MX2014002285A - Inhibidores de la replicacion del vih. - Google Patents
Inhibidores de la replicacion del vih.Info
- Publication number
- MX2014002285A MX2014002285A MX2014002285A MX2014002285A MX2014002285A MX 2014002285 A MX2014002285 A MX 2014002285A MX 2014002285 A MX2014002285 A MX 2014002285A MX 2014002285 A MX2014002285 A MX 2014002285A MX 2014002285 A MX2014002285 A MX 2014002285A
- Authority
- MX
- Mexico
- Prior art keywords
- substituted
- hiv replication
- replication inhibitors
- group
- unsubstituted aryl
- Prior art date
Links
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
- 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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Compuestos de la Fórmula (I), en donde B se selecciona del grupo que consiste de arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido; Y es un residuo enlazador seleccionado del grupo que consiste de una unión directa. R, R1, R2 y R3 se seleccionan cada uno individualmente del grupo que consiste de arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido o heterociclo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161527895P | 2011-08-26 | 2011-08-26 | |
| PCT/US2012/052482 WO2013033003A1 (en) | 2011-08-26 | 2012-08-27 | Hiv replication inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2014002285A true MX2014002285A (es) | 2017-01-06 |
Family
ID=47756783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2014002285A MX2014002285A (es) | 2011-08-26 | 2012-08-27 | Inhibidores de la replicacion del vih. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9120787B2 (es) |
| EP (1) | EP2748150B1 (es) |
| JP (1) | JP5969031B2 (es) |
| CN (1) | CN103827094B (es) |
| AU (1) | AU2012300274B2 (es) |
| BR (1) | BR112014003989A2 (es) |
| CA (1) | CA2844119A1 (es) |
| ES (1) | ES2617332T3 (es) |
| MX (1) | MX2014002285A (es) |
| WO (1) | WO2013033003A1 (es) |
| ZA (1) | ZA201401330B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102573470A (zh) | 2009-11-02 | 2012-07-11 | 宋嘉盛 | 用于介入治疗和根除癌症的ite |
| US10632106B2 (en) | 2009-11-02 | 2020-04-28 | Ariagen, Inc. | Methods of cancer treatment with 2-(1′H-Indole-3′-carbonyl)-thiazole-4-carboxylic acid methyl ester |
| ES2848065T3 (es) | 2014-09-12 | 2021-08-05 | Ariagen Inc | Síntesis eficiente y escalable de éster metílico del ácido 2-(1¿H-indol-3¿-carbonil)-tiazol-4-carboxílico y sus análogos estructurales |
| CN108239083B (zh) | 2016-12-26 | 2021-08-17 | 阿里根公司 | 芳香烃受体调节剂 |
| WO2019099977A2 (en) | 2017-11-20 | 2019-05-23 | Ariagen, Inc. | Indole compounds and their use |
| AU2020258394A1 (en) | 2019-04-15 | 2021-10-28 | Ariagen, Inc. | Chiral indole compounds and their use |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6900214B2 (en) | 2001-03-29 | 2005-05-31 | Bristol-Myers Squibb Company | Cyano-substituted dihydropyrimidine compounds and their use to treat diseases |
| AR048962A1 (es) | 2004-05-17 | 2006-06-14 | Tibotec Pharm Ltd | Combinaciones de 1- fenil-1,5 - dihidro - pirido - (3,2-b) indol -2- onas sustituidas y otros inhibidores de vih |
| WO2009020457A2 (en) * | 2006-06-30 | 2009-02-12 | Smithkline Beecham Corporation | Chemical compounds |
| MY150285A (en) | 2007-12-20 | 2013-12-31 | Bayer Ip Gmbh | 4-(4-cyano-2-thioaryl)dihydropyrimidinones and their use |
| WO2010046780A2 (en) | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Anti viral compounds |
-
2012
- 2012-08-27 BR BR112014003989A patent/BR112014003989A2/pt not_active Application Discontinuation
- 2012-08-27 ES ES12828488.2T patent/ES2617332T3/es active Active
- 2012-08-27 CA CA2844119A patent/CA2844119A1/en not_active Abandoned
- 2012-08-27 WO PCT/US2012/052482 patent/WO2013033003A1/en not_active Ceased
- 2012-08-27 CN CN201280041536.7A patent/CN103827094B/zh not_active Expired - Fee Related
- 2012-08-27 AU AU2012300274A patent/AU2012300274B2/en not_active Ceased
- 2012-08-27 EP EP12828488.2A patent/EP2748150B1/en not_active Not-in-force
- 2012-08-27 JP JP2014527351A patent/JP5969031B2/ja not_active Expired - Fee Related
- 2012-08-27 US US14/238,374 patent/US9120787B2/en active Active
- 2012-08-27 MX MX2014002285A patent/MX2014002285A/es unknown
-
2014
- 2014-02-21 ZA ZA2014/01330A patent/ZA201401330B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20140235582A1 (en) | 2014-08-21 |
| BR112014003989A2 (pt) | 2017-06-13 |
| EP2748150B1 (en) | 2016-11-30 |
| WO2013033003A1 (en) | 2013-03-07 |
| US9120787B2 (en) | 2015-09-01 |
| CN103827094B (zh) | 2017-09-26 |
| EP2748150A1 (en) | 2014-07-02 |
| NZ622558A (en) | 2016-09-30 |
| ZA201401330B (en) | 2019-08-28 |
| ES2617332T3 (es) | 2017-06-16 |
| CA2844119A1 (en) | 2013-03-07 |
| JP2014525416A (ja) | 2014-09-29 |
| CN103827094A (zh) | 2014-05-28 |
| AU2012300274B2 (en) | 2017-06-29 |
| EP2748150A4 (en) | 2015-01-07 |
| AU2012300274A1 (en) | 2014-03-06 |
| JP5969031B2 (ja) | 2016-08-10 |
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