PL2552909T3 - Pochodne 4-aminopirymidyny i ich zastosowanie jako antagonistów receptorów adenozynowych a2a - Google Patents
Pochodne 4-aminopirymidyny i ich zastosowanie jako antagonistów receptorów adenozynowych a2aInfo
- Publication number
- PL2552909T3 PL2552909T3 PL11719879T PL11719879T PL2552909T3 PL 2552909 T3 PL2552909 T3 PL 2552909T3 PL 11719879 T PL11719879 T PL 11719879T PL 11719879 T PL11719879 T PL 11719879T PL 2552909 T3 PL2552909 T3 PL 2552909T3
- Authority
- PL
- Poland
- Prior art keywords
- adenosine
- receptor antagonists
- aminopyrimidine derivatives
- aminopyrimidine
- derivatives
- Prior art date
Links
- 150000005007 4-aminopyrimidines Chemical class 0.000 title 1
- 229940123702 Adenosine A2a receptor antagonist Drugs 0.000 title 1
- 239000002467 adenosine A2a receptor antagonist Substances 0.000 title 1
Classifications
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- 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
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- 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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Ophthalmology & Optometry (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Otolaryngology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Anesthesiology (AREA)
- Physical Education & Sports Medicine (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES201030489A ES2365960B1 (es) | 2010-03-31 | 2010-03-31 | Nuevos antagonistas de los receptores de adenosina. |
| PCT/IB2011/000664 WO2011121418A1 (en) | 2010-03-31 | 2011-03-29 | 4 - aminopyrimidine derivatives and their as as adenosine a2a receptor antagonists |
| EP11719879.6A EP2552909B1 (en) | 2010-03-31 | 2011-03-29 | 4-aminopyrimidine derivatives and their as as adenosine a2a receptor antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2552909T3 true PL2552909T3 (pl) | 2015-08-31 |
Family
ID=44120157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL11719879T PL2552909T3 (pl) | 2010-03-31 | 2011-03-29 | Pochodne 4-aminopirymidyny i ich zastosowanie jako antagonistów receptorów adenozynowych a2a |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8796284B2 (pl) |
| EP (1) | EP2552909B1 (pl) |
| JP (1) | JP5725383B2 (pl) |
| KR (1) | KR101441781B1 (pl) |
| CN (1) | CN102892761B (pl) |
| AU (1) | AU2011234144B2 (pl) |
| BR (1) | BR112012024870B1 (pl) |
| CA (1) | CA2795009C (pl) |
| CY (1) | CY1116328T1 (pl) |
| DK (1) | DK2552909T3 (pl) |
| EA (1) | EA021565B1 (pl) |
| ES (2) | ES2365960B1 (pl) |
| HR (1) | HRP20150366T1 (pl) |
| ME (1) | ME02100B (pl) |
| MX (1) | MX2012011240A (pl) |
| PL (1) | PL2552909T3 (pl) |
| PT (1) | PT2552909E (pl) |
| RS (1) | RS53939B1 (pl) |
| SI (1) | SI2552909T1 (pl) |
| SM (1) | SMT201500097B (pl) |
| WO (1) | WO2011121418A1 (pl) |
| ZA (1) | ZA201207259B (pl) |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012170647A1 (en) * | 2011-06-09 | 2012-12-13 | Assia Chemical Industriew Ltd. | Process for the preparation of etravirine and intermediates in the synthesis thereof |
| DK2922828T3 (da) | 2012-11-21 | 2020-08-31 | Ptc Therapeutics Inc | 4,6-diamino-pyrimidin-derivater som bmi-1-inhibitorer til at behandle cancer |
| ES2480341B1 (es) * | 2013-01-24 | 2015-01-22 | Palobiofarma S.L | Nuevos derivados de pirimidina como inhibidores de la fosfodiesterasa 10 (PDE-10) |
| CA2922657C (en) | 2013-08-30 | 2022-04-12 | Ptc Therapeutics, Inc. | Substituted pyrimidine bmi-1 inhibitors |
| US10584115B2 (en) | 2013-11-21 | 2020-03-10 | Ptc Therapeutics, Inc. | Substituted pyridine and pyrazine BMI-1 inhibitors |
| CN103626741A (zh) * | 2013-11-26 | 2014-03-12 | 苏州大学 | 具有腺苷受体拮抗剂活性的杂环氨基嘧啶化合物 |
| CN103664908A (zh) * | 2013-12-10 | 2014-03-26 | 苏州大学 | 一种具有腺苷受体拮抗活性的氨基嘧啶杂环化合物 |
| US11312690B2 (en) | 2015-07-24 | 2022-04-26 | University Of Lousville Research Foundation, Inc. | Compounds, compositions, methods for treating diseases, and methods for preparing compounds |
| PL3334431T3 (pl) * | 2015-08-11 | 2020-03-31 | Novartis Ag | 5-bromo-2,6-di-(1H-pirazol-1-ilo)pirymidyno-4-amina do zastosowania w leczeniu nowotworu złośliwego |
| PT3334431T (pt) * | 2015-08-11 | 2020-01-06 | Novartis Ag | 5-bromo-2,6-di-(1h-pirazol-l-il)pirimidin-4-amina para uso no tratamento do cancro |
| WO2017173498A1 (en) | 2016-04-06 | 2017-10-12 | Noxopharm Limited | Isoflavonoid composition with improved pharmacokinetics |
| CA3058492A1 (en) | 2016-04-06 | 2017-10-12 | Noxopharm Limited | Radiotherapy improvements |
| CN106543416A (zh) * | 2016-10-21 | 2017-03-29 | 新疆大学 | 含嘧啶的聚合物在dmf溶液中检测硫酸浓度方面的应用 |
| KR20190115053A (ko) * | 2017-02-10 | 2019-10-10 | 노파르티스 아게 | 1-(4-아미노-5-브로모-6-(1h-피라졸-1-일)피리미딘-2-일)-1h-피라졸-4-올 및 암 치료에 있어서의 이의 용도 |
| JOP20190279A1 (ar) * | 2017-05-31 | 2019-11-28 | Novartis Ag | الصور البلورية من 5-برومو -2، 6-داي (1h-بيرازول -1-يل) بيريميدين -4- أمين وأملاح جديدة |
| US20200172628A1 (en) | 2017-06-22 | 2020-06-04 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
| MY204117A (en) | 2017-06-22 | 2024-08-08 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
| CN107286146B (zh) * | 2017-07-05 | 2020-07-31 | 上海肇钰医药科技有限公司 | 作为腺苷a2a受体拮抗剂的4-氨基嘧啶衍生物及其用途 |
| CA3081602A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
| AU2018375738A1 (en) | 2017-11-30 | 2020-06-11 | Novartis Ag | BCMA-targeting chimeric antigen receptor, and uses thereof |
| CN111818923A (zh) * | 2018-02-16 | 2020-10-23 | 艾库斯生物科学有限公司 | 用唑并嘧啶化合物给药 |
| KR102495666B1 (ko) | 2018-03-14 | 2023-02-06 | 서피스 온콜로지, 인크. | Cd39에 결합하는 항체 및 이의 용도 |
| TWI869346B (zh) | 2018-05-30 | 2025-01-11 | 瑞士商諾華公司 | Entpd2抗體、組合療法、及使用該等抗體和組合療法之方法 |
| US20210214459A1 (en) | 2018-05-31 | 2021-07-15 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
| CN118459594A (zh) | 2018-06-01 | 2024-08-09 | 诺华股份有限公司 | 针对bcma的结合分子及其用途 |
| JP7478673B2 (ja) | 2018-06-04 | 2024-05-07 | エクスシエンティア・エルティーディー | アデノシン受容体アンタゴニストとしてのピラゾロピリミジン化合物 |
| AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
| WO2020011245A1 (zh) * | 2018-07-13 | 2020-01-16 | 江苏恒瑞医药股份有限公司 | 一种1,2,4-三嗪-3-胺类衍生物的晶型及制备方法 |
| BR112021002630A2 (pt) | 2018-08-17 | 2021-05-11 | Ptc Therapeutics, Inc. | método para tratar câncer pancreático |
| US11376255B2 (en) | 2018-09-11 | 2022-07-05 | iTeos Belgium SA | Thiocarbamate derivatives as A2A inhibitors, pharmaceutical composition thereof and combinations with anticancer agents |
| WO2020065036A1 (en) | 2018-09-27 | 2020-04-02 | Iteos Therapeutics S.A. | Use of an inhibitor of an ent family transporter in the treatment of cancer and combination thereof with an adenosine receptor antagonist |
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| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
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| WO1999035147A1 (en) | 1998-01-05 | 1999-07-15 | Eisai Co., Ltd. | Purine derivatives and adenosine a2 receptor antagonists serving as preventives/remedies for diabetes |
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| PT1438053E (pt) * | 2001-10-17 | 2008-09-25 | Boehringer Ingelheim Int | Derivados de pirimidina, medicamento contendo estes compostos, sua utilização e processo para a sua preparação |
| TWI330183B (pl) * | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
| AU2004299461A1 (en) * | 2003-12-15 | 2005-06-30 | Almirall Ag | 2, 6 bisheteroaryl-4-aminopyrimidines as adenosine receptor antagonists |
| EP1894930A4 (en) * | 2005-06-23 | 2010-06-23 | Kyowa Hakko Kirin Co Ltd | THIAZOLE DERIVATIVE |
| CN101679371A (zh) * | 2006-12-04 | 2010-03-24 | 艾美罗股份公司 | 作为腺苷受体拮抗剂的取代的嘧啶 |
| US20080221103A1 (en) | 2007-03-09 | 2008-09-11 | Orchid Research Laboratories Ltd. | New heterocyclic compounds |
| EP2132197A2 (en) * | 2007-03-21 | 2009-12-16 | Almirall, S.A. | Substituted pyrimidines as adenosine receptor antagonists |
| AU2008296479A1 (en) * | 2007-08-28 | 2009-03-12 | Dana Farber Cancer Institute | Amino substituted pyrimidine, pyrollopyridine and pyrazolopyrimidine derivatives useful as kinase inhibitors and in treating proliferative disorders and diseases associated with angiogenesis |
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| US8796284B2 (en) | 2014-08-05 |
| KR20130028732A (ko) | 2013-03-19 |
| PT2552909E (pt) | 2015-04-23 |
| EP2552909A1 (en) | 2013-02-06 |
| ES2365960B1 (es) | 2012-06-04 |
| HRP20150366T1 (hr) | 2015-05-22 |
| BR112012024870B1 (pt) | 2020-11-17 |
| ME02100B (me) | 2015-10-20 |
| AU2011234144B2 (en) | 2014-04-24 |
| SMT201500097B (it) | 2015-07-09 |
| SI2552909T1 (sl) | 2015-06-30 |
| CA2795009C (en) | 2016-06-21 |
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| JP2013523711A (ja) | 2013-06-17 |
| ES2534227T3 (es) | 2015-04-20 |
| MX2012011240A (es) | 2012-11-30 |
| DK2552909T3 (en) | 2015-04-13 |
| ES2365960A1 (es) | 2011-10-14 |
| EA021565B1 (ru) | 2015-07-30 |
| CN102892761A (zh) | 2013-01-23 |
| JP5725383B2 (ja) | 2015-05-27 |
| CN102892761B (zh) | 2015-02-04 |
| WO2011121418A9 (en) | 2012-04-05 |
| BR112012024870A2 (pt) | 2016-06-14 |
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| RS53939B1 (sr) | 2015-08-31 |
| AU2011234144A1 (en) | 2012-10-25 |
| EP2552909B1 (en) | 2015-03-11 |
| EA201201343A1 (ru) | 2013-03-29 |
| CA2795009A1 (en) | 2011-10-06 |
| CY1116328T1 (el) | 2017-02-08 |
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