PE20090511A1 - Imidazopiridinonas - Google Patents
ImidazopiridinonasInfo
- Publication number
- PE20090511A1 PE20090511A1 PE2008001300A PE2008001300A PE20090511A1 PE 20090511 A1 PE20090511 A1 PE 20090511A1 PE 2008001300 A PE2008001300 A PE 2008001300A PE 2008001300 A PE2008001300 A PE 2008001300A PE 20090511 A1 PE20090511 A1 PE 20090511A1
- Authority
- PE
- Peru
- Prior art keywords
- pyridin
- ilmethyl
- ona
- imidazo
- tetrahydro
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 101000669402 Homo sapiens Toll-like receptor 7 Proteins 0.000 abstract 1
- 102100039390 Toll-like receptor 7 Human genes 0.000 abstract 1
- 208000036142 Viral infection Diseases 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- FIULGFJIHJJXMT-UHFFFAOYSA-N [C]1[N]C=CC=C1 Chemical group [C]1[N]C=CC=C1 FIULGFJIHJJXMT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
- A61P31/20—Antivirals for DNA viruses
-
- 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
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
REFERIDA A UN COMPUESTO DE FORMULA (I): DONDE R1 ES HETEROCICLICO SATURADO DE 3-8 MIEMBROS EN EL QUE UN MIEMBRO ES -O- TAL COMO TETRAHIDROPIRANILO O TETRAHIDROFURANILO; R2 ES FENILO O PIRIDINILO SUSTITUIDO O NO POR -ALQUILO(C1-C6). SON COMPUESTOS PREFERIDOS: 4-AMINO-1-(6-METIL-PIRIDIN-3-ILMETIL)-6-(TETRAHIDRO-PIRAN-4-ILMETOXI)-1,3-DIHIDRO-IMIDAZO[4,5-c]PIRIDIN-2-ONA; 4-AMINO-1-(6-METIL-PIRIDIN-3-ILMETIL)-6-(TETRAHIDRO-FURAN-3-S/R-ILMETOXI)-1,3-DIHIDRO-IMIDAZO[4,5-c]PIRIDIN-2-ONA; 4-AMINO-1-(6-METIL-PIRIDIN-3-ILMETIL)-6-(TETRAHIDRO-FURAN-3-S-ILMETOXI)-1,3-DIHIDRO-IMIDAZO[4,5-c]PIRIDIN-2-ONA; ENTRE OTROS. TAMBIEN SE REFIERE UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DE TLR7 DE CELULAS MEDIADORAS, UTILES EN EL TRATAMIENTO DE INFECCIONES VIRALES, CANCERES Y TUMORES
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95370707P | 2007-08-03 | 2007-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090511A1 true PE20090511A1 (es) | 2009-05-07 |
Family
ID=40193849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008001300A PE20090511A1 (es) | 2007-08-03 | 2008-08-01 | Imidazopiridinonas |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US20090221631A1 (es) |
| EP (1) | EP2188280B1 (es) |
| JP (1) | JP2010535755A (es) |
| AR (1) | AR067757A1 (es) |
| AT (1) | ATE501136T1 (es) |
| CA (1) | CA2707030A1 (es) |
| CL (1) | CL2008002228A1 (es) |
| DE (1) | DE602008005470D1 (es) |
| ES (1) | ES2359123T3 (es) |
| PA (1) | PA8791701A1 (es) |
| PE (1) | PE20090511A1 (es) |
| TW (1) | TW200914003A (es) |
| UY (1) | UY31261A1 (es) |
| WO (1) | WO2009019553A2 (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AP2011005745A0 (en) * | 2008-12-09 | 2011-06-30 | Gilead Sciences Inc | Modulators of toll-like receptors. |
| BR112012004806B8 (pt) | 2009-09-02 | 2022-10-04 | Novartis Ag | composições imunogênicas que incluem moduladores da atividade de tlr, método para aumento da eficácia da referida composição e uso |
| PL2477987T3 (pl) * | 2009-09-14 | 2018-06-29 | Gilead Sciences, Inc. | Modulatory receptorów toll-podobnych |
| SI2491035T1 (sl) | 2009-10-22 | 2017-10-30 | Gilead Sciences, Inc. | Derivati purina ali deazapurina uporabni za zdravljenje (med drugimi) virusnih okužb |
| JP5689321B2 (ja) * | 2010-01-21 | 2015-03-25 | 石原産業株式会社 | ２−アミノ−４−トリフルオロメチルピリジン類の製造方法 |
| US9315530B2 (en) | 2010-09-01 | 2016-04-19 | Novartis Ag | Adsorption of immunopotentiators to insoluble metal salts |
| EP2471776A1 (de) | 2010-12-28 | 2012-07-04 | Bayer CropScience AG | Pyridin-2-ylpropandinitrile und deren Verwendung als Herbizide |
| CA2828844C (en) * | 2011-03-02 | 2020-07-14 | Novartis Ag | Combination vaccines with lower doses of antigen and/or adjuvant |
| JP2014525429A (ja) | 2011-09-01 | 2014-09-29 | ノバルティス アーゲー | Ｓｔａｐｈｙｌｏｃｏｃｃｕｓａｕｒｅｕｓ抗原のアジュバント添加処方物 |
| JP2015510872A (ja) | 2012-03-07 | 2015-04-13 | ノバルティス アーゲー | Ｓｔｒｅｐｔｏｃｏｃｃｕｓｐｎｅｕｍｏｎｉａｅ抗原の増強された製剤 |
| WO2013131984A1 (en) | 2012-03-07 | 2013-09-12 | Novartis Ag | Adjuvanted formulations of rabies virus immunogens |
| CA2866406A1 (en) | 2012-03-08 | 2013-09-12 | Novartis Ag | Adjuvanted formulations of booster vaccines |
| CN104602705A (zh) | 2012-09-06 | 2015-05-06 | 诺华股份有限公司 | 血清组b脑膜炎球菌和d/t/p的联合疫苗 |
| US10471139B2 (en) * | 2013-08-15 | 2019-11-12 | The University Of Kansas | Toll-like receptor agonists |
| JP6522732B2 (ja) | 2014-07-11 | 2019-05-29 | ギリアード サイエンシーズ， インコーポレイテッド | Ｈｉｖを治療するためのトール様受容体の調節因子 |
| PT3190113T (pt) | 2014-08-15 | 2021-06-17 | Chai Tai Tianqing Pharmaceutical Group Co Ltd | Compostos pirrolopirimidina utilizados como agonistas de tlr7 |
| PT3194401T (pt) | 2014-09-16 | 2020-12-23 | Gilead Sciences Inc | Formas sólidas de modulador de recetor tipo toll |
| CN107043380A (zh) | 2016-02-05 | 2017-08-15 | 正大天晴药业集团股份有限公司 | 一种tlr7激动剂的马来酸盐、其晶型c、晶型d、晶型e、制备方法和用途 |
| WO2019209811A1 (en) | 2018-04-24 | 2019-10-31 | Bristol-Myers Squibb Company | Macrocyclic toll-like receptor 7 (tlr7) agonists |
| US11554120B2 (en) | 2018-08-03 | 2023-01-17 | Bristol-Myers Squibb Company | 1H-pyrazolo[4,3-d]pyrimidine compounds as toll-like receptor 7 (TLR7) agonists and methods and uses therefor |
| TWI838401B (zh) | 2018-09-12 | 2024-04-11 | 瑞士商諾華公司 | 抗病毒性吡啶并吡𠯤二酮化合物 |
| US11667613B2 (en) | 2019-09-26 | 2023-06-06 | Novartis Ag | Antiviral pyrazolopyridinone compounds |
| CN115151548A (zh) | 2020-01-27 | 2022-10-04 | 百时美施贵宝公司 | 作为Toll样受体7(TLR7)激动剂的1H-吡唑并[4,3-d]嘧啶化合物 |
| WO2021154661A1 (en) | 2020-01-27 | 2021-08-05 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| JP2023512229A (ja) | 2020-01-27 | 2023-03-24 | ブリストル－マイヤーズ スクイブ カンパニー | トール様受容体７（ＴＬＲ７）アゴニストとしての１Ｈ－ピラゾロ［４，３－ｄ］ピリミジン化合物 |
| JP2023512230A (ja) | 2020-01-27 | 2023-03-24 | ブリストル－マイヤーズ スクイブ カンパニー | トール様受容体７（ＴＬＲ７）アゴニストとしてのＣ３置換１Ｈ－ピラゾロ［４，３－ｄ］ピリミジン化合物 |
| EP4097104A1 (en) | 2020-01-27 | 2022-12-07 | Bristol-Myers Squibb Company | 1h-pyrazolo[4,3-d]pyrimidine compounds as toll-like receptor 7 (tlr7) agonists |
| US20230041738A1 (en) | 2020-01-27 | 2023-02-09 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| US20230131192A1 (en) | 2020-01-27 | 2023-04-27 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| US20230140430A1 (en) | 2020-01-27 | 2023-05-04 | Bristol-Myers Squibb Company | 1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS |
| JP2023512208A (ja) | 2020-01-27 | 2023-03-24 | ブリストル－マイヤーズ スクイブ カンパニー | トール様受容体７（ＴＬＲ７）アゴニストとしての１Ｈ－ピラゾロ［４，３－ｄ］ピリミジン化合物 |
| CN117736210A (zh) * | 2021-01-28 | 2024-03-22 | 上海翊石医药科技有限公司 | 一类芳杂环类化合物及其制备方法和用途 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2006287157A1 (en) * | 2005-09-02 | 2007-03-08 | Pfizer Inc. | Hydroxy substituted 1H-imidazopyridines and methods |
| JP2009528989A (ja) * | 2006-02-17 | 2009-08-13 | ファイザー・リミテッド | Ｔｌｒ７変調剤としての３−デアザプリン誘導体 |
-
2008
- 2008-07-22 WO PCT/IB2008/001962 patent/WO2009019553A2/en active Application Filing
- 2008-07-22 ES ES08788941T patent/ES2359123T3/es active Active
- 2008-07-22 JP JP2010519534A patent/JP2010535755A/ja not_active Withdrawn
- 2008-07-22 AT AT08788941T patent/ATE501136T1/de not_active IP Right Cessation
- 2008-07-22 DE DE602008005470T patent/DE602008005470D1/de active Active
- 2008-07-22 CA CA2707030A patent/CA2707030A1/en not_active Abandoned
- 2008-07-22 EP EP08788941A patent/EP2188280B1/en not_active Not-in-force
- 2008-07-29 CL CL2008002228A patent/CL2008002228A1/es unknown
- 2008-07-30 PA PA20088791701A patent/PA8791701A1/es unknown
- 2008-07-31 UY UY31261A patent/UY31261A1/es not_active Application Discontinuation
- 2008-07-31 AR ARP080103322A patent/AR067757A1/es not_active Application Discontinuation
- 2008-08-01 PE PE2008001300A patent/PE20090511A1/es not_active Application Discontinuation
- 2008-08-01 TW TW097129257A patent/TW200914003A/zh unknown
-
2009
- 2009-05-15 US US12/184,494 patent/US20090221631A1/en not_active Abandoned
-
2010
- 2010-10-28 US US12/914,530 patent/US20110039884A1/en not_active Abandoned
-
2011
- 2011-11-22 US US13/302,085 patent/US20120302598A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20120302598A1 (en) | 2012-11-29 |
| CA2707030A1 (en) | 2009-02-12 |
| DE602008005470D1 (en) | 2011-04-21 |
| TW200914003A (en) | 2009-04-01 |
| WO2009019553A2 (en) | 2009-02-12 |
| ATE501136T1 (de) | 2011-03-15 |
| JP2010535755A (ja) | 2010-11-25 |
| CL2008002228A1 (es) | 2009-04-17 |
| AR067757A1 (es) | 2009-10-21 |
| US20090221631A1 (en) | 2009-09-03 |
| US20110039884A1 (en) | 2011-02-17 |
| WO2009019553A3 (en) | 2009-04-02 |
| EP2188280B1 (en) | 2011-03-09 |
| EP2188280A2 (en) | 2010-05-26 |
| ES2359123T3 (es) | 2011-05-18 |
| UY31261A1 (es) | 2009-03-31 |
| PA8791701A1 (es) | 2009-04-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD | Application declared void or lapsed |