PL411864A1 - Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-α]pirymidyny jako inhibitory kinazy P13 - Google Patents
Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-α]pirymidyny jako inhibitory kinazy P13Info
- Publication number
- PL411864A1 PL411864A1 PL411864A PL41186415A PL411864A1 PL 411864 A1 PL411864 A1 PL 411864A1 PL 411864 A PL411864 A PL 411864A PL 41186415 A PL41186415 A PL 41186415A PL 411864 A1 PL411864 A1 PL 411864A1
- Authority
- PL
- Poland
- Prior art keywords
- compound
- pyrazolo
- morpholin
- pyrimidine
- kinase
- Prior art date
Links
Classifications
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- 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
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- 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
-
- 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)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Ujawniono związek o wzorze ogólnym (I), w którym Y oznacza -CH2- lub >C=O; R1 oznacza grupę wybraną z grup A1, A2 i A3 zdefiniowanych w opisie; R2 oznacza grupę wybraną z grup B1, B2, B3 i B4 zdefiniowanych w opisie; R3 oznacza H, halogen, lub C1-C4 alkil; R4 oznacza C1-C4 alkil, C3-C4-cykloalkil, C1-C4 alkil podstawiony przez C1-C4 alkoksyl, lub CHF2; jego dopuszczalne farmaceutycznie sole, oraz kompozycja farmaceutyczna zawierająca związek o wzorze (I). Związek jest selektywnym inhibitorem izoformy delta kinazy PI3 i znajduje zastosowanie jako lek w leczeniu chorób układu immunologicznego, chorób o podłożu zapalnym i nowotworów.
Priority Applications (19)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL411864A PL236355B1 (pl) | 2015-04-02 | 2015-04-02 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-α]pirymidyny jako inhibitory kinazy PI3 |
EP16714019.3A EP3277687B1 (en) | 2015-04-02 | 2016-03-30 | 7-(morpholin-4-yl)pyrazole[1,5-a]pyrimidine derivatives which are useful for the treatment of immune or inflammatory diseases or cancer |
AU2016241568A AU2016241568B2 (en) | 2015-04-02 | 2016-03-30 | 7-(morpholin-4-yl)pyrazole[1,5-a]pyrimidine derivatives which are useful for the treatment of immune or inflammatory diseases or cancer |
DK16714019.3T DK3277687T3 (da) | 2015-04-02 | 2016-03-30 | 7-(Morpholin-4-yl)pyrazol[1,5-a]pyrimidinderivater, som kan anvendes til behandling af immunsygdomme eller inflammatoriske sygdomme eller cancer |
BR112017020131-3A BR112017020131B1 (pt) | 2015-04-02 | 2016-03-30 | Composto, seu uso e composição farmacêutica |
PL16714019T PL3277687T3 (pl) | 2015-04-02 | 2016-03-30 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-a]pirymidyny użyteczne do leczenia chorób immunologicznych lub zapalnych lub nowotworów |
PCT/IB2016/051792 WO2016157091A1 (en) | 2015-04-02 | 2016-03-30 | 7-(morpholin-4-yl)pyrazole[1,5-a]pyrimidine derivatives which are useful for the treatment of immune or inflammatory diseases or cancer |
HUE16714019A HUE047822T2 (hu) | 2015-04-02 | 2016-03-30 | Immun- vagy gyulladásos betegségek és rák kezelésére alkalmas 7-(morfolin-4-il)pirazol[1,5-a]pirimidin-származékok |
JP2017551627A JP6665201B2 (ja) | 2015-04-02 | 2016-03-30 | 免疫もしくは炎症性の疾患またはがんの処置に有用な7−(モルホリン−4−イル)ピラゾール[1,5−a]ピリミジン誘導体 |
CN201680017259.4A CN107743489B (zh) | 2015-04-02 | 2016-03-30 | 治疗免疫疾病、炎性疾病或癌症的7-(吗啉-4-基)吡唑并[1,5-a]嘧啶衍生物 |
CA2978828A CA2978828A1 (en) | 2015-04-02 | 2016-03-30 | 7-(morpholin-4-yl)pyrazole[1,5-a]pyrimidine derivatives which are useful for the treatment of immune or inflammatory diseases or cancer |
PT167140193T PT3277687T (pt) | 2015-04-02 | 2016-03-30 | Derivados de 7-(morfolin-4-il)pirazole[1,5-a]pirimidina que são úteis para o tratamento de doenças imunitárias ou inflamatórias ou cancro |
KR1020177031214A KR102559190B1 (ko) | 2015-04-02 | 2016-03-30 | 면역성 또는 염증성 질환 또는 암의 치료를 위해 유용한 7-(모르폴린-4-일)피라졸[1,5-a]피리미딘 유도체 |
EA201792087A EA032826B1 (ru) | 2015-04-02 | 2016-03-30 | ПРОИЗВОДНЫЕ 7-(МОРФОЛИН-4-ИЛ)ПИРАЗОЛО[1,5-a]ПИРИМИДИНА, ПРИГОДНЫЕ ДЛЯ ЛЕЧЕНИЯ ИММУННЫХ ИЛИ ВОСПАЛИТЕЛЬНЫХ ЗАБОЛЕВАНИЙ ИЛИ РАКА |
US15/562,537 US10138247B2 (en) | 2015-04-02 | 2016-03-30 | 7-(morpholin-4-yl)pyrazole[1,5-A]pyrimidine derivatives as PI3 kinase inhibitors |
SI201630560T SI3277687T1 (sl) | 2015-04-02 | 2016-03-30 | 7-(morfolin-4-IL)pirazol(1,5-A)pirimidinski derivati, ki so uporabni za zdravljenje imunskih ali vnetnih bolezni ali raka |
ES16714019T ES2765642T3 (es) | 2015-04-02 | 2016-03-30 | Derivados de 7-(morfolin-4-il)pirazol[1,5-a]pirimidina que son útiles para el tratamiento de enfermedades inmunitarias o inflamatorias o cáncer |
MX2017011423A MX2017011423A (es) | 2015-04-02 | 2016-03-30 | Derivados de 7-(morfolin-4-il)pirazolo[1,5-a]pirimidina que son utiles para el tratamiento de enfermedades inmunes o inflamatorias o cancer. |
HRP20192195TT HRP20192195T1 (hr) | 2015-04-02 | 2019-12-06 | Derivati 7-(morfolin-4-il)pirazol[1,5-a]pirimidina koji su korisni za liječenje imunoloških ili upalnih oboljenja ili karcinoma |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL411864A PL236355B1 (pl) | 2015-04-02 | 2015-04-02 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-α]pirymidyny jako inhibitory kinazy PI3 |
Publications (2)
Publication Number | Publication Date |
---|---|
PL411864A1 true PL411864A1 (pl) | 2016-10-10 |
PL236355B1 PL236355B1 (pl) | 2021-01-11 |
Family
ID=55650626
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL411864A PL236355B1 (pl) | 2015-04-02 | 2015-04-02 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-α]pirymidyny jako inhibitory kinazy PI3 |
PL16714019T PL3277687T3 (pl) | 2015-04-02 | 2016-03-30 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-a]pirymidyny użyteczne do leczenia chorób immunologicznych lub zapalnych lub nowotworów |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL16714019T PL3277687T3 (pl) | 2015-04-02 | 2016-03-30 | Pochodne 7-(morfolin-4-ylo)pirazolo[1,5-a]pirymidyny użyteczne do leczenia chorób immunologicznych lub zapalnych lub nowotworów |
Country Status (18)
Country | Link |
---|---|
US (1) | US10138247B2 (pl) |
EP (1) | EP3277687B1 (pl) |
JP (1) | JP6665201B2 (pl) |
KR (1) | KR102559190B1 (pl) |
CN (1) | CN107743489B (pl) |
AU (1) | AU2016241568B2 (pl) |
BR (1) | BR112017020131B1 (pl) |
CA (1) | CA2978828A1 (pl) |
DK (1) | DK3277687T3 (pl) |
EA (1) | EA032826B1 (pl) |
ES (1) | ES2765642T3 (pl) |
HR (1) | HRP20192195T1 (pl) |
HU (1) | HUE047822T2 (pl) |
MX (1) | MX2017011423A (pl) |
PL (2) | PL236355B1 (pl) |
PT (1) | PT3277687T (pl) |
SI (1) | SI3277687T1 (pl) |
WO (1) | WO2016157091A1 (pl) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11834467B2 (en) | 2020-09-28 | 2023-12-05 | 1ST Biotherapeutics, Inc. | Substituted indazoles as hematopoietic progenitor kinase 1 (HPK1) inhibitors |
CN114957261B (zh) * | 2022-05-17 | 2023-06-23 | 重庆文理学院 | 一种具有抗头颈癌作用的化合物及其制备方法和应用 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ330119A (en) * | 1996-02-07 | 2000-02-28 | Janssen Pharmaceutica Nv | Pyrazolopyrimidines as crf receptor antagonists |
AU2004308399A1 (en) | 2003-12-23 | 2005-07-14 | Activbiotics, Inc. | Rifamycin analogs and uses thereof |
ES2365406T3 (es) * | 2005-02-11 | 2011-10-04 | F. Hoffmann-La Roche Ag | Derivados de pirazolo-pirimidina como antagonistas de mglur2. |
UA96458C2 (ru) * | 2006-09-20 | 2011-11-10 | Эли Лилли Энд Компани | Тиазолпиразолопиримидиновые соединения как антагонисты рецептора crf1 |
JP5638955B2 (ja) * | 2007-10-26 | 2014-12-10 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Pi3キナーゼ阻害剤として有用なプリン誘導体 |
AU2009218515A1 (en) | 2008-02-26 | 2009-09-03 | Novartis Ag | Heterocyclic compounds as inhibitors of CXCR2 |
WO2009146406A1 (en) * | 2008-05-30 | 2009-12-03 | Genentech, Inc. | Purine pi3k inhibitor compounds and methods of use |
AU2009299894A1 (en) * | 2008-10-03 | 2010-04-08 | Merck Serono S.A. | 4 -morpholino-pyrido [3, 2 -d] pyrimidines active on Pi3k |
WO2010074284A1 (ja) * | 2008-12-26 | 2010-07-01 | 味の素株式会社 | ピラゾロピリミジン化合物 |
ES2475091T3 (es) * | 2009-04-16 | 2014-07-10 | Centro Nacional De Investigaciones Oncol�Gicas (Cnio) | Imidazopirazinas como inhibidores de proteína cinasas |
WO2010136491A1 (en) | 2009-05-27 | 2010-12-02 | F. Hoffmann-La Roche Ag | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
CN102459272B (zh) | 2009-05-27 | 2014-08-06 | 健泰科生物技术公司 | 对P110δ具有选择性的为PI3K抑制剂的二环嘧啶化合物和使用方法 |
GB0912745D0 (en) | 2009-07-22 | 2009-08-26 | Wolfson Microelectronics Plc | Improvements relating to DC-DC converters |
BR112012019635A2 (pt) | 2010-02-22 | 2016-05-03 | Hoffmann La Roche | compostos inibidores de pirido[3,2-d] pirimidina pi3k delta e métodos de uso |
AU2011223888B2 (en) | 2010-03-04 | 2015-07-02 | Merck Sharp & Dohme Llc | Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders |
WO2013028263A1 (en) * | 2011-08-24 | 2013-02-28 | Glaxosmithkline Llc | Pyrazolopyrimidine derivatives as pi3 kinase inhibitors |
-
2015
- 2015-04-02 PL PL411864A patent/PL236355B1/pl unknown
-
2016
- 2016-03-30 MX MX2017011423A patent/MX2017011423A/es active IP Right Grant
- 2016-03-30 CN CN201680017259.4A patent/CN107743489B/zh active Active
- 2016-03-30 DK DK16714019.3T patent/DK3277687T3/da active
- 2016-03-30 SI SI201630560T patent/SI3277687T1/sl unknown
- 2016-03-30 JP JP2017551627A patent/JP6665201B2/ja active Active
- 2016-03-30 AU AU2016241568A patent/AU2016241568B2/en not_active Ceased
- 2016-03-30 PL PL16714019T patent/PL3277687T3/pl unknown
- 2016-03-30 PT PT167140193T patent/PT3277687T/pt unknown
- 2016-03-30 EP EP16714019.3A patent/EP3277687B1/en active Active
- 2016-03-30 CA CA2978828A patent/CA2978828A1/en active Pending
- 2016-03-30 EA EA201792087A patent/EA032826B1/ru not_active IP Right Cessation
- 2016-03-30 US US15/562,537 patent/US10138247B2/en active Active
- 2016-03-30 ES ES16714019T patent/ES2765642T3/es active Active
- 2016-03-30 KR KR1020177031214A patent/KR102559190B1/ko active IP Right Grant
- 2016-03-30 HU HUE16714019A patent/HUE047822T2/hu unknown
- 2016-03-30 WO PCT/IB2016/051792 patent/WO2016157091A1/en active Application Filing
- 2016-03-30 BR BR112017020131-3A patent/BR112017020131B1/pt active IP Right Grant
-
2019
- 2019-12-06 HR HRP20192195TT patent/HRP20192195T1/hr unknown
Also Published As
Publication number | Publication date |
---|---|
US20180111939A1 (en) | 2018-04-26 |
WO2016157091A1 (en) | 2016-10-06 |
HRP20192195T1 (hr) | 2020-03-06 |
DK3277687T3 (da) | 2019-12-16 |
ES2765642T3 (es) | 2020-06-10 |
MX2017011423A (es) | 2018-05-17 |
KR102559190B1 (ko) | 2023-07-25 |
PL236355B1 (pl) | 2021-01-11 |
AU2016241568B2 (en) | 2019-09-26 |
BR112017020131A2 (pt) | 2018-05-29 |
EP3277687B1 (en) | 2019-10-30 |
BR112017020131B1 (pt) | 2023-02-28 |
HUE047822T2 (hu) | 2020-05-28 |
AU2016241568A1 (en) | 2017-10-19 |
EA201792087A1 (ru) | 2018-03-30 |
JP6665201B2 (ja) | 2020-03-13 |
CN107743489B (zh) | 2021-05-04 |
KR20170132275A (ko) | 2017-12-01 |
EP3277687A1 (en) | 2018-02-07 |
CA2978828A1 (en) | 2016-10-06 |
PT3277687T (pt) | 2020-01-10 |
CN107743489A (zh) | 2018-02-27 |
EA032826B1 (ru) | 2019-07-31 |
JP2018510192A (ja) | 2018-04-12 |
PL3277687T3 (pl) | 2020-09-21 |
SI3277687T1 (sl) | 2020-02-28 |
US10138247B2 (en) | 2018-11-27 |
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