CY1107953T1 - Ενωσεις υποκαθιστουμενης βενζιμιδαζολης και η χρηση τους για τη θεραπεια του καρκινου - Google Patents

Ενωσεις υποκαθιστουμενης βενζιμιδαζολης και η χρηση τους για τη θεραπεια του καρκινου

Info

Publication number
CY1107953T1
CY1107953T1 CY20081100526T CY081100526T CY1107953T1 CY 1107953 T1 CY1107953 T1 CY 1107953T1 CY 20081100526 T CY20081100526 T CY 20081100526T CY 081100526 T CY081100526 T CY 081100526T CY 1107953 T1 CY1107953 T1 CY 1107953T1
Authority
CY
Cyprus
Prior art keywords
cancer therapy
benzimidazole compounds
substituted benzimidazole
compounds
substituted
Prior art date
Application number
CY20081100526T
Other languages
English (en)
Inventor
François Clerc
François Hamy
Isabelle Depaty
Odile Angouillant-Boniface
Stephanie Deprets
Chantal Carrez
Manfred Roesner
Original Assignee
Aventis Pharma S.A.
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 S.A. filed Critical Aventis Pharma S.A.
Publication of CY1107953T1 publication Critical patent/CY1107953T1/el

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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

Abstract

Νέες ενώσεις βενζιμιδαζόλης του τύπου I και η χρήση τους ως ενώσεις αναστολέων κινάσης που εξαρτώνται από την κυκλίνη καθώς και νέες φαρμακευτικές ενώσεις που τις περιέχουν. (Τύπος I).
CY20081100526T 2001-09-26 2008-05-20 Ενωσεις υποκαθιστουμενης βενζιμιδαζολης και η χρηση τους για τη θεραπεια του καρκινου CY1107953T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01402460A EP1298125A1 (en) 2001-09-26 2001-09-26 Substituted benzimidazole compounds and their use for the treatment of cancer
EP02772370A EP1432417B1 (en) 2001-09-26 2002-09-26 Substituted benzimidazole compounds and their use for the treatment of cancer

Publications (1)

Publication Number Publication Date
CY1107953T1 true CY1107953T1 (el) 2013-09-04

Family

ID=8182891

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20081100526T CY1107953T1 (el) 2001-09-26 2008-05-20 Ενωσεις υποκαθιστουμενης βενζιμιδαζολης και η χρηση τους για τη θεραπεια του καρκινου

Country Status (35)

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

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
JP2007527412A (ja) * 2003-10-24 2007-09-27 エグゼリクシス, インコーポレイテッド Taoキナーゼモジュレーターおよび使用方法
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 (en) 2004-05-18 2005-11-23 Aventis Pharma Deutschland GmbH Novel pyridazinone derivatives as inhibitors of CDK2
CN101128421A (zh) 2004-12-22 2008-02-20 神经化学(国际)有限公司 治疗淀粉样相关疾病用的方法与组合物
CN101300251B (zh) * 2005-09-06 2011-08-03 史密丝克莱恩比彻姆公司 作为plk抑制剂的苯并咪唑噻吩化合物
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
BRPI0717794B8 (pt) 2006-10-12 2021-05-25 Bellus Health International Ltd composto e composição farmacêutica de ácido 3-amino-1-propanosulfônico
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.
WO2009049111A1 (en) * 2007-10-12 2009-04-16 Abbott Laboratories 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
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.
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.
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.
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.
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
CO5570675A2 (es) 2005-10-31
HUP0401756A2 (hu) 2005-01-28
EP1432417B1 (en) 2008-02-20
HRP20040293A2 (en) 2005-06-30
HK1068551A1 (en) 2005-04-29
CA2461622C (en) 2008-12-02
BR0212856A (pt) 2004-09-14
US20050014811A1 (en) 2005-01-20
EA006802B1 (ru) 2006-04-28
MXPA04002042A (es) 2004-06-07
MEP16808A (en) 2010-06-10
IL161059A0 (en) 2004-08-31
PE20030427A1 (es) 2003-06-20
DK1432417T3 (da) 2008-06-16
KR20040048904A (ko) 2004-06-10
SI1432417T1 (sl) 2008-08-31
DE60225159D1 (de) 2008-04-03
AR037096A1 (es) 2004-10-20
PT1432417E (pt) 2008-05-23
EP1432417A2 (en) 2004-06-30
CN1558761A (zh) 2004-12-29
HUP0401756A3 (en) 2005-06-28
MY135339A (en) 2008-03-31
EA200400475A1 (ru) 2004-08-26
PA8555501A1 (es) 2003-06-30
YU21404A (sh) 2006-08-17
HRPK20040293B3 (en) 2007-06-30
US7041668B2 (en) 2006-05-09
UY27452A1 (es) 2003-02-28
ATE386517T1 (de) 2008-03-15
GT200200190A (es) 2003-11-11
NZ531246A (en) 2006-06-30
ES2301682T3 (es) 2008-07-01
WO2003028721A2 (en) 2003-04-10
NO327008B1 (no) 2009-04-06
NO20041214L (no) 2004-06-24
JP4510450B2 (ja) 2010-07-21
WO2003028721A3 (en) 2003-12-11
DE60225159T2 (de) 2009-02-19
EP1298125A1 (en) 2003-04-02
CN100346786C (zh) 2007-11-07
AU2002337151B2 (en) 2007-04-26
PL369527A1 (en) 2005-05-02
ZA200401887B (en) 2005-05-31
CA2461622A1 (en) 2003-04-10
KR100891439B1 (ko) 2009-04-03
JP2005504112A (ja) 2005-02-10
RS50896B (sr) 2010-08-31

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