ATE413877T1 - Indol-derivate und ihre verwendung als kinase- hemmer, insbesondere ikk2-hemmer - Google Patents

Indol-derivate und ihre verwendung als kinase- hemmer, insbesondere ikk2-hemmer

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Publication number
ATE413877T1
ATE413877T1 AT05701855T AT05701855T ATE413877T1 AT E413877 T1 ATE413877 T1 AT E413877T1 AT 05701855 T AT05701855 T AT 05701855T AT 05701855 T AT05701855 T AT 05701855T AT E413877 T1 ATE413877 T1 AT E413877T1
Authority
AT
Austria
Prior art keywords
inhibitors
indole derivatives
kinase inhibitors
particular ikk2
kinase
Prior art date
Application number
AT05701855T
Other languages
English (en)
Inventor
Ian Baldwin
Paul Bamborough
John Christopher
Jeffrey Kerns
Timothy Longstaff
David Miller
Original Assignee
Smithkline Beecham Corp
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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Application granted granted Critical
Publication of ATE413877T1 publication Critical patent/ATE413877T1/de

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
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    • C07ORGANIC CHEMISTRY
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    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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    • C07D401/04Heterocyclic 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
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    • 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
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    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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AT05701855T 2004-01-15 2005-01-13 Indol-derivate und ihre verwendung als kinase- hemmer, insbesondere ikk2-hemmer ATE413877T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0400895.9A GB0400895D0 (en) 2004-01-15 2004-01-15 Chemical compounds

Publications (1)

Publication Number Publication Date
ATE413877T1 true ATE413877T1 (de) 2008-11-15

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Application Number Title Priority Date Filing Date
AT05701855T ATE413877T1 (de) 2004-01-15 2005-01-13 Indol-derivate und ihre verwendung als kinase- hemmer, insbesondere ikk2-hemmer

Country Status (24)

Country Link
US (1) US20080269200A1 (de)
EP (1) EP1703905B1 (de)
JP (2) JP4975447B2 (de)
KR (1) KR20070026357A (de)
CN (1) CN1933830A (de)
AT (1) ATE413877T1 (de)
AU (1) AU2005205090A1 (de)
BR (1) BRPI0506802A (de)
CA (1) CA2552953A1 (de)
DE (1) DE602005010970D1 (de)
DK (1) DK1703905T3 (de)
ES (1) ES2317184T3 (de)
GB (1) GB0400895D0 (de)
HK (1) HK1098047A1 (de)
HR (1) HRP20090071T3 (de)
IL (1) IL176739A0 (de)
MA (1) MA28279A1 (de)
NO (1) NO20063676L (de)
PL (1) PL1703905T3 (de)
PT (1) PT1703905E (de)
RU (1) RU2006129492A (de)
SI (1) SI1703905T1 (de)
WO (1) WO2005067923A1 (de)
ZA (1) ZA200604855B (de)

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PE20060748A1 (es) * 2004-09-21 2006-10-01 Smithkline Beecham Corp Derivados de indolcarboxamida como inhibidores de quinasa ikk2
US8063071B2 (en) 2007-10-31 2011-11-22 GlaxoSmithKline, LLC Chemical compounds
PE20070173A1 (es) * 2005-06-30 2007-03-14 Smithkline Beecham Corp Compuestos de indol carboxamidas como inhibidores de ikk2
US20080242685A1 (en) * 2005-10-25 2008-10-02 Smithkline Beecham Corporation Chemical Compounds
US20080269291A1 (en) * 2005-11-18 2008-10-30 Kerns Jeffrey K Chemical Compounds
EP1959737A4 (de) * 2005-12-16 2010-12-08 Glaxosmithkline Llc Chemische verbindungen
WO2008087933A1 (ja) * 2007-01-15 2008-07-24 Santen Pharmaceutical Co., Ltd. IκBキナーゼβ阻害活性を有する新規インドール誘導体
AR065804A1 (es) 2007-03-23 2009-07-01 Smithkline Beecham Corp Compuesto de indol carboxamida, composicion farmaceutica que lo comprende y uso de dicho compuesto para preparar un medicamento
EA019309B1 (ru) 2008-02-04 2014-02-28 Меркьюри Терапьютикс, Инк. Модуляторы ampk (амф-активируемой протеинкиназы)
EP2253618A1 (de) * 2008-02-27 2010-11-24 Takeda Pharmaceutical Company Limited Verbindung mit 6-gliedrigem aromatischem ring
WO2010007972A1 (ja) * 2008-07-14 2010-01-21 参天製薬株式会社 カルバモイル基、ウレイド基及び置換オキシ基を有する新規インドール誘導体
KR20110125258A (ko) * 2009-03-05 2011-11-18 스미또모 가가꾸 가부시끼가이샤 할로겐 치환 벤젠디메탄올의 제조 방법
EP2406249A1 (de) 2009-03-10 2012-01-18 Glaxo Group Limited Indolderivate als ikk2-inhibitoren
EP2646020B1 (de) * 2010-12-01 2016-09-21 Glaxosmithkline LLC Indole
WO2014036268A2 (en) * 2012-08-29 2014-03-06 Mount Sinai School Of Medicine Indole derivatives as sumo activators
FR3001219A1 (fr) * 2013-01-22 2014-07-25 Centre Nat Rech Scient Inhibiteurs de kinases
WO2014121055A2 (en) 2013-02-04 2014-08-07 Janssen Pharmaceutica Nv Flap modulators
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
UY35630A (es) * 2013-06-26 2015-01-30 Abbvie Inc Carboxamidas primarias como inhibidores de btk
WO2016096778A1 (en) * 2014-12-18 2016-06-23 F. Hoffmann-La Roche Ag Benzazepine sulfonamide compounds
WO2017096045A1 (en) * 2015-12-02 2017-06-08 Kyras Therapeutics, Inc. Multivalent ras binding compounds
WO2018013430A2 (en) 2016-07-12 2018-01-18 Arisan Therapeutics Inc. Heterocyclic compounds for the treatment of arenavirus infection
EP3636642A4 (de) 2017-06-07 2021-03-24 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences Indolessigsäurederivat und herstellungsverfahren sowie pharmazeutische verwendung davon
WO2024059220A2 (en) * 2022-09-15 2024-03-21 Vanderbilt University 6,5 southwestern core compounds as mglu5 negative allosteric modulators and methods of making and using the same

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KR20070026357A (ko) 2007-03-08
WO2005067923A1 (en) 2005-07-28
IL176739A0 (en) 2006-10-31
PT1703905E (pt) 2009-02-04
AU2005205090A1 (en) 2005-07-28
EP1703905A1 (de) 2006-09-27
JP2007517848A (ja) 2007-07-05
HRP20090071T3 (en) 2009-04-30
US20080269200A1 (en) 2008-10-30
SI1703905T1 (sl) 2009-04-30
DK1703905T3 (da) 2009-02-16
JP2012025761A (ja) 2012-02-09
JP4975447B2 (ja) 2012-07-11
CA2552953A1 (en) 2005-07-28
EP1703905B1 (de) 2008-11-12
ES2317184T3 (es) 2009-04-16
DE602005010970D1 (de) 2008-12-24
BRPI0506802A (pt) 2007-05-29
GB0400895D0 (en) 2004-02-18
RU2006129492A (ru) 2008-02-27
MA28279A1 (fr) 2006-11-01
NO20063676L (no) 2006-10-13
ZA200604855B (en) 2007-11-28
PL1703905T3 (pl) 2009-04-30
CN1933830A (zh) 2007-03-21

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