048A (en) 2007-12-16
IL189961A0 (en) 2008-08-07
NZ566568A (en) 2012-05-25
CA2620857A1 (fr) 2007-04-05
CN101273019A (zh) 2008-09-24

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