JP5276676B2 - Erk阻害剤である化合物 - Google Patents
Erk阻害剤である化合物 Download PDFInfo
- Publication number
- JP5276676B2 JP5276676B2 JP2010547732A JP2010547732A JP5276676B2 JP 5276676 B2 JP5276676 B2 JP 5276676B2 JP 2010547732 A JP2010547732 A JP 2010547732A JP 2010547732 A JP2010547732 A JP 2010547732A JP 5276676 B2 JP5276676 B2 JP 5276676B2
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- group
- triazolyl
- moiety
- nitrogen
- 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.)
- Expired - Fee Related
Links
- 0 *C1(C*(CC(*)=*)CC1)[N+](*(c(cc1)cc(C(*)=*2)c1*2=C)=C)[O-] Chemical compound *C1(C*(CC(*)=*)CC1)[N+](*(c(cc1)cc(C(*)=*2)c1*2=C)=C)[O-] 0.000 description 31
- QBRNLWZYIYCURR-UHFFFAOYSA-N C1CC#CCCNCC1 Chemical compound C1CC#CCCNCC1 QBRNLWZYIYCURR-UHFFFAOYSA-N 0.000 description 1
- YLPKHKMIETXKFQ-UHFFFAOYSA-O C=[Br]c(cc1)cc(F)c1C(NNCCO)=[NH2+] Chemical compound C=[Br]c(cc1)cc(F)c1C(NNCCO)=[NH2+] YLPKHKMIETXKFQ-UHFFFAOYSA-O 0.000 description 1
- KGASBNKUKKZCNX-NJNXFGOHSA-N CC(C)(C)OC(N(CC1)C/C1=C/C(Nc(cc1)cc2c1[n](C(c1ccccc1)(c1ccccc1)N)nc2-c1ccnc(OC)c1)=O)=O Chemical compound CC(C)(C)OC(N(CC1)C/C1=C/C(Nc(cc1)cc2c1[n](C(c1ccccc1)(c1ccccc1)N)nc2-c1ccnc(OC)c1)=O)=O KGASBNKUKKZCNX-NJNXFGOHSA-N 0.000 description 1
- NGIGLOKJPWGIJT-QMMMGPOBSA-N CC(C)(C)OC(N(CC1)C[C@H]1OC)=O Chemical compound CC(C)(C)OC(N(CC1)C[C@H]1OC)=O NGIGLOKJPWGIJT-QMMMGPOBSA-N 0.000 description 1
- IZXSSGPNTHGIQR-LLVKDONJSA-N CC(C)(C)OC(N(CC1)C[C@]1(C(O)O)OC)=O Chemical compound CC(C)(C)OC(N(CC1)C[C@]1(C(O)O)OC)=O IZXSSGPNTHGIQR-LLVKDONJSA-N 0.000 description 1
- RKOGJMZTWNLTIY-WAYWQWQTSA-N CC(C)C(C)/C=C\N(CCO)N=C Chemical compound CC(C)C(C)/C=C\N(CCO)N=C RKOGJMZTWNLTIY-WAYWQWQTSA-N 0.000 description 1
- MYVCCYAUMCTCMK-POHAHGRESA-N CC(C)C(C)/N=C\N(C)NC Chemical compound CC(C)C(C)/N=C\N(C)NC MYVCCYAUMCTCMK-POHAHGRESA-N 0.000 description 1
- KCDDACBXIXDFCQ-UHFFFAOYSA-N CC(C)OC1=NC=C(B2OC(C)(C)C(C)(C)O2)CC1 Chemical compound CC(C)OC1=NC=C(B2OC(C)(C)C(C)(C)O2)CC1 KCDDACBXIXDFCQ-UHFFFAOYSA-N 0.000 description 1
- VLYZVCYSEXYCCH-RWYGWLOXSA-N CC(C)Oc(cc1)ncc1-c(c1c2)n[nH]c1ccc2NC(C([C@]1(CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](CCOC)cn3)c(F)c2)=O)CC1)OC)=C)=O Chemical compound CC(C)Oc(cc1)ncc1-c(c1c2)n[nH]c1ccc2NC(C([C@]1(CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](CCOC)cn3)c(F)c2)=O)CC1)OC)=C)=O VLYZVCYSEXYCCH-RWYGWLOXSA-N 0.000 description 1
- OMJGCNYSERINJL-LHEWISCISA-N CC(C)Oc(cc1)ncc1-c1n[nH]c(cc2)c1cc2NC([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](CCO)cn2)=O)CC1)OC)=O Chemical compound CC(C)Oc(cc1)ncc1-c1n[nH]c(cc2)c1cc2NC([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](CCO)cn2)=O)CC1)OC)=O OMJGCNYSERINJL-LHEWISCISA-N 0.000 description 1
- PVCRCTVBYAZWEM-BHVANESWSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2NC([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[nH]c(N)n2)=O)CC1)SC)=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2NC([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[nH]c(N)n2)=O)CC1)SC)=O PVCRCTVBYAZWEM-BHVANESWSA-N 0.000 description 1
- ZHPCVSZRBQKSMV-QNGWXLTQSA-N CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N[IH]([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](CCO)cn2)=O)CC1)SC)=O Chemical compound CC(C)Oc(nc1)ccc1-c1n[nH]c(cc2)c1cc2N[IH]([C@]1(CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](CCO)cn2)=O)CC1)SC)=O ZHPCVSZRBQKSMV-QNGWXLTQSA-N 0.000 description 1
- CBJUNIOKQHLFCC-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1C(c(cc(cc1)N)c1N)=N Chemical compound CC(C)Oc(nc1)ccc1C(c(cc(cc1)N)c1N)=N CBJUNIOKQHLFCC-UHFFFAOYSA-N 0.000 description 1
- SMOGRWUQVHTLDU-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1C(c(cc(cc1)NC=O)c1N)=N Chemical compound CC(C)Oc(nc1)ccc1C(c(cc(cc1)NC=O)c1N)=N SMOGRWUQVHTLDU-UHFFFAOYSA-N 0.000 description 1
- BFGMLSOJSQAOLZ-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1C(c(cc(cc1)N[I]=O)c1N)=N Chemical compound CC(C)Oc(nc1)ccc1C(c(cc(cc1)N[I]=O)c1N)=N BFGMLSOJSQAOLZ-UHFFFAOYSA-N 0.000 description 1
- UKAJPPGQMHOKHT-UHFFFAOYSA-N CC(C)c1ccc(-c2n[n](CCO)cn2)c(F)c1 Chemical compound CC(C)c1ccc(-c2n[n](CCO)cn2)c(F)c1 UKAJPPGQMHOKHT-UHFFFAOYSA-N 0.000 description 1
- GXPILPBZBDJRGD-TWGQIWQCSA-N CCN(/C=N\C(C)C)NC Chemical compound CCN(/C=N\C(C)C)NC GXPILPBZBDJRGD-TWGQIWQCSA-N 0.000 description 1
- AZHQIINOUIVWTM-VWLOTQADSA-O CCOC(CN(CC1)C[C@@]1(C(Nc(cc1)cc(C(c(cn2)ccc2OC(C)C)=[NH2+])c1N)=O)OC)=O Chemical compound CCOC(CN(CC1)C[C@@]1(C(Nc(cc1)cc(C(c(cn2)ccc2OC(C)C)=[NH2+])c1N)=O)OC)=O AZHQIINOUIVWTM-VWLOTQADSA-O 0.000 description 1
- DPPZXEXJVRIIGN-PXNMLYILSA-N CN(/C=N\C(c1cnc(C2=CCNCC2)[s]1)=C)N Chemical compound CN(/C=N\C(c1cnc(C2=CCNCC2)[s]1)=C)N DPPZXEXJVRIIGN-PXNMLYILSA-N 0.000 description 1
- SAPRRBPIAGDKDZ-UHFFFAOYSA-N CN1[I]=NC(c(cc2)ccc2C2=CCNCC2)=N1 Chemical compound CN1[I]=NC(c(cc2)ccc2C2=CCNCC2)=N1 SAPRRBPIAGDKDZ-UHFFFAOYSA-N 0.000 description 1
- BRVXPLIMSDWAHU-UHFFFAOYSA-N COCCOC(N=C1)=CCC1c(c1c2ccc(N)c1)n[n]2[Tl] Chemical compound COCCOC(N=C1)=CCC1c(c1c2ccc(N)c1)n[n]2[Tl] BRVXPLIMSDWAHU-UHFFFAOYSA-N 0.000 description 1
- GDWLUDPQJKSHHV-UHFFFAOYSA-N COCC[n]1nc(-c(ccc(Br)c2)c2F)nc1 Chemical compound COCC[n]1nc(-c(ccc(Br)c2)c2F)nc1 GDWLUDPQJKSHHV-UHFFFAOYSA-N 0.000 description 1
- BISLVBCOVWUMRX-UHFFFAOYSA-N COc1cc(-c2n[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)c(cc3)c2cc3N)ccn1 Chemical compound COc1cc(-c2n[n](C(c3ccccc3)(c3ccccc3)c3ccccc3)c(cc3)c2cc3N)ccn1 BISLVBCOVWUMRX-UHFFFAOYSA-N 0.000 description 1
- CXQIMYHJJCWTER-UHFFFAOYSA-N CS(c(cc1)ccc1-c1n[n](CCO)cn1)S Chemical compound CS(c(cc1)ccc1-c1n[n](CCO)cn1)S CXQIMYHJJCWTER-UHFFFAOYSA-N 0.000 description 1
- HCCUNJKRVXVFCH-UHFFFAOYSA-N CSC(Cc1ccc(N2N=CC=CC2=O)[s]1)S Chemical compound CSC(Cc1ccc(N2N=CC=CC2=O)[s]1)S HCCUNJKRVXVFCH-UHFFFAOYSA-N 0.000 description 1
- YJBVAPNADCWMDK-UHFFFAOYSA-N CSC(c1ccc(-c2n[nH]cn2)c(F)c1)S Chemical compound CSC(c1ccc(-c2n[nH]cn2)c(F)c1)S YJBVAPNADCWMDK-UHFFFAOYSA-N 0.000 description 1
- LYHSSZHGEKMFRD-UHFFFAOYSA-N C[n]1nc(-c([s]2)ccc2Br)nc1 Chemical compound C[n]1nc(-c([s]2)ccc2Br)nc1 LYHSSZHGEKMFRD-UHFFFAOYSA-N 0.000 description 1
- OWJDWSBMXAMPBY-UHFFFAOYSA-N C[n]1nc(-c(cc2)ccc2C2=CCNCC2)nc1 Chemical compound C[n]1nc(-c(cc2)ccc2C2=CCNCC2)nc1 OWJDWSBMXAMPBY-UHFFFAOYSA-N 0.000 description 1
- WNJZGUZYODIDKC-UHFFFAOYSA-N C[n]1nc(-c2ccccc2)nc1 Chemical compound C[n]1nc(-c2ccccc2)nc1 WNJZGUZYODIDKC-UHFFFAOYSA-N 0.000 description 1
- ACZVYRRIAYCOKM-UHFFFAOYSA-N C[n]1nc(-c2cnc(CS)cc2)nc1 Chemical compound C[n]1nc(-c2cnc(CS)cc2)nc1 ACZVYRRIAYCOKM-UHFFFAOYSA-N 0.000 description 1
- ZASQHVAGPKBSHH-UHFFFAOYSA-N Cc(cc1)ccc1-c1n[nH]cn1 Chemical compound Cc(cc1)ccc1-c1n[nH]cn1 ZASQHVAGPKBSHH-UHFFFAOYSA-N 0.000 description 1
- HQQIHKQUVMLUIT-UHFFFAOYSA-N Cc1nc(-c(cc2)ccc2SC)n[n]1C Chemical compound Cc1nc(-c(cc2)ccc2SC)n[n]1C HQQIHKQUVMLUIT-UHFFFAOYSA-N 0.000 description 1
- OLCWFLWEHWLBTO-HSZRJFAPSA-N N#Cc(cc1C2)ccc1N(Cc1cnc[nH]1)C[C@@H](Cc1ccccc1)N2S(c1ccc[s]1)(=O)=O Chemical compound N#Cc(cc1C2)ccc1N(Cc1cnc[nH]1)C[C@@H](Cc1ccccc1)N2S(c1ccc[s]1)(=O)=O OLCWFLWEHWLBTO-HSZRJFAPSA-N 0.000 description 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
- C07D401/14—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
-
- 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
-
- 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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (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 | |
| US61/030,407 | 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 |
|---|---|
| JP2011513225A JP2011513225A (ja) | 2011-04-28 |
| JP5276676B2 true JP5276676B2 (ja) | 2013-08-28 |
Family
ID=40601237
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010547732A Expired - Fee Related JP5276676B2 (ja) | 2008-02-21 | 2009-02-19 | Erk阻害剤である化合物 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8716483B2 (enExample) |
| EP (1) | EP2260031B1 (enExample) |
| JP (1) | JP5276676B2 (enExample) |
| KR (1) | KR20100117123A (enExample) |
| CN (1) | CN102015693B (enExample) |
| AR (1) | AR070460A1 (enExample) |
| AU (1) | AU2009215534B8 (enExample) |
| BR (1) | BRPI0908120A8 (enExample) |
| CA (1) | CA2714479A1 (enExample) |
| CL (1) | CL2009000394A1 (enExample) |
| CO (1) | CO6300939A2 (enExample) |
| EC (1) | ECSP10010415A (enExample) |
| ES (1) | ES2556353T3 (enExample) |
| IL (1) | IL207530A (enExample) |
| MX (1) | MX2010009268A (enExample) |
| MY (1) | MY152271A (enExample) |
| NZ (1) | NZ587504A (enExample) |
| PE (1) | PE20091491A1 (enExample) |
| RU (1) | RU2525389C2 (enExample) |
| SG (1) | SG188179A1 (enExample) |
| TW (1) | TWI398441B (enExample) |
| WO (1) | WO2009105500A1 (enExample) |
| ZA (2) | ZA201005909B (enExample) |
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 |
| ATE485268T1 (de) | 2006-02-16 | 2010-11-15 | Schering Corp | Pyrrolidin-derivate als erk-hemmer |
| EP2316031B1 (en) * | 2008-08-19 | 2016-09-14 | Merck Sharp & Dohme Corp. | IL-8 biomarker for monitoring cancer treatment |
| 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 |
| US8609675B2 (en) | 2009-07-02 | 2013-12-17 | Merck Sharp & Dohme Corp. | Fused Tricyclic Compounds as novel mTOR inhibitors |
| JP2013506669A (ja) | 2009-09-30 | 2013-02-28 | メルク・シャープ・アンド・ドーム・コーポレーション | Erk阻害剤である新規化合物 |
| EP2584903B1 (en) * | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
| US9242981B2 (en) | 2010-09-16 | 2016-01-26 | Merck Sharp & Dohme Corp. | Fused pyrazole derivatives as novel ERK inhibitors |
| BR112013009823A2 (pt) | 2010-10-22 | 2016-07-05 | Bayer Ip Gmbh | novos compostos heterocíclicos como pesticidas |
| AU2011329067A1 (en) * | 2010-11-16 | 2013-05-30 | Medimmune, Llc | Regimens for treatments using anti-IGF antibodies |
| US9000209B2 (en) | 2011-07-22 | 2015-04-07 | Iowa State University Research Foundation, Inc. | Method of regioselective synthesis of substituted benzoates |
| PL2820009T3 (pl) | 2012-03-01 | 2018-09-28 | Array Biopharma, Inc. | Inhibitory kinaz serynowo/treoninowych |
| US20150141470A1 (en) | 2012-05-08 | 2015-05-21 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
| RU2701156C9 (ru) | 2012-07-18 | 2019-12-18 | Саншайн Лейк Фарма Ко., Лтд. | Азотсодержащие гетероциклические производные и их применение в фармацевтических препаратах |
| WO2014052566A1 (en) * | 2012-09-28 | 2014-04-03 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
| EP2900241B1 (en) * | 2012-09-28 | 2018-08-08 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
| CA2897618A1 (en) * | 2013-03-13 | 2014-09-18 | F. Hoffmann-La Roche Ag | Process for making benzoxazepin compounds |
| US8871966B2 (en) | 2013-03-15 | 2014-10-28 | Iowa State University Research Foundation, Inc. | Regiospecific synthesis of terephthalates |
| PT3052096T (pt) | 2013-10-03 | 2018-04-04 | Kura Oncology Inc | Inibidores de erk e métodos de utilização |
| EP3143166A4 (en) | 2014-05-16 | 2018-04-18 | 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 |
| WO2016095088A1 (en) * | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
| WO2016095089A1 (en) * | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
| BR112017012547A2 (pt) * | 2014-12-18 | 2018-03-13 | Merck Sharp & Dohme Corp. | Composições 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-diidropiridin-1(2h)-il)-2-oxoetil)-3-(metiltio) pirrolidina-3-carboxamida para preparações farmacêuticas |
| BR112017012558A2 (pt) * | 2014-12-19 | 2018-01-02 | Merck Sharp & Dohme | Composições 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-diidropiridin-1(2h)-il)-2-oxoetil)-3-(metiltio) pirrolidina-3-carboxamida para preparações farmacêuticas |
| HRP20200805T1 (hr) | 2015-04-03 | 2020-10-16 | Recurium Ip Holdings, Llc | Spirociklički spojevi |
| US20180250232A1 (en) * | 2015-09-03 | 2018-09-06 | 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 |
| CN114867529B (zh) | 2019-10-09 | 2024-09-27 | 拜耳公司 | 作为农药的新的杂芳基三唑化合物 |
| JP7326622B2 (ja) | 2019-12-06 | 2023-08-15 | メッドシャイン ディスカバリー インコーポレイテッド | Erk阻害剤としてのスピロ系化合物およびその使用 |
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 |
| WO1997045412A1 (en) | 1996-05-30 | 1997-12-04 | Merck & Co., Inc. | A method of treating cancer |
| GB2323845A (en) | 1997-03-31 | 1998-10-07 | Merck & Co Inc | MEK inhibiting lactones |
| WO1999003498A1 (en) | 1997-07-18 | 1999-01-28 | Novo Nordisk A/S | USE OF FVIIa OR FVIIai FOR THE TREATMENT OF ADVERSE CONDITIONS RELATED TO THE FVIIa MEDIATED INTRACELLULAR SIGNALLING PATHWAY |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| CA2369504C (en) | 2000-02-05 | 2009-01-06 | Vertex Pharmaceuticals Incorporated | Pyrazole compositions useful as inhibitors of erk |
| CA2369502A1 (en) | 2000-02-05 | 2001-08-09 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of erk |
| BR0109188A (pt) | 2000-03-15 | 2003-03-18 | Warner Lambert Co | Diarilaminas 5-amida substituìdas como inibidores de mex |
| TWI310684B (en) | 2000-03-27 | 2009-06-11 | Bristol Myers Squibb Co | Synergistic pharmaceutical kits for treating cancer |
| US7211594B2 (en) | 2000-07-31 | 2007-05-01 | Signal Pharmaceuticals, Llc | Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith |
| US20050009876A1 (en) | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
| US6897231B2 (en) | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
| WO2002022610A1 (en) | 2000-09-15 | 2002-03-21 | Vertex Pharmaceuticals Incorporated | Isoxazoles and their use as inhibitors of erk |
| EP1318814B1 (en) | 2000-09-15 | 2007-05-30 | Vertex Pharmaceuticals Incorporated | Triazole compounds useful as protein kinase inhibitors |
| CA2429258A1 (en) | 2000-11-20 | 2002-06-13 | Scios Inc. | Piperidine/piperazine-type inhibitors of p38 kinase |
| US7625913B2 (en) | 2000-12-21 | 2009-12-01 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| MY130778A (en) | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
| KR20040007497A (ko) | 2001-04-16 | 2004-01-24 | 에자이 가부시키가이샤 | 신규 1h-인다졸 화합물 |
| US6962936B2 (en) | 2001-04-27 | 2005-11-08 | Vertex Pharmaceuticals Incorporated | Triazole-derived kinase inhibitors and uses thereof |
| EP1461334A2 (en) | 2001-04-27 | 2004-09-29 | Vertex Pharmaceuticals Incorporated | Pyrazole derived kinase inhibitors |
| CA2456187A1 (en) | 2001-08-03 | 2003-02-13 | Qing Tang | Pyrazole-derived kinase inhibitors and uses thereof |
| WO2003011855A2 (en) | 2001-08-03 | 2003-02-13 | Vertex Pharmaceuticals Incorporated | Pyrazole-derived kinase inhibitors and uses thereof |
| US7253199B2 (en) | 2001-10-23 | 2007-08-07 | Applied Research Systems Ars Holding N.V. | Azole derivatives and pharmaceutical compositions containing them |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| US7304061B2 (en) | 2002-04-26 | 2007-12-04 | Vertex Pharmaceuticals Incorporated | Heterocyclic inhibitors of ERK2 and uses thereof |
| WO2003099212A2 (en) | 2002-05-24 | 2003-12-04 | The University Of Utah Research Foundation | Mitogen activated protein kinase inhibitor compositions for lymphoma therapy |
| CN1656079A (zh) | 2002-05-31 | 2005-08-17 | 卫材株式会社 | 吡唑化合物和含有该化合物的药物组合物 |
| US7205308B2 (en) | 2002-09-04 | 2007-04-17 | Schering Corporation | Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7196092B2 (en) | 2002-09-04 | 2007-03-27 | Schering Corporation | N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| WO2004026867A2 (en) | 2002-09-19 | 2004-04-01 | Schering Corporation | Imidazopyridines as cyclin dependent kinase inhibitors |
| WO2004083203A1 (en) | 2003-03-13 | 2004-09-30 | Vertex Pharmaceuticals Incorporated | Compositions useful as protein kinase inhibitors |
| GB2400101A (en) | 2003-03-28 | 2004-10-06 | Biofocus Discovery Ltd | Compounds capable of binding to the active site of protein kinases |
| WO2005002673A1 (en) | 2003-07-03 | 2005-01-13 | Astex Therapeutics Limited | Raf kinase inhibitors |
| AU2004293035A1 (en) | 2003-11-19 | 2005-06-09 | Signal Pharmaceuticals, Llc | Methods of treating diseases and disorders by targeting multiple kinases |
| EP1715871A1 (en) | 2003-12-22 | 2006-11-02 | Gilead Sciences, Inc. | Kinase inhibitor phosphonate conjugates |
| US7462612B2 (en) | 2004-03-26 | 2008-12-09 | Vertex Pharmaceuticals Incorporated | Pyridine inhibitors of ERK2 and uses thereof |
| JP2007532615A (ja) | 2004-04-13 | 2007-11-15 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
| BRPI0511124A (pt) | 2004-05-14 | 2007-11-27 | Vertex Pharma | pró-drogas de inibidores de erk proteìna cinase de pirrolilpirimidina |
| DK3305776T3 (da) | 2004-05-14 | 2019-12-09 | Vertex Pharma | Pyrrol-forbindelser som inhibitorer af erk-protein-kinaser og farmaceutiske sammensætninger, der indeholder disse forbindelser |
| WO2006040569A1 (en) | 2004-10-14 | 2006-04-20 | Astex Therapeutics Limited | Thiophene amide compounds for use in the treatment or prophylaxis of cancers |
| EP1833820A1 (en) | 2004-12-23 | 2007-09-19 | Vertex Pharmaceuticals Incorporated | Selective inhibitors of erk protein kinase and uses therof |
| CN100377868C (zh) | 2005-03-24 | 2008-04-02 | 中国科学院物理研究所 | 用于磁性/非磁性/磁性多层薄膜的核心复合膜及其用途 |
| 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 |
| US8217042B2 (en) | 2005-11-11 | 2012-07-10 | Zentaris Gmbh | Pyridopyrazines and their use as modulators of kinases |
| US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
| HRP20110892T1 (hr) * | 2005-12-13 | 2011-12-31 | Schering Corporation | Policiklični derivati indazola koji su inhibitori erk |
| ATE485268T1 (de) | 2006-02-16 | 2010-11-15 | Schering Corp | Pyrrolidin-derivate als erk-hemmer |
| EP2018872A4 (en) | 2006-04-20 | 2010-06-09 | Takeda Pharmaceutical | PHARMACEUTICAL PRODUCT |
| US7601852B2 (en) | 2006-05-11 | 2009-10-13 | Kosan Biosciences Incorporated | Macrocyclic kinase inhibitors |
| US7884107B2 (en) | 2006-06-30 | 2011-02-08 | Merck | Substituted piperidines that increase P53 activity and the uses thereof |
| US7671832B2 (en) | 2006-07-10 | 2010-03-02 | Philips Lumileds Lighting Company, Llc | Multi-colored LED backlight with color-compensated clusters near edge |
| EP2560007A1 (en) | 2007-03-28 | 2013-02-20 | Pharmacyclics, Inc. | Identification of bruton's tyrosine kinase inhibitors |
| AU2008262412A1 (en) * | 2007-06-05 | 2008-12-18 | Merck Sharp & Dohme Corp. | Polycyclic indazole derivatives and their use as ERK inhibitors for the treatment of cancer |
| KR20100032886A (ko) | 2007-06-08 | 2010-03-26 | 아보트 러보러터리즈 | 키나제 억제제로서의 5-헤테로아릴 치환된 인다졸 |
| MX2009014208A (es) | 2007-06-18 | 2010-01-28 | Schering Corp | Compuestos heterociclicos y usos de los mismos como inhibidores de erk. |
| JP2013506669A (ja) | 2009-09-30 | 2013-02-28 | メルク・シャープ・アンド・ドーム・コーポレーション | Erk阻害剤である新規化合物 |
-
2009
- 2009-02-19 MY MYPI20103904 patent/MY152271A/en unknown
- 2009-02-19 SG SG2013013206A patent/SG188179A1/en unknown
- 2009-02-19 BR BRPI0908120A patent/BRPI0908120A8/pt not_active IP Right Cessation
- 2009-02-19 RU RU2010138635/04A patent/RU2525389C2/ru not_active IP Right Cessation
- 2009-02-19 KR KR1020107020896A patent/KR20100117123A/ko not_active Ceased
- 2009-02-19 AU AU2009215534A patent/AU2009215534B8/en not_active Ceased
- 2009-02-19 US US12/918,099 patent/US8716483B2/en active Active
- 2009-02-19 NZ NZ587504A patent/NZ587504A/xx not_active IP Right Cessation
- 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 EP EP09712601.5A patent/EP2260031B1/en active Active
- 2009-02-19 CA CA2714479A patent/CA2714479A1/en not_active Abandoned
- 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 WO PCT/US2009/034447 patent/WO2009105500A1/en not_active Ceased
- 2009-02-20 PE PE2009000250A patent/PE20091491A1/es active IP Right Grant
- 2009-02-20 AR ARP090100604A patent/AR070460A1/es active IP Right Grant
- 2009-02-20 TW TW098105537A patent/TWI398441B/zh not_active IP Right Cessation
- 2009-02-20 CL CL2009000394A patent/CL2009000394A1/es unknown
-
2010
- 2010-08-10 IL IL207530A patent/IL207530A/en active IP Right Grant
- 2010-08-18 ZA ZA2010/05909A patent/ZA201005909B/en unknown
- 2010-08-20 EC EC2010010415A patent/ECSP10010415A/es unknown
- 2010-09-21 CO CO10116702A patent/CO6300939A2/es active IP Right Grant
-
2014
- 2014-01-17 ZA ZA2014/00396A patent/ZA201400396B/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5276676B2 (ja) | Erk阻害剤である化合物 | |
| JP4881957B2 (ja) | Erk阻害剤である多環式インドール誘導体 | |
| EP2483263B1 (en) | Heterocyclic compounds that are erk inhibitors | |
| EP1984331B1 (en) | Pyrrolidine derivatives as erk inhibitors | |
| US8546404B2 (en) | Compounds that are ERK inhibitors | |
| JP2010530421A (ja) | 複素環化合物およびerk阻害剤としてのそれらの使用 | |
| JP2010529122A (ja) | 多環式インダゾール誘導体および癌の治療のためのerk阻害剤としてのそれらの使用 | |
| JP2009523799A (ja) | ファルネシルタンパク質トランスフェラーゼインヒビターとしてのピペラジン誘導体 | |
| HK1114851B (en) | Polycyclic indazole derivatives that are erk inhibitors | |
| HK1117159B (en) | Pyrrolidine derivatives as erk inhibitors | |
| MX2008007801A (en) | Polycyclic indazole derivatives that are erk inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20111005 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20121127 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130222 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130301 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130325 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130422 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130517 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |