ATE234830T1 - 4-alkenyl (und alkinyl)oxoindole als inhibitoren cyclinabhängiger kinasen, insbesondere cdk2 - Google Patents
4-alkenyl (und alkinyl)oxoindole als inhibitoren cyclinabhängiger kinasen, insbesondere cdk2Info
- Publication number
- ATE234830T1 ATE234830T1 AT99963422T AT99963422T ATE234830T1 AT E234830 T1 ATE234830 T1 AT E234830T1 AT 99963422 T AT99963422 T AT 99963422T AT 99963422 T AT99963422 T AT 99963422T AT E234830 T1 ATE234830 T1 AT E234830T1
- Authority
- AT
- Austria
- Prior art keywords
- oxoindoles
- alkinyl
- cyclin
- alkenyl
- 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
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11259198P | 1998-12-17 | 1998-12-17 | |
US14907399P | 1999-08-16 | 1999-08-16 | |
PCT/EP1999/009624 WO2000035908A1 (en) | 1998-12-17 | 1999-12-08 | 4-alkenyl (and alkynyl) oxindoles as inhibitors of cyclin-dependent kinases, in particular cdk2 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE234830T1 true ATE234830T1 (de) | 2003-04-15 |
Family
ID=26810131
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT99963422T ATE234830T1 (de) | 1998-12-17 | 1999-12-08 | 4-alkenyl (und alkinyl)oxoindole als inhibitoren cyclinabhängiger kinasen, insbesondere cdk2 |
Country Status (20)
Country | Link |
---|---|
US (3) | US6130239A (de) |
EP (1) | EP1157019B1 (de) |
JP (1) | JP2002532492A (de) |
KR (1) | KR100649925B1 (de) |
CN (1) | CN1138773C (de) |
AR (1) | AR024847A1 (de) |
AT (1) | ATE234830T1 (de) |
AU (1) | AU770375B2 (de) |
BR (1) | BR9916327A (de) |
CA (1) | CA2354873A1 (de) |
CO (1) | CO5261600A1 (de) |
DE (1) | DE69906152T2 (de) |
DK (1) | DK1157019T3 (de) |
ES (1) | ES2192877T3 (de) |
PE (1) | PE20001537A1 (de) |
PT (1) | PT1157019E (de) |
TR (1) | TR200101860T2 (de) |
TW (1) | TW550262B (de) |
UY (1) | UY25857A1 (de) |
WO (1) | WO2000035908A1 (de) |
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 |
JP2002532492A (ja) * | 1998-12-17 | 2002-10-02 | エフ.ホフマン−ラ ロシュ アーゲー | サイクリン−依存性キナーゼ、特にcdk2のインヒビターとしての4−アルケニル(及びアルキニル)オキシドール |
US6878733B1 (en) | 1999-11-24 | 2005-04-12 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
ATE514676T1 (de) * | 1999-11-24 | 2011-07-15 | Sugen Inc | Ionisierbare indolinon derivate und deren verwendung als ptk liganden |
MXPA02006263A (es) * | 1999-12-22 | 2004-02-26 | Sugen Inc | Metodos de modulacion de la funcion de la cinasa de tirosina c-kit de la proteina con compuestos de indolinona. |
ME00415B (me) * | 2000-02-15 | 2011-10-10 | Pharmacia & Upjohn Co Llc | Pirol supstituisani 2-indol protein kinazni inhibitori |
EP1272483A2 (de) * | 2000-03-24 | 2003-01-08 | Millenium Pharmaceuticals, Inc. | Oxindole als faktor xa inhibitoren |
TWI270545B (en) | 2000-05-24 | 2007-01-11 | Sugen Inc | Mannich base prodrugs of 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
AU2001268154A1 (en) | 2000-06-02 | 2001-12-17 | 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 |
EA006445B9 (ru) * | 2001-08-15 | 2017-02-28 | Фармация Энд Апджон Компани | Кристаллы, содержащие соль яблочной кислоты n-[2-(диэтиламино)этил]-5-[(5-фторо-2-оксо-1,2-дигидро-3h-индол-3-илиден)метил]-2,4-диметил-1h-пиррол-3-карбоксамида, способы их получения и их композиции |
WO2003031438A1 (en) | 2001-10-10 | 2003-04-17 | Sugen, Inc. | 3-[4-(substituted heterocyclyl)-pyrrol-2-ylmethylidene]-2-indolinone derivatives as kinase inhibitors |
EP1458713B1 (de) * | 2001-12-27 | 2005-08-24 | Theravance, Inc. | Indolinon-derivative als protein-kinasehemmer |
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 |
MX2020002944A (es) | 2017-09-14 | 2020-09-28 | Daiichi Sankyo Co Ltd | Compuesto que tiene estructura ciclica. |
AR124154A1 (es) | 2020-11-27 | 2023-02-22 | Rhizen Pharmaceuticals Ag | Inhibidores de cdk |
WO2022149057A1 (en) | 2021-01-05 | 2022-07-14 | Rhizen Pharmaceuticals Ag | Cdk inhibitors |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
WO1991001306A1 (fr) * | 1989-07-25 | 1991-02-07 | Taiho Pharmaceutical Company, Limited | Derive oxoindole |
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 |
EP0850055B1 (de) * | 1995-09-11 | 2005-06-29 | Osteoarthritis Sciences, Inc. | Proteintyrosine-kinaseinhibitoren zur behandlung der osteoarthritis |
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 (de) * | 1996-08-23 | 2002-10-16 | Sugen, Inc. | Indolinon-Verbindungen und deren Verwendung als Protein- Kinase-Modulatoren |
WO1998024432A2 (en) * | 1996-12-05 | 1998-06-11 | Sugen, Inc. | Use of indolinone compounds as modulators of protein kinases |
JP2002511852A (ja) * | 1997-05-07 | 2002-04-16 | スージェン・インコーポレーテッド | 蛋白質キナーゼ活性の調節剤としての2−インドリノン誘導体 |
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 |
EP1066257A2 (de) * | 1998-03-26 | 2001-01-10 | Sugen, Inc. | Heterozyklische stoffklassen für die modulation der tyrosine protein kinase |
TR200003514T2 (tr) * | 1998-05-29 | 2002-05-21 | Sugen Inc. | Pirol ikame edilmiş 2-indolinon protein kinaz inhibitörleri |
AU5468499A (en) * | 1998-08-04 | 2000-02-28 | Sugen, Inc. | 3-methylidenyl-2-indolinone modulators of protein kinase |
US6525072B1 (en) * | 1998-08-31 | 2003-02-25 | Sugen, Inc. | Geometrically restricted 2-indolinone derivatives as modulators of protein kinase activity |
JP2002532492A (ja) * | 1998-12-17 | 2002-10-02 | エフ.ホフマン−ラ ロシュ アーゲー | サイクリン−依存性キナーゼ、特にcdk2のインヒビターとしての4−アルケニル(及びアルキニル)オキシドール |
-
1999
- 1999-12-08 JP JP2000588168A patent/JP2002532492A/ja active Pending
- 1999-12-08 ES ES99963422T patent/ES2192877T3/es not_active Expired - Lifetime
- 1999-12-08 CA CA002354873A patent/CA2354873A1/en not_active Abandoned
- 1999-12-08 AU AU19727/00A patent/AU770375B2/en not_active Ceased
- 1999-12-08 BR BR9916327-6A patent/BR9916327A/pt not_active Application Discontinuation
- 1999-12-08 DE DE69906152T patent/DE69906152T2/de not_active Expired - Fee Related
- 1999-12-08 PT PT99963422T patent/PT1157019E/pt unknown
- 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 TR TR2001/01860T patent/TR200101860T2/xx unknown
- 1999-12-08 CN CNB998145246A patent/CN1138773C/zh not_active Expired - Fee Related
- 1999-12-08 WO PCT/EP1999/009624 patent/WO2000035908A1/en active IP Right Grant
- 1999-12-08 DK DK99963422T patent/DK1157019T3/da active
- 1999-12-08 EP EP99963422A patent/EP1157019B1/de not_active Expired - Lifetime
- 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 UY UY25857A patent/UY25857A1/es not_active Application Discontinuation
- 1999-12-16 TW TW088122068A patent/TW550262B/zh active
-
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 |
---|---|
DK1157019T3 (da) | 2003-07-14 |
US6303793B1 (en) | 2001-10-16 |
AU1972700A (en) | 2000-07-03 |
AU770375B2 (en) | 2004-02-19 |
EP1157019B1 (de) | 2003-03-19 |
CN1138773C (zh) | 2004-02-18 |
UY25857A1 (es) | 2001-07-31 |
US6252086B1 (en) | 2001-06-26 |
JP2002532492A (ja) | 2002-10-02 |
PT1157019E (pt) | 2003-06-30 |
TW550262B (en) | 2003-09-01 |
BR9916327A (pt) | 2001-09-18 |
PE20001537A1 (es) | 2001-01-09 |
DE69906152T2 (de) | 2004-02-12 |
US6130239A (en) | 2000-10-10 |
CO5261600A1 (es) | 2003-03-31 |
CN1330647A (zh) | 2002-01-09 |
ES2192877T3 (es) | 2003-10-16 |
KR20010101274A (ko) | 2001-11-14 |
KR100649925B1 (ko) | 2007-02-28 |
WO2000035908A1 (en) | 2000-06-22 |
EP1157019A1 (de) | 2001-11-28 |
TR200101860T2 (tr) | 2001-12-21 |
CA2354873A1 (en) | 2000-06-22 |
DE69906152D1 (de) | 2003-04-24 |
AR024847A1 (es) | 2002-10-30 |
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