PE20070124A1 - Derivados de heteroaril para tratar virus - Google Patents
Derivados de heteroaril para tratar virusInfo
- Publication number
- PE20070124A1 PE20070124A1 PE2006000725A PE2006000725A PE20070124A1 PE 20070124 A1 PE20070124 A1 PE 20070124A1 PE 2006000725 A PE2006000725 A PE 2006000725A PE 2006000725 A PE2006000725 A PE 2006000725A PE 20070124 A1 PE20070124 A1 PE 20070124A1
- Authority
- PE
- Peru
- Prior art keywords
- heteroaril
- substituted
- derivatives
- quinolin
- pyrrol
- Prior art date
Links
- 241000700605 Viruses Species 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical class N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 abstract 1
- 241000710781 Flaviviridae Species 0.000 abstract 1
- 208000036142 Viral infection Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE L ES UN ENLACE, ALQUILENO C1-C3, ALQUENILENO C2-C3 SUSTITUIDO, CICLOALQUILENO C3-C6, ENTRE OTROS; UNO DE X, X' ESNR1 Y EL OTRO ES SELECCIONADO ENTRE CR2, N, O, S; Q ES CR, N, O, S; R ES H, HALO, ALQUIL C1-C2, ALQUENIL C2-C3, ENTRE OTROS; R1 Y R2 SON CADA UNO H, ALQUIL, ALQUIL SUSTITUIDO, CICLOALQUIL SUSTITUIDO, ALQUINIL, ENTRE OTROS; Z ES H, HALO, ALQUIL, ALQUENIL, ALCOXI, ARIL, CIANO, HETEROARIL, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: SINTESIS DE ACIDO 1-CARBOXIMETIL-4-CICLOHEXIL-5-[2-(2,4-DIMETIL-TIAZOL-5-IL)-QUINOLIN-6-IL]-1H-PIRROL-2-CARBOXILICO; ACIDO TERT-BUTOXICARBONILMETIL-4-CICLOHEXIL-5-[2-(2,4-DIMETIL-TIAZOL-5-IL)-QUINOLIN-6-IL]-1H-PIRROL-2-CARBOXILICO; ENTRE OTROS. REFERIDA TEMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DE INFECCIONES VIRALES EN AMIMALES MEDIADOS POR EL VIRUS FLAVIVIRIDAE
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69370005P | 2005-06-24 | 2005-06-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070124A1 true PE20070124A1 (es) | 2007-03-09 |
Family
ID=37499598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006000725A PE20070124A1 (es) | 2005-06-24 | 2006-06-23 | Derivados de heteroaril para tratar virus |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20060293320A1 (es) |
| EP (1) | EP1910337A2 (es) |
| JP (1) | JP2008546802A (es) |
| KR (1) | KR20080040677A (es) |
| CN (1) | CN101223161A (es) |
| AR (1) | AR054797A1 (es) |
| AU (1) | AU2006261132A1 (es) |
| BR (1) | BRPI0612124A2 (es) |
| CA (1) | CA2613261A1 (es) |
| MA (1) | MA28394B1 (es) |
| MX (1) | MX2007016144A (es) |
| PE (1) | PE20070124A1 (es) |
| TW (1) | TW200726471A (es) |
| WO (1) | WO2006138744A2 (es) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2644933A1 (en) * | 2006-02-27 | 2007-09-07 | Gilead Colorado, Inc. | Combinations comprising a histone deacetylase inhibiting agent and a nuclear hormone receptor ligand for treating cardiovascular conditions |
| UY30892A1 (es) * | 2007-02-07 | 2008-09-02 | Smithkline Beckman Corp | Inhibidores de la actividad akt |
| EP2494991A1 (en) | 2007-05-04 | 2012-09-05 | Vertex Pharmaceuticals Incorporated | Combination therapy for the treatment of HCV infection |
| US20090005374A1 (en) * | 2007-06-26 | 2009-01-01 | Melvin Jr Lawrence S | Imidazopyridinyl thiazolyl histone deacetylase inhibitors |
| WO2010009166A1 (en) * | 2008-07-14 | 2010-01-21 | Gilead Colorado, Inc. | Oxindolyl inhibitor compounds |
| US8134000B2 (en) * | 2008-07-14 | 2012-03-13 | Gilead Sciences, Inc. | Imidazolyl pyrimidine inhibitor compounds |
| NZ590320A (en) * | 2008-07-14 | 2012-12-21 | Gilead Sciences Inc | Fused heterocyclyc inhibitors of histone deacetylase and/or cyclin-dependent kinases |
| CA2731323A1 (en) * | 2008-07-28 | 2010-02-04 | Gilead Sciences, Inc. | Cycloalkylidene and heterocycloalkylidene histone deacetylase inhibitor compounds |
| DK2318007T3 (da) * | 2008-08-15 | 2013-03-25 | N30 Pharmaceuticals Inc | Nye pyrrol-inhibitorer af s-nitrosoglutathion-reduktase som terapeutiske midler |
| JP5524209B2 (ja) | 2008-08-15 | 2014-06-18 | エヌサーティー・ファーマシューティカルズ・インコーポレーテッド | S−ニトロソグルタチオンレダクターゼのピロール阻害剤 |
| DK2315591T3 (en) | 2008-08-15 | 2016-06-06 | Nivalis Therapeutics Inc | NOVEL PYRROLE INHIBITORS OF S-nitrosoglutathione-reductase as therapeutic agents |
| CN102405047B (zh) | 2009-01-30 | 2014-07-09 | 葛兰素史密斯克莱有限责任公司 | 结晶型的n-{(1s)-2-氨基-1-[(3-氟苯基)甲基]乙基}-5-氯-4-(4-氯-1-甲基-1h-吡唑-5-基)-2-噻吩甲酰胺盐酸盐 |
| WO2010144371A1 (en) * | 2009-06-08 | 2010-12-16 | Gilead Colorado, Inc. | Alkanoylamino benzamide aniline hdac inihibitor compounds |
| AU2010259042A1 (en) * | 2009-06-08 | 2011-12-15 | Gilead Sciences, Inc. | Cycloalkylcarbamate benzamide aniline HDAC inhibitor compounds |
| PL2455376T3 (pl) * | 2009-06-11 | 2015-06-30 | Abbvie Bahamas Ltd | Związki heterocykliczne jako inhibitory wirusa zapalenia wątroby typu C (HCV) |
| US8822515B2 (en) | 2009-10-16 | 2014-09-02 | University Of Maryland, Baltimore County | Heterocyclic benzoxazole compositions as inhibitors of hepatitis C virus |
| CA2779244A1 (en) | 2009-10-30 | 2011-05-05 | Boehringer Ingelheim International Gmbh | Dosage regimens for hcv combination therapy comprising bi201335, interferon alpha and ribavirin |
| TWI508968B (zh) * | 2010-02-08 | 2015-11-21 | Biota Scient Management | 用於治療呼吸道融合性病毒感染的化合物 |
| CA2813093A1 (en) * | 2010-09-30 | 2012-04-05 | Boehringer Ingelheim International Gmbh | Combination therapy for treating hcv infection |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4107288A (en) * | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
| EP1304335B1 (en) * | 1990-04-04 | 2009-06-10 | Novartis Vaccines and Diagnostics, Inc. | Hepatitis C virus protease |
| US5145684A (en) * | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| US5738985A (en) * | 1993-04-02 | 1998-04-14 | Ribogene, Inc. | Method for selective inactivation of viral replication |
| IT1272179B (it) * | 1994-02-23 | 1997-06-16 | Angeletti P Ist Richerche Bio | Metodologia per riprodurre in vitro l'attivita' proteolitica della proteasi ns3 del virus hcv. |
| US5861267A (en) * | 1995-05-01 | 1999-01-19 | Vertex Pharmaceuticals Incorporated | Methods, nucleotide sequences and host cells for assaying exogenous and endogenous protease activity |
| US5759795A (en) * | 1996-03-08 | 1998-06-02 | Schering Corporation | Assay for determining inhibitors of ATPase |
| WO1998039487A1 (en) * | 1997-03-05 | 1998-09-11 | Ribogene, Inc. | Novel screening methods to identify agents that selectively inhibit hepatitis c virus replication |
| US6228576B1 (en) * | 1997-12-11 | 2001-05-08 | Smithkline Beecham Corporation | Hepatitis C virus NS5B truncated protein and methods thereof to identify antiviral compounds |
| CO5271680A1 (es) * | 2000-02-21 | 2003-04-30 | Smithkline Beecham Corp | Compuestos |
| EP2335700A1 (en) * | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis C virus polymerase inhibitors with a heterobicylic structure |
| MY151199A (en) * | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
| PL375442A1 (en) * | 2002-07-18 | 2005-11-28 | Bristol-Myers Squibb Company | Modulators of the glucocorticoid receptor and method |
| GB0307891D0 (en) * | 2003-04-04 | 2003-05-14 | Angeletti P Ist Richerche Bio | Chemical compounds,compositions and uses |
| EP1651631A1 (en) * | 2003-08-01 | 2006-05-03 | Genelabs Technologies, Inc. | Bicyclic imidazol derivatives against flaviviridae |
-
2006
- 2006-06-22 AU AU2006261132A patent/AU2006261132A1/en not_active Abandoned
- 2006-06-22 US US11/473,511 patent/US20060293320A1/en not_active Abandoned
- 2006-06-22 EP EP06799960A patent/EP1910337A2/en not_active Withdrawn
- 2006-06-22 MA MA29128A patent/MA28394B1/fr unknown
- 2006-06-22 JP JP2008518457A patent/JP2008546802A/ja active Pending
- 2006-06-22 MX MX2007016144A patent/MX2007016144A/es not_active Application Discontinuation
- 2006-06-22 BR BRPI0612124-1A patent/BRPI0612124A2/pt not_active Application Discontinuation
- 2006-06-22 CA CA002613261A patent/CA2613261A1/en not_active Abandoned
- 2006-06-22 KR KR1020087001748A patent/KR20080040677A/ko not_active Withdrawn
- 2006-06-22 WO PCT/US2006/024554 patent/WO2006138744A2/en not_active Ceased
- 2006-06-22 CN CNA2006800262169A patent/CN101223161A/zh active Pending
- 2006-06-23 PE PE2006000725A patent/PE20070124A1/es not_active Application Discontinuation
- 2006-06-23 TW TW095122749A patent/TW200726471A/zh unknown
- 2006-06-23 AR ARP060102719A patent/AR054797A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2613261A1 (en) | 2006-12-28 |
| KR20080040677A (ko) | 2008-05-08 |
| JP2008546802A (ja) | 2008-12-25 |
| WO2006138744A3 (en) | 2007-04-05 |
| TW200726471A (en) | 2007-07-16 |
| WO2006138744A2 (en) | 2006-12-28 |
| BRPI0612124A2 (pt) | 2010-10-19 |
| EP1910337A2 (en) | 2008-04-16 |
| AR054797A1 (es) | 2007-07-18 |
| AU2006261132A1 (en) | 2006-12-28 |
| CN101223161A (zh) | 2008-07-16 |
| MA28394B1 (fr) | 2007-01-02 |
| MX2007016144A (es) | 2008-03-06 |
| US20060293320A1 (en) | 2006-12-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration | ||
| FD | Application declared void or lapsed |