PL2193131T3 - Związki imidazo[1,2-a]pirazyny w leczeniu infekcji wirusowych takich jak zapalenia wątroby - Google Patents
Związki imidazo[1,2-a]pirazyny w leczeniu infekcji wirusowych takich jak zapalenia wątrobyInfo
- Publication number
- PL2193131T3 PL2193131T3 PL08787346T PL08787346T PL2193131T3 PL 2193131 T3 PL2193131 T3 PL 2193131T3 PL 08787346 T PL08787346 T PL 08787346T PL 08787346 T PL08787346 T PL 08787346T PL 2193131 T3 PL2193131 T3 PL 2193131T3
- Authority
- PL
- Poland
- Prior art keywords
- imidazo
- hepatitis
- treatment
- viral infections
- pyrazine compounds
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0716292.8A GB0716292D0 (en) | 2007-08-21 | 2007-08-21 | Imidazopyrazine compounds |
PCT/EP2008/060896 WO2009024585A2 (en) | 2007-08-21 | 2008-08-20 | Imidazo [1,2-a] pyrazine compounds for treatment of viral infections such as hepatitis |
EP08787346A EP2193131B1 (en) | 2007-08-21 | 2008-08-20 | Imidazo[1,2-a]pyrazine compounds for treatment of viral infections such as hepatitis |
Publications (1)
Publication Number | Publication Date |
---|---|
PL2193131T3 true PL2193131T3 (pl) | 2013-07-31 |
Family
ID=38566736
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL08787346T PL2193131T3 (pl) | 2007-08-21 | 2008-08-20 | Związki imidazo[1,2-a]pirazyny w leczeniu infekcji wirusowych takich jak zapalenia wątroby |
Country Status (21)
Country | Link |
---|---|
US (1) | US8362018B2 (pl) |
EP (2) | EP2567960A3 (pl) |
JP (1) | JP2010536825A (pl) |
KR (1) | KR20100081294A (pl) |
CN (1) | CN101835780B (pl) |
AU (1) | AU2008290531A1 (pl) |
BR (1) | BRPI0815717A2 (pl) |
CA (1) | CA2707521A1 (pl) |
CY (1) | CY1113872T1 (pl) |
DK (1) | DK2193131T3 (pl) |
ES (1) | ES2404415T3 (pl) |
GB (1) | GB0716292D0 (pl) |
HK (1) | HK1143810A1 (pl) |
HR (1) | HRP20130202T1 (pl) |
MX (1) | MX2010001733A (pl) |
NZ (1) | NZ584108A (pl) |
PL (1) | PL2193131T3 (pl) |
PT (1) | PT2193131E (pl) |
SI (1) | SI2193131T1 (pl) |
WO (1) | WO2009024585A2 (pl) |
ZA (1) | ZA201002009B (pl) |
Families Citing this family (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0716292D0 (en) * | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
CA2722923C (en) | 2008-04-29 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Indazole compounds as ccr1 receptor antagonists |
CA2722811C (en) | 2008-05-06 | 2016-07-05 | Boehringer Ingelheim International Gmbh | Pyrazole compounds as ccr1 antagonists |
PE20110854A1 (es) | 2008-09-26 | 2011-12-23 | Boehringer Ingelheim Int | DERIVADOS DE 1-FENIL-1H-PIRAZOLO[3,4-c]PIRIDINA-4-CARBONILAMINA COMO ANTAGONISTAS DE LOS RECEPTORES CCR1 |
TW201107329A (en) | 2009-07-30 | 2011-03-01 | Oncotherapy Science Inc | Fused imidazole derivative having ttk inhibitory action |
EA021015B1 (ru) | 2009-10-21 | 2015-03-31 | Бёрингер Ингельхайм Интернациональ Гмбх | Индазолы и пиразолопиридины в качестве антагонистов рецептора ccr1 |
US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
WO2011051342A1 (en) | 2009-10-30 | 2011-05-05 | Janssen Pharmaceutica Nv | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
EP2509952A1 (en) * | 2009-12-08 | 2012-10-17 | Boehringer Ingelheim International GmbH | Process for synthesis of intermediates useful for making substituted indazole and azaindazole compounds |
AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
EP2547680B1 (en) * | 2010-03-18 | 2015-08-05 | Bayer Intellectual Property GmbH | Imidazopyrazines |
WO2011137109A1 (en) | 2010-04-30 | 2011-11-03 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as ccr1 receptor antagonists |
JP5824040B2 (ja) | 2010-06-01 | 2015-11-25 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換イミダゾピラジン |
CN103403006B (zh) * | 2010-12-17 | 2015-11-25 | 拜耳知识产权有限责任公司 | 在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的6-硫代-取代的咪唑并吡嗪 |
CN103370322B (zh) * | 2010-12-17 | 2016-02-10 | 拜耳知识产权有限责任公司 | 在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的2-取代的咪唑并吡嗪 |
US20140187548A1 (en) | 2010-12-17 | 2014-07-03 | Bayer Intellectual Property Gmbh | 6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
CA2821819A1 (en) * | 2010-12-17 | 2012-06-21 | Marcus Koppitz | 6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
JP2014503521A (ja) * | 2010-12-17 | 2014-02-13 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 過増殖性障害の処置におけるmps−1およびtkk阻害剤としての使用のための、イミダゾピラジン類 |
CN103443100B (zh) * | 2010-12-17 | 2016-03-23 | 拜耳知识产权有限责任公司 | 在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的取代的6-咪唑并吡嗪 |
WO2012087782A1 (en) | 2010-12-23 | 2012-06-28 | Boehringer Ingelheim International Gmbh | Pyrazolopiperidine compounds as ccr1 receptor antagonists |
GB201109763D0 (en) * | 2011-06-10 | 2011-07-27 | Ucl Business Plc | Compounds |
BR112013033375B1 (pt) | 2011-06-27 | 2022-05-10 | Janssen Pharmaceutica N.V | Derivados de 1-aril-4-metil-[1,2,4]triazolo[4,3-a]quinoxa-lina, seu uso, composição farmacêutica que os compreende, processo de preparação dos mesmos, solução estéril e composto intermediário |
WO2013061962A1 (ja) * | 2011-10-24 | 2013-05-02 | 武田薬品工業株式会社 | 二環性化合物 |
AU2013283426B2 (en) | 2012-06-26 | 2018-02-22 | Janssen Pharmaceutica Nv | Combinations comprising PDE 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and PDE 10 inhibitors for use in the treatment of neurological or metabolic disorders |
CN104411314B (zh) | 2012-07-09 | 2017-10-20 | 詹森药业有限公司 | 磷酸二酯酶10的抑制剂 |
WO2016130501A1 (en) | 2015-02-09 | 2016-08-18 | Incyte Corporation | Aza-heteroaryl compounds as pi3k-gamma inhibitors |
KR20170141768A (ko) * | 2015-04-29 | 2017-12-26 | 얀센 파마슈티카 엔.브이. | 이미다조피라진 및 피라졸로피리미딘 및 ampa 수용체 조절제로서의 이의 용도 |
LT3288940T (lt) | 2015-04-29 | 2021-05-10 | Janssen Pharmaceutica Nv | Azabenzimidazolai ir jų panaudojimas kaip ampa receptoriaus moduliatorių |
CA2989722C (en) * | 2015-06-24 | 2023-09-19 | Jacob Westman | Pyrazolo[1,5-a]triazin-4-amine derivatives useful in therapy |
JP6507976B2 (ja) * | 2015-09-30 | 2019-05-08 | 東レ株式会社 | イミダゾール−2−カルボン酸エステル誘導体又はその塩の製造方法 |
MA43169B1 (fr) | 2015-11-06 | 2022-05-31 | Incyte Corp | Composés héterocycliques en tant qu' inhibiteurs pi3k-gamma |
ES2833955T3 (es) | 2016-01-05 | 2021-06-16 | Incyte Corp | Piridinas sustituidas con pirazol/imidazol como inhibidores de PI3K-Gamma |
EA202091849A1 (ru) * | 2016-03-31 | 2020-12-11 | Ромарк Лабораториз Л.С. | Тиазолидные соединения для лечения вирусных инфекций |
TW201803871A (zh) * | 2016-06-24 | 2018-02-01 | 英塞特公司 | 作為PI3K-γ抑制劑之雜環化合物 |
UY37381A (es) | 2016-08-30 | 2018-03-23 | Glaxosmithkline Ip No 2 Ltd | Compuestos que inhiben proteasas 3c y 3cl y métodos de uso de los mismos |
JOP20200086A1 (ar) | 2017-10-18 | 2020-04-30 | Incyte Corp | مشتقات إيميدازول مكثفة بها استبدال بمجموعات هيدروكسي ثلاثية كمثبطات لـ pi3k-جاما |
BR112020014431A2 (pt) | 2018-01-17 | 2020-12-01 | Glaxosmithkline Intellectual Property Development Limited | inibidores de pl4kiiibeta |
TWI811428B (zh) | 2018-08-21 | 2023-08-11 | 日商杏林製藥股份有限公司 | 雙環雜芳香環衍生物 |
PE20211815A1 (es) | 2018-09-05 | 2021-09-14 | Incyte Corp | Formas cristalinas de un inhibidor de fosfoinositida 3-quinasa (pi3k) |
CN109369545B (zh) * | 2018-12-14 | 2020-04-10 | 东营曜康医药科技有限公司 | 2-甲基-5-甲酸吡嗪的合成工艺 |
US20230014730A1 (en) | 2019-09-23 | 2023-01-19 | Nanjing Zhengxiang Pharmaceuticals Co., Ltd. | Phosphodiesterase inhibitors and use |
WO2021249893A1 (en) * | 2020-06-08 | 2021-12-16 | F. Hoffmann-La Roche Ag | Novel imidazo-pyrazine derivatives |
CN113929633A (zh) * | 2021-10-27 | 2022-01-14 | 山东大学 | 一种法匹拉韦的合成方法及其应用 |
CN113831255B (zh) * | 2021-11-25 | 2022-03-11 | 山东诚创蓝海医药科技有限公司 | 一种2-氨基丙二酰胺的制备方法 |
CN115489188B (zh) * | 2022-10-09 | 2023-08-29 | 安徽国风新材料股份有限公司 | 一种家居保护用聚酯薄膜及其制备方法 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2607813B1 (fr) * | 1986-12-05 | 1989-03-31 | Montpellier I Universite | Alkylamino-8 imidazo (1,2-a) pyrazines et derives, leur preparation et leur application en therapeutique |
DE19915178A1 (de) | 1999-04-03 | 2000-10-05 | Univ Mainz Johannes Gutenberg | Hepatitis C Virus Zellkultursystem |
ATE525384T1 (de) | 2000-05-23 | 2011-10-15 | Univ Washington | Varianten des hepatitisvirus |
AU2002225895A1 (en) | 2000-11-07 | 2002-05-21 | Anadys Pharmaceuticals, Inc. | Hepatitis c virus constructs characterized by high efficiency replication |
ES2287074T3 (es) | 2000-12-22 | 2007-12-16 | Boehringer Ingelheim (Canada) Ltd. | Molecula de rna autorreplicante del virus de la hepatitis c. |
EP2050822B1 (en) | 2001-01-23 | 2013-07-31 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hepatitis C virus replicons and replicon enhanced cells |
EP1363702A4 (en) * | 2001-01-30 | 2007-08-22 | Cytopia Pty Ltd | PROCESS FOR INHIBITING KINASES |
AU2007200401A1 (en) * | 2002-09-23 | 2007-02-22 | Schering Corporation | Imidazopyrazines as cyclin dependent kinase inhibitors |
US7576085B2 (en) * | 2002-09-23 | 2009-08-18 | Schering Corporation | Imidazopyrazines as cyclin dependent kinase inhibitors |
KR20050057520A (ko) | 2002-09-23 | 2005-06-16 | 쉐링 코포레이션 | 사이클린 의존성 키나제 억제제로서의 이미다조피라진 |
DE602004024658D1 (de) | 2003-02-13 | 2010-01-28 | Merck & Co Inc | Verfahren zur vermittlung von zellkulturreplikationsaktivität an unterschiedliche hepatitis-c-virus-isolate |
AR043002A1 (es) | 2003-02-18 | 2005-07-13 | Altana Pharma Ag | Imidazopirazinas 6-substituidos |
US7186832B2 (en) | 2003-02-20 | 2007-03-06 | Sugen Inc. | Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors |
US7157460B2 (en) | 2003-02-20 | 2007-01-02 | Sugen Inc. | Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors |
WO2007056468A1 (en) | 2005-11-10 | 2007-05-18 | Schering Corporation | Methods for inhibiting protein kinases |
CA2628455A1 (en) * | 2005-11-10 | 2007-05-24 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
JP5600004B2 (ja) * | 2006-09-05 | 2014-10-01 | エモリー ユニバーシティー | 感染の予防または治療のためのチロシンキナーゼ阻害剤 |
WO2008030795A2 (en) * | 2006-09-05 | 2008-03-13 | Boards Of Regents, The University Of Texas System | Compositions and methods for inhibition of tyrosine kinases |
CA2669465A1 (en) | 2006-11-08 | 2008-05-15 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
WO2008059373A1 (en) | 2006-11-17 | 2008-05-22 | Raqualia Pharma Inc. | Imidazo [1, 2-a] pyrazine derivatives and their use as acid pump antagonists |
US8243049B2 (en) | 2006-12-20 | 2012-08-14 | 3M Innovative Properties Company | Untethered stylus employing low current power converter |
GB0716292D0 (en) * | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
-
2007
- 2007-08-21 GB GBGB0716292.8A patent/GB0716292D0/en not_active Ceased
-
2008
- 2008-08-20 ES ES08787346T patent/ES2404415T3/es active Active
- 2008-08-20 EP EP12188861.4A patent/EP2567960A3/en not_active Withdrawn
- 2008-08-20 BR BRPI0815717-0A2A patent/BRPI0815717A2/pt not_active IP Right Cessation
- 2008-08-20 KR KR1020107005549A patent/KR20100081294A/ko not_active Application Discontinuation
- 2008-08-20 MX MX2010001733A patent/MX2010001733A/es active IP Right Grant
- 2008-08-20 AU AU2008290531A patent/AU2008290531A1/en not_active Abandoned
- 2008-08-20 DK DK08787346.9T patent/DK2193131T3/da active
- 2008-08-20 JP JP2010521417A patent/JP2010536825A/ja not_active Ceased
- 2008-08-20 CA CA2707521A patent/CA2707521A1/en not_active Abandoned
- 2008-08-20 WO PCT/EP2008/060896 patent/WO2009024585A2/en active Application Filing
- 2008-08-20 EP EP08787346A patent/EP2193131B1/en not_active Not-in-force
- 2008-08-20 PT PT87873469T patent/PT2193131E/pt unknown
- 2008-08-20 NZ NZ584108A patent/NZ584108A/en not_active IP Right Cessation
- 2008-08-20 CN CN2008801108961A patent/CN101835780B/zh not_active Expired - Fee Related
- 2008-08-20 PL PL08787346T patent/PL2193131T3/pl unknown
- 2008-08-20 SI SI200830948T patent/SI2193131T1/sl unknown
- 2008-08-20 US US12/674,525 patent/US8362018B2/en not_active Expired - Fee Related
-
2010
- 2010-03-19 ZA ZA2010/02009A patent/ZA201002009B/en unknown
- 2010-11-04 HK HK10110351.0A patent/HK1143810A1/xx not_active IP Right Cessation
-
2013
- 2013-03-08 HR HRP20130202AT patent/HRP20130202T1/hr unknown
- 2013-04-03 CY CY20131100277T patent/CY1113872T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
US20110166147A1 (en) | 2011-07-07 |
GB0716292D0 (en) | 2007-09-26 |
CN101835780B (zh) | 2013-09-18 |
HK1143810A1 (en) | 2011-01-14 |
NZ584108A (en) | 2012-06-29 |
SI2193131T1 (sl) | 2013-06-28 |
KR20100081294A (ko) | 2010-07-14 |
MX2010001733A (es) | 2010-07-06 |
CN101835780A (zh) | 2010-09-15 |
WO2009024585A2 (en) | 2009-02-26 |
EP2193131A2 (en) | 2010-06-09 |
JP2010536825A (ja) | 2010-12-02 |
CY1113872T1 (el) | 2016-07-27 |
WO2009024585A3 (en) | 2009-08-06 |
BRPI0815717A2 (pt) | 2015-02-10 |
CA2707521A1 (en) | 2009-02-26 |
US8362018B2 (en) | 2013-01-29 |
DK2193131T3 (da) | 2013-04-22 |
EP2567960A3 (en) | 2013-06-05 |
ZA201002009B (en) | 2010-12-29 |
ES2404415T3 (es) | 2013-05-27 |
EP2567960A2 (en) | 2013-03-13 |
PT2193131E (pt) | 2013-04-04 |
HRP20130202T1 (hr) | 2013-04-30 |
AU2008290531A1 (en) | 2009-02-26 |
EP2193131B1 (en) | 2013-01-30 |
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