CL2011002258A1 - Compuestos derivados heterociclicos fusionados; composicion farmaceutica que los comprende; y uso de los compuestos para tratar vih. - Google Patents
Compuestos derivados heterociclicos fusionados; composicion farmaceutica que los comprende; y uso de los compuestos para tratar vih.Info
- Publication number
- CL2011002258A1 CL2011002258A1 CL2011002258A CL2011002258A CL2011002258A1 CL 2011002258 A1 CL2011002258 A1 CL 2011002258A1 CL 2011002258 A CL2011002258 A CL 2011002258A CL 2011002258 A CL2011002258 A CL 2011002258A CL 2011002258 A1 CL2011002258 A1 CL 2011002258A1
- Authority
- CL
- Chile
- Prior art keywords
- compounds
- pharmaceutical composition
- fused heterocyclic
- treat hiv
- heterocyclic derivative
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Virology (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- AIDS & HIV (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
Abstract
Compuestos heterocíclicos fusionados; composición farmacéutica que los comprende; y uso para tratar VIH.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16803209P | 2009-04-09 | 2009-04-09 | |
| US26368909P | 2009-11-23 | 2009-11-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2011002258A1 true CL2011002258A1 (es) | 2012-02-10 |
Family
ID=42934876
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2011002258A CL2011002258A1 (es) | 2009-04-09 | 2011-09-12 | Compuestos derivados heterociclicos fusionados; composicion farmaceutica que los comprende; y uso de los compuestos para tratar vih. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8349839B2 (es) |
| EP (1) | EP2417140B1 (es) |
| JP (1) | JP5643290B2 (es) |
| KR (1) | KR20120034592A (es) |
| CN (1) | CN102388051A (es) |
| AR (1) | AR076252A1 (es) |
| AU (1) | AU2010234241A1 (es) |
| BR (1) | BRPI1014821A2 (es) |
| CA (1) | CA2758149A1 (es) |
| CL (1) | CL2011002258A1 (es) |
| EA (1) | EA201101397A1 (es) |
| IL (1) | IL214606A0 (es) |
| MX (1) | MX2011010582A (es) |
| TW (1) | TW201103940A (es) |
| WO (1) | WO2010115264A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013091096A1 (en) | 2011-12-20 | 2013-06-27 | Boehringer Ingelheim International Gmbh | Condensed triclyclic compounds as inhibitors of hiv replication |
| EP3233797B1 (en) * | 2015-01-18 | 2019-05-08 | SRI International Inc. | Map4k4 (hgk) inhibitors |
| US10183934B2 (en) | 2015-02-02 | 2019-01-22 | Forma Therapeutics, Inc. | Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors |
| SG11201706146UA (en) | 2015-02-02 | 2017-08-30 | Forma Therapeutics Inc | 3-alkyl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
| WO2017218950A1 (en) | 2016-06-17 | 2017-12-21 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors |
| JP7569688B2 (ja) | 2017-12-22 | 2024-10-18 | ハイバーセル,インコーポレイテッド | ホスファチジルイノシトールリン酸キナーゼ阻害剤としてのアミノピリジン誘導体 |
| WO2020028482A1 (en) * | 2018-07-31 | 2020-02-06 | The Trustees Of The University Of Pennsylvania | Small molecules that sensitize hiv-1 infected cells to antibody dependent cellular cytotoxicity |
| TW202112767A (zh) | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | 作為磷脂酸肌醇磷酸激酶抑制劑之胺基吡啶衍生物 |
| CN111560022A (zh) * | 2020-05-13 | 2020-08-21 | 深圳职业技术学院 | 四氢苯并呋喃[3,2-d]嘧啶类衍生物及其制备方法及应用 |
| CN116332947A (zh) * | 2021-12-24 | 2023-06-27 | 上海海和药物研究开发股份有限公司 | 具有mat2a抑制活性的嘧啶-2(1h)-酮并二环类化合物及其用途 |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8016A (en) * | 1851-04-01 | Improvement in the manufacture of india-rubber | ||
| JPH06172365A (ja) * | 1992-12-11 | 1994-06-21 | Yamasa Shoyu Co Ltd | 10−チアイソアロキサジン誘導体およびその用途 |
| JPH06220059A (ja) * | 1993-01-28 | 1994-08-09 | Tanabe Seiyaku Co Ltd | 縮合ピリミジン誘導体及びその製法 |
| US6593337B1 (en) * | 1999-10-19 | 2003-07-15 | Bristol-Myers Squibb Pharma Company | Tricyclic compounds useful as HIV reverse transcriptase inhibitors |
| EP1209158A1 (en) | 2000-11-18 | 2002-05-29 | Aventis Pharma Deutschland GmbH | Substituted beta-carbolines |
| TWI270547B (en) * | 2000-06-16 | 2007-01-11 | Boehringer Ingelheim Ca Ltd | Non-nucleoside reverse transcriptase inhibitors |
| WO2003099206A2 (en) | 2002-05-21 | 2003-12-04 | Bristol-Myers Squibb Company | Indole compounds useful as impdh inhibitors |
| US20030139427A1 (en) * | 2002-08-23 | 2003-07-24 | Osi Pharmaceuticals Inc. | Bicyclic pyrimidinyl derivatives and methods of use thereof |
| WO2004046163A1 (ja) | 2002-11-08 | 2004-06-03 | Kaneka Corporation | エルゴステロールの分離方法 |
| US7608726B2 (en) | 2002-11-15 | 2009-10-27 | Tibotec Pharmaceuticals Ltd. | Substituted indolepyridinium as anti-infective compounds |
| US7642277B2 (en) | 2002-12-04 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
| AU2004234087A1 (en) * | 2003-04-28 | 2004-11-11 | Tibotec Pharmaceuticals Ltd. | HIV integrase inhibitors |
| US20060074124A1 (en) * | 2003-09-12 | 2006-04-06 | Andrew Napper | Methods of treating a disorder |
| WO2005041664A1 (en) * | 2003-10-20 | 2005-05-12 | Merck & Co., Inc. | Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors |
| WO2005076861A2 (en) * | 2004-02-04 | 2005-08-25 | University Of Virginia Patent Foundation | Compounds that inhibit hiv particle formation |
| AR049637A1 (es) | 2004-05-17 | 2006-08-23 | Tibotec Pharm Ltd | 1-fenil-1,5-dihidro-pirido[3,2-b]indol-2-onas sustituidas en las posiciones 6, 7, 8, 9 |
| TW200607503A (en) | 2004-05-17 | 2006-03-01 | Tibotec Pharm Ltd | 1-heterocyclyl-1, 5-dihydro-pyrido[3, 2-b]indol-2-ones |
| US20070238727A1 (en) | 2004-05-17 | 2007-10-11 | Tibotec Bvba | 5-Substituted 1-Phenyl-1,5-Dihydro-Pyrido[3,2-B]Indol-2-Ones and Analogs as Anti-Virals |
| MXPA06013315A (es) * | 2004-05-17 | 2007-02-02 | Tibotec Pharm Ltd | 1,5-dihidro-pirido[3,2-b]indol-2-onas 4-sustituidas. |
| MXPA06013316A (es) * | 2004-05-17 | 2007-02-02 | Tibotec Pharm Ltd | Combinaciones de 1-fenil-1,5-dihidro-pirido-[3,2-b]indol-2-onas sustituidas y otros inhibidores de virus de inmunodeficiencia humana. |
| EP1773840B1 (de) * | 2004-07-23 | 2010-01-20 | The Medicines Company (Leipzig) GmbH | Substituierte pyrido[3',2':4,5]thieno[3,2-d]pyrimidine und pyrido[3',2':4,5]furo[3,2-d]-pyrimidine zur verwendung als inhibitoren der pda-4 und/oder tnf-alpha freisetzung |
| EP1797062B8 (en) | 2004-09-30 | 2011-05-25 | Boehringer Ingelheim International GmbH | Alkynyl based dervatives of benzophenone as non-nucleoside reverse transcriptase inhibitors |
| JP2008515982A (ja) | 2004-10-13 | 2008-05-15 | メルク エンド カムパニー インコーポレーテッド | 高眼圧症を治療するための眼科組成物 |
| AU2005315319B2 (en) | 2004-12-17 | 2011-07-07 | Glenmark Pharmaceuticals S.A. | Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders |
| US20060276440A1 (en) | 2005-01-03 | 2006-12-07 | An Wenqian F | Treatment of inflammatory disorders |
| WO2007025090A2 (en) | 2005-08-25 | 2007-03-01 | Kalypsys, Inc. | Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase |
| WO2007088214A2 (en) * | 2006-02-03 | 2007-08-09 | Tibotec Pharmaceuticals Ltd. | Treating hiv infection, wherein hiv has a k65r mutation |
| WO2008037783A1 (en) | 2006-09-29 | 2008-04-03 | Tibotec Pharmaceuticals Ltd. | Process for preparing 2-oxo-2,5-dihydro-1h-pyrido[3,2-b]indole-3-carbonitriles |
| DE102006062203A1 (de) * | 2006-12-22 | 2008-06-26 | Curacyte Discovery Gmbh | Substituierte 5H-Pyrimido[5,4-b]indole als Induktoren der Apoptose bei B-CLL Zellen |
| ATE490249T1 (de) | 2007-02-19 | 2010-12-15 | Glaxosmithkline Llc | Purinderivate als immunmodulatoren |
| US20100210692A1 (en) | 2007-03-28 | 2010-08-19 | Farmer Stephen R | Methods of treatment using sirt modulators and compositions containing sirt1 modulators |
| EP2231656A1 (en) | 2007-12-19 | 2010-09-29 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
-
2010
- 2010-04-07 WO PCT/CA2010/000478 patent/WO2010115264A1/en not_active Ceased
- 2010-04-07 EP EP10761139.4A patent/EP2417140B1/en active Active
- 2010-04-07 AU AU2010234241A patent/AU2010234241A1/en not_active Abandoned
- 2010-04-07 EA EA201101397A patent/EA201101397A1/ru unknown
- 2010-04-07 KR KR1020117023696A patent/KR20120034592A/ko not_active Withdrawn
- 2010-04-07 CA CA2758149A patent/CA2758149A1/en not_active Abandoned
- 2010-04-07 CN CN2010800156236A patent/CN102388051A/zh active Pending
- 2010-04-07 JP JP2012503835A patent/JP5643290B2/ja active Active
- 2010-04-07 MX MX2011010582A patent/MX2011010582A/es unknown
- 2010-04-07 BR BRPI1014821A patent/BRPI1014821A2/pt not_active Application Discontinuation
- 2010-04-08 AR ARP100101202A patent/AR076252A1/es unknown
- 2010-04-08 US US12/756,276 patent/US8349839B2/en active Active
- 2010-04-08 TW TW099110936A patent/TW201103940A/zh unknown
-
2011
- 2011-08-11 IL IL214606A patent/IL214606A0/en unknown
- 2011-09-12 CL CL2011002258A patent/CL2011002258A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW201103940A (en) | 2011-02-01 |
| AR076252A1 (es) | 2011-05-26 |
| JP5643290B2 (ja) | 2014-12-17 |
| EP2417140B1 (en) | 2014-11-26 |
| US8349839B2 (en) | 2013-01-08 |
| WO2010115264A1 (en) | 2010-10-14 |
| JP2012523380A (ja) | 2012-10-04 |
| EP2417140A1 (en) | 2012-02-15 |
| EA201101397A1 (ru) | 2012-05-30 |
| CN102388051A (zh) | 2012-03-21 |
| BRPI1014821A2 (pt) | 2016-04-05 |
| IL214606A0 (en) | 2011-09-27 |
| EP2417140A4 (en) | 2013-02-20 |
| US20100261714A1 (en) | 2010-10-14 |
| CA2758149A1 (en) | 2010-10-14 |
| KR20120034592A (ko) | 2012-04-12 |
| AU2010234241A1 (en) | 2011-09-08 |
| MX2011010582A (es) | 2011-10-19 |
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