AR063602A1 - Derivados de espiroindolinona, formulaciones farmaceuticas que los contienen y su uso en la obtencion de un medicamento para el tratamiento de trastornos oncologicos. - Google Patents
Derivados de espiroindolinona, formulaciones farmaceuticas que los contienen y su uso en la obtencion de un medicamento para el tratamiento de trastornos oncologicos.Info
- Publication number
- AR063602A1 AR063602A1 ARP070104959A ARP070104959A AR063602A1 AR 063602 A1 AR063602 A1 AR 063602A1 AR P070104959 A ARP070104959 A AR P070104959A AR P070104959 A ARP070104959 A AR P070104959A AR 063602 A1 AR063602 A1 AR 063602A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- hydrogen
- pharmaceutical formulations
- spiroindolinone
- derivatives
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940126601 medicinal product Drugs 0.000 title 1
- 230000000771 oncological effect Effects 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 150000002431 hydrogen Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 230000001093 anti-cancer Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- -1 nitro, ethynyl Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D209/54—Spiro-condensed
-
- 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
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Los compuestos presentan actividad anticancerígena y se emplean en formulaciones farmacéuticas y en medicamentos. Reivindicación 1: Un compuesto de las fórmulas (1) o (2) en las que X se selecciona del grupo formado por hidrógeno, halógeno, ciano, nitro, etinilo y ciclopropilo; Y es hidrógeno; R1, R2, R3 y R4 se seleccionan del grupo formado por hidrógeno, alquilo inferior, alcoxilo inferior, alquilo inferior sustituido, alquenilo inferior, alquinilo inferior, arilo, arilo sustituido heteroarilo, heteroarilo sustituido, heterociclo, heterociclo sustituido, cicloalquilo, cicloalquilo sustituido, cicloalquenilo y cicloalquenilo sustituido, con la condición de que uno de R1/R2 o de R3/R4 sea hidrógeno y el otro no sea hidrógeno, y las sales y ésteres farmacéuticamente aceptables de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85803906P | 2006-11-09 | 2006-11-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR063602A1 true AR063602A1 (es) | 2009-02-04 |
Family
ID=38942414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070104959A AR063602A1 (es) | 2006-11-09 | 2007-11-07 | Derivados de espiroindolinona, formulaciones farmaceuticas que los contienen y su uso en la obtencion de un medicamento para el tratamiento de trastornos oncologicos. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7638548B2 (es) |
| EP (1) | EP2089360B1 (es) |
| JP (1) | JP2010509260A (es) |
| KR (1) | KR20090095563A (es) |
| CN (1) | CN101535255A (es) |
| AR (1) | AR063602A1 (es) |
| AT (1) | ATE512135T1 (es) |
| AU (1) | AU2007316740A1 (es) |
| CA (1) | CA2668398A1 (es) |
| CL (1) | CL2007003202A1 (es) |
| ES (1) | ES2364784T3 (es) |
| IL (1) | IL198319A0 (es) |
| MX (1) | MX2009004766A (es) |
| PE (1) | PE20081346A1 (es) |
| TW (1) | TW200829551A (es) |
| WO (1) | WO2008055812A1 (es) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8134001B2 (en) * | 2007-12-14 | 2012-03-13 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US7776875B2 (en) * | 2007-12-19 | 2010-08-17 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| US7723372B2 (en) * | 2008-03-19 | 2010-05-25 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| EP2350001A4 (en) * | 2008-10-14 | 2011-11-16 | Univ Singapore | NEW BENZYLIDENE INDOLINOES AND THEIR MEDICAL AND DIAGNOSTIC USES |
| US20100190814A1 (en) * | 2009-01-26 | 2010-07-29 | Li Chen | Spiroindolinone derivative prodrugs |
| US7928233B2 (en) * | 2009-02-10 | 2011-04-19 | Hoffmann-La Roche Inc. | Spiroindolinone pyridine derivatives |
| US8217051B2 (en) * | 2009-02-17 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US8076482B2 (en) | 2009-04-23 | 2011-12-13 | Hoffmann-La Roche Inc. | 3,3′-spiroindolinone derivatives |
| KR20120099462A (ko) * | 2009-11-12 | 2012-09-10 | 더 리젠츠 오브 더 유니버시티 오브 미시건 | 스피로-옥신돌 mdm2 길항제 |
| US8088815B2 (en) * | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
| US8288431B2 (en) * | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
| US8217044B2 (en) | 2010-04-28 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone pyrrolidines |
| MX2013005238A (es) | 2010-11-12 | 2013-09-02 | Univ Michigan | Antagonistas de mdm2 de espiro-oxindol. |
| DK2684880T3 (en) | 2011-03-10 | 2018-05-22 | Daiichi Sankyo Co Ltd | DISPIROPYRROLIDINE DERIVATIVES |
| CN102180828A (zh) * | 2011-03-31 | 2011-09-14 | 四川大学 | 手性吲哚啉酮螺五环骨架化合物及不对称合成 |
| BR112013028983A2 (pt) | 2011-05-11 | 2017-02-07 | Sanofi Sa | antagonistas mdm2 espiro-oxindol |
| 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 |
| US8846657B2 (en) | 2012-12-20 | 2014-09-30 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as HDM2 inhibitors |
| CN103992334A (zh) * | 2014-05-29 | 2014-08-20 | 中国人民解放军第二军医大学 | 吲哚酮螺四氢硫代吡喃类抗肿瘤衍生物及其制备方法 |
| KR102595395B1 (ko) | 2015-02-20 | 2023-10-27 | 다이이찌 산쿄 가부시키가이샤 | 암의 병용 치료법 |
| HK1251165A1 (en) | 2015-04-13 | 2019-01-25 | Daiichi Sankyo Company, Limited | Treatment method combining mdm2 inhibitor and btk inhibitor |
| CN113788818A (zh) | 2016-04-06 | 2021-12-14 | 密执安大学评议会 | Mdm2蛋白质降解剂 |
| AU2017246453A1 (en) | 2016-04-06 | 2018-11-08 | The Regents Of The University Of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
| CN118436801A (zh) | 2016-05-20 | 2024-08-06 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| 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 |
| EP3863720A1 (en) | 2018-10-08 | 2021-08-18 | The Regents Of The University Of Michigan | Small molecule mdm2 protein degraders |
| MX2022011602A (es) | 2020-03-19 | 2023-01-04 | Kymera Therapeutics Inc | Degradadores de la proteína de homólogo de ratón de minuto 2 (mdm2) y usos de los mismos. |
| CN113149890B (zh) * | 2021-04-27 | 2023-01-03 | 华东理工大学 | 合成3-螺-2-吲哚酮类化合物的方法 |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| CN116354786A (zh) * | 2021-12-27 | 2023-06-30 | 北京化工大学 | 一种碗状并苯类化合物,制备及应用 |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0947511A1 (en) | 1998-03-30 | 1999-10-06 | F. Hoffmann-La Roche Ag | Derivatives of phenoxy acetic acid and of phenoxymethyl tetrazole having antitumor activity |
| HUP9902374A3 (en) * | 1999-07-15 | 2002-11-28 | Sanofi Aventis | Process for producing spiro[(4-cyclohexanone)-[3h]indol-2'[1'h]-on derivatives and intermediates |
| EA019566B1 (ru) * | 2005-02-22 | 2014-04-30 | Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган | Низкомолекулярные ингибиторы mdm2 |
| US7553833B2 (en) * | 2007-05-17 | 2009-06-30 | Hoffmann-La Roche Inc. | 3,3-spiroindolinone derivatives |
-
2007
- 2007-10-04 US US11/867,155 patent/US7638548B2/en not_active Expired - Fee Related
- 2007-10-30 MX MX2009004766A patent/MX2009004766A/es active IP Right Grant
- 2007-10-30 EP EP07822025A patent/EP2089360B1/en not_active Not-in-force
- 2007-10-30 ES ES07822025T patent/ES2364784T3/es active Active
- 2007-10-30 AT AT07822025T patent/ATE512135T1/de not_active IP Right Cessation
- 2007-10-30 CN CNA2007800416354A patent/CN101535255A/zh active Pending
- 2007-10-30 WO PCT/EP2007/061671 patent/WO2008055812A1/en not_active Ceased
- 2007-10-30 CA CA002668398A patent/CA2668398A1/en not_active Abandoned
- 2007-10-30 JP JP2009535672A patent/JP2010509260A/ja active Pending
- 2007-10-30 AU AU2007316740A patent/AU2007316740A1/en not_active Abandoned
- 2007-10-30 KR KR1020097009486A patent/KR20090095563A/ko not_active Ceased
- 2007-11-06 CL CL200703202A patent/CL2007003202A1/es unknown
- 2007-11-07 TW TW096142122A patent/TW200829551A/zh unknown
- 2007-11-07 AR ARP070104959A patent/AR063602A1/es unknown
- 2007-11-07 PE PE2007001533A patent/PE20081346A1/es not_active Application Discontinuation
-
2009
- 2009-04-23 IL IL198319A patent/IL198319A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010509260A (ja) | 2010-03-25 |
| CA2668398A1 (en) | 2008-05-15 |
| KR20090095563A (ko) | 2009-09-09 |
| TW200829551A (en) | 2008-07-16 |
| CN101535255A (zh) | 2009-09-16 |
| US20080114013A1 (en) | 2008-05-15 |
| CL2007003202A1 (es) | 2008-03-07 |
| AU2007316740A1 (en) | 2008-05-15 |
| ATE512135T1 (de) | 2011-06-15 |
| IL198319A0 (en) | 2010-02-17 |
| PE20081346A1 (es) | 2008-10-24 |
| EP2089360B1 (en) | 2011-06-08 |
| US7638548B2 (en) | 2009-12-29 |
| ES2364784T3 (es) | 2011-09-14 |
| EP2089360A1 (en) | 2009-08-19 |
| MX2009004766A (es) | 2009-05-21 |
| WO2008055812A1 (en) | 2008-05-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |