CN101878216B - 作为蛋白激酶抑制剂的嘧啶衍生物 - Google Patents
作为蛋白激酶抑制剂的嘧啶衍生物 Download PDFInfo
- Publication number
- CN101878216B CN101878216B CN2008801182902A CN200880118290A CN101878216B CN 101878216 B CN101878216 B CN 101878216B CN 2008801182902 A CN2008801182902 A CN 2008801182902A CN 200880118290 A CN200880118290 A CN 200880118290A CN 101878216 B CN101878216 B CN 101878216B
- Authority
- CN
- China
- Prior art keywords
- compound
- methyl
- cyclopentyl
- pyrimido
- diazepine
- 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
- SBYHFKPVCBCYGV-UHFFFAOYSA-N C(C1)C2CCN1CC2 Chemical compound C(C1)C2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- ONIVTPSMIVIGHU-UHFFFAOYSA-N CC(C)(CN(C1CCCC1)c(nc(Nc(ccc(C(N)=O)c1)c1OC)nc1)c1N1C)C1=O Chemical compound CC(C)(CN(C1CCCC1)c(nc(Nc(ccc(C(N)=O)c1)c1OC)nc1)c1N1C)C1=O ONIVTPSMIVIGHU-UHFFFAOYSA-N 0.000 description 1
- QYWMDSSWIGWXSE-UHFFFAOYSA-N CC(C1)N(C2CCCC2)c(nc(Nc(cc2)ccc2C(O)=O)nc2)c2NC1=O Chemical compound CC(C1)N(C2CCCC2)c(nc(Nc(cc2)ccc2C(O)=O)nc2)c2NC1=O QYWMDSSWIGWXSE-UHFFFAOYSA-N 0.000 description 1
- KZLQLABUFJNPSZ-UHFFFAOYSA-N CC(C1)N(C2CCCC2)c(nc(Nc(ccc(C(NC2CCN(C)CC2)=O)c2)c2OC)nc2)c2N(C)C1=O Chemical compound CC(C1)N(C2CCCC2)c(nc(Nc(ccc(C(NC2CCN(C)CC2)=O)c2)c2OC)nc2)c2N(C)C1=O KZLQLABUFJNPSZ-UHFFFAOYSA-N 0.000 description 1
- YAMIMLRPPHTJPC-UHFFFAOYSA-N CC(CN(C1CCCC1)c(nc(nc1)Cl)c1[N+]([O-])=O)C(OC)=O Chemical compound CC(CN(C1CCCC1)c(nc(nc1)Cl)c1[N+]([O-])=O)C(OC)=O YAMIMLRPPHTJPC-UHFFFAOYSA-N 0.000 description 1
- CKKCYWXFAHYHMM-UHFFFAOYSA-N CCC(CC)N(CC1)c2nc(Nc(c(OC)c3)ccc3C(NC3CCN(C)CC3)=O)ncc2N(CC)C1=O Chemical compound CCC(CC)N(CC1)c2nc(Nc(c(OC)c3)ccc3C(NC3CCN(C)CC3)=O)ncc2N(CC)C1=O CKKCYWXFAHYHMM-UHFFFAOYSA-N 0.000 description 1
- GPXQMZVGHFRABO-UHFFFAOYSA-N CN(CC1)CCN1NC(c(cc1)cc(F)c1Nc(nc1)nc(N(CC23CC2)C2CCCC2)c1N(C)C3=O)=O Chemical compound CN(CC1)CCN1NC(c(cc1)cc(F)c1Nc(nc1)nc(N(CC23CC2)C2CCCC2)c1N(C)C3=O)=O GPXQMZVGHFRABO-UHFFFAOYSA-N 0.000 description 1
- PEXIBZBONDDAHU-UHFFFAOYSA-N CN(c(cn1)c(N(CC2)C3CCOCC3)nc1Cl)C2=O Chemical compound CN(c(cn1)c(N(CC2)C3CCOCC3)nc1Cl)C2=O PEXIBZBONDDAHU-UHFFFAOYSA-N 0.000 description 1
- UHCROXCVKZSKQH-UHFFFAOYSA-N COc1cc(C(O)=O)ccc1Nc(nc1)nc(N(CC2)C3CCCCC3)c1NC2=O Chemical compound COc1cc(C(O)=O)ccc1Nc(nc1)nc(N(CC2)C3CCCCC3)c1NC2=O UHCROXCVKZSKQH-UHFFFAOYSA-N 0.000 description 1
Images
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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- 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
- C07D487/10—Spiro-condensed systems
-
- 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
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0719038A GB0719038D0 (en) | 2007-09-28 | 2007-09-28 | Compound |
| GB0719038.2 | 2007-09-28 | ||
| GB0806844A GB0806844D0 (en) | 2008-04-15 | 2008-04-15 | Compound |
| GB0806844.7 | 2008-04-15 | ||
| PCT/GB2008/003305 WO2009040556A1 (en) | 2007-09-28 | 2008-09-29 | Pyrimidine derivatives as protein kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101878216A CN101878216A (zh) | 2010-11-03 |
| CN101878216B true CN101878216B (zh) | 2013-07-10 |
Family
ID=40199600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801182902A Active CN101878216B (zh) | 2007-09-28 | 2008-09-29 | 作为蛋白激酶抑制剂的嘧啶衍生物 |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US8563542B2 (enExample) |
| EP (2) | EP2610256B1 (enExample) |
| JP (2) | JP5410432B2 (enExample) |
| CN (1) | CN101878216B (enExample) |
| CA (1) | CA2700979C (enExample) |
| ES (2) | ES2585110T3 (enExample) |
| PL (2) | PL2610256T3 (enExample) |
| RU (2) | RU2478100C2 (enExample) |
| WO (1) | WO2009040556A1 (enExample) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ570530A (en) | 2006-02-14 | 2011-09-30 | Vertex Pharma | Pharmaceutical compositions comprising 6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4)diazepine derivatives |
| CN101952291A (zh) | 2007-08-15 | 2011-01-19 | 弗特克斯药品有限公司 | 用作人蛋白激酶plk1至plk4的抑制剂以治疗增殖疾病的4-(9-(3,3-二氟环戊基)-5,7,7-三甲基-6-氧代-6,7,8,9-四氢-5h-嘧啶并[4,5-b][1,4]二氮杂䓬-2-基氨基)-3-甲氧基苯甲酰胺衍生物 |
| US8026234B2 (en) | 2007-09-25 | 2011-09-27 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| EP2610256B1 (en) | 2007-09-28 | 2016-04-27 | Cyclacel Limited | Pyrimidine derivatives as protein kinase inhibitors |
| AU2009271658B2 (en) | 2008-06-23 | 2014-04-10 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors |
| WO2010008459A1 (en) * | 2008-06-23 | 2010-01-21 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors |
| SG10201405826RA (en) | 2009-06-17 | 2014-12-30 | Vertex Pharma | Inhibitors of influenza viruses replication |
| CN103492391A (zh) | 2009-09-25 | 2014-01-01 | 沃泰克斯药物股份有限公司 | 用于制备用作蛋白激酶抑制剂的嘧啶衍生物的方法 |
| MX2012003484A (es) | 2009-09-25 | 2012-04-20 | Vertex Pharma | Metodos para preparar derivados de pirimidina utiles como inhibidores de proteina cinasa. |
| AU2011260323A1 (en) | 2010-06-04 | 2012-11-15 | F. Hoffmann-La Roche Ag | Aminopyrimidine derivatives as LRRK2 modulators |
| DK2638031T3 (en) | 2010-11-10 | 2017-12-11 | Genentech Inc | PYRAZOLAMINOPYRIMIDINE DERIVATIVES AS LRRK2 MODULATORS |
| RU2013132681A (ru) | 2010-12-16 | 2015-01-27 | Вертекс Фармасьютикалз Инкорпорейтед | Ингибиторы репликации вирусов гриппа |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
| GB201205752D0 (en) * | 2012-03-30 | 2012-05-16 | Cyclacel Ltd | Treatment |
| EP3388436B1 (en) | 2013-03-15 | 2020-08-12 | Dana-Farber Cancer Institute, Inc. | Pyrimido-diazepinone compounds and methods of treating disorders |
| MX2016001037A (es) | 2013-07-25 | 2016-11-10 | Dana Farber Cancer Inst Inc | Inhibidores de factores de transcripción y usos. |
| PT3068776T (pt) | 2013-11-13 | 2019-08-26 | Vertex Pharma | Inibidores da replicação de vírus da gripe |
| WO2015073481A1 (en) | 2013-11-13 | 2015-05-21 | Vertex Pharmaceuticals Incorporated | Methods of preparing inhibitors of influenza viruses replication |
| EP3099693A4 (en) * | 2014-01-31 | 2017-08-16 | Dana-Farber Cancer Institute, Inc. | Uses of diazepane derivatives |
| US10150756B2 (en) | 2014-01-31 | 2018-12-11 | Dana-Farber Cancer Institute, Inc. | Diaminopyrimidine benzenesulfone derivatives and uses thereof |
| KR101517414B1 (ko) * | 2014-04-24 | 2015-05-04 | 고려대학교 산학협력단 | 염증성 질환의 예방 또는 치료용 약학 조성물 |
| RU2017104897A (ru) | 2014-08-08 | 2018-09-10 | Дана-Фарбер Кэнсер Инститьют, Инк. | Производные диазепана и их применения |
| ES2764178T3 (es) | 2014-12-16 | 2020-06-02 | Kayla Therapeutics | Dinucleótidos cíclicos fluorados para inducción de citocinas |
| EP3294735B8 (en) | 2015-05-13 | 2022-01-05 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| JP6704416B2 (ja) | 2015-05-13 | 2020-06-03 | 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Vertex Pharmaceuticals Incorporated | インフルエンザウイルスの複製の阻害剤を調製する方法 |
| CA2986441A1 (en) | 2015-06-12 | 2016-12-15 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| PE20181287A1 (es) | 2015-09-11 | 2018-08-07 | Dana Farber Cancer Inst Inc | Ciano tienotriazolpirazinas y usos de las mismas |
| RU2018112953A (ru) | 2015-09-11 | 2019-10-14 | Дана-Фарбер Кэнсер Инститьют, Инк. | Ацетамидтиенотриазолодиазепины и пути их применения |
| US10738016B2 (en) | 2015-10-13 | 2020-08-11 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | BRD4-kinase inhibitors as cancer therapeutics |
| US10913752B2 (en) | 2015-11-25 | 2021-02-09 | Dana-Farber Cancer Institute, Inc. | Bivalent bromodomain inhibitors and uses thereof |
| CN107151250B (zh) * | 2016-03-04 | 2020-03-27 | 安徽省新星药物开发有限责任公司 | 嘧啶类七元环化合物、其制备方法、药用组合物及其应用 |
| JP6968819B2 (ja) * | 2016-04-07 | 2021-11-17 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッドDana−Farber Cancer Institute, Inc. | ピリミド−ジアゼピノンキナーゼ骨格化合物およびpi3k媒介性障害の治療方法 |
| CN112218851A (zh) * | 2017-11-02 | 2021-01-12 | 卡里科生命科学有限责任公司 | 整合应激通路的调节剂 |
| WO2019090088A1 (en) | 2017-11-02 | 2019-05-09 | Calico Life Sciences Llc | Modulators of the integrated stress pathway |
| US20220281880A1 (en) * | 2019-08-16 | 2022-09-08 | Cyclacel Limited | Crystalline forms of pyrimidino diazepine derivative |
| ES3047933T3 (en) * | 2019-08-16 | 2025-12-05 | Cyclacel Pharmaceuticals Inc | Process for the preparation of a pyrimidino-diazepine derivative |
| CA3150316A1 (en) * | 2019-09-27 | 2021-04-01 | Dana-Farber Cancer Institute, Inc. | ERK5 DEGRADING AGENTS USED AS THERAPEUTIC AGENTS IN CANCER AND INFLAMMATORY DISEASES |
| US20250215101A1 (en) | 2022-04-08 | 2025-07-03 | Inhibrx Biosciences, Inc. | DR5 Agonist and PLK1 Inhibitor or CDK Inhibitor Combination Therapy |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9117635D0 (en) | 1991-08-15 | 1991-10-02 | British Telecomm | Phase shifter |
| GB0302220D0 (en) | 2003-01-30 | 2003-03-05 | Cyclacel Ltd | Use |
| US6861422B2 (en) | 2003-02-26 | 2005-03-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
| HRP20050735B1 (hr) | 2003-02-26 | 2013-08-31 | Boehringer Ingelheim Pharma Gmbh & Co.Kg | Dihidropteridinoni, metoda za njihovu proizvodnju i upotrebu u obliku lijekova |
| US8710009B2 (en) | 2004-05-26 | 2014-04-29 | The Texas A&M University System | HSP20 inhibits amyloidogenesis and neurotoxicity |
| CA2582235A1 (en) * | 2004-10-04 | 2006-04-20 | Millennium Pharmaceuticals, Inc. | Lactam compounds useful as protein kinase inhibitors |
| JP5204650B2 (ja) | 2005-06-24 | 2013-06-05 | イーライ リリー アンド カンパニー | アンドロゲン受容体調節物質として有用なテトラヒドロカルバゾール誘導体 |
| US7439358B2 (en) | 2006-02-08 | 2008-10-21 | Boehringer Ingelheim International Gmbh | Specific salt, anhydrous and crystalline form of a dihydropteridione derivative |
| NZ570530A (en) * | 2006-02-14 | 2011-09-30 | Vertex Pharma | Pharmaceutical compositions comprising 6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4)diazepine derivatives |
| TW200808325A (en) * | 2006-07-06 | 2008-02-16 | Astrazeneca Ab | Novel compounds |
| SI2139892T1 (sl) * | 2007-03-22 | 2011-12-30 | Takede Pharmaceutical Company Ltd | Substituirani pirimidodiazepini, uporabni kot PLK1 inhibitorji |
| US8026234B2 (en) * | 2007-09-25 | 2011-09-27 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| EP2610256B1 (en) | 2007-09-28 | 2016-04-27 | Cyclacel Limited | Pyrimidine derivatives as protein kinase inhibitors |
| US20090291938A1 (en) * | 2007-11-19 | 2009-11-26 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| WO2010083505A1 (en) | 2009-01-19 | 2010-07-22 | The Trustees Of The University Of Pennsylvania | Method of treating cancer using a survivin inhibitor |
| GB201205752D0 (en) | 2012-03-30 | 2012-05-16 | Cyclacel Ltd | Treatment |
-
2008
- 2008-09-29 EP EP13156251.4A patent/EP2610256B1/en active Active
- 2008-09-29 ES ES13156251.4T patent/ES2585110T3/es active Active
- 2008-09-29 ES ES08806455T patent/ES2457394T3/es active Active
- 2008-09-29 PL PL13156251.4T patent/PL2610256T3/pl unknown
- 2008-09-29 RU RU2010116759/04A patent/RU2478100C2/ru active
- 2008-09-29 EP EP20080806455 patent/EP2205603B1/en active Active
- 2008-09-29 JP JP2010526364A patent/JP5410432B2/ja active Active
- 2008-09-29 CA CA2700979A patent/CA2700979C/en active Active
- 2008-09-29 US US12/680,353 patent/US8563542B2/en active Active
- 2008-09-29 WO PCT/GB2008/003305 patent/WO2009040556A1/en not_active Ceased
- 2008-09-29 CN CN2008801182902A patent/CN101878216B/zh active Active
- 2008-09-29 PL PL08806455T patent/PL2205603T3/pl unknown
-
2013
- 2013-02-26 RU RU2013108456A patent/RU2623221C2/ru active
- 2013-06-05 US US13/910,349 patent/US9133199B2/en active Active
- 2013-11-06 JP JP2013230231A patent/JP5863196B2/ja not_active Expired - Fee Related
-
2015
- 2015-08-07 US US14/820,711 patent/US9493471B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2610256B1 (en) | 2016-04-27 |
| PL2610256T3 (pl) | 2016-11-30 |
| PL2205603T3 (pl) | 2014-07-31 |
| US9493471B2 (en) | 2016-11-15 |
| CN101878216A (zh) | 2010-11-03 |
| HK1146042A1 (en) | 2011-05-13 |
| WO2009040556A1 (en) | 2009-04-02 |
| JP5863196B2 (ja) | 2016-02-16 |
| ES2585110T3 (es) | 2016-10-03 |
| US20150344486A1 (en) | 2015-12-03 |
| US8563542B2 (en) | 2013-10-22 |
| JP2014076994A (ja) | 2014-05-01 |
| EP2205603B1 (en) | 2014-01-15 |
| JP2010540509A (ja) | 2010-12-24 |
| CA2700979C (en) | 2017-06-20 |
| US20140066436A1 (en) | 2014-03-06 |
| CA2700979A1 (en) | 2009-04-02 |
| RU2478100C2 (ru) | 2013-03-27 |
| JP5410432B2 (ja) | 2014-02-05 |
| RU2013108456A (ru) | 2014-09-10 |
| HK1187895A1 (en) | 2014-04-17 |
| EP2205603A1 (en) | 2010-07-14 |
| RU2010116759A (ru) | 2011-11-10 |
| ES2457394T3 (es) | 2014-04-25 |
| US20110046093A1 (en) | 2011-02-24 |
| EP2610256A1 (en) | 2013-07-03 |
| US9133199B2 (en) | 2015-09-15 |
| RU2623221C2 (ru) | 2017-06-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101878216B (zh) | 作为蛋白激酶抑制剂的嘧啶衍生物 | |
| AU2007284542B2 (en) | Tricyclic compounds and its use as tyrosine kinase modulators | |
| US9249145B2 (en) | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors | |
| CN106456580B (zh) | 作为蛋白质脱乙酰酶抑制剂和蛋白质脱乙酰酶-蛋白质激酶双重抑制剂的杂环异羟肟酸及其使用方法 | |
| US11274098B2 (en) | Tricyclic compounds for use in treatment of proliferative disorders | |
| KR20190012167A (ko) | 이소퀴놀린-3-일 카르복스아마이드 및 이의 제제와 용도 | |
| TW201940479A (zh) | 作為jak抑制劑之聯吡唑衍生物 | |
| JP2013543007A (ja) | Jak阻害剤としての複素環置換ピロロピリジンおよびピロロピリミジン | |
| TW200808325A (en) | Novel compounds | |
| CN103797010A (zh) | 作为jak抑制剂的氮杂环丁烷基苯基、吡啶基或吡嗪基甲酰胺衍生物 | |
| US20060166993A1 (en) | Substituted imidazotriazines | |
| CN101687855A (zh) | 酞嗪酮衍生物及其作为治疗癌症的药物的用途 | |
| US20170233395A1 (en) | 2,4-disubstituted 7h-pyrrolo[2,3-d]pyrimidine derivative, preparation method and medicinal use thereof | |
| TW200835495A (en) | Substituted 8-piperidinyl-2-pyridinyl-pyrimido[1,2-a] pyrimidin-6-one and 8-piperidinyl-2-pyrimidinyl-pyrimido[1,2-a] pyrimidin-6-one derivatives | |
| JP2007504159A (ja) | プロテインキナーゼ阻害剤としての化合物および組成物 | |
| CN108463222A (zh) | 用于治疗疾病的杂环化合物 | |
| JP2005519087A (ja) | 1−[アルキル]、1−[(ヘテロアリール)アルキル]および1−[(アリール)アルキル]−7−(ピリミジン−4−イル)−イミダゾ[1,2−a]ピリミジン−5(1H)−オン誘導体 | |
| JP6916195B2 (ja) | キナーゼ活性の阻害剤としての化合物 | |
| US9290503B2 (en) | Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders | |
| US20240051946A1 (en) | Targeted protein degradation of parp14 for use in therapy | |
| HK1146042B (en) | Pyrimidine derivatives as protein kinase inhibitors | |
| HK1187895B (en) | Pyrimidine derivatives as protein kinase inhibitors | |
| HK1260375B (zh) | 用於治疗疾病的杂环化合物 | |
| HK1229722B (zh) | 作为蛋白质脱乙酰酶抑制剂和蛋白质脱乙酰酶-蛋白质激酶双重抑制剂的杂环异羟肟酸及其使用方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant |