MA32764B1 - Inhibiteurs de l'intégrase du vih - Google Patents
Inhibiteurs de l'intégrase du vihInfo
- Publication number
- MA32764B1 MA32764B1 MA33804A MA33804A MA32764B1 MA 32764 B1 MA32764 B1 MA 32764B1 MA 33804 A MA33804 A MA 33804A MA 33804 A MA33804 A MA 33804A MA 32764 B1 MA32764 B1 MA 32764B1
- Authority
- MA
- Morocco
- Prior art keywords
- hiv
- compounds
- inhibitors
- antigrade
- prophylaxis
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—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
- A61K31/495—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- 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
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
L'INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I) QUI SONT DES INHIBITEURS DE L'INTÉGRASE DU VIH ET DES INHIBITEURS DE LA RÉPLICATION DU VIH. DANS LA FORMULE (I), X1, X2, Y, R1A, R1B, R2 ET R3 SONT DÉFINIS DANS LA DESCRIPTION. CES COMPOSÉS SONT UTILES DANS LA PROPHYLAXIE OU LE TRAITEMENT D'UNE INFECTION PROVOQUÉE PAR LE VIH ET LA PROPHYLAXIE, LE TRAITEMENT OU LE RETARDEMENT DU DÉCLENCHEMENT OU DE LA PROGRESSION DU SIDA. LES COMPOSÉS SELON L'INVENTION SONT UTILISÉS POUR LUTTER CONTRE UNE INFECTION VIH ET LE SIDA SOUS FORME DESDITS COMPOSÉS EUX-MÊMES (OU D'HYDRATES OU DE SOLVATES DE CEUX-CI) OU DE LEURS SELS PHARMACEUTIQUEMENT ACCEPTABLES. CES COMPOSÉS ET LEURS SELS PEUVENT ÊTRE EMPLOYÉS EN TANT QU'INGRÉDIENTS DANS DES COMPOSITIONS PHARMACEUTIQUES, ÉVENTUELLEMENT COMBINÉS À D'AUTRES ANTIVIRAUX, IMMUNOMODULATEURS, ANTIBIOTIQUES OR VACCINS.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19527108P | 2008-10-06 | 2008-10-06 | |
PCT/US2009/059306 WO2010042391A2 (fr) | 2008-10-06 | 2009-10-02 | Inhibiteurs de l'intégrase du vih |
Publications (1)
Publication Number | Publication Date |
---|---|
MA32764B1 true MA32764B1 (fr) | 2011-11-01 |
Family
ID=41682332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA33804A MA32764B1 (fr) | 2008-10-06 | 2011-05-02 | Inhibiteurs de l'intégrase du vih |
Country Status (22)
Country | Link |
---|---|
US (2) | US8513234B2 (fr) |
EP (1) | EP2349276B1 (fr) |
JP (2) | JP4880097B1 (fr) |
KR (1) | KR20110066224A (fr) |
CN (1) | CN102239172A (fr) |
AR (1) | AR073769A1 (fr) |
AU (1) | AU2009302663B2 (fr) |
BR (1) | BRPI0920605A8 (fr) |
CA (1) | CA2738814C (fr) |
CO (1) | CO6382127A2 (fr) |
CR (1) | CR20110184A (fr) |
DO (1) | DOP2011000093A (fr) |
EA (1) | EA201170537A1 (fr) |
EC (1) | ECSP11010959A (fr) |
IL (1) | IL212019A0 (fr) |
MA (1) | MA32764B1 (fr) |
MX (1) | MX2011003637A (fr) |
NI (1) | NI201100069A (fr) |
PE (1) | PE20110344A1 (fr) |
TW (1) | TW201020251A (fr) |
WO (2) | WO2010042392A2 (fr) |
ZA (1) | ZA201102620B (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8283366B2 (en) | 2010-01-22 | 2012-10-09 | Ambrilia Biopharma, Inc. | Derivatives of pyridoxine for inhibiting HIV integrase |
WO2014008636A1 (fr) * | 2012-07-11 | 2014-01-16 | Merck Sharp & Dohme Corp. | Composés macrocycliques en tant qu'inhibiteurs de l'intégrase du vih |
CN102936188B (zh) * | 2012-11-19 | 2015-07-15 | 湖北吉和昌化工科技有限公司 | 一种丙炔醇缩水甘油醚的合成方法 |
WO2014172188A2 (fr) | 2013-04-16 | 2014-10-23 | Merck Sharp & Dohme Corp. | Composés dérivés de 4-pyridone et leurs utilisations en tant qu'inhibiteurs de la vih intégrase |
CN107722106A (zh) * | 2016-08-11 | 2018-02-23 | 重庆大学 | Hiv抑制剂 |
CN111684715B (zh) | 2018-02-08 | 2023-05-02 | 株式会社索思未来 | 放大电路、加法电路、接收电路以及集成电路 |
WO2020197991A1 (fr) | 2019-03-22 | 2020-10-01 | Gilead Sciences, Inc. | Composés de carbamoylpyridone tricyclique pontés et leur utilisation pharmaceutique |
CR20220418A (es) | 2020-02-24 | 2022-10-10 | Gilead Sciences Inc | Compuestos tetracíclicos para el tratamiento de infecciones por vih |
CN111454214B (zh) * | 2020-05-27 | 2023-04-07 | 龙曦宁(上海)医药科技有限公司 | 一种2-甲氧基1-嘧啶乙胺盐酸盐的合成方法 |
HUE064467T2 (hu) | 2021-01-19 | 2024-03-28 | Gilead Sciences Inc | Szubsztituált piridotriazin-származékok és alkalmazásuk |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE530520T1 (de) * | 2001-08-10 | 2011-11-15 | Shionogi & Co | Antivirales mittel |
CA2463975A1 (fr) * | 2001-10-26 | 2003-05-01 | Maria Emilia Di Francesco | Inhibiteurs de l'integrase du vih a base de dihydroxypyrimidine carboxamide |
CA2463976C (fr) * | 2001-10-26 | 2007-02-13 | Benedetta Crescenzi | Inhibiteurs de l'integrase du vih a base d'hydroxypyrimidinone carboxamide n-substitue |
CA2472372C (fr) * | 2002-01-17 | 2010-08-17 | Melissa Egbertson | Carboxamides hydroxynaphthyridinone utiles comme inhibiteurs de l'integrase du vih |
AU2003292436B2 (en) * | 2002-12-27 | 2009-07-30 | Msd Italia S.R.L. | Tetrahydro-4H-pyrido[1,2-A]pyrimidines and related compounds useful as HIV integrase inhibitors |
WO2004062613A2 (fr) * | 2003-01-13 | 2004-07-29 | Bristol-Myers Squibb Company | Inhibiteurs d'integrase hiv |
US7037908B2 (en) * | 2003-04-24 | 2006-05-02 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
TW200510425A (en) * | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
AR046938A1 (es) | 2003-12-12 | 2006-01-04 | Merck & Co Inc | Procedimiento para preparar hexahidropirimido[1,2-a]azepin-2-carboxilatos y compuetos similares |
TW200526635A (en) * | 2003-12-22 | 2005-08-16 | Shionogi & Co | Hydroxypyrimidinone derivative having HIV integrase inhibitory activity |
US20080249112A1 (en) * | 2004-04-06 | 2008-10-09 | Chiron Corporation | Mitotic Kinesin Inhibitors |
US7273859B2 (en) * | 2004-05-12 | 2007-09-25 | Bristol-Myers Squibb Company | HIV integrase inhibitors: cyclic pyrimidinone compounds |
US7115601B2 (en) * | 2004-05-18 | 2006-10-03 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
US7192948B2 (en) * | 2004-05-28 | 2007-03-20 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
US7157447B2 (en) * | 2004-05-28 | 2007-01-02 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
US7176196B2 (en) * | 2004-05-28 | 2007-02-13 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
US7173022B2 (en) * | 2004-05-28 | 2007-02-06 | Bristol-Myers Squibb Company | Bicyclic heterocycles as HIV integrase inhibitors |
WO2006060225A2 (fr) * | 2004-11-23 | 2006-06-08 | Merck & Co., Inc. | Processus destine a la synthese asymetrique d'hexahydropyrimido[1,2-a] azepine-2-carboxamides et de composes correspondants |
US7981879B2 (en) * | 2005-03-31 | 2011-07-19 | Instituto di Ricerchi di Biologia Molecolare P. Angeletti S.p.A. | HIV integrase inhibitors |
US7494984B2 (en) * | 2005-08-31 | 2009-02-24 | Bristol-Myers Squibb Company | Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors |
WO2007059125A2 (fr) * | 2005-11-15 | 2007-05-24 | Bristol-Myers Squibb Company | Inhibiteurs de l'integrase du vih |
WO2007058646A1 (fr) | 2005-11-15 | 2007-05-24 | Bristol-Myers Squibb Company | Inhibiteurs d’integrase du vih : composes cycliques de la pyrimidinone |
US7902182B2 (en) * | 2005-11-16 | 2011-03-08 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
US8039458B2 (en) * | 2005-11-17 | 2011-10-18 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
WO2007064316A1 (fr) | 2005-11-30 | 2007-06-07 | Bristol-Myers Squibb Company | Heterocycles bicycliques en tant qu'inhibiteurs de l'integrase du vih |
US7897593B2 (en) * | 2006-05-30 | 2011-03-01 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
US7893055B2 (en) * | 2006-06-28 | 2011-02-22 | Bristol-Myers Squibb Company | HIV integrase inhibitors |
-
2009
- 2009-10-02 AU AU2009302663A patent/AU2009302663B2/en not_active Ceased
- 2009-10-02 EA EA201170537A patent/EA201170537A1/ru unknown
- 2009-10-02 WO PCT/US2009/059308 patent/WO2010042392A2/fr active Application Filing
- 2009-10-02 EP EP09740569.0A patent/EP2349276B1/fr active Active
- 2009-10-02 WO PCT/US2009/059306 patent/WO2010042391A2/fr active Application Filing
- 2009-10-02 CN CN2009801489012A patent/CN102239172A/zh active Pending
- 2009-10-02 CA CA2738814A patent/CA2738814C/fr not_active Expired - Fee Related
- 2009-10-02 KR KR1020117010300A patent/KR20110066224A/ko not_active Application Discontinuation
- 2009-10-02 US US12/572,341 patent/US8513234B2/en active Active
- 2009-10-02 JP JP2011530255A patent/JP4880097B1/ja not_active Expired - Fee Related
- 2009-10-02 PE PE2011000840A patent/PE20110344A1/es not_active Application Discontinuation
- 2009-10-02 MX MX2011003637A patent/MX2011003637A/es not_active Application Discontinuation
- 2009-10-02 BR BRPI0920605A patent/BRPI0920605A8/pt not_active IP Right Cessation
- 2009-10-05 AR ARP090103831A patent/AR073769A1/es unknown
- 2009-10-06 TW TW098133878A patent/TW201020251A/zh unknown
-
2011
- 2011-03-29 IL IL212019A patent/IL212019A0/en unknown
- 2011-04-04 DO DO2011000093A patent/DOP2011000093A/es unknown
- 2011-04-05 NI NI201100069A patent/NI201100069A/es unknown
- 2011-04-06 CR CR20110184A patent/CR20110184A/es unknown
- 2011-04-06 EC EC2011010959A patent/ECSP11010959A/es unknown
- 2011-04-08 ZA ZA2011/02620A patent/ZA201102620B/en unknown
- 2011-04-11 CO CO11044772A patent/CO6382127A2/es not_active Application Discontinuation
- 2011-05-02 MA MA33804A patent/MA32764B1/fr unknown
- 2011-09-30 JP JP2011215915A patent/JP5600311B2/ja not_active Expired - Fee Related
-
2013
- 2013-08-19 US US13/970,130 patent/US20130338141A1/en not_active Abandoned
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