MA31466B1 - Derives de benzimidazole - Google Patents

Derives de benzimidazole

Info

Publication number
MA31466B1
MA31466B1 MA32454A MA32454A MA31466B1 MA 31466 B1 MA31466 B1 MA 31466B1 MA 32454 A MA32454 A MA 32454A MA 32454 A MA32454 A MA 32454A MA 31466 B1 MA31466 B1 MA 31466B1
Authority
MA
Morocco
Prior art keywords
benzimidazole derivatives
mammals
compounds
treatment
cell growth
Prior art date
Application number
MA32454A
Other languages
Arabic (ar)
English (en)
Inventor
Christopher Scott Jones
GRECA Susan LA
Qifang Li
Michael John Munchhof
Lawrence Alan Reiter
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MA31466B1 publication Critical patent/MA31466B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La présente invention concerne un composé de formule i (i) ou un de ses sels pharmaceutiquement acceptables, dans laquelle r1, r2, r3a, r3b, r4, r5, x, m et n sont tels que définis dans le présent document. De tels nouveaux dérivés de benzamidazole sont utiles dans le traitement de la croissance cellulaire anormale, telle que le cancer, chez les mammifères. L'invention concerne également un procédé d'utilisation de tels composés dans le traitement de la croissance cellulaire anormale chez les mammifères, notamment les humains, et des compositions pharmaceutiques qui contiennent de tels composés.
MA32454A 2007-06-29 2009-12-29 Derives de benzimidazole MA31466B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US94728707P 2007-06-29 2007-06-29
US4164508P 2008-04-02 2008-04-02
PCT/IB2008/001575 WO2009004427A2 (fr) 2007-06-29 2008-06-16 Dérivés de benzamidazole

Publications (1)

Publication Number Publication Date
MA31466B1 true MA31466B1 (fr) 2010-06-01

Family

ID=40161351

Family Applications (1)

Application Number Title Priority Date Filing Date
MA32454A MA31466B1 (fr) 2007-06-29 2009-12-29 Derives de benzimidazole

Country Status (46)

Country Link
US (2) US8148401B2 (fr)
EP (1) EP2170860B9 (fr)
JP (2) JP4567099B2 (fr)
KR (1) KR101143246B1 (fr)
CN (1) CN101687841B (fr)
AP (1) AP2377A (fr)
AR (1) AR067346A1 (fr)
AU (1) AU2008272641B2 (fr)
BR (1) BRPI0813412B8 (fr)
CA (1) CA2690953C (fr)
CL (1) CL2008001922A1 (fr)
CO (1) CO6160232A2 (fr)
CR (1) CR11150A (fr)
CU (1) CU23847B1 (fr)
CY (2) CY1118650T1 (fr)
DK (1) DK2170860T5 (fr)
DO (1) DOP2009000278A (fr)
EA (1) EA016888B1 (fr)
EC (1) ECSP099803A (fr)
ES (1) ES2609258T3 (fr)
FR (1) FR20C1038I2 (fr)
GE (1) GEP20125702B (fr)
GT (1) GT200900328A (fr)
HK (1) HK1139658A1 (fr)
HN (1) HN2008000974A (fr)
HR (1) HRP20161562T2 (fr)
HU (2) HUE030052T4 (fr)
IL (1) IL202420A (fr)
LT (2) LT2170860T (fr)
MA (1) MA31466B1 (fr)
ME (1) ME00962B (fr)
MY (1) MY148636A (fr)
NI (1) NI200900219A (fr)
NL (1) NL301057I2 (fr)
NO (1) NO2020027I1 (fr)
NZ (1) NZ581889A (fr)
PA (1) PA8785401A1 (fr)
PE (2) PE20121010A1 (fr)
PL (1) PL2170860T3 (fr)
PT (1) PT2170860T (fr)
RS (1) RS55395B9 (fr)
SI (1) SI2170860T1 (fr)
TN (1) TN2009000544A1 (fr)
TW (1) TWI371451B (fr)
UY (1) UY31164A1 (fr)
WO (1) WO2009004427A2 (fr)

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US8907089B2 (en) 2009-08-26 2014-12-09 Takeda Pharmaceutical Company Limited Fused heterocyclic ring derivative and use thereof
US8628554B2 (en) 2010-06-13 2014-01-14 Virender K. Sharma Intragastric device for treating obesity
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US9526648B2 (en) 2010-06-13 2016-12-27 Synerz Medical, Inc. Intragastric device for treating obesity
US10420665B2 (en) 2010-06-13 2019-09-24 W. L. Gore & Associates, Inc. Intragastric device for treating obesity
ES2543151T3 (es) 2010-10-20 2015-08-17 Pfizer Inc Derivados de 2-piridina como moduladores del receptor Smoothened
JP5452459B2 (ja) 2010-12-16 2014-03-26 株式会社Ｎｔｔドコモ ホーム基地局及びハンドオーバ方法
US10059723B2 (en) 2011-02-28 2018-08-28 Biomarin Pharmaceutical Inc. Histone deacetylase inhibitors
US8957066B2 (en) 2011-02-28 2015-02-17 Biomarin Pharmaceutical Inc. Histone deacetylase inhibitors
CA3061239A1 (fr) 2011-02-28 2012-09-07 Biomarin Pharmaceutical Inc. Inhibiteurs de l'histone deacetylase
US9051305B2 (en) 2011-03-08 2015-06-09 Eutropics Pharmaceuticals, Inc. Compositions and methods useful for treating diseases
FR2980477B1 (fr) 2011-09-23 2013-10-18 Centre Nat Rech Scient Nouveaux composes modulateurs de la voie de signalisation des proteines hedgehog, leurs formes marquees, et applications
CA2849820C (fr) * 2011-09-26 2019-08-27 Merck Patent Gmbh Composes de benzylpiperidine utilises comme antagonistes des recepteurs a l'acide lysophosphatidique (lpa)
IN2014DN11205A (fr) 2012-06-20 2015-10-02 Eutropics Pharmaceuticals Inc
WO2014081953A1 (fr) 2012-11-21 2014-05-30 Richard David J Méthodes et compositions utiles dans le traitement de maladies faisant appel à des protéines de la famille bcl-2 et des dérivés d'isoquinoléine et de quinoléine
CA2903490C (fr) 2013-03-15 2021-04-13 Biomarin Pharmaceutical Inc. Inhibiteurs de hdac
EP2996689A1 (fr) 2013-04-17 2016-03-23 Albert-Ludwigs-Universität Freiburg Composés destinés à être utilisés comme inhibiteurs de bromodomaine
US10732182B2 (en) 2013-08-01 2020-08-04 Eutropics Pharmaceuticals, Inc. Method for predicting cancer sensitivity
GB2519344A (en) * 2013-10-18 2015-04-22 Redx Pharma Ltd Compounds
US10640803B2 (en) 2013-10-30 2020-05-05 Eutropics Pharmaceuticals, Inc. Methods for determining chemosensitivity and chemotoxicity
EP3666768B1 (fr) * 2015-04-24 2022-06-15 Pfizer Inc. Procédé de préparation d'une forme cristalline du 1-((2r,4r) -2-(1h-benzo [ d ] imidazol-2-yl ) -1-méthylpipéridin-4-yl) -3-(4-cyanophényl) urée maléate; le complexe (1:1) entre l'imidazole et le 1-((2r,4r)-2-(1h-benzo[d]imidazol-2-yl)-1-méthylpipéridin-4-yl)-3-(4-cyanophényl)urée
US10779980B2 (en) 2016-04-27 2020-09-22 Synerz Medical, Inc. Intragastric device for treating obesity
JP2020164722A (ja) * 2019-03-29 2020-10-08 デクセリアルズ株式会社 接着剤組成物
EP4097093B8 (fr) 2020-01-28 2024-02-28 Assia Chemical Industries LTD Procédés de préparation de glasdegib et de sel de celui-ci et formes à l'état solide de maléate de glasdegib et procédé de préparation associé
CN113248475B (zh) * 2020-02-11 2023-03-17 中国科学院上海药物研究所 一类杂环取代的苯并咪唑二聚体或其药学上可接受的盐、组合物及其用途
EP4126237B1 (fr) 2020-03-26 2024-04-10 LEK Pharmaceuticals d.d. Forme dimaléate de 1-((2r,4r)-2-(1h-benzo[d]imidazol-2-yl)-1-méthylpipéridine?-4-yl)-3-(4-cyanophényl)urée
CN115997122A (zh) 2020-06-26 2023-04-21 拉夸里亚创药株式会社 类维生素a与癌治疗剂的组合疗法有效的癌患者的选择方法、及类维生素a与癌治疗剂的组合药物
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WO2006124780A2 (fr) * 2005-05-12 2006-11-23 Kalypsys, Inc. Inhibiteurs de la b-raf kinase
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CA2672815A1 (fr) 2006-12-15 2008-06-26 Pfizer Products Inc. Derives du benzamidazole
DK2170860T5 (en) * 2007-06-29 2017-03-20 Pfizer benzimidazole
EP2303275A4 (fr) 2008-06-17 2012-05-09 Univ Duke Modulateurs du récepteur smoothened
EP2328871B1 (fr) 2008-08-25 2020-04-01 Novartis AG Modulateurs de la voie hedgehog

Also Published As

Publication number Publication date
NL301057I1 (nl) 2020-07-22
FR20C1038I1 (fr) 2020-10-02
CR11150A (es) 2010-02-08
LTPA2020528I1 (lt) 2020-09-25
AP2009005089A0 (en) 2009-12-31
SI2170860T1 (sl) 2017-01-31
JP4567099B2 (ja) 2010-10-20
CL2008001922A1 (es) 2009-01-02
HK1139658A1 (en) 2010-09-24
RS55395B1 (sr) 2017-04-28
HUE030052T2 (hu) 2017-04-28
GEP20125702B (en) 2012-12-10
US20120157495A1 (en) 2012-06-21
NI200900219A (es) 2010-03-11
PE20090772A1 (es) 2009-06-24
US8431597B2 (en) 2013-04-30
HRP20161562T2 (hr) 2017-04-21
EA016888B1 (ru) 2012-08-30
HUS2000031I1 (hu) 2020-09-28
HRP20161562T1 (hr) 2016-12-30
CU20090225A7 (es) 2012-02-15
ME00962B (fr) 2012-06-20
GT200900328A (es) 2011-08-29
NL301057I2 (nl) 2020-09-10
TWI371451B (en) 2012-09-01
IL202420A (en) 2014-05-28
KR20100028120A (ko) 2010-03-11
CO6160232A2 (es) 2010-05-20
AP2377A (en) 2012-03-07
EP2170860A2 (fr) 2010-04-07
PE20121010A1 (es) 2012-08-06
WO2009004427A3 (fr) 2009-06-04
PA8785401A1 (es) 2009-01-23
EA200971104A1 (ru) 2010-06-30
DK2170860T5 (en) 2017-03-20
MY148636A (en) 2013-05-15
CA2690953C (fr) 2012-10-02
NZ581889A (en) 2011-05-27
CY2020028I1 (el) 2020-11-25
WO2009004427A2 (fr) 2009-01-08
DK2170860T3 (en) 2017-01-09
CA2690953A1 (fr) 2009-01-08
AU2008272641A1 (en) 2009-01-08
AU2008272641B2 (en) 2013-08-29
LTC2170860I2 (lt) 2022-03-10
PT2170860T (pt) 2017-01-04
RS55395B9 (sr) 2020-01-31
LT2170860T (lt) 2017-01-10
CU23847B1 (es) 2012-10-15
CN101687841A (zh) 2010-03-31
ES2609258T3 (es) 2017-04-19
HUE030052T4 (en) 2017-06-28
US20090005416A1 (en) 2009-01-01
IL202420A0 (en) 2010-06-30
KR101143246B1 (ko) 2012-05-18
BRPI0813412B1 (pt) 2020-01-21
EP2170860B9 (fr) 2017-02-22
TW200911792A (en) 2009-03-16
CY2020028I2 (el) 2020-11-25
AR067346A1 (es) 2009-10-07
FR20C1038I2 (fr) 2021-08-13
JP2010280693A (ja) 2010-12-16
PL2170860T3 (pl) 2017-05-31
BRPI0813412A2 (pt) 2014-12-30
US8148401B2 (en) 2012-04-03
CY1118650T1 (el) 2017-07-12
TN2009000544A1 (fr) 2011-03-31
EP2170860B1 (fr) 2016-11-02
JP2010531869A (ja) 2010-09-30
HN2008000974A (es) 2011-01-24
BRPI0813412B8 (pt) 2021-05-25
UY31164A1 (es) 2009-01-30
ECSP099803A (es) 2010-01-29
NO2020027I1 (no) 2020-08-11
CN101687841B (zh) 2013-07-10
DOP2009000278A (es) 2009-12-31

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