JP6216791B2 - 阻害剤化合物 - Google Patents
阻害剤化合物 Download PDFInfo
- Publication number
- JP6216791B2 JP6216791B2 JP2015530495A JP2015530495A JP6216791B2 JP 6216791 B2 JP6216791 B2 JP 6216791B2 JP 2015530495 A JP2015530495 A JP 2015530495A JP 2015530495 A JP2015530495 A JP 2015530495A JP 6216791 B2 JP6216791 B2 JP 6216791B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- alkyl
- methoxy
- pyrazol
- phenyl
- 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
- ZLJIRNNOBVWOOS-UHFFFAOYSA-N C=[O]c(cc(cc1)S)c1N Chemical compound C=[O]c(cc(cc1)S)c1N ZLJIRNNOBVWOOS-UHFFFAOYSA-N 0.000 description 1
- MJSREVGITAJCEL-UHFFFAOYSA-N CC(C)(CNc1nccc2c1nc(Nc(ccc(-c1nnn[n]1C)n1)c1OC)nc2)OC Chemical compound CC(C)(CNc1nccc2c1nc(Nc(ccc(-c1nnn[n]1C)n1)c1OC)nc2)OC MJSREVGITAJCEL-UHFFFAOYSA-N 0.000 description 1
- KEJBZRCOUASHPK-UHFFFAOYSA-N CC(C)Oc(cc(cc1)-c2c[n](C)nc2)c1NC=O Chemical compound CC(C)Oc(cc(cc1)-c2c[n](C)nc2)c1NC=O KEJBZRCOUASHPK-UHFFFAOYSA-N 0.000 description 1
- KTDLIDFCMGOUKC-NSHDSACASA-N CC1(C)OB(C2=CN(CC(F)F)N(C)C2)O[C@]1(C)N Chemical compound CC1(C)OB(C2=CN(CC(F)F)N(C)C2)O[C@]1(C)N KTDLIDFCMGOUKC-NSHDSACASA-N 0.000 description 1
- 0 CCOC1=CC(c2nnc[n]2C)=CCC1Nc1nc(c(*)nc(C)c2)c2cn1 Chemical compound CCOC1=CC(c2nnc[n]2C)=CCC1Nc1nc(c(*)nc(C)c2)c2cn1 0.000 description 1
- YEOQHUXOUKTVPT-UHFFFAOYSA-N CCOc(cc(cc1)-c2nnc[n]2C)c1N Chemical compound CCOc(cc(cc1)-c2nnc[n]2C)c1N YEOQHUXOUKTVPT-UHFFFAOYSA-N 0.000 description 1
- AZOWLGREMRBIRN-UHFFFAOYSA-N CCc(cc(cc1)-c2c[n](C)nc2)c1N Chemical compound CCc(cc(cc1)-c2c[n](C)nc2)c1N AZOWLGREMRBIRN-UHFFFAOYSA-N 0.000 description 1
- PAFQTDKYYROHMA-UHFFFAOYSA-N CN(C)CC[n]1ncc(I)c1 Chemical compound CN(C)CC[n]1ncc(I)c1 PAFQTDKYYROHMA-UHFFFAOYSA-N 0.000 description 1
- YHXOZAUTEWFRER-UHFFFAOYSA-N CN(CC1)CCC1[n]1ncc(-c2cccc3c2cc(Nc(ccc(C(N(C2)CC2OC)=O)c2)c2OC)nc3)c1 Chemical compound CN(CC1)CCC1[n]1ncc(-c2cccc3c2cc(Nc(ccc(C(N(C2)CC2OC)=O)c2)c2OC)nc3)c1 YHXOZAUTEWFRER-UHFFFAOYSA-N 0.000 description 1
- UALRJETVVDVJCD-XIWNQAKTSA-O CN/C=C(\C=[NH2+])/c(cc1OC)ccc1Nc1nc(c(Cl)ncc2)c2cn1 Chemical compound CN/C=C(\C=[NH2+])/c(cc1OC)ccc1Nc1nc(c(Cl)ncc2)c2cn1 UALRJETVVDVJCD-XIWNQAKTSA-O 0.000 description 1
- XKTMLTZHDGOSNL-UHFFFAOYSA-N CN1CCN(CC[n]2ncc(-c(cc3OC)ccc3Nc3nc(c(NC4CCCCC4)ncc4)c4cn3)c2)CC1 Chemical compound CN1CCN(CC[n]2ncc(-c(cc3OC)ccc3Nc3nc(c(NC4CCCCC4)ncc4)c4cn3)c2)CC1 XKTMLTZHDGOSNL-UHFFFAOYSA-N 0.000 description 1
- KRQMSXPCFNMXGS-UHFFFAOYSA-N CN1CCN(CC[n]2ncc(I)c2)CC1 Chemical compound CN1CCN(CC[n]2ncc(I)c2)CC1 KRQMSXPCFNMXGS-UHFFFAOYSA-N 0.000 description 1
- SKSRYWGHQFQRME-UHFFFAOYSA-N COc(nc(cc1)SC)c1[N+]([O-])=O Chemical compound COc(nc(cc1)SC)c1[N+]([O-])=O SKSRYWGHQFQRME-UHFFFAOYSA-N 0.000 description 1
- RBRQRTSULICSFP-UHFFFAOYSA-N CS(c1nc2c(N3CC4(COC4)CC3)nccc2cn1)(=O)=O Chemical compound CS(c1nc2c(N3CC4(COC4)CC3)nccc2cn1)(=O)=O RBRQRTSULICSFP-UHFFFAOYSA-N 0.000 description 1
- PVHIGFHNYQVMRW-UHFFFAOYSA-N CSc1nc2c(C3CC3)nccc2cn1 Chemical compound CSc1nc2c(C3CC3)nccc2cn1 PVHIGFHNYQVMRW-UHFFFAOYSA-N 0.000 description 1
- PCTUEDXGUWSKSV-UHFFFAOYSA-N C[n](nc1)nc1C(C=CC1[N+]([O-])=O)=NC1OC Chemical compound C[n](nc1)nc1C(C=CC1[N+]([O-])=O)=NC1OC PCTUEDXGUWSKSV-UHFFFAOYSA-N 0.000 description 1
- SEROCBXXHACDIM-UHFFFAOYSA-N C[n]1ncc(-c(c2c3)cccc2cnc3Nc(ccc(OC)c2)c2OC)c1 Chemical compound C[n]1ncc(-c(c2c3)cccc2cnc3Nc(ccc(OC)c2)c2OC)c1 SEROCBXXHACDIM-UHFFFAOYSA-N 0.000 description 1
- WURIOZMXFUGBMX-UHFFFAOYSA-N C[n]1ncc(-c(cc2OC)ccc2Nc2nc(c(-c3c[n](C)nc3)ncc3)c3cn2)c1 Chemical compound C[n]1ncc(-c(cc2OC)ccc2Nc2nc(c(-c3c[n](C)nc3)ncc3)c3cn2)c1 WURIOZMXFUGBMX-UHFFFAOYSA-N 0.000 description 1
- SYXBXYLYOCLOHD-UHFFFAOYSA-N C[n]1nnnc1-c(cc1)nc(OC)c1N Chemical compound C[n]1nnnc1-c(cc1)nc(OC)c1N SYXBXYLYOCLOHD-UHFFFAOYSA-N 0.000 description 1
- ALNODCCNKFRLDE-UHFFFAOYSA-N Nc(c(Cl)c1)ccc1N1CC=[O]CC1 Chemical compound Nc(c(Cl)c1)ccc1N1CC=[O]CC1 ALNODCCNKFRLDE-UHFFFAOYSA-N 0.000 description 1
- DZMNECGHHBBVBC-UHFFFAOYSA-N Oc(c1c2)nccc1cnc2OCc1ccccc1 Chemical compound Oc(c1c2)nccc1cnc2OCc1ccccc1 DZMNECGHHBBVBC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic 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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1216017.2 | 2012-09-07 | ||
| GBGB1216017.2A GB201216017D0 (en) | 2012-09-07 | 2012-09-07 | Inhibitor compounds |
| PCT/GB2013/052360 WO2014037750A1 (en) | 2012-09-07 | 2013-09-09 | Inhibitor compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017182377A Division JP6496376B2 (ja) | 2012-09-07 | 2017-09-22 | 阻害剤化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015527387A JP2015527387A (ja) | 2015-09-17 |
| JP2015527387A5 JP2015527387A5 (OSRAM) | 2017-09-07 |
| JP6216791B2 true JP6216791B2 (ja) | 2017-10-18 |
Family
ID=47137117
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015530495A Active JP6216791B2 (ja) | 2012-09-07 | 2013-09-09 | 阻害剤化合物 |
| JP2017182377A Expired - Fee Related JP6496376B2 (ja) | 2012-09-07 | 2017-09-22 | 阻害剤化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017182377A Expired - Fee Related JP6496376B2 (ja) | 2012-09-07 | 2017-09-22 | 阻害剤化合物 |
Country Status (22)
| Country | Link |
|---|---|
| US (6) | US9409907B2 (OSRAM) |
| EP (2) | EP2892889B1 (OSRAM) |
| JP (2) | JP6216791B2 (OSRAM) |
| CN (1) | CN104837829B (OSRAM) |
| AU (2) | AU2013311434B2 (OSRAM) |
| BR (1) | BR112015004489B1 (OSRAM) |
| CA (1) | CA2884006C (OSRAM) |
| CY (1) | CY1119714T1 (OSRAM) |
| DK (2) | DK3293183T3 (OSRAM) |
| ES (2) | ES2742442T3 (OSRAM) |
| GB (1) | GB201216017D0 (OSRAM) |
| HR (1) | HRP20171835T1 (OSRAM) |
| HU (1) | HUE036259T2 (OSRAM) |
| LT (1) | LT2892889T (OSRAM) |
| NO (1) | NO2892889T3 (OSRAM) |
| PL (1) | PL2892889T3 (OSRAM) |
| PT (1) | PT2892889T (OSRAM) |
| RS (1) | RS56750B1 (OSRAM) |
| RU (1) | RU2673079C2 (OSRAM) |
| SI (1) | SI2892889T1 (OSRAM) |
| SM (1) | SMT201700596T1 (OSRAM) |
| WO (1) | WO2014037750A1 (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2018027967A (ja) * | 2012-09-07 | 2018-02-22 | キャンサー・リサーチ・テクノロジー・リミテッド | 阻害剤化合物 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9017724B2 (en) | 2004-02-24 | 2015-04-28 | The General Hospital Corporation | Catalytic radiofluorination |
| CA2718035C (en) | 2008-03-21 | 2017-10-24 | The General Hospital Corporation | Inositol derivatives for the detection and treatment of alzheimer' s disease and related disorders |
| GB201104267D0 (en) | 2011-03-14 | 2011-04-27 | Cancer Rec Tech Ltd | Pyrrolopyridineamino derivatives |
| GB201216018D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Pharmacologically active compounds |
| US9550770B2 (en) * | 2013-08-23 | 2017-01-24 | Neupharma, Inc. | Substituted quinazolines for inhibiting kinase activity |
| GB201403536D0 (en) | 2014-02-28 | 2014-04-16 | Cancer Rec Tech Ltd | Inhibitor compounds |
| JP6616934B2 (ja) * | 2014-05-22 | 2019-12-04 | 株式会社 資生堂 | レナリドミドの光学分割方法 |
| CA2976227C (en) | 2015-02-17 | 2023-10-24 | Neupharma, Inc. | Quinazoline derivatives and their use in treatment of cancer |
| WO2016166255A1 (en) | 2015-04-17 | 2016-10-20 | Netherlands Translational Research Center B.V. | Prognostic biomarkers for ttk inhibitor chemotherapy |
| MY192487A (en) | 2015-05-29 | 2022-08-23 | Teijin Pharma Ltd | Pyrido[3,4-d]pyrimidine derivative and pharmaceutically acceptable salt thereof |
| KR102591886B1 (ko) * | 2015-07-21 | 2023-10-20 | 광저우 맥시노벨 파마수티컬스 씨오., 엘티디. | 축합고리 피리미딘계 화합물, 중간체, 이의 제조 방법, 조성물 및 응용 |
| GB201522532D0 (en) * | 2015-12-21 | 2016-02-03 | Cancer Rec Tech Ltd | Novel pyrrolo[3,2-c]pyridine-6-amino derivatives |
| EP3497087B1 (en) | 2016-08-15 | 2021-11-10 | Neupharma, Inc. | Pyrrolo[1,2-c]pyrimidine, imidazo[1,5-c]pyrimidine, quinazoline, purine and imidazo[1,5-a][1,3,5]triazine derivatives as tyrosine kinase inhibitors for the treatment of cancer |
| CA3041854C (en) | 2016-11-28 | 2025-05-13 | Teijin Pharma Limited | PYRIDO DERIVATIVE CRYSTAL [3,4-D]PYRIMIDINE OR ITS SOLVA |
| US11084814B2 (en) | 2016-11-28 | 2021-08-10 | Teijin Pharma Limited | Pyrido[3, 4-d]pyrimidine derivative and pharmaceutically acceptable salt thereof |
| AU2018287988A1 (en) * | 2017-06-20 | 2019-10-10 | Breast Cancer Now | Methods and medical uses |
| GB201709840D0 (en) | 2017-06-20 | 2017-08-02 | Inst Of Cancer Research: Royal Cancer Hospital | Methods and medical uses |
| EP3701304B1 (en) | 2017-10-26 | 2022-05-04 | CommScope Connectivity Belgium BVBA | Telecommunications system |
| GB201809458D0 (en) | 2018-06-08 | 2018-07-25 | Crt Pioneer Fund Lp | Salt form |
| GB201809460D0 (en) | 2018-06-08 | 2018-07-25 | Crt Pioneer Fund Lp | Salt form |
| LT4053118T (lt) | 2019-10-30 | 2024-12-10 | Genfleet Therapeutics (Shanghai) Inc. | Pakeistas heterociklinis junginys su sujungtais žiedais, jo paruošimo būdas ir naudojimas farmacijoje |
| JP2023510918A (ja) * | 2020-01-15 | 2023-03-15 | ブループリント メディシンズ コーポレイション | Map4k1阻害剤 |
| KR102396930B1 (ko) * | 2020-01-15 | 2022-05-12 | 한국과학기술연구원 | 피리도[3,4-d]피리미딘 유도체 및 이를 포함하는 치료용 약학 조성물 |
| TW202202498A (zh) * | 2020-07-01 | 2022-01-16 | 大陸商四川海思科製藥有限公司 | 一種並環雜環衍生物及其在醫藥上的應用 |
| WO2022015423A1 (en) * | 2020-07-16 | 2022-01-20 | Dermavant Sciences GmbH | ISOQUINOLINE COMPOUNDS AND THEIR USE IN TREATING AhR IMBALANCE |
| CN115942937B (zh) * | 2020-08-17 | 2025-07-25 | 浙江扬厉医药技术有限公司 | 嘧啶并环类化合物 |
| JP2023549540A (ja) | 2020-11-18 | 2023-11-27 | デシフェラ・ファーマシューティカルズ,エルエルシー | Gcn2およびperkキナーゼ阻害剤およびその使用方法 |
| CN115583946A (zh) * | 2021-07-06 | 2023-01-10 | 赛诺哈勃药业(成都)有限公司 | 杂环化合物及其作为cdk抑制剂的用途 |
| AU2022412837A1 (en) * | 2021-12-16 | 2024-06-13 | Teijin Pharma Limited | Cdk9 inhibitor and use thereof |
| WO2024238574A1 (en) * | 2023-05-15 | 2024-11-21 | Aleksia Therapeutics, Inc. | Cdk inhibitor compounds |
| WO2025038785A1 (en) * | 2023-08-16 | 2025-02-20 | Biotheryx, Inc. | Sos1 protein degraders, pharmaceutical compositions, and therapeutic applications |
| CN117800875B (zh) * | 2023-12-21 | 2024-10-22 | 泰州精英化成医药科技有限公司 | 一种反式-(N-Boc-4-氨基环己基)乙酸的制备方法 |
| WO2025155740A1 (en) * | 2024-01-17 | 2025-07-24 | Iambic Therapeutics, Inc. | Combinations comprising aza-quinazoline compounds for use in the treatment of cancer |
Family Cites Families (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2697710A (en) | 1953-01-02 | 1954-12-21 | Burroughs Wellcome Co | Pyrido (2,3-d) pyrimidines and method of preparing same |
| US3021332A (en) | 1954-01-04 | 1962-02-13 | Burroughs Wellcome Co | Pyrido (2, 3-d) pyrimidine compounds and method of making |
| TJ342B (en) | 1994-11-14 | 2002-10-06 | Warner Lambert Co | Derivatives of 6-aryl pyrido Ä2,3-dÜ pyrimidines and naphthyridines pharmaceutical composition possess inhibiting effect of cellular proliferation pr ovoking protein tyrosine kinase and method of inhibiting cellular proliferation |
| AP2002002586A0 (en) | 2000-01-25 | 2002-09-30 | Warner Lambert Co | Pyrido[2,3-d] pyrimidine-2,7-diamine kinase inhibitors. |
| US7053070B2 (en) | 2000-01-25 | 2006-05-30 | Warner-Lambert Company | Pyrido[2,3-d]pyrimidine-2,7-diamine kinase inhibitors |
| WO2001082916A2 (en) | 2000-05-03 | 2001-11-08 | Tularik Inc. | Combination therapeutic compositions and methods of use |
| WO2002090360A1 (en) | 2001-05-10 | 2002-11-14 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| WO2003000011A2 (en) | 2001-06-21 | 2003-01-03 | Ariad Pharmaceuticals, Inc. | Novel pyridopyrimidines and uses thereof |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| AU2002353147A1 (en) | 2001-12-13 | 2003-06-30 | Abbott Laboratories | 3-(phenyl-alkoxy)-5-(phenyl)-pyridine derivatives and related compounds as kinase inhibitors for the treatment of cancer |
| ES2314224T3 (es) | 2002-03-07 | 2009-03-16 | F. Hoffmann-La Roche Ag | Inhibidores pirimidina y piridina biciclicos de p38 quinasa. |
| CA2492112A1 (en) * | 2002-08-06 | 2004-02-19 | F. Hoffmann-La Roche Ag | 6-alkoxy-pyrido-pyrimidines as p-38 map kinase inhibitors |
| US20040092521A1 (en) | 2002-11-12 | 2004-05-13 | Altenbach Robert J. | Bicyclic-substituted amines as histamine-3 receptor ligands |
| WO2004043458A1 (en) | 2002-11-12 | 2004-05-27 | Abbott Laboratories | Bicyclic-substituted amines as histamine-3 receptor ligands |
| MXPA05007503A (es) | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
| US20050256118A1 (en) | 2004-05-12 | 2005-11-17 | Altenbach Robert J | Bicyclic-substituted amines having cyclic-substituted monocyclic substituents |
| US7098222B2 (en) | 2004-05-12 | 2006-08-29 | Abbott Laboratories | Bicyclic-substituted amines having cyclic-substituted monocyclic substituents |
| DE602006008945D1 (de) | 2005-06-28 | 2009-10-15 | Sanofi Aventis | Isochinolinderivate als inhibitoren von rho-kinase |
| US7910595B2 (en) * | 2005-12-21 | 2011-03-22 | Abbott Laboratories | Anti-viral compounds |
| TW200808739A (en) * | 2006-04-06 | 2008-02-16 | Novartis Vaccines & Diagnostic | Quinazolines for PDK1 inhibition |
| JP2009535393A (ja) | 2006-05-01 | 2009-10-01 | ファイザー・プロダクツ・インク | 置換2−アミノ縮合複素環式化合物 |
| JO3235B1 (ar) | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | مركبات بيررولوبيريميدين و استعمالاتها |
| CA2673003A1 (en) | 2006-12-22 | 2008-07-03 | Novartis Ag | Quinazolines for pdk1 inhibition |
| WO2008135232A1 (en) | 2007-05-02 | 2008-11-13 | Riccardo Cortese | Use and compositions of purine derivatives for the treatment of proliferative disorders |
| WO2009032703A1 (en) | 2007-08-28 | 2009-03-12 | Irm Llc | 2- (het) arylamino-6-aminopyridine derivatives and fused forms thereof as anaplastic lymphoma kinase inhibitors |
| US20100311965A1 (en) * | 2007-12-28 | 2010-12-09 | Carna Biosciences Inc. | 2-aminoquinazoline derivative |
| GB0803018D0 (en) | 2008-02-19 | 2008-03-26 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| GB0812969D0 (en) | 2008-07-15 | 2008-08-20 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| EP2427195B1 (en) | 2009-05-07 | 2019-05-01 | Intellikine, LLC | Heterocyclic compounds and uses thereof |
| EP2519517B1 (en) | 2009-12-29 | 2015-03-25 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
| EP2542081A4 (en) | 2010-03-01 | 2013-07-31 | Gtx Inc | COMPOSITIONS FOR CANCER TREATMENT |
| GB201011182D0 (en) | 2010-07-02 | 2010-08-18 | Wireless Fibre Systems Ltd | Riser wireless communications system |
| EP2598508B1 (en) | 2010-07-30 | 2015-04-22 | Nerviano Medical Sciences S.r.l. | Isoxazolo-quinazolines as modulators of protein kinase activity |
| ES2377610B1 (es) | 2010-09-01 | 2013-02-05 | Institut Químic de Sarriá CETS Fundació Privada | Preparación de compuestos pirido[2,3-d]pirimidin-7(8h)-ona sustituidos. |
| JP2013540145A (ja) | 2010-10-21 | 2013-10-31 | ウニベルシテート デス ザールランデス | コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤 |
| EP2637669A4 (en) | 2010-11-10 | 2014-04-02 | Infinity Pharmaceuticals Inc | Heterocyclic compounds and their use |
| BR112013013790A2 (pt) | 2010-12-17 | 2016-09-13 | Hoffmann La Roche | compostos heterocíclos nitrogenosos 6,6-fundidos substituídos e usos dos mesmos |
| WO2012088438A1 (en) | 2010-12-22 | 2012-06-28 | Eutropics Pharmaceuticals, Inc. | Compositions and methods useful for treating diseases |
| TWI450891B (zh) | 2010-12-29 | 2014-09-01 | Dev Center Biotechnology | 新穎微管蛋白抑制劑 |
| BR112013018515B1 (pt) * | 2011-01-26 | 2021-06-29 | Nerviano Medical Sciences S.R.I | Derivados de pirrol tricíclico, processo para sua preparação e seu uso como inibidores da quinase |
| GB201104267D0 (en) | 2011-03-14 | 2011-04-27 | Cancer Rec Tech Ltd | Pyrrolopyridineamino derivatives |
| US9745191B2 (en) | 2011-04-11 | 2017-08-29 | Saudi Arabian Oil Company | Auto thermal reforming (ATR) catalytic structures |
| MX359664B (es) | 2011-07-29 | 2018-10-05 | Univ Colorado Regents | Tratamiento de cáncer de mama. |
| US9580390B2 (en) | 2011-10-12 | 2017-02-28 | University Health Network | Indazole compounds as kinase inhibitors and method of treating cancer with same |
| GB201216018D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Pharmacologically active compounds |
| GB201216017D0 (en) * | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Inhibitor compounds |
| EP2961409A1 (en) | 2013-02-26 | 2016-01-06 | Senex Biotechnology, Inc. | Inhibitors of cdk8/19 for use in treating estrogen receptor positive breast cancer |
| US9675586B2 (en) | 2013-12-06 | 2017-06-13 | Genentech, Inc. | Estrogen receptor modulator for the treatment of locally advanced or metastatic estrogen receptor positive breast cancer |
| GB201403536D0 (en) | 2014-02-28 | 2014-04-16 | Cancer Rec Tech Ltd | Inhibitor compounds |
| BR112016020897A2 (pt) | 2014-03-11 | 2018-01-23 | Council Queensland Inst Medical Res | ?determinação da agressividade de câncer, prognóstico e capacidade de reação a tratamento? |
| CA2955009A1 (en) | 2014-07-14 | 2016-01-21 | Signal Pharmaceuticals, Llc | Methods of treating a cancer using substituted pyrrolopyrimidine compounds, compositions thereof |
| WO2016073771A2 (en) | 2014-11-06 | 2016-05-12 | Ohio State Innovation Foundation | Pyrrolopyrimidine derivatives as mps1/ttk kinase inhibitors |
| GB201522532D0 (en) | 2015-12-21 | 2016-02-03 | Cancer Rec Tech Ltd | Novel pyrrolo[3,2-c]pyridine-6-amino derivatives |
| AU2018287988A1 (en) | 2017-06-20 | 2019-10-10 | Breast Cancer Now | Methods and medical uses |
| GB201709840D0 (en) | 2017-06-20 | 2017-08-02 | Inst Of Cancer Research: Royal Cancer Hospital | Methods and medical uses |
-
2012
- 2012-09-07 GB GBGB1216017.2A patent/GB201216017D0/en not_active Ceased
-
2013
- 2013-09-09 RS RS20171314A patent/RS56750B1/sr unknown
- 2013-09-09 JP JP2015530495A patent/JP6216791B2/ja active Active
- 2013-09-09 LT LTEP13760106.8T patent/LT2892889T/lt unknown
- 2013-09-09 BR BR112015004489-1A patent/BR112015004489B1/pt not_active IP Right Cessation
- 2013-09-09 EP EP13760106.8A patent/EP2892889B1/en active Active
- 2013-09-09 ES ES17192253T patent/ES2742442T3/es active Active
- 2013-09-09 HU HUE13760106A patent/HUE036259T2/hu unknown
- 2013-09-09 ES ES13760106.8T patent/ES2655194T3/es active Active
- 2013-09-09 DK DK17192253.7T patent/DK3293183T3/da active
- 2013-09-09 WO PCT/GB2013/052360 patent/WO2014037750A1/en not_active Ceased
- 2013-09-09 CA CA2884006A patent/CA2884006C/en active Active
- 2013-09-09 PL PL13760106T patent/PL2892889T3/pl unknown
- 2013-09-09 AU AU2013311434A patent/AU2013311434B2/en not_active Ceased
- 2013-09-09 HR HRP20171835TT patent/HRP20171835T1/hr unknown
- 2013-09-09 DK DK13760106.8T patent/DK2892889T3/en active
- 2013-09-09 PT PT137601068T patent/PT2892889T/pt unknown
- 2013-09-09 RU RU2015112580A patent/RU2673079C2/ru active
- 2013-09-09 SM SM20170596T patent/SMT201700596T1/it unknown
- 2013-09-09 NO NO13760106A patent/NO2892889T3/no unknown
- 2013-09-09 CN CN201380057967.7A patent/CN104837829B/zh not_active Expired - Fee Related
- 2013-09-09 US US14/426,549 patent/US9409907B2/en active Active
- 2013-09-09 EP EP17192253.7A patent/EP3293183B1/en active Active
- 2013-09-09 SI SI201330829T patent/SI2892889T1/sl unknown
-
2016
- 2016-04-06 US US15/091,980 patent/US9834552B2/en active Active
- 2016-04-06 US US15/091,887 patent/US9890157B2/en active Active
-
2017
- 2017-09-22 JP JP2017182377A patent/JP6496376B2/ja not_active Expired - Fee Related
- 2017-11-27 AU AU2017268488A patent/AU2017268488B2/en not_active Ceased
- 2017-12-29 CY CY20171101358T patent/CY1119714T1/el unknown
-
2018
- 2018-01-08 US US15/864,499 patent/US10479788B2/en active Active
-
2019
- 2019-10-10 US US16/598,717 patent/US11046688B2/en not_active Expired - Fee Related
-
2021
- 2021-05-13 US US17/319,231 patent/US11897877B2/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2018027967A (ja) * | 2012-09-07 | 2018-02-22 | キャンサー・リサーチ・テクノロジー・リミテッド | 阻害剤化合物 |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6216791B2 (ja) | 阻害剤化合物 | |
| JP6027989B2 (ja) | Mps1阻害剤としてのピロロピリジンアミノ誘導体 | |
| JP6297570B2 (ja) | 薬理活性化合物 | |
| JP6440728B2 (ja) | N2−フェニル−ピリド[3,4−d]ピリミジン−2,8−ジアミン誘導体およびmps1阻害剤としてのそれらの使用 | |
| HK1211921B (en) | Inhibitor compounds |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20160707 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20170420 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20170425 |
|
| A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20170725 |
|
| 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: 20170825 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20170925 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6216791 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |