DE60225159D1 - Substituierte benzimidazole und ihre anwendung in der krebsbehandlung - Google Patents

Substituierte benzimidazole und ihre anwendung in der krebsbehandlung

Info

Publication number
DE60225159D1
DE60225159D1 DE60225159T DE60225159T DE60225159D1 DE 60225159 D1 DE60225159 D1 DE 60225159D1 DE 60225159 T DE60225159 T DE 60225159T DE 60225159 T DE60225159 T DE 60225159T DE 60225159 D1 DE60225159 D1 DE 60225159D1
Authority
DE
Germany
Prior art keywords
application
cancer treatment
substituted benzimidazole
benzimidazole
substituted
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
DE60225159T
Other languages
English (en)
Other versions
DE60225159T2 (de
Inventor
Francois Clerc
Francois Hamy
Isabelle Depaty
Odile Angouillant-Boniface
Stephanie Deprets
Chantal Carrez
Manfred Roesner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aventis Pharma SA
Original Assignee
Aventis Pharma SA
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 Aventis Pharma SA filed Critical Aventis Pharma SA
Publication of DE60225159D1 publication Critical patent/DE60225159D1/de
Application granted granted Critical
Publication of DE60225159T2 publication Critical patent/DE60225159T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • 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
    • C07D235/32Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
DE60225159T 2001-09-26 2002-09-26 Substituierte benzimidazole und ihre anwendung in der krebsbehandlung Expired - Lifetime DE60225159T2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP01402460A EP1298125A1 (de) 2001-09-26 2001-09-26 Substituierte Benzimidazolverbindungen und ihre Verwendung zur Behandlung von Krebs
EP01402460 2001-09-26
PCT/EP2002/011353 WO2003028721A2 (en) 2001-09-26 2002-09-26 Substituted benzimidazole compounds and their use for the treatment of cancer

Publications (2)

Publication Number Publication Date
DE60225159D1 true DE60225159D1 (de) 2008-04-03
DE60225159T2 DE60225159T2 (de) 2009-02-19

Family

ID=8182891

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60225159T Expired - Lifetime DE60225159T2 (de) 2001-09-26 2002-09-26 Substituierte benzimidazole und ihre anwendung in der krebsbehandlung

Country Status (35)

Country Link
US (1) US7041668B2 (de)
EP (2) EP1298125A1 (de)
JP (1) JP4510450B2 (de)
KR (1) KR100891439B1 (de)
CN (1) CN100346786C (de)
AR (1) AR037096A1 (de)
AT (1) ATE386517T1 (de)
AU (1) AU2002337151B2 (de)
BR (1) BR0212856A (de)
CA (1) CA2461622C (de)
CO (1) CO5570675A2 (de)
CY (1) CY1107953T1 (de)
DE (1) DE60225159T2 (de)
DK (1) DK1432417T3 (de)
EA (1) EA006802B1 (de)
ES (1) ES2301682T3 (de)
GT (1) GT200200190A (de)
HK (1) HK1068551A1 (de)
HR (1) HRPK20040293B3 (de)
HU (1) HUP0401756A3 (de)
IL (1) IL161059A0 (de)
ME (1) MEP16808A (de)
MX (1) MXPA04002042A (de)
MY (1) MY135339A (de)
NO (1) NO327008B1 (de)
NZ (1) NZ531246A (de)
PA (1) PA8555501A1 (de)
PE (1) PE20030427A1 (de)
PL (1) PL369527A1 (de)
PT (1) PT1432417E (de)
RS (1) RS50896B (de)
SI (1) SI1432417T1 (de)
UY (1) UY27452A1 (de)
WO (1) WO2003028721A2 (de)
ZA (1) ZA200401887B (de)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070010573A1 (en) 2003-06-23 2007-01-11 Xianqi Kong Methods and compositions for treating amyloid-related diseases
AU2011250847B2 (en) * 2003-06-23 2013-06-20 Bhi Limited Partnership Methods and compositions for treating amyloid-related diseases
US20070208166A1 (en) * 2003-10-24 2007-09-06 Exelixis, Inc. Tao Kinase Modulators And Method Of Use
DE102004010207A1 (de) 2004-03-02 2005-09-15 Aventis Pharma S.A. Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate
FR2868421B1 (fr) * 2004-04-01 2008-08-01 Aventis Pharma Sa Nouveaux benzothiazoles et leur utilisation comme medicaments
EP1598348A1 (de) 2004-05-18 2005-11-23 Aventis Pharma Deutschland GmbH Pyridazinonderivate als CDK2-Inhibitoren
EP1836161B1 (de) 2004-12-22 2016-07-20 BHI Limited Partnership Verfahren und zusammensetzungen zur behandlung von amyloidassoziierten krankheiten
UA92180C2 (en) * 2005-09-06 2010-10-11 Смиткляйн Бичам Корпорейшн Benzimidazole thiophene compounds as plk inhibitors
FR2891273B1 (fr) * 2005-09-27 2007-11-23 Aventis Pharma Sa NOUVEAUX DERIVES BENZIMIDAZOLES ET BENZOTHIAZOLES, LEUR PREPARATION ET LEUR UTILISATION PHARMACEUTIQUE NOTAMMENT COMME INHIBITEURS DE CMet
DK3851447T3 (da) 2006-10-12 2023-12-04 Bellus Health Inc Fremgangsmåder, forbindelser, sammensætninger og vehikler til administration af 3-amino-1-propansulfonsyre
PA8792501A1 (es) 2007-08-09 2009-04-23 Sanofi Aventis Nuevos derivados de 6-triazolopiridacina-sulfanil benzotiazol y bencimidazol,su procedimiento de preparación,su aplicación como medicamentos,composiciones farmacéuticas y nueva utilización principalmente como inhibidores de met.
CA3006332A1 (en) * 2007-10-12 2009-04-16 Abbvie Ireland Unlimited Company 2-((r)-2-methylpyrrolidin-2-yl)-1h-benzimidazole-4-carboxamide crystalline form 1
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
FR2941949B1 (fr) 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-cycloalkyl ou 6-nh-cycloalkyl- triazolopyridazine-sulfanyl)benzothiazoles et benzimidazoles preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941950B1 (fr) 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941951B1 (fr) 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-nh-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941952B1 (fr) 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-substitue-triazolopyridazine-sulfanyl) 5-fluoro-benzothiazoles et 5-fluoro-benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
WO2011091152A1 (en) * 2010-01-22 2011-07-28 Pablo Gastaminza Inhibitors of hepatitis c virus infection
JP6941598B2 (ja) 2015-08-25 2021-09-29 アルナイラム ファーマシューティカルズ, インコーポレイテッドAlnylam Pharmaceuticals, Inc. プロタンパク質転換酵素サブチリシン/ケキシン(pcsk9)遺伝子関連障害を治療するための方法および組成物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2441201C2 (de) * 1974-08-28 1986-08-07 Hoechst Ag, 6230 Frankfurt Anthelminthisch wirksame 2-Carbalkoxyamino-5(6)-phenyl-sulfonyloxy-benzimidazole und Verfahren zu ihrer Herstellung
DE2541752A1 (de) * 1975-09-19 1977-03-24 Hoechst Ag Anthelminthisch wirksame 2-carbalkoxyamino-5(6)-phenyl-sulfonyloxy- benzimidazole und verfahren zu ihrer herstellung
DE3247615A1 (de) * 1982-12-23 1984-07-05 Hoechst Ag, 6230 Frankfurt Substituierte phenylsulfonyloxybenzimidazolcarbaminate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
GB9900752D0 (en) * 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
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

Also Published As

Publication number Publication date
ES2301682T3 (es) 2008-07-01
IL161059A0 (en) 2004-08-31
YU21404A (sh) 2006-08-17
CN100346786C (zh) 2007-11-07
PA8555501A1 (es) 2003-06-30
EP1432417A2 (de) 2004-06-30
WO2003028721A2 (en) 2003-04-10
HK1068551A1 (en) 2005-04-29
PT1432417E (pt) 2008-05-23
HUP0401756A2 (hu) 2005-01-28
EA006802B1 (ru) 2006-04-28
WO2003028721A3 (en) 2003-12-11
CA2461622A1 (en) 2003-04-10
CA2461622C (en) 2008-12-02
RS50896B (sr) 2010-08-31
AR037096A1 (es) 2004-10-20
PE20030427A1 (es) 2003-06-20
JP4510450B2 (ja) 2010-07-21
HRP20040293A2 (en) 2005-06-30
NZ531246A (en) 2006-06-30
SI1432417T1 (sl) 2008-08-31
NO327008B1 (no) 2009-04-06
MY135339A (en) 2008-03-31
KR20040048904A (ko) 2004-06-10
US20050014811A1 (en) 2005-01-20
PL369527A1 (en) 2005-05-02
HUP0401756A3 (en) 2005-06-28
CN1558761A (zh) 2004-12-29
US7041668B2 (en) 2006-05-09
HRPK20040293B3 (en) 2007-06-30
NO20041214L (no) 2004-06-24
EA200400475A1 (ru) 2004-08-26
EP1432417B1 (de) 2008-02-20
ZA200401887B (en) 2005-05-31
AU2002337151B2 (en) 2007-04-26
JP2005504112A (ja) 2005-02-10
UY27452A1 (es) 2003-02-28
EP1298125A1 (de) 2003-04-02
CO5570675A2 (es) 2005-10-31
ATE386517T1 (de) 2008-03-15
DE60225159T2 (de) 2009-02-19
DK1432417T3 (da) 2008-06-16
GT200200190A (es) 2003-11-11
KR100891439B1 (ko) 2009-04-03
MXPA04002042A (es) 2004-06-07
MEP16808A (en) 2010-06-10
BR0212856A (pt) 2004-09-14
CY1107953T1 (el) 2013-09-04

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition