NO20080457L - Chemical connections - Google Patents
Chemical connectionsInfo
- Publication number
- NO20080457L NO20080457L NO20080457A NO20080457A NO20080457L NO 20080457 L NO20080457 L NO 20080457L NO 20080457 A NO20080457 A NO 20080457A NO 20080457 A NO20080457 A NO 20080457A NO 20080457 L NO20080457 L NO 20080457L
- Authority
- NO
- Norway
- Prior art keywords
- compound
- ikk2
- directed
- compounds
- formula
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 5
- 102100021854 Inhibitor of nuclear factor kappa-B kinase subunit beta Human genes 0.000 abstract 3
- 101710205525 Inhibitor of nuclear factor kappa-B kinase subunit beta Proteins 0.000 abstract 3
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 208000035475 disorder Diseases 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- VFHUJFBEFDVZPJ-UHFFFAOYSA-N 1h-indole-2-carboxamide Chemical class C1=CC=C2NC(C(=O)N)=CC2=C1 VFHUJFBEFDVZPJ-UHFFFAOYSA-N 0.000 abstract 1
- 230000002411 adverse Effects 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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- 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
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- Health & Medical Sciences (AREA)
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Abstract
Foreliggende oppfinnelse er rettet mot nye indolkarboksamidderivater. Spesifikt er oppfinnelsen rettet mot forbindelser ifølge formel I: Formel (I) hvor RI, R2, R3, U og V er definert nedenfor, og mot farmasøytisk akseptable salter derav. Forbindelsene ifølge oppfinnelsen er inhibitorer av IKK2 og kan være nyttige i behandlingen av forstyrrelser assosiert med uheldig IKK2 (også kjent som IKKP) aktivitet, slik som reumatoid artritt, astma og COPD (kronisk obstruktiv lungesykdom). Oppfinnelsen er følgelig ytterligere rettet mot farmasøytiske sammensetninger omfattende en forbindelse ifølge oppfinnelsen. Oppfinnelsen er også ytterligere rettet mot fremgangsmåter for å inhibere IKK2-aktivitet og behandling av forstyrrelser assosiert dermed, ved anvendelse av en forbindelse ifølge foreliggende oppfinnelse eller en farmasøytisk sammensetning omfattende en forbindelse ifølge oppfinnelsen.The present invention is directed to novel indolecarboxamide derivatives. Specifically, the invention is directed to compounds of formula I: Formula (I) wherein R1, R2, R3, U and V are defined below, and to pharmaceutically acceptable salts thereof. The compounds of the invention are inhibitors of IKK2 and may be useful in the treatment of disorders associated with adverse IKK2 (also known as IKKP) activity, such as rheumatoid arthritis, asthma and COPD (chronic obstructive pulmonary disease). Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is also further directed to methods for inhibiting IKK2 activity and the treatment of disorders associated therewith, using a compound of the present invention or a pharmaceutical composition comprising a compound of the invention.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69525605P | 2005-06-30 | 2005-06-30 | |
| PCT/US2006/025402 WO2007005534A2 (en) | 2005-06-30 | 2006-06-28 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20080457L true NO20080457L (en) | 2008-01-29 |
Family
ID=37605008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20080457A NO20080457L (en) | 2005-06-30 | 2008-01-24 | Chemical connections |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP1896014A4 (en) |
| JP (1) | JP5059756B2 (en) |
| KR (1) | KR20080021077A (en) |
| CN (1) | CN101247804B (en) |
| AR (1) | AR055343A1 (en) |
| AU (1) | AU2006266028B2 (en) |
| BR (1) | BRPI0611674A2 (en) |
| CA (1) | CA2613068A1 (en) |
| EA (1) | EA014083B1 (en) |
| IL (1) | IL187786A0 (en) |
| MA (1) | MA29566B1 (en) |
| MX (1) | MX2007016541A (en) |
| NO (1) | NO20080457L (en) |
| NZ (1) | NZ563687A (en) |
| PE (1) | PE20070173A1 (en) |
| TW (1) | TWI380973B (en) |
| UA (1) | UA99699C2 (en) |
| WO (1) | WO2007005534A2 (en) |
| ZA (1) | ZA200709948B (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0315950D0 (en) | 2003-06-11 | 2003-08-13 | Xention Discovery Ltd | Compounds |
| PE20060748A1 (en) | 2004-09-21 | 2006-10-01 | Smithkline Beecham Corp | INDOLCARBOXAMIDE DERIVATIVES AS KINASE INHIBITORS IKK2 |
| GB0525164D0 (en) * | 2005-12-09 | 2006-01-18 | Xention Discovery Ltd | Compounds |
| JP2009519968A (en) * | 2005-12-16 | 2009-05-21 | スミスクライン・ビーチャム・コーポレイション | Chemical substance |
| PE20081889A1 (en) * | 2007-03-23 | 2009-03-05 | Smithkline Beecham Corp | INDOL CARBOXAMIDES AS INHIBITORS OF IKK2 |
| ES2490867T3 (en) * | 2008-12-19 | 2014-09-04 | Bristol-Myers Squibb Company | Carbazole and carboline kinase inhibitors |
| EP2406249A1 (en) * | 2009-03-10 | 2012-01-18 | Glaxo Group Limited | Indole derivatives as ikk2 inhibitors |
| WO2014210255A1 (en) * | 2013-06-26 | 2014-12-31 | Abbvie Inc. | Primary carboxamides as btk inhibitors |
| KR102030305B1 (en) * | 2014-10-24 | 2019-10-08 | 브리스톨-마이어스 스큅 컴퍼니 | Indole carboxamide compounds useful as kinase inhibitors |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1272842A (en) * | 1997-08-06 | 2000-11-08 | 伊莱利利公司 | 2-acylaminopropanamines as tachykinin receptor antagonists |
| DE19807993A1 (en) | 1998-02-26 | 1999-09-02 | Bayer Ag | Treating tumor necrosis factor mediated inflammatory disease, e.g. arteriosclerosis, using new or known beta-carboline derivatives |
| ME00370B (en) | 1999-06-23 | 2011-05-10 | Sanofi Aventis Deutschland | Substituted benzimidazole |
| DE19928424A1 (en) | 1999-06-23 | 2000-12-28 | Aventis Pharma Gmbh | New aminoacid residue substituted benzimidazole derivative I(kappa)B-kinase inhibitors, useful for treating NF(kappa)B-related disorders e.g. rheumatoid arthritis, asthma, Alzheimer's disease and cancer |
| DE19951360A1 (en) | 1999-10-26 | 2001-05-03 | Aventis Pharma Gmbh | Substituted indoles |
| GB0003154D0 (en) | 2000-02-12 | 2000-04-05 | Astrazeneca Uk Ltd | Novel compounds |
| EP1209158A1 (en) | 2000-11-18 | 2002-05-29 | Aventis Pharma Deutschland GmbH | Substituted beta-carbolines |
| EP1134221A1 (en) | 2000-03-15 | 2001-09-19 | Aventis Pharma Deutschland GmbH | Substituted beta-carbolines as lkB kinase inhibitors |
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-
2006
- 2006-06-28 KR KR1020077030656A patent/KR20080021077A/en not_active Ceased
- 2006-06-28 BR BRPI0611674-4A patent/BRPI0611674A2/en not_active IP Right Cessation
- 2006-06-28 UA UAA200714940A patent/UA99699C2/en unknown
- 2006-06-28 JP JP2008519569A patent/JP5059756B2/en not_active Expired - Fee Related
- 2006-06-28 CA CA002613068A patent/CA2613068A1/en not_active Abandoned
- 2006-06-28 TW TW095123240A patent/TWI380973B/en not_active IP Right Cessation
- 2006-06-28 EA EA200800183A patent/EA014083B1/en not_active IP Right Cessation
- 2006-06-28 AR ARP060102790A patent/AR055343A1/en not_active Application Discontinuation
- 2006-06-28 CN CN2006800304481A patent/CN101247804B/en not_active Expired - Fee Related
- 2006-06-28 AU AU2006266028A patent/AU2006266028B2/en not_active Ceased
- 2006-06-28 WO PCT/US2006/025402 patent/WO2007005534A2/en not_active Ceased
- 2006-06-28 MX MX2007016541A patent/MX2007016541A/en active IP Right Grant
- 2006-06-28 PE PE2006000761A patent/PE20070173A1/en not_active Application Discontinuation
- 2006-06-28 NZ NZ563687A patent/NZ563687A/en not_active IP Right Cessation
- 2006-06-28 EP EP06785861A patent/EP1896014A4/en not_active Withdrawn
-
2007
- 2007-11-19 ZA ZA2007/09948A patent/ZA200709948B/en unknown
- 2007-11-29 IL IL187786A patent/IL187786A0/en unknown
- 2007-12-26 MA MA30513A patent/MA29566B1/en unknown
-
2008
- 2008-01-24 NO NO20080457A patent/NO20080457L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2006266028A1 (en) | 2007-01-11 |
| BRPI0611674A2 (en) | 2009-04-28 |
| IL187786A0 (en) | 2008-08-07 |
| CN101247804A (en) | 2008-08-20 |
| ZA200709948B (en) | 2009-03-25 |
| CA2613068A1 (en) | 2007-01-11 |
| EA200800183A1 (en) | 2008-08-29 |
| EP1896014A2 (en) | 2008-03-12 |
| MX2007016541A (en) | 2008-03-07 |
| UA99699C2 (en) | 2012-09-25 |
| AU2006266028B2 (en) | 2012-03-15 |
| KR20080021077A (en) | 2008-03-06 |
| JP5059756B2 (en) | 2012-10-31 |
| NZ563687A (en) | 2011-07-29 |
| JP2009500338A (en) | 2009-01-08 |
| EP1896014A4 (en) | 2010-07-21 |
| AR055343A1 (en) | 2007-08-22 |
| CN101247804B (en) | 2012-09-26 |
| WO2007005534A3 (en) | 2007-04-26 |
| WO2007005534A8 (en) | 2008-01-17 |
| PE20070173A1 (en) | 2007-03-14 |
| MA29566B1 (en) | 2008-06-02 |
| WO2007005534A2 (en) | 2007-01-11 |
| TW200738588A (en) | 2007-10-16 |
| TWI380973B (en) | 2013-01-01 |
| EA014083B1 (en) | 2010-08-30 |
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