EA201690908A1 - Pyrazolopyrmidine compounds - Google Patents
Pyrazolopyrmidine compoundsInfo
- Publication number
- EA201690908A1 EA201690908A1 EA201690908A EA201690908A EA201690908A1 EA 201690908 A1 EA201690908 A1 EA 201690908A1 EA 201690908 A EA201690908 A EA 201690908A EA 201690908 A EA201690908 A EA 201690908A EA 201690908 A1 EA201690908 A1 EA 201690908A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- pyrazolopyrmidine
- compounds
- methods
- pharmaceutically acceptable
- acceptable salt
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
В настоящем изобретении предложено соединение, представленное следующей структурной формулой:или его фармацевтически приемлемая соль. Также описаны фармацевтические композиции и способы их применения.The present invention provides a compound represented by the following structural formula: or a pharmaceutically acceptable salt thereof. Also described pharmaceutical compositions and methods for their use.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CA2013/000957 WO2014075168A1 (en) | 2012-11-16 | 2013-11-15 | Pyrazolopyrimidine compounds |
PCT/CA2014/051091 WO2015070349A1 (en) | 2012-11-16 | 2014-11-14 | Pyrazolopyrimidine compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201690908A1 true EA201690908A1 (en) | 2016-09-30 |
EA029372B1 EA029372B1 (en) | 2018-03-30 |
Family
ID=56617958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201690908A EA029372B1 (en) | 2013-11-15 | 2014-11-14 | Pyrazolopyrimidine compounds |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP6095857B2 (en) |
EA (1) | EA029372B1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK3484888T3 (en) * | 2016-07-18 | 2023-05-30 | Univ Health Network | SOLID FORMS OF TTK INHIBITOR |
JP7473483B2 (en) * | 2018-05-23 | 2024-04-23 | ユニバーシティー ヘルス ネットワーク | Methods for treating cancer characterized by high expression levels of the spindle- and kinetochore-associated complex subunit 3 (SKA3) gene - Patents.com |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004052315A2 (en) * | 2002-12-11 | 2004-06-24 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
EP1608652A1 (en) * | 2003-03-31 | 2005-12-28 | Vernalis (Cambridge) Limited | Pyrazolopyrimidine compounds and their use in medicine |
KR100899245B1 (en) * | 2003-12-23 | 2009-05-26 | 노파르티스 아게 | Bicyclic heterocyclic p-38 kinase inhibitors |
CN101360499B (en) * | 2005-10-06 | 2015-10-07 | 默沙东公司 | The purposes of pyrazolo [1,5-A] pyrimidine derivatives in the kinase whose medicine of preparation Profilin |
EP1873157A1 (en) * | 2006-06-21 | 2008-01-02 | Bayer Schering Pharma Aktiengesellschaft | Pyrazolopyrimidines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
US8461162B2 (en) * | 2007-07-20 | 2013-06-11 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyrimidine derivatives |
ES2555261T3 (en) * | 2010-06-01 | 2015-12-30 | Bayer Intellectual Property Gmbh | Imidazopyrazines substituted |
CN103429592A (en) * | 2010-12-17 | 2013-12-04 | 拜耳知识产权有限责任公司 | 6-substituted imidazopyrazines for use as MPS-1 and TKK inhibitors in the treatment of hyperproliferative disorders |
CA2821829A1 (en) * | 2010-12-17 | 2012-06-21 | Bayer Intellectual Property Gmbh | Imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
ES2545135T3 (en) * | 2011-04-06 | 2015-09-08 | Bayer Pharma Aktiengesellschaft | Substituted Imidazopyridines and intermediates thereof |
WO2014075168A1 (en) * | 2012-11-16 | 2014-05-22 | University Health Network | Pyrazolopyrimidine compounds |
-
2014
- 2014-11-14 EA EA201690908A patent/EA029372B1/en not_active IP Right Cessation
- 2014-11-14 JP JP2016530227A patent/JP6095857B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
JP2016537354A (en) | 2016-12-01 |
EA029372B1 (en) | 2018-03-30 |
JP6095857B2 (en) | 2017-03-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG TJ TM |