AR067813A1 - Fenilendiaminas sustituidas como inhibidores de l ainteraccion entre mdm2 y p53 - Google Patents
Fenilendiaminas sustituidas como inhibidores de l ainteraccion entre mdm2 y p53Info
- Publication number
- AR067813A1 AR067813A1 ARP080103415A ARP080103415A AR067813A1 AR 067813 A1 AR067813 A1 AR 067813A1 AR P080103415 A ARP080103415 A AR P080103415A AR P080103415 A ARP080103415 A AR P080103415A AR 067813 A1 AR067813 A1 AR 067813A1
- Authority
- AR
- Argentina
- Prior art keywords
- mdm2
- phenilendiamins
- ainteraction
- inhibitors
- replaced
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 title 1
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000815 N-oxide group Chemical group 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
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
- C07D401/02—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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Su uso como un inhibidor de una interaccion entre p53-MDM2 así como también proporciona composiciones farmacéuticas que comprenden dichos compuestos Reivindicacion 1: Un compuesto de formula (1), una forma de N-oxido, una sal de adicion, una forma estereoquímicamente isomérica o un solvato del mismo, o su forma polimorfica.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07113878 | 2007-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR067813A1 true AR067813A1 (es) | 2009-10-21 |
Family
ID=38872012
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080103415A AR067813A1 (es) | 2007-08-06 | 2008-08-05 | Fenilendiaminas sustituidas como inhibidores de l ainteraccion entre mdm2 y p53 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8853406B2 (es) |
| EP (1) | EP2185541B1 (es) |
| AR (1) | AR067813A1 (es) |
| CL (1) | CL2008002316A1 (es) |
| ES (1) | ES2534899T3 (es) |
| PA (1) | PA8792401A1 (es) |
| PE (1) | PE20090512A1 (es) |
| TW (1) | TW200922557A (es) |
| UY (1) | UY31273A1 (es) |
| WO (1) | WO2009019274A1 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO2704B1 (en) | 2007-09-21 | 2013-03-03 | جانسين فارماسوتيكا ان في | Interference inhibition factors between MD2 and B53 |
| MY152018A (en) | 2009-02-04 | 2014-08-15 | Janssen Pharmaceutica Nv | Indole derivatives as anticancer agents |
| WO2014085486A2 (en) | 2012-11-30 | 2014-06-05 | Waters Technologies Corporation | Methods and apparatus for the analysis of vitamin d metabolites |
| KR102196882B1 (ko) | 2012-12-20 | 2020-12-30 | 머크 샤프 앤드 돔 코포레이션 | Hdm2 억제제로서의 치환된 이미다조피리딘 |
| TW201932456A (zh) | 2013-01-15 | 2019-08-16 | 美商英塞特控股公司 | 適用作pim激酶抑制劑之噻唑甲醯胺及吡啶甲醯胺化合物 |
| TWI734699B (zh) | 2015-09-09 | 2021-08-01 | 美商英塞特公司 | Pim激酶抑制劑之鹽 |
| US9920032B2 (en) | 2015-10-02 | 2018-03-20 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
| ES2858151T3 (es) | 2016-05-20 | 2021-09-29 | Hoffmann La Roche | Conjugados de PROTAC-anticuerpo y procedimientos de uso |
| CN110291087B (zh) | 2016-12-01 | 2024-07-09 | 阿尔维纳斯运营股份有限公司 | 作为雌激素受体降解剂的四氢萘和四氢异喹啉衍生物 |
| KR20220054347A (ko) | 2019-08-26 | 2022-05-02 | 아비나스 오퍼레이션스, 인코포레이티드 | 에스트로겐 수용체 분해제로서의 테트라히드로나프탈렌 유도체로 유방암을 치료하는 방법 |
| AR123492A1 (es) * | 2020-09-14 | 2022-12-07 | Arvinas Operations Inc | Formas cristalinas y amorfas de un compuesto para la degradación dirigida del receptor de estrógeno |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AUPO863197A0 (en) | 1997-08-18 | 1997-09-11 | Fujisawa Pharmaceutical Co., Ltd. | Novel derivatives |
| US6309492B1 (en) | 1998-09-16 | 2001-10-30 | Marc A. Seidner | Polymer fill coating for laminate or composite wood products and method of making same |
| UA71587C2 (uk) * | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
| BR9915940A (pt) | 1998-12-02 | 2001-09-11 | Pfizer Prod Inc | Métodos e composições para restaurar a estabilidade conformacional de uma proteìna da famìlia p53 |
| AU1734401A (en) | 1999-12-09 | 2001-06-18 | Mitsubishi Pharma Corporation | Carboxyamido derivatives |
| JP2004508421A (ja) | 2000-09-15 | 2004-03-18 | アノーメッド インコーポレイティド | ケモカインレセプター結合性ヘテロ環式化合物 |
| ES2566056T3 (es) | 2001-03-29 | 2016-04-08 | Eli Lilly And Company | N-(2-ariletil)bencilaminas como antagonistas del receptor 5-HT6 |
| AU2002357728A1 (en) | 2001-11-09 | 2003-05-19 | The Regents Of The University Of California | Alpha-helix mimicry by a class of organic molecules |
| PL370176A1 (en) | 2001-11-13 | 2005-05-16 | 3-Dimensional Pharmaceuticals, Inc. | Substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
| ES2301717T3 (es) | 2001-12-18 | 2008-07-01 | F. Hoffmann-La Roche Ag | Cis-2,4,5-trifenil-imidazolinas y su utilizacion para el tratamiento de tumores. |
| GB0215650D0 (en) | 2002-07-05 | 2002-08-14 | Cyclacel Ltd | Bisarylsufonamide compounds |
| JP5156378B2 (ja) | 2004-09-22 | 2013-03-06 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | MDM2とp53の間の相互作用の阻害剤 |
-
2008
- 2008-08-05 PA PA20088792401A patent/PA8792401A1/es unknown
- 2008-08-05 WO PCT/EP2008/060291 patent/WO2009019274A1/en not_active Ceased
- 2008-08-05 AR ARP080103415A patent/AR067813A1/es not_active Application Discontinuation
- 2008-08-05 ES ES08786899.8T patent/ES2534899T3/es active Active
- 2008-08-05 US US12/672,381 patent/US8853406B2/en active Active
- 2008-08-05 EP EP08786899.8A patent/EP2185541B1/en active Active
- 2008-08-05 TW TW097129590A patent/TW200922557A/zh unknown
- 2008-08-06 CL CL2008002316A patent/CL2008002316A1/es unknown
- 2008-08-06 PE PE2008001310A patent/PE20090512A1/es not_active Application Discontinuation
- 2008-08-06 UY UY31273A patent/UY31273A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2185541B1 (en) | 2015-01-28 |
| ES2534899T3 (es) | 2015-04-30 |
| PE20090512A1 (es) | 2009-04-29 |
| CL2008002316A1 (es) | 2009-07-17 |
| UY31273A1 (es) | 2009-03-02 |
| WO2009019274A1 (en) | 2009-02-12 |
| TW200922557A (en) | 2009-06-01 |
| PA8792401A1 (es) | 2009-03-31 |
| US8853406B2 (en) | 2014-10-07 |
| EP2185541A1 (en) | 2010-05-19 |
| US20110130418A1 (en) | 2011-06-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR067813A1 (es) | Fenilendiaminas sustituidas como inhibidores de l ainteraccion entre mdm2 y p53 | |
| EA201070278A1 (ru) | Ингибиторы гамма-секретазы | |
| CY1109916T1 (el) | Βενζιμιδαζολο-θειοφαινικες ενωσεις ως plk αναστολεις | |
| EA201100037A1 (ru) | Органические соединения | |
| EA200971051A1 (ru) | Ингибиторы p70 s6 киназы | |
| CR20110684A (es) | Derivados de imidazolidin-2-ona 1,3-disustituida como inhibidores de cyp17 | |
| ECSP077335A (es) | Inhibidores de la interaccion entre mdm2 y p53 | |
| CL2011002781A1 (es) | Compuestos (e)-2-(4-(2-(5-(1-(3,5-dicloropiridin-4-il)etoxi)-1h-indazol-3-il)vinil)-1h-pirazol-1-il)etanol y (r)-(e)-2-(4-(2-(5-(1-(3,5-dicloropiridin-4-il)etoxi)-1h-indazol-3-il)vinil)-1h-pirazol-1-il)etanol; composicion farmaceutica que los comprende; y uso en el tratamiento del cancer. | |
| CL2008002369A1 (es) | Compuestos derivados de piridin-3-il-oxipiridin-2-il-amino, inhibidores de alk5; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto en el tratamiento del cancer. | |
| JO3425B1 (ar) | مشتقات البابيريدينيل-اندول واستخدامها كعامل متمم لمثبطات b | |
| CR20110028A (es) | Derivados de pirimidina como inhibidores de cinasa | |
| DK2078010T3 (da) | Polycyklisk heteroaryl-substituerede triazoler, der er anvendelige som axl-hæmmere | |
| GT200900027A (es) | Compuestos organicos | |
| CL2011000957A1 (es) | Compuesto derivados de isoindolina sustituidos, inhibidores de citosinas tnf-a; composicion farmaceutica; utiles en el tratamiento del cancer. | |
| EA201000775A1 (ru) | Ингибиторы бета-лактамазы | |
| UA103319C2 (en) | Thiazole- and oxazole-benzene sulfonamide compounds | |
| DK2134691T3 (da) | Quinolinonderivativer som parp- og tank-inhibitorer | |
| CL2009000426A1 (es) | Compuestos derivados de carbociclil/heterociclil-piridin-2-il-urea, inhibidores de topoisomerasa iv bacteriana; composicion farmaceutica; y su uso para el tratamiento de infecciones bacterianas | |
| EA200970156A1 (ru) | Пиридизиноновые производные | |
| CL2011003147A1 (es) | Compuestos derivados de n-(1-4-(1h-pirazol-5-il)ftalazina-1-il) piperidina-4-il) benzamida; composicion farmaceutica que los contiene, utiles como antagonista de la trayectoria de hedgehog, en el tratamiento del cancer. | |
| ECSP088676A (es) | Pirazolquinolonas como potentes inhibidores de parp | |
| CL2009000923A1 (es) | Compuestos derivados de 1-(aminoacetil)-n-(1-cicloalquil)pirrolidina-2-carboxamida sustituidas; composicion farmaceutica; utiles para tratar la hepatitis c. | |
| UY30310A1 (es) | Derivados 2-azetidinona, sales, solvatos, composiciones farmacéuticas conteniéndolos, procesos de preparacion y aplicaciones | |
| EA201071224A1 (ru) | Ингибиторы limk2, композиции, содержащие их, и способы их применения | |
| ATE544759T1 (de) | 5-pyridinon-substituierte indazole und pharmazeutische zusammensetzungen davon |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |