BRPI0506802A - derivados de indol e uso destes como inibidores de quinase em inibidores de ikk2 particulares - Google Patents

derivados de indol e uso destes como inibidores de quinase em inibidores de ikk2 particulares

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Publication number
BRPI0506802A
BRPI0506802A BRPI0506802-9A BRPI0506802A BRPI0506802A BR PI0506802 A BRPI0506802 A BR PI0506802A BR PI0506802 A BRPI0506802 A BR PI0506802A BR PI0506802 A BRPI0506802 A BR PI0506802A
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BR
Brazil
Prior art keywords
inhibitors
indole derivatives
kinase inhibitors
particular ikk2
kinase
Prior art date
Application number
BRPI0506802-9A
Other languages
English (en)
Inventor
Ian Robert Baldwin
Paul Bamborough
John Andrew Christopher
Timothy Longstaff
Jeffrey K Kerns
David Drysdale Miller
Original Assignee
Smithkline Beecham Corp
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Publication date
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of BRPI0506802A publication Critical patent/BRPI0506802A/pt

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    • 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
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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
    • C07D209/30Indoles; 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
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    • 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
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Abstract

DERIVADOS DE INDOL E USO DESTES COMO INIBIDORES DE QUINASE EM INIBIDORES DE IKK2 PARTICULARES Compostos de carboxamida indol da fórmula (I) : são fornecidos como inibidores de atividade quinase, em particular atividade IKK2, bem como composições e medicamentos contendo-as, para o uso em desordens inflamatórias e reparo do tecido.
BRPI0506802-9A 2004-01-15 2005-01-13 derivados de indol e uso destes como inibidores de quinase em inibidores de ikk2 particulares BRPI0506802A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0400895.9A GB0400895D0 (en) 2004-01-15 2004-01-15 Chemical compounds
PCT/GB2005/000085 WO2005067923A1 (en) 2004-01-15 2005-01-13 Indole derivatives and use thereof as kinase inhibitors in particular ikk2 inhibitors

Publications (1)

Publication Number Publication Date
BRPI0506802A true BRPI0506802A (pt) 2007-05-29

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ID=31726240

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0506802-9A BRPI0506802A (pt) 2004-01-15 2005-01-13 derivados de indol e uso destes como inibidores de quinase em inibidores de ikk2 particulares

Country Status (24)

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

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US20080293802A1 (en) * 2005-12-16 2008-11-27 Smithline Beecham Corporation Chemical Compounds
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CN102341367B (zh) * 2009-03-05 2014-05-07 住友化学株式会社 卤素取代苯二甲醇的制造方法
US8354539B2 (en) 2009-03-10 2013-01-15 Glaxo Group Limited Indole derivatives as IKK2 inhibitors
US8765792B2 (en) 2010-12-01 2014-07-01 Glaxosmithkline Llc Indoles
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
EP3070085B1 (en) 2013-02-04 2019-01-09 Janssen Pharmaceutica NV Flap modulators
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
SI3013337T1 (sl) * 2013-06-26 2019-02-28 Abbvie Inc. Primarni karboksamidi kot inhibitorji BTK
CN107148417B (zh) * 2014-12-18 2020-09-08 豪夫迈·罗氏有限公司 苯并氮杂*磺酰胺化合物
US20170158702A1 (en) * 2015-12-02 2017-06-08 Kyras Therapeutics, Inc. Multivalent ras binding compounds
US11352328B2 (en) 2016-07-12 2022-06-07 Arisan Therapeutics Inc. Heterocyclic compounds for the treatment of arenavirus
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PT1703905E (pt) 2009-02-04
GB0400895D0 (en) 2004-02-18
JP2007517848A (ja) 2007-07-05
RU2006129492A (ru) 2008-02-27
CN1933830A (zh) 2007-03-21
IL176739A0 (en) 2006-10-31
EP1703905B1 (en) 2008-11-12
EP1703905A1 (en) 2006-09-27
ZA200604855B (en) 2007-11-28
US20080269200A1 (en) 2008-10-30
HK1098047A1 (en) 2007-07-13
CA2552953A1 (en) 2005-07-28
JP2012025761A (ja) 2012-02-09
DE602005010970D1 (de) 2008-12-24
MA28279A1 (fr) 2006-11-01
AU2005205090A1 (en) 2005-07-28
WO2005067923A1 (en) 2005-07-28
JP4975447B2 (ja) 2012-07-11
HRP20090071T3 (en) 2009-04-30
DK1703905T3 (da) 2009-02-16
KR20070026357A (ko) 2007-03-08
ATE413877T1 (de) 2008-11-15
ES2317184T3 (es) 2009-04-16

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