ES2556353T3 - Compuestos que son inhibidores de las ERK - Google Patents
Compuestos que son inhibidores de las ERK Download PDFInfo
- Publication number
- ES2556353T3 ES2556353T3 ES09712601.5T ES09712601T ES2556353T3 ES 2556353 T3 ES2556353 T3 ES 2556353T3 ES 09712601 T ES09712601 T ES 09712601T ES 2556353 T3 ES2556353 T3 ES 2556353T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- substituted
- alkyl
- heteroaryl
- triazolyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- LNKGKDPOYPEVSU-QNGWXLTQSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2NC(C#C[C@]1(CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](C)cn3)[s]2)=O)CC1)SC)=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2NC(C#C[C@]1(CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](C)cn3)[s]2)=O)CC1)SC)=O LNKGKDPOYPEVSU-QNGWXLTQSA-N 0.000 description 1
- RLPHZKNHLMYKNY-QNGWXLTQSA-N CC(C)Oc1nccc(-c2n[nH]c(cc3)c2cc3NC([C@]2(CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC2)SC)=O)c1 Chemical compound CC(C)Oc1nccc(-c2n[nH]c(cc3)c2cc3NC([C@]2(CN(CC(N(CC3)CC=C3c(cc3)ccc3-c3n[n](C)cn3)=O)CC2)SC)=O)c1 RLPHZKNHLMYKNY-QNGWXLTQSA-N 0.000 description 1
- 0 C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@@]2(*(Nc(cc2)cc3c2[n]nc3-c2cc(OC)ncc2)O)SC)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@@]2(*(Nc(cc2)cc3c2[n]nc3-c2cc(OC)ncc2)O)SC)=O)nc1 0.000 description 1
- PHKCGAPUNRYERA-DHUJRADRSA-N C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@@]2(C(Nc(cc2)cc3c2[nH]nc3-c2ccnc(OC)c2)=O)SC)=O)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C(CC2)=CCN2C(CN(CC2)C[C@@]2(C(Nc(cc2)cc3c2[nH]nc3-c2ccnc(OC)c2)=O)SC)=O)nc1 PHKCGAPUNRYERA-DHUJRADRSA-N 0.000 description 1
Classifications
-
- 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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3040708P | 2008-02-21 | 2008-02-21 | |
| US30407P | 2008-02-21 | ||
| PCT/US2009/034447 WO2009105500A1 (en) | 2008-02-21 | 2009-02-19 | Compounds that are erk inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2556353T3 true ES2556353T3 (es) | 2016-01-15 |
| ES2556353T8 ES2556353T8 (es) | 2017-10-13 |
Family
ID=40601237
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES09712601.5T Active ES2556353T3 (es) | 2008-02-21 | 2009-02-19 | Compuestos que son inhibidores de las ERK |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8716483B2 (en:Method) |
| EP (1) | EP2260031B1 (en:Method) |
| JP (1) | JP5276676B2 (en:Method) |
| KR (1) | KR20100117123A (en:Method) |
| CN (1) | CN102015693B (en:Method) |
| AR (1) | AR070460A1 (en:Method) |
| AU (1) | AU2009215534B8 (en:Method) |
| BR (1) | BRPI0908120A8 (en:Method) |
| CA (1) | CA2714479A1 (en:Method) |
| CL (1) | CL2009000394A1 (en:Method) |
| CO (1) | CO6300939A2 (en:Method) |
| EC (1) | ECSP10010415A (en:Method) |
| ES (1) | ES2556353T3 (en:Method) |
| IL (1) | IL207530A (en:Method) |
| MX (1) | MX2010009268A (en:Method) |
| MY (1) | MY152271A (en:Method) |
| NZ (1) | NZ587504A (en:Method) |
| PE (1) | PE20091491A1 (en:Method) |
| RU (1) | RU2525389C2 (en:Method) |
| SG (1) | SG188179A1 (en:Method) |
| TW (1) | TWI398441B (en:Method) |
| WO (1) | WO2009105500A1 (en:Method) |
| ZA (2) | ZA201005909B (en:Method) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
| KR20080103996A (ko) | 2006-02-16 | 2008-11-28 | 쉐링 코포레이션 | Erk 억제제로서 피롤리딘 유도체 |
| US9229008B2 (en) | 2008-08-19 | 2016-01-05 | Merck Sharp & Dohme Corp. | IL-8 level as a determinant of responsivity of a cancer to treatment |
| WO2010021978A2 (en) * | 2008-08-19 | 2010-02-25 | Schering Corporation | Il-8 biomarker |
| EP2448942B1 (en) | 2009-07-02 | 2014-09-24 | Merck Sharp & Dohme Corp. | FUSED TRICYCLIC COMPOUNDS AS mTOR INHIBITORS |
| WO2011041152A1 (en) | 2009-09-30 | 2011-04-07 | Schering Corporation | Novel compounds that are erk inhibitors |
| US8999957B2 (en) * | 2010-06-24 | 2015-04-07 | Merck Sharp & Dohme Corp. | Heterocyclic compounds as ERK inhibitors |
| US9242981B2 (en) | 2010-09-16 | 2016-01-26 | Merck Sharp & Dohme Corp. | Fused pyrazole derivatives as novel ERK inhibitors |
| EP2630133A1 (de) | 2010-10-22 | 2013-08-28 | Bayer Intellectual Property GmbH | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
| JP2014500874A (ja) * | 2010-11-16 | 2014-01-16 | メディミューン,エルエルシー | 抗igf抗体を用いた治療レジメン |
| WO2013015918A1 (en) | 2011-07-22 | 2013-01-31 | Iowa State University Research Foundation, Inc. | Method of regioselective synthesis of substituted benzoates |
| MX354675B (es) | 2012-03-01 | 2018-03-15 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa. |
| WO2013169858A1 (en) | 2012-05-08 | 2013-11-14 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
| KR102057877B1 (ko) * | 2012-07-18 | 2019-12-20 | 노스 앤드 사우스 브라더 파마시 인베스트먼트 컴파니 리미티드 | 질소함유 헤테로고리 유도체 및 그의 약물에서의 용도 |
| BR112015006990A2 (pt) * | 2012-09-28 | 2017-07-04 | Merck Sharp & Dohme | composto, composição farmacêutica, e, uso de pelo menos um composto |
| US9226922B2 (en) | 2012-09-28 | 2016-01-05 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
| AR095365A1 (es) * | 2013-03-13 | 2015-10-14 | Hoffmann La Roche | Procedimiento para preparar compuestos benzoxazepina |
| US8871966B2 (en) | 2013-03-15 | 2014-10-28 | Iowa State University Research Foundation, Inc. | Regiospecific synthesis of terephthalates |
| JP6427197B2 (ja) | 2013-10-03 | 2018-11-21 | クラ オンコロジー, インコーポレイテッド | Erkの阻害剤および使用方法 |
| US10428387B2 (en) | 2014-05-16 | 2019-10-01 | University Of Massachusetts | Treating chronic myelogenous leukemia (CML) |
| WO2016025639A1 (en) * | 2014-08-13 | 2016-02-18 | Celgene Avilomics Research, Inc. | Combinations of an erk inhibitor and a chemotherapeutic agent and related methods |
| WO2016095089A1 (en) | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
| WO2016095088A1 (en) | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
| AU2015362844B2 (en) * | 2014-12-18 | 2019-10-24 | Merck Sharp & Dohme Corp. | (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3- (methylthio)pyrrolidine-3-carboxamide compositions for pharmaceutical preparations |
| MX2017008078A (es) * | 2014-12-19 | 2017-09-28 | Merck Sharp & Dohme | Composiciones de (s)-n-(3-(6-isopropoxipiridin-3-il)-1h-indazol-5- il)-1-(2-(4-(4-(1-metil-1h-1,2,4-triazol-3-il)fenil)-3,6-dihidrop iridin-1(2h)-il)-2-oxoetil)-3-(metiltio)pirrolidin-3-carboxamida para preparaciones farmaceuticas. |
| JP6737533B2 (ja) * | 2015-04-03 | 2020-08-12 | リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー | スピロ環式化合物 |
| WO2017040362A1 (en) * | 2015-09-03 | 2017-03-09 | Merck Sharp & Dohme Corp. | Process for preparing spray dried solid dispersions of (s)-n-(3-(6-isopropoxypyridin-3-yl)-1h-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2h)-yl)-2-oxoethyl)-3- (methylthio)pyrrolidine-3-carboxamide for pharmaceutical preparations |
| CN106432182B (zh) * | 2016-09-06 | 2019-04-30 | 铜仁学院 | 特地唑胺中间体的合成方法 |
| CN109020789B (zh) * | 2017-06-12 | 2021-08-13 | 浙江医药股份有限公司新昌制药厂 | 一种制备2-甲氧基丙烯的方法 |
| WO2021067266A1 (en) * | 2019-10-01 | 2021-04-08 | Recurium Ip Holdings, Llc | Pyrrolidinyl-based compounds |
| PH12022550874A1 (en) | 2019-10-09 | 2023-03-27 | Bayer Ag | Novel heteroaryl-triazole compounds as pesticides |
| CA3160899C (en) | 2019-12-06 | 2024-04-16 | Medshine Discovery Inc. | Spiro compound serving as erk inhibitor, and application thereof |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2306108A (en) | 1995-10-13 | 1997-04-30 | Merck & Co Inc | Treatment of Raf-mediated cancers with imidazole derivatives |
| AU3215197A (en) | 1996-05-30 | 1998-01-05 | Merck & Co., Inc. | A method of treating cancer |
| GB2323845A (en) | 1997-03-31 | 1998-10-07 | Merck & Co Inc | MEK inhibiting lactones |
| DE69841434D1 (de) | 1997-07-18 | 2010-02-25 | Novo Nordisk Healthcare Ag | VERWENDUNG VON FVIIa ODER FVIIAi ZUR BEHANDLUNG VON ENDOTHELIALER FEHLFUNKTION BZW ZUR INHIBIERUNG DER ANGIOGENESE |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| SK14082001A3 (sk) | 2000-02-05 | 2002-03-05 | Vertex Pharmaceuticals Incorporated | Deriváty pyrazolu ako inhibítory ERK a farmaceutická kompozícia, ktorá ich obsahuje |
| CA2369502A1 (en) | 2000-02-05 | 2001-08-09 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of erk |
| CA2403017A1 (en) | 2000-03-15 | 2001-09-20 | Warner-Lambert Company | 5-amide substituted diarylamines as mex inhibitors |
| TWI310684B (en) | 2000-03-27 | 2009-06-11 | Bristol Myers Squibb Co | Synergistic pharmaceutical kits for treating cancer |
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| AU2001290940A1 (en) | 2000-09-15 | 2002-03-26 | Vertex Pharmaceuticals Incorporated | Isoxazoles and their use as inhibitors of erk |
| DE60125980T2 (de) * | 2000-11-20 | 2007-10-25 | Scios Inc., Sunnyvale | P38kinase-inhibitoren vom piperidin/piperazin-typ |
| MXPA03005610A (es) | 2000-12-21 | 2003-10-06 | Vertex Pharma | Compuestos de pirazol utiles como inhibidores de la proteina cinasa. |
| MY130778A (en) | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
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| AU2003233605A1 (en) | 2002-05-24 | 2003-12-12 | The University Of Utah Research Foundation | Mitogen activated protein kinase inhibitor compositions for lymphoma therapy |
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| US7205308B2 (en) | 2002-09-04 | 2007-04-17 | Schering Corporation | Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors |
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| JP4845379B2 (ja) | 2002-09-19 | 2011-12-28 | シェーリング コーポレイション | サイクリン依存性キナーゼインヒビターとしてのイミダゾピリジン |
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| JP4993604B2 (ja) | 2004-05-14 | 2012-08-08 | バーテックス ファーマシューティカルズ インコーポレイテッド | ピロリルピリミジンerkプロテインキナーゼインヒビターのプロドラッグ |
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| WO2006136008A1 (en) | 2005-05-24 | 2006-12-28 | University Health Network | Salicylic acid hydrazones as inhibitors of the erk mapkinase pathway and for the treatment of cancer |
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| PL1966151T3 (pl) * | 2005-12-13 | 2012-02-29 | Merck Sharp & Dohme | Policykliczne pochodne indazoli jako inhibitory ERK |
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| KR20080103996A (ko) | 2006-02-16 | 2008-11-28 | 쉐링 코포레이션 | Erk 억제제로서 피롤리딘 유도체 |
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| US20110038876A1 (en) | 2007-06-18 | 2011-02-17 | Robert Sun | Heterocyclic compounds and use thereof as erk inhibitors |
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-
2009
- 2009-02-19 CN CN200980113870.7A patent/CN102015693B/zh not_active Expired - Fee Related
- 2009-02-19 ES ES09712601.5T patent/ES2556353T3/es active Active
- 2009-02-19 JP JP2010547732A patent/JP5276676B2/ja not_active Expired - Fee Related
- 2009-02-19 MX MX2010009268A patent/MX2010009268A/es active IP Right Grant
- 2009-02-19 SG SG2013013206A patent/SG188179A1/en unknown
- 2009-02-19 MY MYPI20103904 patent/MY152271A/en unknown
- 2009-02-19 WO PCT/US2009/034447 patent/WO2009105500A1/en not_active Ceased
- 2009-02-19 BR BRPI0908120A patent/BRPI0908120A8/pt not_active IP Right Cessation
- 2009-02-19 US US12/918,099 patent/US8716483B2/en active Active
- 2009-02-19 CA CA2714479A patent/CA2714479A1/en not_active Abandoned
- 2009-02-19 AU AU2009215534A patent/AU2009215534B8/en not_active Ceased
- 2009-02-19 EP EP09712601.5A patent/EP2260031B1/en active Active
- 2009-02-19 KR KR1020107020896A patent/KR20100117123A/ko not_active Ceased
- 2009-02-19 RU RU2010138635/04A patent/RU2525389C2/ru not_active IP Right Cessation
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- 2009-02-20 AR ARP090100604A patent/AR070460A1/es active IP Right Grant
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2010
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2014
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