TR200101858T2 - JNK protein kinaz inhibitörleri olarak 4-ariloksindoller - Google Patents
JNK protein kinaz inhibitörleri olarak 4-ariloksindollerInfo
- Publication number
- TR200101858T2 TR200101858T2 TR2001/01858T TR200101858T TR200101858T2 TR 200101858 T2 TR200101858 T2 TR 200101858T2 TR 2001/01858 T TR2001/01858 T TR 2001/01858T TR 200101858 T TR200101858 T TR 200101858T TR 200101858 T2 TR200101858 T2 TR 200101858T2
- Authority
- TR
- Turkey
- Prior art keywords
- aryloxindoles
- protein kinase
- kinase inhibitors
- jnk protein
- jnk
- Prior art date
Links
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 1
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 229940121363 anti-inflammatory agent Drugs 0.000 abstract 1
- 239000002260 anti-inflammatory agent Substances 0.000 abstract 1
- 108060006633 protein kinase Proteins 0.000 abstract 1
- 201000003068 rheumatic fever Diseases 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- 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
- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
Abstract
Bu bulus yeni formül (I)4-ariloksindolleri ile ilgilidir ki burada R2,R3 X ve A tarifnamede belirtildigi gibidir ve bunlar protein kinazlari, özellikle de JNK protein kinazlari inhibe eder ya da hafifletir ve bu nedenle iltihaba karsi maddeler olarak ve özellikle romatizmal artirit tedavisinde kullanislidirlar.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11259098P | 1998-12-17 | 1998-12-17 | |
US14902899P | 1999-08-16 | 1999-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
TR200101858T2 true TR200101858T2 (tr) | 2001-12-21 |
Family
ID=26810127
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TR2001/01858T TR200101858T2 (tr) | 1998-12-17 | 1999-12-09 | JNK protein kinaz inhibitörleri olarak 4-ariloksindoller |
Country Status (10)
Country | Link |
---|---|
US (1) | US6307056B1 (tr) |
EP (1) | EP1149093A1 (tr) |
JP (1) | JP2002532493A (tr) |
KR (1) | KR20010101266A (tr) |
CN (1) | CN1136217C (tr) |
AU (1) | AU760039B2 (tr) |
BR (1) | BR9916223A (tr) |
CA (1) | CA2354591A1 (tr) |
TR (1) | TR200101858T2 (tr) |
WO (1) | WO2000035909A1 (tr) |
Families Citing this family (42)
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US20040072888A1 (en) | 1999-08-19 | 2004-04-15 | Bennett Brydon L. | Methods for treating inflammatory conditions or inhibiting JNK |
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WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
JP2004518669A (ja) * | 2000-12-20 | 2004-06-24 | スージェン・インコーポレーテッド | 4−アリール置換インドリノン |
WO2002051442A1 (fr) * | 2000-12-26 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Co-prescriptions |
US6987184B2 (en) | 2001-02-15 | 2006-01-17 | Signal Pharmaceuticals, Llc | Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related |
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GB0112834D0 (en) | 2001-05-25 | 2001-07-18 | Smithkline Beecham Plc | Medicaments |
AU2002303892A1 (en) | 2001-05-30 | 2002-12-09 | Jingrong Cui | 5-aralkylsulfonyl-3- (pyrrol-2-ylmethylidene)-2-indolinone derivatives as kinase inhibitors |
WO2003010164A1 (en) | 2001-07-23 | 2003-02-06 | Applied Research Systems Ars Holding N.V. | Arylsulfonamide derivatives as c-jun-n-terminal kinases (jnk's) inhibitors |
US20030119839A1 (en) * | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
JP2005533748A (ja) | 2002-03-08 | 2005-11-10 | シグナル ファーマシューティカルズ,インコーポレイテッド | 増殖性障害および癌を治療、予防、または管理するための併用療法 |
AU2003214414B2 (en) | 2002-03-28 | 2008-10-09 | Eisai R & D Management Co., Ltd. | Azaindoles as inhibitors of c-Jun N-terminal kinases |
EP1490364B1 (en) | 2002-03-28 | 2007-09-26 | Eisai R&D Management Co., Ltd. | 7-azaindoles as inhibitors of c-jun n-terminal kinases for the treatment of neurodegenerative disorders |
AU2003231950A1 (en) * | 2002-05-30 | 2003-12-19 | Celgene Corporation | Modulating cell differentiation and treating myeloproliferative disorders with JNK/MKK inhibitors |
AU2003241925A1 (en) | 2002-05-31 | 2003-12-19 | Eisai R&D Management Co., Ltd. | Pyrazole compound and medicinal composition containing the same |
CA2487948A1 (en) | 2002-06-14 | 2003-12-24 | Applied Research Systems Ars Holding N.V. | Azole methylidene cyanide derivatives and their use as protein kinase modulators |
ZA200504898B (en) * | 2002-12-20 | 2006-11-29 | Pharmacia Corp | Acyclic pyrazole compounds |
GB0305142D0 (en) | 2003-03-06 | 2003-04-09 | Eisai London Res Lab Ltd | Synthesis |
EP1628975A2 (en) | 2003-05-16 | 2006-03-01 | Eisai Co., Ltd. | Jnk inhibitors |
US7504401B2 (en) | 2003-08-29 | 2009-03-17 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
BRPI0415773A (pt) | 2003-10-24 | 2006-12-26 | Schering Ag | derivados de indolinona e sua aplicação no tratamento de estados de doença tais como cáncer |
US20060094753A1 (en) | 2004-10-29 | 2006-05-04 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases for the treatment of glaucomatous retinopathy and ocular diseases |
GT200500321A (es) | 2004-11-09 | 2006-09-04 | Compuestos y composiciones como inhibidores de proteina kinase. | |
KR20080044836A (ko) | 2005-07-15 | 2008-05-21 | 라보라뚜와르 세로노 에스. 에이. | 자궁내막증 치료용 jnk 억제제 |
BRPI0613042A2 (pt) | 2005-07-15 | 2010-12-14 | Serono Lab | inibidores de jnk para o tratamento de endometriose |
GB0516156D0 (en) | 2005-08-05 | 2005-09-14 | Eisai London Res Lab Ltd | JNK inhibitors |
EP1932840B1 (en) | 2005-10-03 | 2014-04-09 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic compound and pharmaceutical application thereof |
DK3031909T3 (da) | 2005-10-13 | 2021-11-22 | Celularity Inc | Immuno modulering ved brug af placentastamceller |
KR20080097190A (ko) | 2005-12-29 | 2008-11-04 | 안트로제네시스 코포레이션 | 태반 줄기세포의 수집과 보존을 위한 개선된 조성물과 이조성물의 이용 방법 |
CN101688177A (zh) | 2007-02-12 | 2010-03-31 | 人类起源公司 | 来自贴壁胎盘干细胞的肝细胞和软骨细胞;以及cd34+、cd45-胎盘干细胞富集的细胞群 |
CN103356710A (zh) | 2007-02-12 | 2013-10-23 | 人类起源公司 | 利用胎盘干细胞治疗炎性疾病 |
US9707562B2 (en) | 2013-03-13 | 2017-07-18 | Denovo Sciences, Inc. | System for capturing and analyzing cells |
RU2015143526A (ru) * | 2013-03-13 | 2017-04-19 | Бостон Байомедикал, Инк. | Производные 3-(арил или гетероарил)метилениндолин-2-она в качестве ингибиторов киназного пути раковых стволовых клеток для лечения рака |
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TWI826690B (zh) * | 2019-05-23 | 2023-12-21 | 美商基利科學股份有限公司 | 經取代之烯吲哚酮化物及其用途 |
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-
1999
- 1999-12-09 EP EP99966933A patent/EP1149093A1/en not_active Withdrawn
- 1999-12-09 TR TR2001/01858T patent/TR200101858T2/tr unknown
- 1999-12-09 AU AU22815/00A patent/AU760039B2/en not_active Ceased
- 1999-12-09 BR BR9916223-7A patent/BR9916223A/pt not_active IP Right Cessation
- 1999-12-09 CN CNB998145858A patent/CN1136217C/zh not_active Expired - Fee Related
- 1999-12-09 KR KR1020017007597A patent/KR20010101266A/ko not_active Application Discontinuation
- 1999-12-09 CA CA002354591A patent/CA2354591A1/en not_active Abandoned
- 1999-12-09 WO PCT/EP1999/009673 patent/WO2000035909A1/en not_active Application Discontinuation
- 1999-12-09 JP JP2000588169A patent/JP2002532493A/ja active Pending
- 1999-12-15 US US09/464,466 patent/US6307056B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CA2354591A1 (en) | 2000-06-22 |
EP1149093A1 (en) | 2001-10-31 |
AU760039B2 (en) | 2003-05-08 |
KR20010101266A (ko) | 2001-11-14 |
JP2002532493A (ja) | 2002-10-02 |
BR9916223A (pt) | 2001-09-04 |
CN1136217C (zh) | 2004-01-28 |
US6307056B1 (en) | 2001-10-23 |
WO2000035909A1 (en) | 2000-06-22 |
CN1330648A (zh) | 2002-01-09 |
AU2281500A (en) | 2000-07-03 |
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