TW200728276A - Oxindole derivatives - Google Patents
Oxindole derivativesInfo
- Publication number
- TW200728276A TW200728276A TW095122208A TW95122208A TW200728276A TW 200728276 A TW200728276 A TW 200728276A TW 095122208 A TW095122208 A TW 095122208A TW 95122208 A TW95122208 A TW 95122208A TW 200728276 A TW200728276 A TW 200728276A
- Authority
- TW
- Taiwan
- Prior art keywords
- compounds
- oxindole derivatives
- cancer
- manufacture
- general formula
- 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
- A61K31/4015—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 having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
-
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- 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
- C07D209/30—Indoles; 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
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69375205P | 2005-06-24 | 2005-06-24 | |
US79561606P | 2006-04-27 | 2006-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200728276A true TW200728276A (en) | 2007-08-01 |
Family
ID=37114613
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW095122208A TW200728276A (en) | 2005-06-24 | 2006-06-21 | Oxindole derivatives |
Country Status (16)
Country | Link |
---|---|
US (1) | US7576082B2 (zh) |
EP (1) | EP1896412A2 (zh) |
JP (1) | JP2008543917A (zh) |
KR (1) | KR100990344B1 (zh) |
CN (1) | CN101203489B (zh) |
AR (1) | AR054799A1 (zh) |
AU (1) | AU2006260934B2 (zh) |
BR (1) | BRPI0612535A2 (zh) |
CA (1) | CA2612451A1 (zh) |
DO (1) | DOP2006000141A (zh) |
IL (1) | IL188039A0 (zh) |
MX (1) | MX2007016038A (zh) |
PA (1) | PA8680701A1 (zh) |
TW (1) | TW200728276A (zh) |
UY (1) | UY29633A1 (zh) |
WO (1) | WO2006136606A2 (zh) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008034736A2 (en) * | 2006-09-21 | 2008-03-27 | F. Hoffmann-La Roche Ag | Oxindole derivatives as anticancer agents |
PE20081897A1 (es) | 2007-03-29 | 2009-02-09 | Novartis Ag | 3-imidazolil-indoles para el tratamiento de enfermedades proliferativas |
WO2009011872A1 (en) | 2007-07-17 | 2009-01-22 | Merck & Co., Inc. | Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment |
JO2704B1 (en) * | 2007-09-21 | 2013-03-03 | جانسين فارماسوتيكا ان في | Interference inhibition factors between MD2 and B53 |
US7928233B2 (en) * | 2009-02-10 | 2011-04-19 | Hoffmann-La Roche Inc. | Spiroindolinone pyridine derivatives |
WO2010109008A1 (en) | 2009-03-26 | 2010-09-30 | Topotarget A/S | Prodrugs of substituted 3-(4-hydroxyphenyl)-indolin-2-ones |
WO2011060049A2 (en) * | 2009-11-12 | 2011-05-19 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
US8088815B2 (en) | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
US8288431B2 (en) | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
WO2011106650A2 (en) * | 2010-02-27 | 2011-09-01 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Novel p53-mdm2/p53-mdm4 antagonists to treat proliferative disease |
US8217044B2 (en) | 2010-04-28 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone pyrrolidines |
FR2967072B1 (fr) | 2010-11-05 | 2013-03-29 | Univ Dundee | Procede pour ameliorer la production de virus et semences vaccinales influenza |
CN103298818B (zh) | 2010-11-12 | 2016-06-29 | 密歇根大学董事会 | 螺-吲哚酮mdm2拮抗剂 |
CN103380125B (zh) | 2010-12-21 | 2015-11-25 | 拜耳知识产权有限责任公司 | 制备三嗪基取代的羟吲哚的方法 |
CN103502218B (zh) | 2011-03-04 | 2016-08-17 | 生命科技公司 | 用于缀合生物分子的化合物和方法 |
SG10201601802YA (en) | 2011-03-10 | 2016-04-28 | Daiichi Sankyo Co Ltd | Dispiropyrrolidine derivatives |
CN103717605B (zh) | 2011-05-11 | 2016-05-18 | 密执安州立大学董事会 | 螺-羟吲哚mdm2拮抗剂 |
US9365576B2 (en) | 2012-05-24 | 2016-06-14 | Novartis Ag | Pyrrolopyrrolidinone compounds |
TWI586668B (zh) | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
TW201429969A (zh) | 2012-12-20 | 2014-08-01 | Merck Sharp & Dohme | 作爲hdm2抑制劑之經取代咪唑吡啶 |
WO2014115080A1 (en) | 2013-01-22 | 2014-07-31 | Novartis Ag | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction |
EP2948451B1 (en) | 2013-01-22 | 2017-07-12 | Novartis AG | Substituted purinone compounds |
JO3383B1 (ar) * | 2013-03-14 | 2019-03-13 | Lilly Co Eli | مثبطات cdc7 |
JP6373978B2 (ja) | 2013-05-27 | 2018-08-15 | ノバルティス アーゲー | イミダゾピロリジノン誘導体および疾患の処置におけるその使用 |
WO2014191911A1 (en) | 2013-05-28 | 2014-12-04 | Novartis Ag | Pyrazolo-pyrrolidin-4-one derivatives and their use in the treatment of disease |
WO2014191906A1 (en) | 2013-05-28 | 2014-12-04 | Novartis Ag | Pyrazolo-pyrrolidin-4-one derivatives as bet inhibitors and their use in the treatment of disease |
CA2931249A1 (en) | 2013-11-21 | 2015-05-28 | Novartis Ag | Pyrrolopyrrolone derivatives and their use as bet inhibitors |
US9718775B2 (en) | 2014-03-14 | 2017-08-01 | Milliken & Company | Oxindole compounds and compositions comprising the same |
CN107427501B (zh) | 2015-02-20 | 2023-12-01 | 第一三共株式会社 | 通过联合使用治疗癌症的方法 |
WO2016167236A1 (ja) | 2015-04-13 | 2016-10-20 | 第一三共株式会社 | Mdm2阻害剤とbtk阻害剤との併用治療法 |
EP3440082A1 (en) | 2016-04-06 | 2019-02-13 | The Regents of The University of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
UA123786C2 (uk) | 2016-04-06 | 2021-06-02 | Дзе Ріджентс Оф Дзе Юніверсіті Оф Мічіган | Деструктори білка mdm2 |
JP6991585B2 (ja) | 2016-05-02 | 2022-01-12 | ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン | メニン阻害剤としてのピペリジン |
EP3458101B1 (en) | 2016-05-20 | 2020-12-30 | H. Hoffnabb-La Roche Ag | Protac antibody conjugates and methods of use |
TW201818934A (zh) | 2016-10-17 | 2018-06-01 | 日商第一三共股份有限公司 | Mdm2抑制劑與dna甲基轉移酶抑制劑之倂用治療法 |
EP3600313A4 (en) | 2017-03-31 | 2020-09-23 | The Regents of The University of Michigan | PIPERIDINES AS COVALENT MENINE INHIBITORS |
CN108610277A (zh) * | 2018-03-20 | 2018-10-02 | 贵州大学 | 3-叔胺四取代氧化吲哚化合物及其制备方法 |
JP2022504541A (ja) | 2018-10-08 | 2022-01-13 | ザ リージェンツ オブ ザ ユニバーシティー オブ ミシガン | 低分子mdm2タンパク質デグレーダー |
KR20230005160A (ko) | 2020-03-19 | 2023-01-09 | 카이메라 쎄라퓨틱스 인코포레이티드 | Mdm2 분해제 및 이의 용도 |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
CN113880750B (zh) * | 2021-10-28 | 2023-02-10 | 上海交通大学 | 一种手性3-取代-3-芳基氧化吲哚类化合物的合成方法 |
CN114213396B (zh) * | 2022-01-27 | 2023-03-24 | 深圳市乐土生物医药有限公司 | 一种吲哚-2-酮类化合物及其制备方法与用途 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2759935A (en) | 1953-02-18 | 1956-08-21 | Bristol Lab Inc | Substituted 3-phenyloxindoles |
US3441570A (en) | 1966-01-20 | 1969-04-29 | Parke Davis & Co | 3-tertiary aminoalkylamino-3-phenyl oxindole compounds |
US3686210A (en) | 1970-01-13 | 1972-08-22 | American Home Prod | 2-acylamido-3-aryl-3h-indol-3-ol esters and related compounds |
GB1494340A (en) * | 1974-12-03 | 1977-12-07 | Wyeth John & Brother Ltd | Process for preparation of substituted n-phenylcarbamate esters |
US4020179A (en) | 1975-05-15 | 1977-04-26 | Richardson-Merrell Inc. | 7-Substituted-2-indolinones |
JPS55129284A (en) | 1979-03-27 | 1980-10-06 | Shionogi & Co Ltd | 3-(1-imipazolyl)indolin-2-one |
US5565483A (en) * | 1995-06-07 | 1996-10-15 | Bristol-Myers Squibb Company | 3-substituted oxindole derivatives as potassium channel modulators |
JP3748935B2 (ja) * | 1996-03-18 | 2006-02-22 | 大鵬薬品工業株式会社 | オキシインドール誘導体 |
AU3460797A (en) | 1996-07-16 | 1998-02-09 | Takeda Chemical Industries Ltd. | Bicyclic compounds for controlling micturition |
WO1998054167A1 (fr) | 1997-05-28 | 1998-12-03 | Mitsubishi-Tokyo Pharmaceuticals, Inc. | Composes d'indole |
US6511974B1 (en) | 1997-07-30 | 2003-01-28 | Wyeth | Tricyclic vasopressin agonists |
JP2000191661A (ja) | 1998-12-25 | 2000-07-11 | Mitsubishi-Tokyo Pharmaceuticals Inc | 環状アミド化合物 |
EP1183033B1 (en) | 1999-05-21 | 2006-03-01 | Bristol-Myers Squibb Company | Pyrrolotriazine inhibitors of kinases |
FR2804114B1 (fr) | 2000-01-25 | 2002-03-08 | Sanofi Synthelabo | Nouveaux derives de 1,3-dihydro-2h-indol-2-one, un procede pour leur preparation et les compositions pharmaceutiques en contenant |
FR2827604B1 (fr) | 2001-07-17 | 2003-09-19 | Sanofi Synthelabo | Nouveaux derives de 1-phenylsulfonyl-1,3-dihydro-2h-indol-2- one, un procede pour leur preparation et les compositions pharmaceutiques en contenant |
US7250442B2 (en) | 2002-03-15 | 2007-07-31 | Eli Lilly And Company | Dihydroindol-2-one derivatives as steroid hormone nuclear receptor modulators |
US8030499B2 (en) | 2005-01-28 | 2011-10-04 | Taisho Pharmaceutical Co., Ltd. | 1,3-dihydro-2H-indole-2-one compound and pyrrolidine-2-one compound fused with aromatic heterocycle |
-
2006
- 2006-06-20 US US11/471,363 patent/US7576082B2/en not_active Expired - Fee Related
- 2006-06-21 PA PA20068680701A patent/PA8680701A1/es unknown
- 2006-06-21 TW TW095122208A patent/TW200728276A/zh unknown
- 2006-06-21 DO DO2006000141A patent/DOP2006000141A/es unknown
- 2006-06-22 CN CN2006800224947A patent/CN101203489B/zh not_active Expired - Fee Related
- 2006-06-22 JP JP2008517511A patent/JP2008543917A/ja not_active Ceased
- 2006-06-22 MX MX2007016038A patent/MX2007016038A/es active IP Right Grant
- 2006-06-22 EP EP06777423A patent/EP1896412A2/en not_active Withdrawn
- 2006-06-22 KR KR1020077030158A patent/KR100990344B1/ko not_active IP Right Cessation
- 2006-06-22 CA CA002612451A patent/CA2612451A1/en not_active Abandoned
- 2006-06-22 AU AU2006260934A patent/AU2006260934B2/en not_active Ceased
- 2006-06-22 BR BRPI0612535-2A patent/BRPI0612535A2/pt not_active IP Right Cessation
- 2006-06-22 WO PCT/EP2006/063475 patent/WO2006136606A2/en not_active Application Discontinuation
- 2006-06-23 AR ARP060102722A patent/AR054799A1/es not_active Application Discontinuation
- 2006-06-27 UY UY29633A patent/UY29633A1/es not_active Application Discontinuation
-
2007
- 2007-12-10 IL IL188039A patent/IL188039A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
KR100990344B1 (ko) | 2010-10-29 |
WO2006136606A3 (en) | 2007-04-26 |
EP1896412A2 (en) | 2008-03-12 |
CA2612451A1 (en) | 2006-12-28 |
US20060293319A1 (en) | 2006-12-28 |
AR054799A1 (es) | 2007-07-18 |
KR20080022117A (ko) | 2008-03-10 |
BRPI0612535A2 (pt) | 2010-11-23 |
AU2006260934B2 (en) | 2012-03-29 |
WO2006136606A2 (en) | 2006-12-28 |
IL188039A0 (en) | 2008-03-20 |
MX2007016038A (es) | 2008-03-10 |
PA8680701A1 (es) | 2007-01-17 |
DOP2006000141A (es) | 2006-12-31 |
UY29633A1 (es) | 2007-01-31 |
CN101203489B (zh) | 2011-08-31 |
US7576082B2 (en) | 2009-08-18 |
JP2008543917A (ja) | 2008-12-04 |
AU2006260934A1 (en) | 2006-12-28 |
CN101203489A (zh) | 2008-06-18 |
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