ES2780650T3 - Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer - Google Patents
Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer Download PDFInfo
- Publication number
- ES2780650T3 ES2780650T3 ES16791420T ES16791420T ES2780650T3 ES 2780650 T3 ES2780650 T3 ES 2780650T3 ES 16791420 T ES16791420 T ES 16791420T ES 16791420 T ES16791420 T ES 16791420T ES 2780650 T3 ES2780650 T3 ES 2780650T3
- Authority
- ES
- Spain
- Prior art keywords
- methyl
- compound
- formula
- pharmaceutically acceptable
- pyrazin
- 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
- JODQIWFFKDQLJG-SSDOTTSWSA-N CC(C)(C)OC(N1S(O)(O)OC[C@H]1COC)=O Chemical compound CC(C)(C)OC(N1S(O)(O)OC[C@H]1COC)=O JODQIWFFKDQLJG-SSDOTTSWSA-N 0.000 description 1
- AIVYLYCLCDWKEU-RWNHWRGESA-N CC(C)(C)OC(N1[S+](O)OC[C@@H]1COC)=O Chemical compound CC(C)(C)OC(N1[S+](O)OC[C@@H]1COC)=O AIVYLYCLCDWKEU-RWNHWRGESA-N 0.000 description 1
- UFVXAJVQXHAGDA-UHFFFAOYSA-N CCOC(c1nc(-c2ccnc(Cl)n2)c[nH]1)=O Chemical compound CCOC(c1nc(-c2ccnc(Cl)n2)c[nH]1)=O UFVXAJVQXHAGDA-UHFFFAOYSA-N 0.000 description 1
- KKBUAKLLEWKSNE-LBPRGKRZSA-N CCOC(c1nc(-c2nc(Cl)ncc2C)c[n]1C[C@H](C)NCc1cc(C(F)(F)F)ncn1)=O Chemical compound CCOC(c1nc(-c2nc(Cl)ncc2C)c[n]1C[C@H](C)NCc1cc(C(F)(F)F)ncn1)=O KKBUAKLLEWKSNE-LBPRGKRZSA-N 0.000 description 1
- SCTSUDKWBUYKGM-LBPRGKRZSA-N CCOC(c1nc(-c2nc(Cl)ncc2C)c[n]1C[C@H](C)NCc1nc(C(F)(F)F)ncc1)=O Chemical compound CCOC(c1nc(-c2nc(Cl)ncc2C)c[n]1C[C@H](C)NCc1nc(C(F)(F)F)ncc1)=O SCTSUDKWBUYKGM-LBPRGKRZSA-N 0.000 description 1
- SJNDZZROBMMJHR-UHFFFAOYSA-N CCOC(c1nc(-c2nc(Cl)ncc2Cl)c[n]1COCC[Si+](C)(C)C)=O Chemical compound CCOC(c1nc(-c2nc(Cl)ncc2Cl)c[n]1COCC[Si+](C)(C)C)=O SJNDZZROBMMJHR-UHFFFAOYSA-N 0.000 description 1
- GSJWTBPXHPDMHL-JTQLQIEISA-N CCOC(c1nc(-c2nc(Cl)ncc2Cl)c[n]1C[C@H](C)N(C(OC(C)(C)C)=O)S(O)(=O)=O)=O Chemical compound CCOC(c1nc(-c2nc(Cl)ncc2Cl)c[n]1C[C@H](C)N(C(OC(C)(C)C)=O)S(O)(=O)=O)=O GSJWTBPXHPDMHL-JTQLQIEISA-N 0.000 description 1
- MFXVDDUSPPQUJQ-AWEZNQCLSA-N C[C@@H](C[n]1c2nc(-c(nc(Nc3ccn[n]3C)nc3)c3Cl)c1)N(Cc1cccc(C)n1)C2=O Chemical compound C[C@@H](C[n]1c2nc(-c(nc(Nc3ccn[n]3C)nc3)c3Cl)c1)N(Cc1cccc(C)n1)C2=O MFXVDDUSPPQUJQ-AWEZNQCLSA-N 0.000 description 1
- CHIZSKFEQQPYIG-HNNXBMFYSA-N C[C@@H](C[n]1c2nc(-c3c(C)cnc(Nc4ccn[n]4C)n3)c1)N(Cc(cc1)cc(OC)c1F)C2=O Chemical compound C[C@@H](C[n]1c2nc(-c3c(C)cnc(Nc4ccn[n]4C)n3)c1)N(Cc(cc1)cc(OC)c1F)C2=O CHIZSKFEQQPYIG-HNNXBMFYSA-N 0.000 description 1
- VTWRYQNQNQTDJU-INIZCTEOSA-N C[C@@H](C[n]1c2nc(-c3c(C)cnc(Nc4ccn[n]4C)n3)c1)N(Cc1cccc(OC)c1)C2=O Chemical compound C[C@@H](C[n]1c2nc(-c3c(C)cnc(Nc4ccn[n]4C)n3)c1)N(Cc1cccc(OC)c1)C2=O VTWRYQNQNQTDJU-INIZCTEOSA-N 0.000 description 1
- OWPHFRAKUXEJOP-JTQLQIEISA-N C[C@@H](C[n]1c2nc(-c3nc(Cl)ncc3)c1)N(Cc(cc1)cc(F)c1F)C2=O Chemical compound C[C@@H](C[n]1c2nc(-c3nc(Cl)ncc3)c1)N(Cc(cc1)cc(F)c1F)C2=O OWPHFRAKUXEJOP-JTQLQIEISA-N 0.000 description 1
- BUVJSMCNKIHFCD-NSHDSACASA-N C[C@@H](C[n]1c2nc(-c3nc(Cl)ncc3C)c1)N(Cc1nc(C(F)F)ccc1)C2=O Chemical compound C[C@@H](C[n]1c2nc(-c3nc(Cl)ncc3C)c1)N(Cc1nc(C(F)F)ccc1)C2=O BUVJSMCNKIHFCD-NSHDSACASA-N 0.000 description 1
- DHPAIROIAXACNO-ZDUSSCGKSA-N Cc(c(-c1c[n](C[C@@H](COC)N(Cc(cc2)cc(F)c2F)C2=O)c2n1)n1)cnc1Cl Chemical compound Cc(c(-c1c[n](C[C@@H](COC)N(Cc(cc2)cc(F)c2F)C2=O)c2n1)n1)cnc1Cl DHPAIROIAXACNO-ZDUSSCGKSA-N 0.000 description 1
- DRPYDUUPNVEQCA-CYBMUJFWSA-N Cc(c(-c1c[n](C[C@H](COC)N(Cc2nc(C(F)F)ccc2)C2=O)c2n1)n1)cnc1Cl Chemical compound Cc(c(-c1c[n](C[C@H](COC)N(Cc2nc(C(F)F)ccc2)C2=O)c2n1)n1)cnc1Cl DRPYDUUPNVEQCA-CYBMUJFWSA-N 0.000 description 1
- LDWCHEJBPZNGIS-UHFFFAOYSA-N Cc(cn1)c(-c2c[n](CCNC3=O)c3n2)nc1Cl Chemical compound Cc(cn1)c(-c2c[n](CCNC3=O)c3n2)nc1Cl LDWCHEJBPZNGIS-UHFFFAOYSA-N 0.000 description 1
- HVIGNZUDBVLTLU-MRXNPFEDSA-N Cc1c(-c2c[n](C[C@H](COC)N(Cc(cc3)cc(F)c3F)C3=O)c3n2)nc(Nc2ccn[n]2C)nc1 Chemical compound Cc1c(-c2c[n](C[C@H](COC)N(Cc(cc3)cc(F)c3F)C3=O)c3n2)nc(Nc2ccn[n]2C)nc1 HVIGNZUDBVLTLU-MRXNPFEDSA-N 0.000 description 1
- KMPXZNPDWGUHKX-GOSISDBHSA-N Cc1c(-c2c[n](C[C@H](COC)N(Cc3cc(OC)ccc3)C3=O)c3n2)nc(Nc2ccn[n]2C)nc1 Chemical compound Cc1c(-c2c[n](C[C@H](COC)N(Cc3cc(OC)ccc3)C3=O)c3n2)nc(Nc2ccn[n]2C)nc1 KMPXZNPDWGUHKX-GOSISDBHSA-N 0.000 description 1
- CQNIYQCVDLBGPY-UHFFFAOYSA-N FC(c1ccnc(Cl)c1)F Chemical compound FC(c1ccnc(Cl)c1)F CQNIYQCVDLBGPY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562252726P | 2015-11-09 | 2015-11-09 | |
| US201662401351P | 2016-09-29 | 2016-09-29 | |
| PCT/EP2016/076932 WO2017080979A1 (en) | 2015-11-09 | 2016-11-08 | Dihydroimidazopyrazinone derivatives useful in the treatment of cancer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2780650T3 true ES2780650T3 (es) | 2020-08-26 |
Family
ID=57241113
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES16791420T Active ES2780650T3 (es) | 2015-11-09 | 2016-11-08 | Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer |
Country Status (35)
| Country | Link |
|---|---|
| US (2) | US9902731B2 (OSRAM) |
| EP (1) | EP3374359B1 (OSRAM) |
| JP (1) | JP6877423B2 (OSRAM) |
| KR (1) | KR20180074788A (OSRAM) |
| CN (1) | CN108349983B (OSRAM) |
| AU (1) | AU2016351813B2 (OSRAM) |
| BR (1) | BR112018008397B1 (OSRAM) |
| CA (1) | CA3003549A1 (OSRAM) |
| CL (1) | CL2018001226A1 (OSRAM) |
| CO (1) | CO2018004857A2 (OSRAM) |
| CR (1) | CR20180316A (OSRAM) |
| CY (1) | CY1123627T1 (OSRAM) |
| DK (1) | DK3374359T3 (OSRAM) |
| EA (1) | EA038028B1 (OSRAM) |
| ES (1) | ES2780650T3 (OSRAM) |
| HR (1) | HRP20200342T1 (OSRAM) |
| IL (1) | IL258953A (OSRAM) |
| LT (1) | LT3374359T (OSRAM) |
| ME (1) | ME03770B (OSRAM) |
| MX (1) | MX376639B (OSRAM) |
| MY (1) | MY197626A (OSRAM) |
| NI (1) | NI201800058A (OSRAM) |
| PE (1) | PE20181288A1 (OSRAM) |
| PH (1) | PH12018500987A1 (OSRAM) |
| PL (1) | PL3374359T3 (OSRAM) |
| PT (1) | PT3374359T (OSRAM) |
| RS (1) | RS60155B1 (OSRAM) |
| SG (1) | SG11201803066VA (OSRAM) |
| SI (1) | SI3374359T1 (OSRAM) |
| SM (1) | SMT202000152T1 (OSRAM) |
| SV (1) | SV2018005687A (OSRAM) |
| TN (1) | TN2018000119A1 (OSRAM) |
| TW (1) | TWI730012B (OSRAM) |
| WO (1) | WO2017080979A1 (OSRAM) |
| ZA (1) | ZA201803742B (OSRAM) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL291017B2 (en) | 2015-10-21 | 2023-11-01 | Otsuka Pharma Co Ltd | Benzolactam compounds as protein kinase inhibitors |
| SI3374359T1 (sl) * | 2015-11-09 | 2020-04-30 | Astrazeneca Ab | Derivati dihidroimidazopirazinona uporabni pri zdravljenju raka |
| GB201706327D0 (en) | 2017-04-20 | 2017-06-07 | Otsuka Pharma Co Ltd | A pharmaceutical compound |
| WO2020073862A1 (zh) * | 2018-10-10 | 2020-04-16 | 深圳市塔吉瑞生物医药有限公司 | 一种二氢咪唑并吡嗪酮化合物及包含该化合物的组合物及其用途 |
| KR20210145773A (ko) | 2019-03-28 | 2021-12-02 | 지앙수 헨그루이 메디슨 컴퍼니 리미티드 | 티에노헤테로고리형 유도체, 이의 제조 방법 및 이의 의약적 용도 |
| EP3978498A1 (en) | 2019-05-24 | 2022-04-06 | Jiangsu Hengrui Medicine Co., Ltd. | Substituted fused bicyclic derivative, preparation method therefor, and application thereof in medicines |
| TWI879771B (zh) | 2019-06-06 | 2025-04-11 | 大陸商和記黃埔醫藥（上海）有限公司 | 三環類化合物及其用途 |
| MX2022006856A (es) | 2019-12-05 | 2022-07-11 | Astrazeneca Ab | Proceso e intermediarios para la produccion de formula (i). |
| EP4071155A4 (en) * | 2019-12-06 | 2024-01-17 | D3 Bio (Wuxi) Co., Ltd. | THIAZOLOLACTAM COMPOUND USED AS ERK INHIBITOR AND USE THEREOF |
| CA3194077A1 (en) | 2020-09-29 | 2022-04-07 | Xianqiang ZHOU | Crystal form of pyrrolo heterocyclic derivative and preparation method therefor |
| CN117529321A (zh) * | 2021-06-18 | 2024-02-06 | 上海德琪医药科技有限公司 | Erk抑制剂和kras抑制剂的组合及其用途 |
| WO2022268065A1 (en) * | 2021-06-22 | 2022-12-29 | Fochon Biosciences, Ltd. | Compounds as erk inhibitors |
| CN117677398A (zh) | 2021-07-27 | 2024-03-08 | 东丽株式会社 | 用于癌的治疗和/或预防的药品 |
| US20250129090A1 (en) | 2021-11-04 | 2025-04-24 | Skyhawk Therapeutics, Inc. | Compositions useful for modulating splicing |
| EP4514806B1 (en) | 2022-04-27 | 2025-12-17 | Skyhawk Therapeutics, Inc. | Compositions useful for modulating splicing |
| WO2023220435A1 (en) | 2022-05-12 | 2023-11-16 | Skyhawk Therapeutics, Inc. | Compositions useful for modulating splicing |
| WO2024006971A2 (en) * | 2022-07-01 | 2024-01-04 | The Scripps Research Institute | Antimalarial compounds |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
| WO2004041826A1 (en) * | 2002-11-06 | 2004-05-21 | Merck Sharp & Dohme Limited | Imidazopyrazinones and imidazotriazinones derivates as gaba-a receptor anxiolytic |
| GB0520958D0 (en) * | 2005-10-14 | 2005-11-23 | Cyclacel Ltd | Compound |
| US8278337B2 (en) * | 2006-12-20 | 2012-10-02 | Merck Sharp & Dohme | Substituted pyridines that are JNK inhibitors |
| EP2655376B1 (en) * | 2010-12-22 | 2017-08-23 | Janssen Pharmaceutica NV | 5,6-DIHYDRO-IMIDAZO[1,2-a]PYRAZIN-8-YLAMINE DERIVATIVES USEFUL AS INHIBITORS OF BETA-SECRETASE (BACE) |
| AU2012323085B2 (en) * | 2011-10-10 | 2017-03-09 | H. Lundbeck A/S | PDE9i with imidazo pyrazinone backbone |
| JP2013166727A (ja) * | 2012-02-16 | 2013-08-29 | Dainippon Sumitomo Pharma Co Ltd | ジヒドロイミダゾピラジノン誘導体 |
| AU2013225737B2 (en) | 2012-03-01 | 2018-03-01 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
| US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
| JP6449293B2 (ja) * | 2013-12-06 | 2019-01-09 | ジェネンテック， インコーポレイテッド | セリン／トレオニンキナーゼ阻害剤 |
| WO2015103133A1 (en) | 2013-12-30 | 2015-07-09 | Genentech, Inc. | Serine/threonine kinase inhibitors |
| EP3089980B1 (en) | 2013-12-30 | 2018-01-31 | Array Biopharma, Inc. | Serine/threonine kinase inhibitors |
| PL3129025T3 (pl) | 2014-04-09 | 2019-11-29 | Genentech Inc | Sposób wytwarzania środków leczniczych |
| US10412619B2 (en) * | 2014-11-14 | 2019-09-10 | Qualcomm Incorporated | Buffer status report for eDCS |
| WO2016162325A1 (en) * | 2015-04-07 | 2016-10-13 | Astrazeneca Ab | Substituted 3,4-dihydropyrrolo[1,2-a]pyrazin-1 (2h)-one derivatives as kinase inhibitors |
| WO2016192063A1 (en) | 2015-06-03 | 2016-12-08 | Changzhou Jiekai Pharmatech Co. Ltd | Heterocyclic compounds as erk inhibitors |
| AU2015396809B2 (en) | 2015-06-03 | 2019-07-11 | Js Innopharm (Shanghai) Ltd. | Heterocyclic compounds for treating psoriasis |
| SI3374359T1 (sl) * | 2015-11-09 | 2020-04-30 | Astrazeneca Ab | Derivati dihidroimidazopirazinona uporabni pri zdravljenju raka |
-
2016
- 2016-11-08 SI SI201630668T patent/SI3374359T1/sl unknown
- 2016-11-08 BR BR112018008397-6A patent/BR112018008397B1/pt active IP Right Grant
- 2016-11-08 HR HRP20200342TT patent/HRP20200342T1/hr unknown
- 2016-11-08 KR KR1020187016091A patent/KR20180074788A/ko not_active Withdrawn
- 2016-11-08 RS RS20200392A patent/RS60155B1/sr unknown
- 2016-11-08 MX MX2018005725A patent/MX376639B/es active IP Right Grant
- 2016-11-08 US US15/345,537 patent/US9902731B2/en active Active
- 2016-11-08 EA EA201891063A patent/EA038028B1/ru unknown
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