TR200101860T2 - Sikline bağlı kinaz inhibitörleri olarak 4-alkenil (ve alkinil) oksidoller - Google Patents
Sikline bağlı kinaz inhibitörleri olarak 4-alkenil (ve alkinil) oksidollerInfo
- Publication number
- TR200101860T2 TR200101860T2 TR2001/01860T TR200101860T TR200101860T2 TR 200101860 T2 TR200101860 T2 TR 200101860T2 TR 2001/01860 T TR2001/01860 T TR 2001/01860T TR 200101860 T TR200101860 T TR 200101860T TR 200101860 T2 TR200101860 T2 TR 200101860T2
- Authority
- TR
- Turkey
- Prior art keywords
- cyclin
- alkynyl
- alkenyl
- oxidols
- kinase inhibitors
- Prior art date
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
- C07D401/14—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
- A61K31/403—Heterocyclic 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
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- 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
-
- 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
Abstract
R1,R2,R3,a,b ve X tarifnamede tanimlandiklari gibi olmak üzere, asagidaki (I) ve (II) formüllerine sahip yeni 4-alkenil-ve 4-alkinil oksindoller ve bunlarin, ilaç sanayiinde kullanilmaya uygun tuzlari, sikline bagli kinazlari (CDK'lar) özellikle CDK2'yi önlemektedir ve bunlar, hücre çogalmasina bagli bozukluklarin, özellikle de gügüs ve kalin bagirsak tümörlerinin tedavi edilmesinde ya da kontrol altina alinmasinda, hücre çogalmasini önleyici etkenler olarak yararlidir.(FORMÜL VAR)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11259198P | 1998-12-17 | 1998-12-17 | |
US14907399P | 1999-08-16 | 1999-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
TR200101860T2 true TR200101860T2 (tr) | 2001-12-21 |
Family
ID=26810131
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TR2001/01860T TR200101860T2 (tr) | 1998-12-17 | 1999-12-08 | Sikline bağlı kinaz inhibitörleri olarak 4-alkenil (ve alkinil) oksidoller |
Country Status (20)
Country | Link |
---|---|
US (3) | US6130239A (tr) |
EP (1) | EP1157019B1 (tr) |
JP (1) | JP2002532492A (tr) |
KR (1) | KR100649925B1 (tr) |
CN (1) | CN1138773C (tr) |
AR (1) | AR024847A1 (tr) |
AT (1) | ATE234830T1 (tr) |
AU (1) | AU770375B2 (tr) |
BR (1) | BR9916327A (tr) |
CA (1) | CA2354873A1 (tr) |
CO (1) | CO5261600A1 (tr) |
DE (1) | DE69906152T2 (tr) |
DK (1) | DK1157019T3 (tr) |
ES (1) | ES2192877T3 (tr) |
PE (1) | PE20001537A1 (tr) |
PT (1) | PT1157019E (tr) |
TR (1) | TR200101860T2 (tr) |
TW (1) | TW550262B (tr) |
UY (1) | UY25857A1 (tr) |
WO (1) | WO2000035908A1 (tr) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6569868B2 (en) | 1998-04-16 | 2003-05-27 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
BR9916327A (pt) * | 1998-12-17 | 2001-09-18 | Hoffmann La Roche | Oxindóis de 4-alquenila (e alquinila) como inibidores de cinases dependentes de ciclina, em particular, cdk2 |
US6878733B1 (en) | 1999-11-24 | 2005-04-12 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
WO2001037820A2 (en) * | 1999-11-24 | 2001-05-31 | Sugen, Inc. | Ionizable indolinone derivatives and their use as ptk ligands |
CA2395461C (en) * | 1999-12-22 | 2010-05-25 | Sugen, Inc. | Methods of modulating c-kit tyrosine kinase function with indolinone compounds |
CA2399358C (en) * | 2000-02-15 | 2006-03-21 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
EP1272483A2 (en) * | 2000-03-24 | 2003-01-08 | Millenium Pharmaceuticals, Inc. | OXINDOLE INHIBITORS OF FACTOR Xa |
MY128450A (en) | 2000-05-24 | 2007-02-28 | Upjohn Co | 1-(pyrrolidin-1-ylmethyl)-3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
EP1294688A2 (en) | 2000-06-02 | 2003-03-26 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
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 |
US6504034B2 (en) | 2001-01-23 | 2003-01-07 | Hoffmann-La Roche Inc. | Naphthostyrils |
AR042586A1 (es) * | 2001-02-15 | 2005-06-29 | Sugen Inc | 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa |
FR2822155B1 (fr) | 2001-03-13 | 2003-12-12 | Aventis Pharma Sa | Composes derives des oxindoles et leur application therapeutique en cancerologie |
RS53251B (sr) * | 2001-08-15 | 2014-08-29 | Pharmacia & Upjohn Company Llc | Kristali koji sadrže n-[2-dietilamino)etil]-5-[(5-fluoro-2-okso-3h-indol-3-iliden)metil]-2,4-dimetil-1h-pirol-3- karboksamid so jabučne kiseline, procesi za njihovu pripremu i njihovi preparati |
JP2005508953A (ja) | 2001-10-10 | 2005-04-07 | スージェン・インコーポレーテッド | キナーゼ阻害剤としての3−[4−(置換ヘテロサイクリル)−ピロール−2−イルメチリデン]−2−インドリノン誘導体 |
AU2002360753B2 (en) * | 2001-12-27 | 2008-08-21 | Theravance, Inc. | Indolinone derivatives useful as protein kinase inhibitors |
FR2948940B1 (fr) * | 2009-08-04 | 2011-07-22 | Servier Lab | Nouveaux derives dihydroindolones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
WO2012178015A2 (en) * | 2011-06-24 | 2012-12-27 | Zenobia Therapeutics, Inc. | Lrrk2 inhibitors |
CN106187904B (zh) * | 2015-05-25 | 2021-07-06 | 中国医学科学院药物研究所 | 含丙炔酰胺基的2-苯基咪唑类衍生物及其制法和药物组合物与用途 |
UA126589C2 (uk) | 2017-09-14 | 2022-11-02 | Даїті Санкіо Компані, Лімітед | Сполука, яка має циклічну структуру |
TW202237585A (zh) | 2020-11-27 | 2022-10-01 | 瑞士商瑞森製藥公司 | Cdk抑制劑 |
WO2022149057A1 (en) | 2021-01-05 | 2022-07-14 | Rhizen Pharmaceuticals Ag | Cdk inhibitors |
Family Cites Families (31)
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US4556672A (en) * | 1984-03-19 | 1985-12-03 | Pfizer Inc. | 3-Substituted 2-oxindole-1-carboxamides as analgesic and anti-inflammatory agents |
US5086186A (en) * | 1989-05-25 | 1992-02-04 | Pfizer Inc. | N-trichloroacetyl-2-oxindole-1-carboxamides |
EP0429685B1 (en) * | 1989-07-25 | 1997-10-29 | Taiho Pharmaceutical Company, Limited | Oxoindole derivative |
WO1991009598A1 (en) * | 1990-01-05 | 1991-07-11 | Pfizer Inc. | Azaoxindole derivatives |
GB9004483D0 (en) * | 1990-02-28 | 1990-04-25 | Erba Carlo Spa | New aryl-and heteroarylethenylene derivatives and process for their preparation |
WO1992007830A2 (en) * | 1990-10-29 | 1992-05-14 | Pfizer Inc. | Oxindole peptide antagonists |
GB9115160D0 (en) * | 1991-07-12 | 1991-08-28 | Erba Carlo Spa | Methylen-oxindole derivatives and process for their preparation |
US5322950A (en) * | 1991-12-05 | 1994-06-21 | Warner-Lambert Company | Imidazole with angiotensin II antagonist properties |
FR2694004B1 (fr) * | 1992-07-21 | 1994-08-26 | Adir | Nouvelles 3-(Hydroxybenzylidényl)-indoline-2-ones et 3-(hydroxybenzylidényl)-indoline-2-thiones, leurs procédés de préparation, et les compositions pharmaceutiques qui les contiennent. |
GB9226855D0 (en) * | 1992-12-23 | 1993-02-17 | Erba Carlo Spa | Vinylene-azaindole derivatives and process for their preparation |
GB9313638D0 (en) * | 1993-07-01 | 1993-08-18 | Erba Carlo Spa | Arylidene and heteroarylidene oxindole derivatives and process for their preparation |
GB9326136D0 (en) * | 1993-12-22 | 1994-02-23 | Erba Carlo Spa | Biologically active 3-substituted oxindole derivatives useful as anti-angiogenic agents |
GB9412719D0 (en) * | 1994-06-24 | 1994-08-17 | Erba Carlo Spa | Substituted azaindolylidene compounds and process for their preparation |
GB9423997D0 (en) * | 1994-11-28 | 1995-01-11 | Erba Carlo Spa | Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation |
GB9501567D0 (en) * | 1995-01-26 | 1995-03-15 | Pharmacia Spa | Hydrosoluble 3-arylidene-2-oxindole derivatives as tyrosine kinase inhibitors |
GB9507298D0 (en) * | 1995-04-07 | 1995-05-31 | Pharmacia Spa | Substituted indolylmethylene-oxindale analogues as tyrosine kinase inhibitors |
US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
JPH11512708A (ja) * | 1995-09-11 | 1999-11-02 | オステオアルスリィティス サイエンシズ,インコーポレイテッド | 変形性関節炎を治療するためのプロテインチロシンキナーゼインヒビター |
US5733920A (en) * | 1995-10-31 | 1998-03-31 | Mitotix, Inc. | Inhibitors of cyclin dependent kinases |
GB9610964D0 (en) * | 1996-05-24 | 1996-07-31 | Pharmacia & Upjohn Spa | Substituted tetralylmethylen-oxindole analogues as tyrosine kinase inhibitors |
GB9611797D0 (en) * | 1996-06-06 | 1996-08-07 | Pharmacia Spa | Substituted quinolylmethylen-oxindole analogues as tyrosine kinase inhibitors |
EP1247803A3 (en) * | 1996-08-23 | 2002-10-16 | Sugen, Inc. | Indolinone compounds suitable for modulation of protein kinases |
AU7622698A (en) * | 1996-12-05 | 1998-06-29 | Sugen, Inc. | Use of indolinone compounds as modulators of protein kinases |
CA2289102A1 (en) * | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
GB9716557D0 (en) * | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
WO2000008202A2 (en) * | 1998-08-04 | 2000-02-17 | Sugen, Inc. | 3-methylidenyl-2-indolinone modulators of protein kinase |
JP2002507598A (ja) * | 1998-03-26 | 2002-03-12 | スージェン・インコーポレーテッド | チロシン蛋白質キナーゼを調節するためのヘテロ環式化合物のファミリー |
HUP0103617A2 (hu) * | 1998-05-29 | 2002-02-28 | Sugen, Inc. | Protein kinázt gátló, pirrolilcsoporttal helyettesített 2-indolszármazékok, e vegyületeket tartalmazó gyógyászati készítmények, valamint e vegyületek alkalmazása |
WO2000012084A1 (en) * | 1998-08-31 | 2000-03-09 | Sugen, Inc. | Geometrically restricted 2-indolinone derivatives as modulators of protein kinase activity |
BR9916327A (pt) * | 1998-12-17 | 2001-09-18 | Hoffmann La Roche | Oxindóis de 4-alquenila (e alquinila) como inibidores de cinases dependentes de ciclina, em particular, cdk2 |
-
1999
- 1999-12-08 BR BR9916327-6A patent/BR9916327A/pt not_active Application Discontinuation
- 1999-12-08 ES ES99963422T patent/ES2192877T3/es not_active Expired - Lifetime
- 1999-12-08 JP JP2000588168A patent/JP2002532492A/ja active Pending
- 1999-12-08 AU AU19727/00A patent/AU770375B2/en not_active Ceased
- 1999-12-08 TR TR2001/01860T patent/TR200101860T2/tr unknown
- 1999-12-08 CA CA002354873A patent/CA2354873A1/en not_active Abandoned
- 1999-12-08 KR KR1020017007610A patent/KR100649925B1/ko not_active IP Right Cessation
- 1999-12-08 AT AT99963422T patent/ATE234830T1/de not_active IP Right Cessation
- 1999-12-08 CN CNB998145246A patent/CN1138773C/zh not_active Expired - Fee Related
- 1999-12-08 DE DE69906152T patent/DE69906152T2/de not_active Expired - Fee Related
- 1999-12-08 DK DK99963422T patent/DK1157019T3/da active
- 1999-12-08 EP EP99963422A patent/EP1157019B1/en not_active Expired - Lifetime
- 1999-12-08 WO PCT/EP1999/009624 patent/WO2000035908A1/en active IP Right Grant
- 1999-12-08 PT PT99963422T patent/PT1157019E/pt unknown
- 1999-12-14 PE PE1999001251A patent/PE20001537A1/es not_active Application Discontinuation
- 1999-12-14 CO CO99078069A patent/CO5261600A1/es not_active Application Discontinuation
- 1999-12-15 US US09/464,502 patent/US6130239A/en not_active Expired - Fee Related
- 1999-12-15 AR ARP990106414A patent/AR024847A1/es not_active Application Discontinuation
- 1999-12-16 TW TW088122068A patent/TW550262B/zh active
- 1999-12-16 UY UY25857A patent/UY25857A1/es not_active Application Discontinuation
-
2000
- 2000-04-14 US US09/549,864 patent/US6252086B1/en not_active Expired - Fee Related
- 2000-05-05 US US09/566,054 patent/US6303793B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP1157019B1 (en) | 2003-03-19 |
CN1138773C (zh) | 2004-02-18 |
CO5261600A1 (es) | 2003-03-31 |
PT1157019E (pt) | 2003-06-30 |
BR9916327A (pt) | 2001-09-18 |
UY25857A1 (es) | 2001-07-31 |
US6303793B1 (en) | 2001-10-16 |
KR20010101274A (ko) | 2001-11-14 |
EP1157019A1 (en) | 2001-11-28 |
ATE234830T1 (de) | 2003-04-15 |
CN1330647A (zh) | 2002-01-09 |
AU1972700A (en) | 2000-07-03 |
KR100649925B1 (ko) | 2007-02-28 |
WO2000035908A1 (en) | 2000-06-22 |
AR024847A1 (es) | 2002-10-30 |
ES2192877T3 (es) | 2003-10-16 |
PE20001537A1 (es) | 2001-01-09 |
US6252086B1 (en) | 2001-06-26 |
JP2002532492A (ja) | 2002-10-02 |
AU770375B2 (en) | 2004-02-19 |
DK1157019T3 (da) | 2003-07-14 |
CA2354873A1 (en) | 2000-06-22 |
DE69906152T2 (de) | 2004-02-12 |
TW550262B (en) | 2003-09-01 |
DE69906152D1 (de) | 2003-04-24 |
US6130239A (en) | 2000-10-10 |
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