SI2201012T1 - Derivati pirolo(2,3-D)pirimidina kot inhibitorji proteina kinaze B - Google Patents
Derivati pirolo(2,3-D)pirimidina kot inhibitorji proteina kinaze BInfo
- Publication number
- SI2201012T1 SI2201012T1 SI200831281T SI200831281T SI2201012T1 SI 2201012 T1 SI2201012 T1 SI 2201012T1 SI 200831281 T SI200831281 T SI 200831281T SI 200831281 T SI200831281 T SI 200831281T SI 2201012 T1 SI2201012 T1 SI 2201012T1
- Authority
- SI
- Slovenia
- Prior art keywords
- pyrrološ2
- dćpyrimidin
- inhibitors
- derivatives
- protein kinase
- Prior art date
Links
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
- A61K31/495—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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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)
- Epidemiology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (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 (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97919207P | 2007-10-11 | 2007-10-11 | |
| US4786208P | 2008-04-25 | 2008-04-25 | |
| EP08806741.8A EP2201012B1 (en) | 2007-10-11 | 2008-10-09 | Pyrrolo[2,3-d]pyrimidin derivatives as protein kinase b inhibitors |
| PCT/GB2008/050925 WO2009047563A1 (en) | 2007-10-11 | 2008-10-09 | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI2201012T1 true SI2201012T1 (sl) | 2014-10-30 |
Family
ID=40251789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI200831281T SI2201012T1 (sl) | 2007-10-11 | 2008-10-09 | Derivati pirolo(2,3-D)pirimidina kot inhibitorji proteina kinaze B |
Country Status (38)
| Country | Link |
|---|---|
| US (8) | US8101623B2 (sl) |
| EP (1) | EP2201012B1 (sl) |
| JP (2) | JP4705695B2 (sl) |
| KR (1) | KR101494734B1 (sl) |
| CN (1) | CN101861321B (sl) |
| AR (1) | AR068846A1 (sl) |
| AU (1) | AU2008309383B2 (sl) |
| BR (1) | BRPI0818533B8 (sl) |
| CA (1) | CA2701057C (sl) |
| CL (1) | CL2008003023A1 (sl) |
| CO (1) | CO6270328A2 (sl) |
| CR (1) | CR11359A (sl) |
| CU (1) | CU23886B1 (sl) |
| CY (1) | CY1116929T1 (sl) |
| DK (1) | DK2201012T3 (sl) |
| DO (1) | DOP2010000103A (sl) |
| EA (1) | EA018512B1 (sl) |
| ES (1) | ES2522365T3 (sl) |
| GT (1) | GT201000082A (sl) |
| HK (1) | HK1143154A1 (sl) |
| HN (1) | HN2010000653A (sl) |
| HR (1) | HRP20140807T1 (sl) |
| IL (1) | IL204721A (sl) |
| ME (1) | ME01999B (sl) |
| MX (1) | MX2010003927A (sl) |
| MY (1) | MY150059A (sl) |
| NI (1) | NI201000050A (sl) |
| NZ (1) | NZ585261A (sl) |
| PE (2) | PE20130152A1 (sl) |
| PL (1) | PL2201012T3 (sl) |
| PT (1) | PT2201012E (sl) |
| RS (1) | RS53552B1 (sl) |
| SA (1) | SA08290625B1 (sl) |
| SI (1) | SI2201012T1 (sl) |
| TW (1) | TWI453021B (sl) |
| UY (1) | UY31384A1 (sl) |
| WO (1) | WO2009047563A1 (sl) |
| ZA (1) | ZA201002318B (sl) |
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| EP2057187B1 (en) | 2006-08-10 | 2016-12-28 | Oncotherapy Science, Inc. | Genes and polypeptides relating to breast cancers |
| RS53552B1 (en) | 2007-10-11 | 2015-02-27 | Astrazeneca Ab | DERIVATI PIROLO [2,3-D] PIRIMIDINA KAO INHIBITORI PROTEIN KINAZE B |
| WO2011002772A1 (en) * | 2009-06-29 | 2011-01-06 | Oncotherapy Science, Inc. | Imidazopyridine derivatives and pbk inhibitors containing the same |
| GB201020161D0 (en) | 2010-11-26 | 2011-01-12 | Almac Discovery Ltd | Pharmaceutical compounds |
| WO2012080735A1 (en) | 2010-12-16 | 2012-06-21 | Convergence Pharmaceuticals Limited | Ask1 inhibiting pyrrolopyrimidine derivatives |
| SG10201600077RA (en) | 2011-01-11 | 2016-02-26 | Glaxosmithkline Llc | Combination |
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| JP6309454B2 (ja) | 2011-11-30 | 2018-04-11 | アストラゼネカ アクチボラグ | 癌の併用処置 |
| AU2013204533B2 (en) * | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
| RU2644769C2 (ru) | 2013-01-23 | 2018-02-14 | Астразенека Аб | Химические соединения |
| EP2815749A1 (en) | 2013-06-20 | 2014-12-24 | IP Gesellschaft für Management mbH | Solid form of 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione having specified X-ray diffraction pattern |
| CA2938626A1 (en) | 2013-07-26 | 2015-01-29 | John Rothman | Compositions to improve the therapeutic benefit of bisantrene |
| JP6295578B2 (ja) * | 2013-09-30 | 2018-03-20 | 凸版印刷株式会社 | 反応容器、核酸解析装置、および核酸解析方法 |
| RU2016116915A (ru) * | 2013-10-01 | 2017-11-13 | Новартис Аг | Комбинация |
| EP3392244A1 (en) | 2014-02-13 | 2018-10-24 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| AU2015217073B2 (en) | 2014-02-13 | 2019-08-22 | Incyte Holdings Corporation | Cyclopropylamines as LSD1 inhibitors |
| WO2015123437A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| EP3105226B1 (en) | 2014-02-13 | 2019-09-04 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| ES2691223T3 (es) * | 2014-05-28 | 2018-11-26 | Astrazeneca Ab | Proceso para la preparación de AZD5363 e intermedio novedoso utilizado en el mismo |
| US9695167B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors |
| TWI687419B (zh) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | 作為ｌｓｄ１抑制劑之咪唑并吡啶及咪唑并吡嗪 |
| US9695180B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors |
| US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
| EA201792205A1 (ru) | 2015-04-03 | 2018-02-28 | Инсайт Корпорейшн | Гетероциклические соединения как ингибиторы lsd1 |
| WO2017027678A1 (en) * | 2015-08-12 | 2017-02-16 | Incyte Corporation | Salts of an lsd1 inhibitor |
| TW201726140A (zh) | 2015-09-17 | 2017-08-01 | 瑞典商阿斯特捷利康公司 | 治療癌症之新型生物標記及方法 |
| BR112018071585B1 (pt) | 2016-04-22 | 2024-01-02 | Incyte Corporation | Formulações de um inibidor de lsd1, seus usos e método de preparação das mesmas |
| WO2020047198A1 (en) | 2018-08-31 | 2020-03-05 | Incyte Corporation | Salts of an lsd1 inhibitor and processes for preparing the same |
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| WO2024100236A1 (en) | 2022-11-11 | 2024-05-16 | Astrazeneca Ab | Combination therapies for the treatment of cancer |
| WO2024104561A1 (en) | 2022-11-15 | 2024-05-23 | Astrazeneca Ab | Therapeutic combinations of capivasertib and venetoclax |
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| RS53552B1 (en) | 2007-10-11 | 2015-02-27 | Astrazeneca Ab | DERIVATI PIROLO [2,3-D] PIRIMIDINA KAO INHIBITORI PROTEIN KINAZE B |
-
2008
- 2008-10-09 RS RS20140457A patent/RS53552B1/en unknown
- 2008-10-09 WO PCT/GB2008/050925 patent/WO2009047563A1/en active Application Filing
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