MA35804B1 - Modulation de l'expression du virus de l'hepatite b (vhb) - Google Patents
Modulation de l'expression du virus de l'hepatite b (vhb)Info
- Publication number
- MA35804B1 MA35804B1 MA36432A MA36432A MA35804B1 MA 35804 B1 MA35804 B1 MA 35804B1 MA 36432 A MA36432 A MA 36432A MA 36432 A MA36432 A MA 36432A MA 35804 B1 MA35804 B1 MA 35804B1
- Authority
- MA
- Morocco
- Prior art keywords
- formula
- compounds
- aids
- virus
- vhb
- Prior art date
Links
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
- C07D491/06—Peri-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
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4741—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen 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
-
- 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
- C07D417/08—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 linked by a carbon chain containing alicyclic rings
-
- 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
- C07D417/10—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 linked by a carbon chain containing aromatic rings
-
- 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
-
- 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
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Dispersion Chemistry (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Dermatology (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Tropical Medicine & Parasitology (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)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
L'invention concerne des composés de la formule i ou un sel pharmaceutiquement acceptable de ceux-ci. L'invention concerne également des compositions pharmaceutiques comprenant un composé de la formule i, des procédés de préparation de composés de la formule i, des intermédiaires utiles pour préparer des composés de la formule i et des procédés thérapeutiques pour traiter la prolifération du virus vih, traiter le sida ou retarder l'apparition de symptômes du sida ou du complexe lié au sida (arc) chez un mammifère à l'aide de composés de la formule i.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161477922P | 2011-04-21 | 2011-04-21 | |
PCT/US2012/034593 WO2012145728A1 (fr) | 2011-04-21 | 2012-04-20 | Composés benzothiazoles et leur utilisation pharmaceutique |
Publications (1)
Publication Number | Publication Date |
---|---|
MA35804B1 true MA35804B1 (fr) | 2014-12-01 |
Family
ID=46028194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36432A MA35804B1 (fr) | 2011-04-21 | 2013-11-14 | Modulation de l'expression du virus de l'hepatite b (vhb) |
Country Status (24)
Country | Link |
---|---|
US (3) | US9006229B2 (fr) |
EP (2) | EP2699558B1 (fr) |
JP (2) | JP5918848B2 (fr) |
KR (1) | KR20140027295A (fr) |
CN (2) | CN105712948A (fr) |
AP (2) | AP2013007249A0 (fr) |
AU (2) | AU2012245187B2 (fr) |
BR (1) | BR112013027096A2 (fr) |
CA (1) | CA2833377C (fr) |
CL (1) | CL2013003019A1 (fr) |
CO (1) | CO6801774A2 (fr) |
CR (1) | CR20130560A (fr) |
EA (1) | EA024952B1 (fr) |
EC (1) | ECSP13013021A (fr) |
ES (2) | ES2615734T3 (fr) |
IL (1) | IL228925A0 (fr) |
MA (1) | MA35804B1 (fr) |
MX (1) | MX2013012266A (fr) |
PE (1) | PE20141066A1 (fr) |
PH (1) | PH12015502056A1 (fr) |
PT (1) | PT2699558T (fr) |
SG (1) | SG194512A1 (fr) |
UA (1) | UA111841C2 (fr) |
WO (1) | WO2012145728A1 (fr) |
Families Citing this family (120)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA021377B9 (ru) | 2008-12-09 | 2015-09-30 | Джилид Сайэнс, Инк. | Модуляторы толл-подобных рецепторов |
BR112013000043A2 (pt) | 2010-07-02 | 2019-09-24 | Gilead Sciences Inc | derivados de ácido naft-2-ilacético para tratar aids |
NZ604716A (en) | 2010-07-02 | 2014-12-24 | Gilead Sciences Inc | 2-quinolinyl-acetic acid derivatives as hiv antiviral compounds |
SG194512A1 (en) | 2011-04-21 | 2013-12-30 | Gilead Sciences Inc | Benzothiazole compounds and their pharmaceutical use |
JP6205354B2 (ja) | 2011-07-06 | 2017-09-27 | ギリアード サイエンシーズ, インコーポレイテッド | Hivの処置のための化合物 |
US9284323B2 (en) | 2012-01-04 | 2016-03-15 | Gilead Sciences, Inc. | Naphthalene acetic acid derivatives against HIV infection |
WO2013103724A1 (fr) | 2012-01-04 | 2013-07-11 | Gilead Sciences, Inc. | Dérivés d'acide 2-(tert-butoxy)-2-(7-méthylquinoléin-6-yl)acétique pour traiter le sida |
CN103204825B (zh) | 2012-01-17 | 2015-03-04 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的苯并噻唑化合物及其制备方法和用途 |
ES2571479T3 (es) | 2012-04-20 | 2016-05-25 | Gilead Sciences Inc | Derivados del ácido benzotiazol-6-il acético y su uso para tratar una infección por VIH |
ES2926068T3 (es) | 2012-12-21 | 2022-10-21 | Gilead Sciences Inc | Compuestos de carbamoilpiridona policíclicos y su uso farmacéutico |
TW201443037A (zh) | 2013-01-09 | 2014-11-16 | Gilead Sciences Inc | 治療用化合物 |
JP5860197B1 (ja) | 2013-01-09 | 2016-02-16 | ギリアード サイエンシーズ, インコーポレイテッド | ウイルス感染症を処置するための治療用化合物 |
PT2943487T (pt) | 2013-01-09 | 2016-12-15 | Gilead Sciences Inc | Heteroarilos de 5 membros e sua utilização como agentes antivirais |
TW201441197A (zh) * | 2013-01-31 | 2014-11-01 | Shionogi & Co | Hiv複製抑制劑 |
TWI694071B (zh) | 2013-03-01 | 2020-05-21 | 美商基利科學股份有限公司 | 治療反轉錄病毒科(Retroviridae)病毒感染之治療性化合物 |
EP2821082A1 (fr) | 2013-07-05 | 2015-01-07 | Laboratoire Biodim | Procédé de production d'un lentivirus inactivé, notamment le VIH, vaccin, kit et procédé d'utilisation |
EP2821104A1 (fr) | 2013-07-05 | 2015-01-07 | Laboratoire Biodim | Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques |
NO2865735T3 (fr) | 2013-07-12 | 2018-07-21 | ||
PT3252058T (pt) | 2013-07-12 | 2021-03-09 | Gilead Sciences Inc | Compostos policíclicos-carbamoílpiridona e seu uso para o tratamento de infecções por hiv |
EP3105236B1 (fr) | 2014-02-12 | 2017-10-18 | ViiV Healthcare UK (No.5) Limited | Utilisation de macrocycles de benzothiazole comme qu'inhibiteurs de la réplication du virus de l'immunodéficience humaine |
WO2015130964A1 (fr) | 2014-02-28 | 2015-09-03 | Gilead Sciences, Inc. | Composés thérapeutiques |
WO2015174511A1 (fr) | 2014-05-16 | 2015-11-19 | 塩野義製薬株式会社 | Dérivé hétérocyclique tricyclique présentant un effet d'inhibition de la réplication du vih |
TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
NO2717902T3 (fr) | 2014-06-20 | 2018-06-23 | ||
TWI806081B (zh) | 2014-07-11 | 2023-06-21 | 美商基利科學股份有限公司 | 用於治療HIV之toll樣受體調節劑 |
WO2016033009A1 (fr) * | 2014-08-27 | 2016-03-03 | Bristol-Myers Squibb Company | Imidazo [1,2-a] pyridine substitués pour une utilisation en tant qu'inhibiteurs de la réplication du virus de l'immunodéficience humaine |
US20160067255A1 (en) | 2014-09-04 | 2016-03-10 | Gilead Sciences, Inc. | Methods of treating or preventing hiv in patients using a combination of tenofovir alafenamide and dolutegravir |
UY36298A (es) | 2014-09-16 | 2016-04-29 | Gilead Science Inc | Formas sólidas de un modulador del receptor tipo toll |
TWI738321B (zh) | 2014-12-23 | 2021-09-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
TWI699355B (zh) | 2014-12-24 | 2020-07-21 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
US9701677B2 (en) | 2014-12-24 | 2017-07-11 | Gilead Sciences, Inc. | Fused pyrimidine compounds |
AU2015371257B2 (en) | 2014-12-24 | 2018-09-06 | Gilead Sciences, Inc. | Isoquinoline compounds for the treatment of HIV |
RS62434B1 (sr) | 2014-12-26 | 2021-11-30 | Univ Emory | Antivirusni n4-hidroksicitidin derivati |
CA2978188C (fr) | 2015-03-04 | 2020-05-12 | Gilead Sciences, Inc. | Composes 4,6-diamino-pyrido[3,2-d]pyrimidine modulateurs du recepteur de type toll |
ES2837383T3 (es) | 2015-04-02 | 2021-06-30 | Gilead Sciences Inc | Compuestos de carbamoilpiridonas policíclicos y su utilización farmacéutica |
WO2016194806A1 (fr) | 2015-05-29 | 2016-12-08 | 塩野義製薬株式会社 | Dérivé tricyclique contenant de l'azote présentant une activité inhibitrice de la réplication du vih |
MA42684A (fr) | 2015-08-26 | 2018-07-04 | Gilead Sciences Inc | Modulateurs deutérés du récepteur toll |
EP3349757A1 (fr) | 2015-09-15 | 2018-07-25 | Gilead Sciences, Inc. | Modulateurs de récepteurs de type toll pour le traitement du vih |
AU2016330895A1 (en) | 2015-09-30 | 2018-05-10 | Gilead Sciences, Inc. | Compounds and combinations for the treatment of HIV |
UA125819C2 (uk) | 2015-12-15 | 2022-06-15 | Гіліад Сайєнсіз, Інк. | ВИДІЛЕНЕ МОНОКЛОНАЛЬНЕ АНТИТІЛО, ЩО ЗВ'ЯЗУЄТЬСЯ З gp120 ВІРУСУ ІМУНОДЕФІЦИТУ ЛЮДИНИ |
MX369307B (es) | 2016-08-19 | 2019-11-05 | Gilead Sciences Inc | Compuestos terapeuticos utiles para tratamiento profilactico o terapeutico de infeccion por virus de inmunodeficiencia humana. |
WO2018042331A1 (fr) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinaisons, utilisations et traitements correspondants |
WO2018042332A1 (fr) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinaisons, utilisations et traitements correspondants |
US10640499B2 (en) | 2016-09-02 | 2020-05-05 | Gilead Sciences, Inc. | Toll like receptor modulator compounds |
WO2018045144A1 (fr) | 2016-09-02 | 2018-03-08 | Gilead Sciences, Inc. | Composés modulateurs du recepteur de type toll |
WO2018051250A1 (fr) | 2016-09-14 | 2018-03-22 | Viiv Healthcare Company | Combinaison comprenant du ténofovir alafénamide, du bictégravir et du 3tc |
EP3519409B1 (fr) | 2016-09-28 | 2024-09-18 | Gilead Sciences, Inc. | Dérivés d'acide benzothiazol-6-yl-acétique et leur utilisation pour le traitement d'une infection par le vih |
ES2881949T3 (es) | 2016-10-27 | 2021-11-30 | Gilead Sciences Inc | Forma cristalina de base libre de darunavir |
US20200055839A1 (en) | 2017-01-03 | 2020-02-20 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
JP2020503352A (ja) | 2017-01-03 | 2020-01-30 | ヴィーブ ヘルスケア ユーケー(ナンバー5)リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのピリジン−3−イル酢酸誘導体 |
TWI784370B (zh) | 2017-01-31 | 2022-11-21 | 美商基利科學股份有限公司 | 替諾福韋埃拉酚胺(tenofovir alafenamide)之晶型 |
JOP20180009A1 (ar) | 2017-02-06 | 2019-01-30 | Gilead Sciences Inc | مركبات مثبط فيروس hiv |
TWI728250B (zh) | 2017-06-21 | 2021-05-21 | 美商基利科學股份有限公司 | 靶向hiv gp120及cd3之多特異性抗體 |
PL3661937T3 (pl) | 2017-08-01 | 2021-12-20 | Gilead Sciences, Inc. | Formy krystaliczne ((s)-((((2r,5r)-5-(6-amino-9h-puryn-9-ylo)-4-fluoro-2,5-dihydrofuran-2-ylo)oksy)metylo)(fenoksy)fosforylo)-l-alaninianu etylu (gs-9131) do leczenia zakażeń wirusowych |
TW202024061A (zh) | 2017-08-17 | 2020-07-01 | 美商基利科學股份有限公司 | Hiv蛋白質膜抑制劑之固體形式 |
AR112412A1 (es) | 2017-08-17 | 2019-10-23 | Gilead Sciences Inc | Formas de sal de colina de un inhibidor de la cápside del vih |
US11229638B2 (en) | 2017-08-22 | 2022-01-25 | Gilead Sciences, Inc. | Therapeutic heterocyclic compounds |
JOP20180092A1 (ar) | 2017-10-13 | 2019-04-13 | Gilead Sciences Inc | مثبطات hiv بروتياز |
EP3700573A1 (fr) | 2017-10-24 | 2020-09-02 | Gilead Sciences, Inc. | Méthodes de traitement de patients co-infectés par un virus et la tuberculose |
CN111372592A (zh) | 2017-12-07 | 2020-07-03 | 埃默里大学 | N4-羟基胞苷及衍生物和与其相关的抗病毒用途 |
CN111511754B (zh) | 2017-12-20 | 2023-09-12 | 捷克共和国有机化学与生物化学研究所 | 活化sting转接蛋白的具有膦酸酯键的2’3’环状二核苷酸 |
AU2018392213B2 (en) | 2017-12-20 | 2021-03-04 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3' cyclic dinucleotides with phosphonate bond activating the STING adaptor protein |
EP3740209A1 (fr) | 2018-01-19 | 2020-11-25 | Gilead Sciences, Inc. | Métabolites du bictégravir |
AU2019221568B2 (en) | 2018-02-15 | 2021-04-22 | Gilead Sciences, Inc. | Pyridine derivatives and their use for treating HIV infection |
EP3752496B1 (fr) | 2018-02-16 | 2023-07-05 | Gilead Sciences, Inc. | Procédés et intermédiaires pour préparer un composé thérapeutique utile dans le traitement d'une infection virale par retroviridae |
TW202005654A (zh) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2,2,─環二核苷酸 |
TWI818007B (zh) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-環二核苷酸 |
TWI833744B (zh) | 2018-04-06 | 2024-03-01 | 捷克科學院有機化學與生物化學研究所 | 3'3'-環二核苷酸 |
WO2019211799A1 (fr) | 2018-05-03 | 2019-11-07 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | Analogue de dinucléotide 2'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle |
SG11202012043RA (en) | 2018-07-03 | 2021-01-28 | Gilead Sciences Inc | Antibodies that target hiv gp120 and methods of use |
WO2020010200A1 (fr) | 2018-07-06 | 2020-01-09 | Gilead Sciences, Inc. | Composés hétérocycliques thérapeutiques |
CN112384283B (zh) | 2018-07-06 | 2023-08-15 | 吉利德科学公司 | 治疗性的杂环化合物 |
KR20210033492A (ko) | 2018-07-16 | 2021-03-26 | 길리애드 사이언시즈, 인코포레이티드 | Hiv의 치료를 위한 캡시드 억제제 |
TWI829205B (zh) | 2018-07-30 | 2024-01-11 | 美商基利科學股份有限公司 | 抗hiv化合物 |
EP3852761A1 (fr) | 2018-09-19 | 2021-07-28 | Gilead Sciences, Inc. | Inhibiteurs d'intégrase pour la prévention du vih |
EP3860717A1 (fr) | 2018-10-03 | 2021-08-11 | Gilead Sciences, Inc. | Dérivés d'imidozopyrimidine |
US11071730B2 (en) | 2018-10-31 | 2021-07-27 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds |
EP3873903B1 (fr) | 2018-10-31 | 2024-01-24 | Gilead Sciences, Inc. | Composés de 6-azabenzimidazole substitués en tant qu'inhibiteurs de hpk1 |
WO2020176510A1 (fr) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Agonistes de protéine kinase c |
WO2020176505A1 (fr) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Agonistes de protéine kinase c |
US11766447B2 (en) | 2019-03-07 | 2023-09-26 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3′3′-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator |
CN113543851A (zh) | 2019-03-07 | 2021-10-22 | 捷克共和国有机化学与生物化学研究所 | 2’3’-环二核苷酸及其前药 |
KR20210137518A (ko) | 2019-03-07 | 2021-11-17 | 인스티튜트 오브 오가닉 케미스트리 앤드 바이오케미스트리 에이에스 씨알 브이.브이.아이. | 3'3'-사이클릭 다이뉴클레오티드 및 이의 프로드럭 |
EP4122537A1 (fr) | 2019-03-22 | 2023-01-25 | Gilead Sciences, Inc. | Composés tricycliques pontés de carbamoylpyridone et leur utilisation pharmaceutique |
TW202212339A (zh) | 2019-04-17 | 2022-04-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
WO2020214647A1 (fr) | 2019-04-17 | 2020-10-22 | Gilead Sciences, Inc. | Formes solides d'un inhibiteur de protéase du vih |
TW202210480A (zh) | 2019-04-17 | 2022-03-16 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
TW202104210A (zh) | 2019-04-17 | 2021-02-01 | 美商基利科學股份有限公司 | Hiv蛋白酶抑制劑 |
TW202231277A (zh) | 2019-05-21 | 2022-08-16 | 美商基利科學股份有限公司 | 鑑別對使用gp120 v3聚醣導向之抗體的治療敏感之hiv病患的方法 |
WO2020237025A1 (fr) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1 |
RU2717101C1 (ru) | 2019-06-03 | 2020-03-18 | Андрей Александрович Иващенко | Анелированные 9-гидрокси-1,8-диоксо-1,3,4,8-тетрагидро-2Н-пиридо[1,2-a]пиразин-7-карбоксамиды - ингибиторы интегразы ВИЧ, способы их получения и применения |
WO2020255038A1 (fr) | 2019-06-18 | 2020-12-24 | Janssen Sciences Ireland Unlimited Company | Association de vaccins contre le virus de l'hépatite b (vhb) et de dérivés de pyridopyrimidine |
CA3142513A1 (fr) | 2019-06-25 | 2020-12-30 | Gilead Sciences, Inc. | Proteines de fusion flt3l-fc et procedes d'utilisation |
KR20220047277A (ko) | 2019-07-16 | 2022-04-15 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 백신, 및 이의 제조 및 사용 방법 |
US20220257619A1 (en) | 2019-07-18 | 2022-08-18 | Gilead Sciences, Inc. | Long-acting formulations of tenofovir alafenamide |
WO2021034804A1 (fr) | 2019-08-19 | 2021-02-25 | Gilead Sciences, Inc. | Formulations pharmaceutiques de ténofovir alafénamide |
CN114727999A (zh) | 2019-11-26 | 2022-07-08 | 吉利德科学公司 | 用于预防hiv的衣壳抑制剂 |
CN117736207A (zh) | 2019-12-24 | 2024-03-22 | 卡尔那生物科学株式会社 | 二酰基甘油激酶调节化合物 |
AU2021225809B2 (en) | 2020-02-24 | 2023-08-24 | Gilead Sciences, Inc. | Tetracyclic compounds for treating HIV infection |
JP2023518433A (ja) | 2020-03-20 | 2023-05-01 | ギリアード サイエンシーズ, インコーポレイテッド | 4’-c-置換-2-ハロ-2’-デオキシアデノシンヌクレオシドのプロドラッグ並びにその製造法及び使用法 |
EP4153181A1 (fr) | 2020-05-21 | 2023-03-29 | Gilead Sciences, Inc. | Compositions pharmaceutiques contenant du bictégravir |
CN115996925A (zh) | 2020-06-25 | 2023-04-21 | 吉利德科学公司 | 用于治疗hiv的衣壳抑制剂 |
PE20230779A1 (es) | 2020-08-07 | 2023-05-09 | Gilead Sciences Inc | Profarmacos de analogos de nucleotidos de fosfonamida y su uso farmaceutico |
KR20230079137A (ko) | 2020-09-30 | 2023-06-05 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리사이클릭 카르바모일피리돈 화합물 및 이의 용도 |
TW202406932A (zh) | 2020-10-22 | 2024-02-16 | 美商基利科學股份有限公司 | 介白素2-Fc融合蛋白及使用方法 |
KR20230107288A (ko) | 2020-11-11 | 2023-07-14 | 길리애드 사이언시즈, 인코포레이티드 | gp120 CD4 결합 부위-지향 항체를 이용한 요법에 감수성인 HIV 환자를 식별하는 방법 |
CR20230315A (es) | 2021-01-19 | 2023-09-01 | Gilead Sciences Inc | Compuestos de piridotriazina sustituidos y usos de estos |
TW202313094A (zh) | 2021-05-18 | 2023-04-01 | 美商基利科學股份有限公司 | 使用FLT3L—Fc融合蛋白之方法 |
EP4359411A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés modulant les diacylglycérol kinases |
EP4359415A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés modulant les diacylglycérol kinases |
US11932634B2 (en) | 2021-06-23 | 2024-03-19 | Gilead Sciences, Inc. | Diacylglycerol kinase modulating compounds |
CN117396478A (zh) | 2021-06-23 | 2024-01-12 | 吉利德科学公司 | 二酰基甘油激酶调节化合物 |
KR20240117588A (ko) | 2021-12-03 | 2024-08-01 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 바이러스 감염 치료용 화합물 |
EP4440702A1 (fr) | 2021-12-03 | 2024-10-09 | Gilead Sciences, Inc. | Composés thérapeutiques contre l'infection par le virus du vih |
WO2023102523A1 (fr) | 2021-12-03 | 2023-06-08 | Gilead Sciences, Inc. | Composés thérapeutiques pour l'infection par le virus du vih |
TWI843506B (zh) | 2022-04-06 | 2024-05-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
WO2024006982A1 (fr) | 2022-07-01 | 2024-01-04 | Gilead Sciences, Inc. | Composés thérapeutiques utiles pour le traitement prophylactique ou thérapeutique d'une infection par le virus du vih |
WO2024015741A1 (fr) | 2022-07-12 | 2024-01-18 | Gilead Sciences, Inc. | Polypeptides immunogènes du vih et vaccins et utilisations de ceux-ci |
WO2024044477A1 (fr) | 2022-08-26 | 2024-02-29 | Gilead Sciences, Inc. | Régime de dosage et de planification pour anticorps largement neutralisants |
WO2024076915A1 (fr) | 2022-10-04 | 2024-04-11 | Gilead Sciences, Inc. | Analogues de 4'-thionucléosides et leur utilisation pharmaceutique |
Family Cites Families (90)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3895028A (en) * | 1972-09-12 | 1975-07-15 | Tokyo Tanabe Co | Alpha-(2-phenylbenzothiazol-5-yl)propionic acid |
JPS4994667A (fr) * | 1973-01-23 | 1974-09-09 | ||
FR2453163A1 (fr) | 1979-04-03 | 1980-10-31 | Rolland Sa A | Derives de benzothiazole, leur procede de preparation et leurs applications en therapeutique |
US4816570A (en) | 1982-11-30 | 1989-03-28 | The Board Of Regents Of The University Of Texas System | Biologically reversible phosphate and phosphonate protective groups |
GB8403739D0 (en) | 1984-02-13 | 1984-03-14 | Roussel Lab Ltd | Chemical compounds |
US4968788A (en) | 1986-04-04 | 1990-11-06 | Board Of Regents, The University Of Texas System | Biologically reversible phosphate and phosphonate protective gruops |
JPH03287558A (ja) | 1990-04-05 | 1991-12-18 | Teijin Ltd | 酵素阻害剤 |
DK0533833T3 (da) | 1990-06-13 | 1996-04-22 | Arnold Glazier | Phosphorprolægemidler |
EP0481214B1 (fr) | 1990-09-14 | 1998-06-24 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Pro-médicaments dérivés de phosphonates |
MX9308016A (es) | 1992-12-22 | 1994-08-31 | Lilly Co Eli | Compuestos inhibidores de la proteasa del virus de la inmunodeficiencia humana, procedimiento para su preparacion y formulacion farmaceutica que los contiene. |
US5733906A (en) | 1993-10-12 | 1998-03-31 | Eli Lilly And Company | Inhibitors of HIV Protease useful for the treatment of Aids |
DE69434931T2 (de) | 1993-04-02 | 2007-11-22 | Rigel Pharmaceuticals, Inc., South San Francisco | Methode zur selektiven inaktivierung der viralen replication |
JP3287558B2 (ja) | 1993-07-27 | 2002-06-04 | 株式会社半導体エネルギー研究所 | 半導体装置の作製方法 |
US5434188A (en) | 1994-03-07 | 1995-07-18 | Warner-Lambert Company | 1-ether and 1-thioether-naphthalene-2-carboxamides as inhibitors of cell adhesion and as inhibitors of the activation of HIV |
DE4428932A1 (de) | 1994-08-16 | 1996-02-22 | Hoechst Ag | Substituierte-Chinolinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung |
AU747500B2 (en) | 1998-04-09 | 2002-05-16 | Merck & Co., Inc. | Oxidation process using periodic acid |
WO2000063152A1 (fr) | 1999-02-22 | 2000-10-26 | The Government Of The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Analogues acetyles et correspondants d'acide chicorique en tant qu'inhibiteurs de l'integrase du vih |
US20020052323A1 (en) | 2000-08-30 | 2002-05-02 | Jinhai Wang | Quinoline-(C=O)-(multiple amino acids)-leaving group compounds for pharmaceutical compositions and reagents |
WO2002042773A2 (fr) | 2000-11-21 | 2002-05-30 | Sunesis Pharmaceuticals, Inc. | Methode de fixation etendue pour l'identification rapide de ligands |
FR2819507B1 (fr) | 2001-01-17 | 2007-09-28 | Inst Rech Developpement Ird | Quinoleines substituees pour le traitement de co-infections a protozoaires et a retrovirus |
FR2839646B1 (fr) | 2002-05-17 | 2008-04-11 | Bioalliance Pharma | Utilisation de derives de quinoleine a effet anti-integrase et ses applications |
KR20050025647A (ko) * | 2002-08-02 | 2005-03-14 | 티보텍 파마슈티칼즈 리미티드 | 광범위 2-아미노-벤조티아졸 설폰아미드 hiv프로테아제 저해제 |
CN101445493A (zh) * | 2002-08-02 | 2009-06-03 | 泰博特克药品有限公司 | 广谱2-氨基-苯并噻唑磺酰胺类hiv蛋白酶抑制剂 |
EP1541558B1 (fr) | 2002-08-13 | 2008-08-13 | Shionogi & Co., Ltd. | Composes heterocycliques a activite inhibitrice de l'integrase du vih |
EP2371955A1 (fr) | 2002-09-26 | 2011-10-05 | K.U. Leuven Research & Development | Cofacteur d'intégrase |
CA2470365C (fr) | 2002-11-20 | 2011-05-17 | Japan Tobacco Inc. | Composes 4-oxoquinoliniques et leur utilisation comme inhibiteur de la vih-integrase |
UA80571C2 (en) | 2002-11-22 | 2007-10-10 | Lilly Co Eli | Quinolinyl-pyrrolopyrazoles |
ES2423800T3 (es) | 2003-03-28 | 2013-09-24 | Novartis Vaccines And Diagnostics, Inc. | Uso de compuestos orgánicos para la inmunopotenciación |
WO2006001958A2 (fr) | 2004-05-21 | 2006-01-05 | Merck & Co., Inc. | Modulateurs heterocycliques et carbocycliques d'amino cyclopentyle de l'activite du recepteur de la chimiokine |
US7087610B2 (en) * | 2004-06-03 | 2006-08-08 | Bristol-Myers Squibb Company | Benzothiazole antiviral agents |
JP2008503588A (ja) | 2004-06-22 | 2008-02-07 | スミスクライン ビーチャム コーポレーション | 化学化合物 |
TWI306401B (en) | 2004-08-13 | 2009-02-21 | Nat Health Research Institutes | Benzothiazolium compounds |
US20060094755A1 (en) | 2004-10-28 | 2006-05-04 | Bioflexis, Llc | Novel quinoline-based metal chelators as antiviral agents |
TWI370820B (en) | 2005-04-27 | 2012-08-21 | Takeda Pharmaceutical | Fused heterocyclic compounds |
WO2006124780A2 (fr) | 2005-05-12 | 2006-11-23 | Kalypsys, Inc. | Inhibiteurs de la b-raf kinase |
US7473784B2 (en) * | 2005-08-01 | 2009-01-06 | Bristol-Myers Squibb Company | Benzothiazole and azabenzothiazole compounds useful as kinase inhibitors |
US7939545B2 (en) * | 2006-05-16 | 2011-05-10 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
JP2009538899A (ja) | 2006-05-30 | 2009-11-12 | ファイザー・プロダクツ・インク | トリアゾロピリダジン誘導体 |
JO2841B1 (en) * | 2006-06-23 | 2014-09-15 | تيبوتيك فارماسيوتيكالز ليمتد | 2-(substituted-amino) -benzothiazole sulfonamide as protease inhibitors HIV (HIV) |
US8435774B2 (en) | 2006-06-28 | 2013-05-07 | Qiagen Gmbh | Enhancing reactivation of thermostable reversibly inactivated enzymes |
WO2008053478A2 (fr) | 2006-10-30 | 2008-05-08 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Compositions et procédés pour inhiber la réplication et l'activité de l'intégrase du vih-1 |
KR101475091B1 (ko) | 2006-12-13 | 2014-12-22 | 에프. 호프만-라 로슈 아게 | 비뉴클레오시드 역전사 효소 억제제로서 2-(피페리딘-4-일)-4-페녹시- 또는 페닐아미노-피리미딘 유도체 |
BRPI0819328A8 (pt) * | 2007-11-15 | 2016-02-10 | Boehringer Ingelheim Int | Compostos inibidores de replicação de vírus da imunodeficiência humana, composição farmacêutica e uso dos ditos compostos |
ATE541841T1 (de) | 2007-11-15 | 2012-02-15 | Boehringer Ingelheim Int | Inhibitoren der replikation des human immunodeficiency virus |
EP2220046B1 (fr) | 2007-11-16 | 2014-06-18 | Gilead Sciences, Inc. | Inhibiteurs de la réplication du virus de l'immunodéficience humaine |
JP5269087B2 (ja) | 2007-11-16 | 2013-08-21 | ギリアード サイエンシス インコーポレーテッド | ヒト免疫不全ウイルス複製のインヒビター |
GB0801940D0 (en) | 2008-02-01 | 2008-03-12 | Univ Leuven Kath | Inhibitors of lentiviral replication |
EP2265270A1 (fr) | 2008-02-04 | 2010-12-29 | OSI Pharmaceuticals, Inc. | Inhibiteurs de 2-aminopyridine kinases |
UY32251A (es) | 2008-11-20 | 2010-05-31 | Glaxosmithkline Llc | Compuestos quimicos |
US8338441B2 (en) | 2009-05-15 | 2012-12-25 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
GB0908394D0 (en) | 2009-05-15 | 2009-06-24 | Univ Leuven Kath | Novel viral replication inhibitors |
KR20120049852A (ko) | 2009-06-30 | 2012-05-17 | 시가 테크놀로지스, 인크. | 뎅기 바이러스 감염의 치료 및 예방 |
GB0913636D0 (en) | 2009-08-05 | 2009-09-16 | Univ Leuven Kath | Novel viral replication inhibitors |
US9095596B2 (en) | 2009-10-15 | 2015-08-04 | Southern Research Institute | Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such |
US20120316161A1 (en) | 2009-12-23 | 2012-12-13 | Katholieke Universiteit Leuven | Novel antiviral compounds |
US20110223131A1 (en) | 2010-02-24 | 2011-09-15 | Gilead Sciences, Inc. | Antiviral compounds |
NZ603644A (en) | 2010-05-24 | 2014-10-31 | Univ Rochester | Bicyclic heteroaryl kinase inhibitors and methods of use |
BR112013000043A2 (pt) | 2010-07-02 | 2019-09-24 | Gilead Sciences Inc | derivados de ácido naft-2-ilacético para tratar aids |
NZ604716A (en) | 2010-07-02 | 2014-12-24 | Gilead Sciences Inc | 2-quinolinyl-acetic acid derivatives as hiv antiviral compounds |
US8633200B2 (en) | 2010-09-08 | 2014-01-21 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
CA2817896A1 (fr) | 2010-11-15 | 2012-05-24 | Viiv Healthcare Uk Limited | Inhibiteurs de la replication du vih |
EP2640705A2 (fr) | 2010-11-15 | 2013-09-25 | Katholieke Universiteit Leuven | Nouveaux composés antiviraux |
TWI538905B (zh) | 2010-12-22 | 2016-06-21 | H 朗德貝克公司 | 雙環[3.2.1]辛基醯胺衍生物及其用途 |
AU2012209373A1 (en) | 2011-01-24 | 2013-04-11 | Glaxosmithkline Llc | Isoquinoline compounds and methods for treating HIV |
WO2012138669A1 (fr) | 2011-04-04 | 2012-10-11 | Gilead Sciences, Inc. | Formes à l'état solide d'un inhibiteur du vih |
WO2012138670A1 (fr) | 2011-04-04 | 2012-10-11 | Gilead Sciences, Inc. | Procédé de préparation d'un inhibiteur de l'intégrase du vih |
EP2508511A1 (fr) | 2011-04-07 | 2012-10-10 | Laboratoire Biodim | Inhibiteurs de la réplication virale, leur procédé de préparation et leurs utilisations thérapeutiques |
ES2742261T3 (es) | 2011-04-15 | 2020-02-13 | Hivih | Inhibidores de la replicación viral, su proceso de preparación y sus usos terapéuticos |
SG194512A1 (en) | 2011-04-21 | 2013-12-30 | Gilead Sciences Inc | Benzothiazole compounds and their pharmaceutical use |
WO2012143144A1 (fr) | 2011-04-21 | 2012-10-26 | Origenis Gmbh | Pyrazolo[4,3-d]pyrimidines utiles en tant qu'inhibiteurs de kinases |
PT2699575E (pt) | 2011-04-21 | 2015-07-29 | Bayer Ip Gmbh | Triazolopiridinas |
KR101649610B1 (ko) | 2011-04-21 | 2016-08-19 | 오리제니스 게엠베하 | 키나아제 억제제로서의 헤테로사이클릭 화합물 |
WO2013002357A1 (fr) | 2011-06-30 | 2013-01-03 | 塩野義製薬株式会社 | Inhibiteur de réplication du vih |
US8791108B2 (en) | 2011-08-18 | 2014-07-29 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
WO2013043553A1 (fr) | 2011-09-22 | 2013-03-28 | Glaxosmithkline Llc | Composés pyrrolopyridinones et méthodes de traitement du vih |
WO2013058448A1 (fr) | 2011-10-20 | 2013-04-25 | 한국해양연구원 | Gènes de medaka marin répondant à l'exposition à des substances chimiques perturbant le système endocrinien et procédé destiné à diagnostiquer une pollution d'un écosystème aquatique les utilisant |
WO2013062028A1 (fr) | 2011-10-25 | 2013-05-02 | 塩野義製薬株式会社 | Inhibiteur de la réplication du vih |
US8332160B1 (en) * | 2011-11-17 | 2012-12-11 | Amyris Biotechnologies, Inc. | Systems and methods for engineering nucleic acid constructs using scoring techniques |
US9284323B2 (en) | 2012-01-04 | 2016-03-15 | Gilead Sciences, Inc. | Naphthalene acetic acid derivatives against HIV infection |
WO2013103724A1 (fr) | 2012-01-04 | 2013-07-11 | Gilead Sciences, Inc. | Dérivés d'acide 2-(tert-butoxy)-2-(7-méthylquinoléin-6-yl)acétique pour traiter le sida |
CN117736134A (zh) | 2012-01-12 | 2024-03-22 | 耶鲁大学 | 通过e3泛素连接酶增强靶蛋白质及其他多肽降解的化合物和方法 |
US8629276B2 (en) | 2012-02-15 | 2014-01-14 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US9034882B2 (en) | 2012-03-05 | 2015-05-19 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US9006235B2 (en) | 2012-03-06 | 2015-04-14 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
WO2013157622A1 (fr) | 2012-04-19 | 2013-10-24 | 塩野義製薬株式会社 | Inhibiteur de la réplication du vih |
ES2571479T3 (es) | 2012-04-20 | 2016-05-25 | Gilead Sciences Inc | Derivados del ácido benzotiazol-6-il acético y su uso para tratar una infección por VIH |
JP6129962B2 (ja) | 2012-07-12 | 2017-05-17 | ヴィーブ ヘルスケア ユーケー リミテッド | 化合物及びhivを治療するための方法 |
US8906929B2 (en) | 2012-08-16 | 2014-12-09 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US20140094609A1 (en) | 2012-10-03 | 2014-04-03 | Gilead Sciences, Inc. | Process for the preparation of an hiv integrase inhibitor |
WO2014055618A1 (fr) | 2012-10-03 | 2014-04-10 | Gilead Sciences, Inc. | Formes à l'état solide d'inhibiteur du vih : hémisuccinate d'acide (2s)-2-tert-butoxy-2-(4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-2-méthylquinolin-3-yl)acétique |
-
2012
- 2012-04-20 SG SG2013077110A patent/SG194512A1/en unknown
- 2012-04-20 EP EP12719182.3A patent/EP2699558B1/fr active Active
- 2012-04-20 UA UAA201312204A patent/UA111841C2/uk unknown
- 2012-04-20 CA CA2833377A patent/CA2833377C/fr active Active
- 2012-04-20 AP AP2013007249A patent/AP2013007249A0/xx unknown
- 2012-04-20 EP EP16196723.7A patent/EP3181555B1/fr active Active
- 2012-04-20 AP AP2015008931A patent/AP2015008931A0/xx unknown
- 2012-04-20 EA EA201391395A patent/EA024952B1/ru unknown
- 2012-04-20 CN CN201610177497.3A patent/CN105712948A/zh active Pending
- 2012-04-20 WO PCT/US2012/034593 patent/WO2012145728A1/fr active Application Filing
- 2012-04-20 JP JP2014506609A patent/JP5918848B2/ja active Active
- 2012-04-20 ES ES12719182.3T patent/ES2615734T3/es active Active
- 2012-04-20 ES ES16196723T patent/ES2707997T3/es active Active
- 2012-04-20 KR KR1020137030857A patent/KR20140027295A/ko not_active Application Discontinuation
- 2012-04-20 PT PT127191823T patent/PT2699558T/pt unknown
- 2012-04-20 BR BR112013027096A patent/BR112013027096A2/pt not_active IP Right Cessation
- 2012-04-20 US US14/112,473 patent/US9006229B2/en active Active
- 2012-04-20 MX MX2013012266A patent/MX2013012266A/es unknown
- 2012-04-20 CN CN201280029211.7A patent/CN103797001B/zh active Active
- 2012-04-20 AU AU2012245187A patent/AU2012245187B2/en active Active
- 2012-04-20 PE PE2013002347A patent/PE20141066A1/es not_active Application Discontinuation
-
2013
- 2013-10-17 CL CL2013003019A patent/CL2013003019A1/es unknown
- 2013-10-17 IL IL228925A patent/IL228925A0/en unknown
- 2013-10-31 CR CR20130560A patent/CR20130560A/es unknown
- 2013-11-14 MA MA36432A patent/MA35804B1/fr unknown
- 2013-11-14 EC ECSP13013021 patent/ECSP13013021A/es unknown
- 2013-11-14 CO CO13268123A patent/CO6801774A2/es unknown
-
2015
- 2015-02-26 US US14/632,771 patent/US9464096B2/en active Active
- 2015-09-11 PH PH12015502056A patent/PH12015502056A1/en unknown
-
2016
- 2016-01-27 JP JP2016012970A patent/JP2016065110A/ja active Pending
- 2016-09-06 US US15/257,482 patent/US9879023B2/en active Active
- 2016-09-29 AU AU2016234985A patent/AU2016234985C1/en active Active
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA35804B1 (fr) | Modulation de l'expression du virus de l'hepatite b (vhb) | |
MA34400B1 (fr) | Dérivés d'acide 2-quinolinyl-acétique en tant que composés antiviraux contre le vih | |
SA519402405B1 (ar) | مركبات مثبط فيروس نقص المناعة البشري | |
MA34397B1 (fr) | Dérivés d'acide napht-2-ylacétique dans le traitement du sida | |
MA42795A (fr) | Composés thérapeutiques utiles pour le traitement prophylactique ou thérapeutique d'une infection par le virus du vih | |
MA35132B1 (fr) | 4-aryl-n-phényl-1,3,5-triazine-2- amines contenant un groupe sulfoximine | |
MA35750B1 (fr) | Dérivés de nucléoside substitué 2',4'-difluoro-2'-méthyle en tant qu'inhibiteurs de la réplication de l'arn du vhc (virus de l'hépatite c) | |
MA37400B1 (fr) | Composés hétérocyclyle en tant qu'inhibiteurs de mek | |
MA35833B1 (fr) | Dérivés de bétuline | |
JOP20180092A1 (ar) | مثبطات hiv بروتياز | |
MA34392B1 (fr) | Pyrimidines en tant qu'agents antiviraux | |
MX349950B (es) | Profarmacos de treprostinil enlazados a un portador. | |
PH12018502026A1 (en) | Substituted indole compound derivatives as dengue viral replication inhibitors | |
GEP201706698B (en) | Inhibitors of influenza viruses replication | |
MA37712B1 (fr) | Inhibiteurs macrocycliques de virus flaviviridae | |
WO2013160810A3 (fr) | Nouveaux dérivés d'acide bétulinique à titre d'inhibiteurs du vih | |
MA40768A (fr) | Dérivés d'indole mono ou di-substitué en tant qu'inhibiteurs de réplication du virus de la dengue | |
MA40769B1 (fr) | Indoles mono ou di-substitués utilisés en tant qu'inhibiteurs de réplication du virus de la dengue | |
MA38315B1 (fr) | Composés tétracycliques substitués par un hétérocycle et procédés pour les utiliser pour le traitement de maladies virales | |
MA35444B1 (fr) | Ligands du récepteur ep1 | |
MA34547B1 (fr) | Traitement d'association pour traiter une infection par le vhc | |
MA43913B1 (fr) | Modulateurs allostériques positifs du récepteur m1 muscarinique | |
EA201170605A1 (ru) | Циклоундекадепсипептидные соединения и применение указанных соединений в качестве лекарственного средства | |
MA43052B1 (fr) | Inhibiteurs de la kallicréine plasmatique humaine | |
EP4248960A3 (fr) | Nouveaux dérivés de triterpène en tant qu'inhibiteurs du vih |