PE20090143A1 - Inhibidores no nucleosidos de transcriptasa inversa - Google Patents
Inhibidores no nucleosidos de transcriptasa inversaInfo
- Publication number
- PE20090143A1 PE20090143A1 PE2008000622A PE2008000622A PE20090143A1 PE 20090143 A1 PE20090143 A1 PE 20090143A1 PE 2008000622 A PE2008000622 A PE 2008000622A PE 2008000622 A PE2008000622 A PE 2008000622A PE 20090143 A1 PE20090143 A1 PE 20090143A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- nucleosid
- fluor
- inhibitors
- chloro
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring 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
- 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
- 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)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS NO NUCLEOSIDOS DE FORMULA I, DONDE X ES CH2 O NH; Y ES CH2 U O; X1 ES N O CH; R1 ES C(=O)Ar, OAr, FLUOR O H; R2 ES OAr, HIDROGENO, HALOGENO, ALQUILO(C1-C6), ALCOXI(C1-C6) O CICLOALQUILO(C3-C5); R3 Y R4 SON H, HALOGENO, ALQUILO(C1-C6), ALCOXI(C1-C6) O CICLOALQUILO(C3-C5); Ra ES H, CH2OH, CH2OC(=O)(CH2)nC(=O)OH, ENTRE OTROS; n ES DE 2 A 5; Rb ES FENILO O ALQUILO INFERIOR(C1-C6); Ar ES FENILO SUSTITUIDO POR 1-3 HALOGENO, CIANO, HALOALQUILO(C1-C6) O ALQUILO(C1-C6). SON SELECCIONADOS 3-CLORO-5-[6-CLORO-2-FLUOR-3-(1H-PIRAZOLO[3,4-b]PIRIDIN-3-ILMETOXI)-FENOXI]-BENZONITRILO, 3-[3-BROMO-2-FLUOR-6-(1H-PIRAZOLO[3,4-c]PIRIDAZIN-3-IL-METOXI)-FENOXI]-5-CLORO-BENZONITRILO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA TRASCRIPTASA INVERSA DEL VIH Y ENCUENTRAN SU UTILIDAD EN EL TRATAMIENTO O PREVENCION DE INFECCION POR VIH-1, SIDA O ARC
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92244907P | 2007-04-09 | 2007-04-09 | |
US96134607P | 2007-07-20 | 2007-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20090143A1 true PE20090143A1 (es) | 2009-02-26 |
Family
ID=39798124
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008000622A PE20090143A1 (es) | 2007-04-09 | 2008-04-07 | Inhibidores no nucleosidos de transcriptasa inversa |
Country Status (15)
Country | Link |
---|---|
US (1) | US20080293664A1 (es) |
EP (1) | EP2134711A2 (es) |
JP (1) | JP2010523613A (es) |
KR (1) | KR20100015435A (es) |
CN (1) | CN101679414A (es) |
AR (1) | AR066404A1 (es) |
AU (1) | AU2008235549A1 (es) |
BR (1) | BRPI0810496A2 (es) |
CA (1) | CA2683046A1 (es) |
CL (1) | CL2008000996A1 (es) |
IL (1) | IL200886A0 (es) |
MX (1) | MX2009010932A (es) |
PE (1) | PE20090143A1 (es) |
TW (1) | TW200906410A (es) |
WO (1) | WO2008122534A2 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080132510A1 (en) * | 2005-01-21 | 2008-06-05 | Bingsong Han | Imidazolylmethyl and Pyrazolylmethyl Heteroaryl Derivatives |
ES2463720T3 (es) * | 2007-11-16 | 2014-05-29 | Gilead Sciences, Inc. | Inhibidores de la replicación del virus de inmunodeficiencia humana |
KR101610415B1 (ko) * | 2007-12-21 | 2016-04-07 | 에프. 호프만-라 로슈 아게 | 헤테로사이클릭 항바이러스 화합물 |
CN103025696B (zh) | 2010-07-15 | 2015-08-12 | 阿尔比马尔公司 | 用于制备4-溴代-2-甲氧基苯甲醛的方法 |
US9497234B2 (en) * | 2012-12-27 | 2016-11-15 | Facebook, Inc. | Implicit social graph connections |
WO2016004305A2 (en) * | 2014-07-02 | 2016-01-07 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0128287D0 (en) * | 2001-11-26 | 2002-01-16 | Smithkline Beecham Plc | Novel method and compounds |
GB0206723D0 (en) * | 2002-03-21 | 2002-05-01 | Glaxo Group Ltd | Novel compounds |
TW200505441A (en) * | 2003-03-24 | 2005-02-16 | Hoffmann La Roche | Non-nucleoside reverse transcriptase inhibitorsⅠ |
JP4485520B2 (ja) * | 2003-03-24 | 2010-06-23 | エフ.ホフマン−ラ ロシュ アーゲー | 逆転写酵素阻害剤としてのベンジル−ピリダジノン類 |
JP4627315B2 (ja) * | 2004-03-23 | 2011-02-09 | エフ.ホフマン−ラ ロシュ アーゲー | 非ヌクレオシド逆転写酵素阻害剤としてのベンジルピリダジノン誘導体 |
US7625949B2 (en) * | 2004-04-23 | 2009-12-01 | Roche Palo Alto Llc | Methods for treating retroviral infections |
US7166738B2 (en) * | 2004-04-23 | 2007-01-23 | Roche Palo Alto Llc | Non-nucleoside reverse transcriptase inhibitors |
BRPI0513858B8 (pt) * | 2004-07-27 | 2021-05-25 | Hoffmann La Roche | compostos de benziltriazolona como inibidores não-nucleosídeos da transcriptase reversa, seu processo de preparação, seu uso e composição farmacêutica que os compreende |
AR057455A1 (es) * | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
CN101501002B (zh) * | 2006-08-16 | 2012-06-27 | 弗·哈夫曼-拉罗切有限公司 | 非核苷逆转录酶抑制剂 |
-
2008
- 2008-03-31 KR KR1020097021022A patent/KR20100015435A/ko not_active Application Discontinuation
- 2008-03-31 BR BRPI0810496A patent/BRPI0810496A2/pt not_active Application Discontinuation
- 2008-03-31 EP EP08735604A patent/EP2134711A2/en not_active Withdrawn
- 2008-03-31 AU AU2008235549A patent/AU2008235549A1/en not_active Abandoned
- 2008-03-31 CA CA002683046A patent/CA2683046A1/en not_active Abandoned
- 2008-03-31 MX MX2009010932A patent/MX2009010932A/es not_active Application Discontinuation
- 2008-03-31 WO PCT/EP2008/053806 patent/WO2008122534A2/en active Application Filing
- 2008-03-31 CN CN200880011097A patent/CN101679414A/zh active Pending
- 2008-03-31 JP JP2010502486A patent/JP2010523613A/ja active Pending
- 2008-04-07 CL CL200800996A patent/CL2008000996A1/es unknown
- 2008-04-07 PE PE2008000622A patent/PE20090143A1/es not_active Application Discontinuation
- 2008-04-07 AR ARP080101433A patent/AR066404A1/es unknown
- 2008-04-08 US US12/082,069 patent/US20080293664A1/en not_active Abandoned
- 2008-04-08 TW TW097112675A patent/TW200906410A/zh unknown
-
2009
- 2009-09-13 IL IL200886A patent/IL200886A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
JP2010523613A (ja) | 2010-07-15 |
KR20100015435A (ko) | 2010-02-12 |
US20080293664A1 (en) | 2008-11-27 |
AU2008235549A1 (en) | 2008-10-16 |
CL2008000996A1 (es) | 2008-10-10 |
WO2008122534A3 (en) | 2009-02-05 |
EP2134711A2 (en) | 2009-12-23 |
AR066404A1 (es) | 2009-08-19 |
CA2683046A1 (en) | 2008-10-16 |
WO2008122534A2 (en) | 2008-10-16 |
CN101679414A (zh) | 2010-03-24 |
BRPI0810496A2 (pt) | 2018-11-06 |
IL200886A0 (en) | 2010-05-17 |
TW200906410A (en) | 2009-02-16 |
MX2009010932A (es) | 2009-10-29 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |