MA37959A2 - Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih - Google Patents

Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih

Info

Publication number
MA37959A2
MA37959A2 MA37959A MA37959A MA37959A2 MA 37959 A2 MA37959 A2 MA 37959A2 MA 37959 A MA37959 A MA 37959A MA 37959 A MA37959 A MA 37959A MA 37959 A2 MA37959 A2 MA 37959A2
Authority
MA
Morocco
Prior art keywords
reverse transcriptase
inhibitors
pyrimidin
phenoxy
derivatives
Prior art date
Application number
MA37959A
Other languages
English (en)
Inventor
Kenneth L Arrington
Christopher Burgey
Robert Gilfillan
Yongxin Han
Mehul Patel
Chun Sing Li
Yaozong Li
Yunfu Luo
Jiayi Xu
Original Assignee
Merck Sharp & Dohme
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MA37959A2 publication Critical patent/MA37959A2/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/56One oxygen atom and one sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

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)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

L'invention concerne des composés de formule i qui sont des inhibiteurs de la transcriptase inverse du vih ; r
MA37959A 2012-10-08 2013-10-07 Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih MA37959A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2012001358 2012-10-08
PCT/US2013/063612 WO2014058747A1 (fr) 2012-10-08 2013-10-07 Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih

Publications (1)

Publication Number Publication Date
MA37959A2 true MA37959A2 (fr) 2017-12-29

Family

ID=49354986

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37959A MA37959A2 (fr) 2012-10-08 2013-10-07 Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih

Country Status (46)

Country Link
US (3) US9469634B2 (fr)
EP (3) EP3295942B1 (fr)
JP (2) JP5877281B2 (fr)
KR (1) KR101696128B1 (fr)
CN (1) CN104822670B (fr)
AP (1) AP2015008355A0 (fr)
AR (1) AR092876A1 (fr)
AU (1) AU2013329552B8 (fr)
BR (1) BR112015007742B8 (fr)
CA (1) CA2887312C (fr)
CL (1) CL2015000880A1 (fr)
CO (1) CO7350655A2 (fr)
CR (1) CR20150183A (fr)
CY (3) CY1119655T1 (fr)
DK (3) DK3656384T3 (fr)
DO (1) DOP2015000082A (fr)
EA (1) EA033436B1 (fr)
EC (1) ECSP15018618A (fr)
ES (3) ES2770774T3 (fr)
GE (1) GEP20186838B (fr)
GT (1) GT201500088A (fr)
HR (3) HRP20220502T1 (fr)
HU (3) HUE037231T2 (fr)
IL (1) IL238090B (fr)
JO (1) JO3470B1 (fr)
LT (3) LT2903977T (fr)
MA (1) MA37959A2 (fr)
MD (1) MD4625C1 (fr)
ME (1) ME02918B (fr)
MX (1) MX355040B (fr)
MY (1) MY192716A (fr)
NI (1) NI201500048A (fr)
NO (1) NO2903977T3 (fr)
NZ (1) NZ706729A (fr)
PE (1) PE20151787A1 (fr)
PH (1) PH12015500764B1 (fr)
PL (3) PL3656384T3 (fr)
PT (3) PT2903977T (fr)
RS (3) RS59863B1 (fr)
SG (1) SG11201502620UA (fr)
SI (3) SI3295942T1 (fr)
TN (1) TN2015000106A1 (fr)
TW (2) TWI598343B (fr)
UA (1) UA114006C2 (fr)
WO (1) WO2014058747A1 (fr)
ZA (1) ZA201503143B (fr)

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140031250A1 (en) 2010-10-07 2014-01-30 David Tsai Ting Biomarkers of Cancer
JO3470B1 (ar) 2012-10-08 2020-07-05 Merck Sharp & Dohme مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv
US9340800B2 (en) 2013-09-06 2016-05-17 President And Fellows Of Harvard College Extended DNA-sensing GRNAS
US20160221965A1 (en) 2013-09-16 2016-08-04 Bayer Pharma Aktiengesellschaft Disubstituted trifluoromethyl pyrimidinones and their use
RU2693622C2 (ru) * 2014-04-01 2019-07-03 Мерк Шарп И Доум Корп. Пролекарственные средства ингибиторов обратной транскриптазы вич
EP3760208B1 (fr) 2014-06-25 2024-05-29 The General Hospital Corporation Ciblage de hsatii (human satellite ii)
MX389591B (es) 2014-08-29 2025-03-20 Tes Pharma S R L INHIBIDORES DE ACIDO A-AMINO-ß-CARBOXIMUCONICO SEMIALDEHIDO DESCARBOXILASA
FR3027901B1 (fr) * 2014-10-31 2018-03-16 Universite De Reims Champagne Ardenne Nouveaux procedes appartenant a la famille des pyridazinones.
US10350165B2 (en) * 2014-12-12 2019-07-16 Ojai Energetics Pbc Methods and systems for forming stable droplets
EP4434589A3 (fr) 2015-10-23 2025-05-14 President and Fellows of Harvard College Protéines cas9 évoluées pour l'édition génétique
JP7231935B2 (ja) 2016-08-03 2023-03-08 プレジデント アンド フェローズ オブ ハーバード カレッジ アデノシン核酸塩基編集因子およびそれらの使用
US11661590B2 (en) 2016-08-09 2023-05-30 President And Fellows Of Harvard College Programmable CAS9-recombinase fusion proteins and uses thereof
WO2018039438A1 (fr) 2016-08-24 2018-03-01 President And Fellows Of Harvard College Incorporation d'acides aminés non naturels dans des protéines au moyen de l'édition de bases
AU2017342543B2 (en) 2016-10-14 2024-06-27 President And Fellows Of Harvard College AAV delivery of nucleobase editors
WO2018119359A1 (fr) 2016-12-23 2018-06-28 President And Fellows Of Harvard College Édition du gène récepteur ccr5 pour protéger contre l'infection par le vih
US11898179B2 (en) 2017-03-09 2024-02-13 President And Fellows Of Harvard College Suppression of pain by gene editing
CN110662556A (zh) 2017-03-09 2020-01-07 哈佛大学的校长及成员们 癌症疫苗
JP2020510439A (ja) 2017-03-10 2020-04-09 プレジデント アンド フェローズ オブ ハーバード カレッジ シトシンからグアニンへの塩基編集因子
WO2018176009A1 (fr) 2017-03-23 2018-09-27 President And Fellows Of Harvard College Éditeurs de nucléobase comprenant des protéines de liaison à l'adn programmable par acides nucléiques
US11560566B2 (en) 2017-05-12 2023-01-24 President And Fellows Of Harvard College Aptazyme-embedded guide RNAs for use with CRISPR-Cas9 in genome editing and transcriptional activation
US11732274B2 (en) 2017-07-28 2023-08-22 President And Fellows Of Harvard College Methods and compositions for evolving base editors using phage-assisted continuous evolution (PACE)
WO2019139645A2 (fr) 2017-08-30 2019-07-18 President And Fellows Of Harvard College Éditeurs de bases à haut rendement comprenant une gam
CA3075727A1 (fr) * 2017-09-18 2019-03-21 Goldfinch Bio, Inc. Pyridazinones et leurs procedes d'utilisation
KR20200121782A (ko) 2017-10-16 2020-10-26 더 브로드 인스티튜트, 인코퍼레이티드 아데노신 염기 편집제의 용도
US12406749B2 (en) 2017-12-15 2025-09-02 The Broad Institute, Inc. Systems and methods for predicting repair outcomes in genetic engineering
US20210213041A1 (en) 2018-02-06 2021-07-15 The General Hospital Corporation Repeat rna as biomarkers of tumor immune response
EA202092590A1 (ru) 2018-04-30 2021-04-08 Рибон Терапьютикс Инк. Пиридазиноны в качестве ингибиторов parp7
US12157760B2 (en) 2018-05-23 2024-12-03 The Broad Institute, Inc. Base editors and uses thereof
US12522807B2 (en) 2018-07-09 2026-01-13 The Broad Institute, Inc. RNA programmable epigenetic RNA modifiers and uses thereof
MD3852533T2 (ro) 2018-09-18 2024-08-31 Gfb Abc Llc Piridazinone și metode de utilizare ale acestora
WO2020092453A1 (fr) 2018-10-29 2020-05-07 The Broad Institute, Inc. Éditeurs de nucléobases comprenant geocas9 et utilisations associées
MA54549A (fr) * 2018-12-18 2022-03-30 Merck Sharp & Dohme Dérivés de pyrimidone en tant qu'agents cytotoxiques sélectifs contre des cellules infectées par le vih
WO2020154500A1 (fr) 2019-01-23 2020-07-30 The Broad Institute, Inc. Protéines chargées supernégativement et utilisations associées
MX2021011426A (es) 2019-03-19 2022-03-11 Broad Inst Inc Metodos y composiciones para editar secuencias de nucleótidos.
SG11202110585SA (en) 2019-04-11 2021-10-28 Goldfinch Bio Inc Spray-dried formulation of a pyridazinone trpc5 inhibitor
WO2020214842A1 (fr) 2019-04-17 2020-10-22 The Broad Institute, Inc. Éditeurs de base d'adénine présentant des effets hors cible réduits
WO2020223229A1 (fr) 2019-04-29 2020-11-05 Ribon Therapeutics, Inc. Formes solides d'un inhibiteur de parp7
CN114026081B (zh) * 2019-05-22 2025-02-11 默沙东有限责任公司 作为针对hiv感染的细胞的选择性细胞毒性剂的吡啶酮衍生物
CN114258398A (zh) 2019-06-13 2022-03-29 总医院公司 工程化的人内源性病毒样颗粒及使用其递送至细胞的方法
IL291903A (en) * 2019-10-04 2022-06-01 Goldfinch Bio Inc Biomarker-based treatment of focal segmental tuberous sclerosis and diabetic kidney disease
US12435330B2 (en) 2019-10-10 2025-10-07 The Broad Institute, Inc. Methods and compositions for prime editing RNA
KR20220109401A (ko) 2019-10-30 2022-08-04 리본 테라퓨틱스 인코포레이티드 Parp7 억제제로서의 피리다진온
TWI902729B (zh) 2019-11-28 2025-11-01 日商鹽野義製藥股份有限公司 以組合整合酶阻礙劑及抗hiv藥為特徵之hiv感染症的預防及治療用醫藥
TW202146416A (zh) 2019-12-11 2021-12-16 德商拜耳廠股份有限公司 吡唑并三𠯤
WO2021226558A1 (fr) 2020-05-08 2021-11-11 The Broad Institute, Inc. Méthodes et compositions d'édition simultanée des deux brins d'une séquence nucléotidique double brin cible
BR112023001272A2 (pt) 2020-07-24 2023-04-04 Massachusetts Gen Hospital Partículas semelhantes a vírus aprimoradas e métodos de uso das mesmas para entrega às células
JP2023543803A (ja) 2020-09-24 2023-10-18 ザ ブロード インスティテュート,インコーポレーテッド プライム編集ガイドrna、その組成物、及びその使用方法
WO2022150790A2 (fr) 2021-01-11 2022-07-14 The Broad Institute, Inc. Variants d'éditeur primaire, constructions et procédés pour améliorer l'efficacité et la précision d'une édition primaire
WO2023275230A1 (fr) * 2021-07-01 2023-01-05 Janssen Pharmaceutica Nv Acétamides 5-oxo-pyrido[2,3-d]pyridazin-6(5h)-yl
US20250270593A1 (en) 2021-08-06 2025-08-28 The Broad Institute, Inc. Improved prime editors and methods of use
WO2023076898A1 (fr) 2021-10-25 2023-05-04 The Broad Institute, Inc. Procédés et compositions pour l'édition d'un génome à l'aide d'une édition primaire et d'une recombinase
IL313146A (en) 2021-12-03 2024-07-01 Harvard College Self-assembling virus-like particles for delivery of prime editors and methods of making and using same
WO2023205687A1 (fr) 2022-04-20 2023-10-26 The Broad Institute, Inc. Procédés et compositions d'édition primaire améliorés
WO2023240137A1 (fr) 2022-06-08 2023-12-14 The Board Institute, Inc. Variants de cas14a1 évolués, compositions et méthodes de fabrication et d'utilisation de ceux-ci dans l'édition génomique
WO2024077267A1 (fr) 2022-10-07 2024-04-11 The Broad Institute, Inc. Méthodes et compositions d'édition d'amorce pour traiter des troubles de répétition de triplet
EP4619515A1 (fr) 2022-11-17 2025-09-24 The Broad Institute, Inc. Distribution d'éditeur primaire par vaa
EP4662306A2 (fr) 2023-02-09 2025-12-17 The Broad Institute Inc. Recombinases évoluées pour éditer un génome en combinaison avec une édition primaire
WO2024206125A1 (fr) 2023-03-24 2024-10-03 The Broad Institute, Inc. Utilisation de l'édition primaire pour le traitement de la drépanocytose
US20250026759A1 (en) 2023-07-07 2025-01-23 Merck Sharp & Dohme Llc Tetrahydroquinazoline derivatives as selective cytotoxic agents
WO2025081042A1 (fr) 2023-10-12 2025-04-17 Renagade Therapeutics Management Inc. Système d'édition de précision basé sur un modèle de nickase-rétron et méthodes d'utilisation
WO2025193566A1 (fr) * 2024-03-15 2025-09-18 Merck Sharp & Dohme Llc Dérivés de n-oxyde utilisés en tant qu'agents cytotoxiques sélectifs

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5519021A (en) 1992-08-07 1996-05-21 Merck & Co., Inc. Benzoxazinones as inhibitors of HIV reverse transcriptase
EP1073637B1 (fr) 1998-04-27 2006-08-02 Centre National De La Recherche Scientifique Derives de 3-(amino- ou aminoalkyl)pyridinone et utilisation de ceux-ci dans le traitement de pathologies associees au vih
IT1305313B1 (it) 1998-07-17 2001-05-04 Colla Paolo 3,4 - diidro- 6- benzil-4-oxopirimidine sostituite e relativo processodi produzione e impiego nella terapia delle infezioni da hiv-1.
SE9904045D0 (sv) 1999-11-09 1999-11-09 Astra Ab Compounds
DK1318997T3 (da) 2000-09-15 2006-09-25 Vertex Pharma Pyrazolforbindelser der er nyttige som proteinkinase-inhibitorer
CL2004000192A1 (es) 2003-02-07 2005-03-18 Janssen Pharmaceutica Nv Uso de compuestos derivados de 2-aminopirimidina para preparar un medicamento para la prevencion de una infeccion por vih relaciones sexuales o un contacto intimo en la pareja.
TW200423930A (en) 2003-02-18 2004-11-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitors
EP1608629A1 (fr) 2003-03-24 2005-12-28 F. Hoffmann-La Roche Ag Benzyl-pyridazinones en tant qu inhibiteurs de transcriptase inverse
TW200505441A (en) 2003-03-24 2005-02-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitorsⅠ
US20050282839A1 (en) 2004-01-12 2005-12-22 Gilead Sciences, Inc. Pyrimidyl phosphonate antiviral compounds and methods of use
CA2559552A1 (fr) 2004-03-23 2005-09-29 F. Hoffmann-La Roche Ag Derives benzyl-pyridazinone servant d'inhibiteurs d'une transcriptase inverse non nucleosidique
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
DK1742908T3 (da) 2004-04-23 2010-01-18 Hoffmann La Roche Ikke nukleosid revers transkriptase inhibitorer
EP1831157A2 (fr) 2004-12-22 2007-09-12 Pfizer Limited Inhibiteurs non-nucléosidiques de la transcriptase inverse du vih-1
AR057455A1 (es) 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
BRPI0617720A2 (pt) 2005-10-19 2011-08-02 Hoffmann La Roche compostos inibidores de nnrt de fenil-acetamida, usos dos referidos compostos e composição farmacêutica que os contém
ES2320042T3 (es) 2005-10-19 2009-05-18 F. Hoffmann-La Roche Ag Inhibidores de transcriptasa reversa con nucleosidos de n-fenil fenilacetamida.
MX2009005449A (es) 2006-11-24 2009-06-02 Takeda Pharmaceutical Compuesto heteromonociclico y uso del mismo.
US7803940B2 (en) 2006-11-24 2010-09-28 Takeda Pharmaceutical Company Limited Heteromonocyclic compound or a salt thereof having strong antihypertensive action, insulin sensitizing activity and the like production thereof and use thereof for prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases
TW200831085A (en) 2006-12-13 2008-08-01 Merck & Co Inc Non-nucleoside reverse transcriptase inhibitors
AU2008326784B2 (en) 2007-11-20 2014-04-24 Merck Sharp & Dohme Corp. Non-nucleoside reverse transcriptase inhibitors
CN101918372B (zh) * 2008-01-08 2014-03-26 默沙东公司 用于制备n-取代的羟基嘧啶酮羧酰胺类化合物的方法
CN102971308B (zh) 2010-03-30 2015-02-04 默克加拿大有限公司 非核苷类逆转录酶抑制剂
US20130040914A1 (en) 2010-04-08 2013-02-14 Samson M. Jolly Prodrugs of an hiv reverse transcriptase inhibitor
JO3470B1 (ar) 2012-10-08 2020-07-05 Merck Sharp & Dohme مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv
RU2693622C2 (ru) 2014-04-01 2019-07-03 Мерк Шарп И Доум Корп. Пролекарственные средства ингибиторов обратной транскриптазы вич

Also Published As

Publication number Publication date
LT3656384T (lt) 2022-05-10
PT3656384T (pt) 2022-03-22
US20140100231A1 (en) 2014-04-10
PT2903977T (pt) 2017-11-14
BR112015007742B8 (pt) 2021-03-23
LT2903977T (lt) 2017-12-11
AU2013329552B2 (en) 2016-09-15
PH12015500764A1 (en) 2015-07-27
EA033436B1 (ru) 2019-10-31
US20160145255A1 (en) 2016-05-26
MD20150047A2 (ro) 2015-08-31
PE20151787A1 (es) 2015-12-03
MD4625B1 (ro) 2019-04-30
NZ706729A (en) 2018-09-28
KR20150065186A (ko) 2015-06-12
HRP20171819T1 (hr) 2017-12-29
WO2014058747A1 (fr) 2014-04-17
KR101696128B1 (ko) 2017-01-13
US20170349585A1 (en) 2017-12-07
AU2013329552C1 (en) 2016-12-22
EP2903977A1 (fr) 2015-08-12
GT201500088A (es) 2017-09-28
US9469634B2 (en) 2016-10-18
HRP20220502T1 (hr) 2022-05-27
PT3295942T (pt) 2020-02-18
TW201623256A (zh) 2016-07-01
US9718819B2 (en) 2017-08-01
US10189831B2 (en) 2019-01-29
JO3470B1 (ar) 2020-07-05
NO2903977T3 (fr) 2018-02-17
BR112015007742B1 (pt) 2021-01-19
TWI598343B (zh) 2017-09-11
RS63112B1 (sr) 2022-05-31
CY1122585T1 (el) 2021-01-27
ME02918B (fr) 2018-10-20
CN104822670A (zh) 2015-08-05
PL3295942T3 (pl) 2020-05-18
MX2015004448A (es) 2016-02-17
MX355040B (es) 2018-03-28
ES2770774T3 (es) 2020-07-03
HK1252786A1 (en) 2019-05-31
ZA201503143B (en) 2016-06-29
NI201500048A (es) 2016-06-29
HUE058903T2 (hu) 2022-09-28
HUE037231T2 (hu) 2018-08-28
RS56543B1 (sr) 2018-02-28
CY1119655T1 (el) 2018-04-04
SI3295942T1 (sl) 2020-03-31
PL3656384T3 (pl) 2022-04-04
CA2887312A1 (fr) 2014-04-17
HUE048670T2 (hu) 2020-08-28
SG11201502620UA (en) 2015-05-28
MY192716A (en) 2022-09-05
SI3656384T1 (sl) 2022-05-31
JP2016128470A (ja) 2016-07-14
AP2015008355A0 (en) 2015-04-30
MD4625C1 (ro) 2019-11-30
CO7350655A2 (es) 2015-08-10
AU2013329552B8 (en) 2017-01-12
TN2015000106A1 (en) 2016-06-29
CA2887312C (fr) 2017-02-28
JP6097422B2 (ja) 2017-03-15
UA114006C2 (xx) 2017-04-10
CN104822670B (zh) 2018-01-12
AU2013329552A1 (en) 2015-04-16
CL2015000880A1 (es) 2015-08-28
AR092876A1 (es) 2015-05-06
TW201420576A (zh) 2014-06-01
RS59863B1 (sr) 2020-03-31
IL238090B (en) 2019-02-28
EA201590674A1 (ru) 2016-02-29
HRP20200158T1 (hr) 2020-08-07
EP2903977B1 (fr) 2017-09-20
JP5877281B2 (ja) 2016-03-02
PH12015500764B1 (en) 2019-04-05
JP2015533123A (ja) 2015-11-19
GEP20186838B (en) 2018-04-10
LT3295942T (lt) 2020-02-10
EP3295942A1 (fr) 2018-03-21
ES2909190T3 (es) 2022-05-05
SI2903977T1 (sl) 2017-12-29
BR112015007742A2 (pt) 2017-08-08
EP3656384A1 (fr) 2020-05-27
ES2645638T3 (es) 2017-12-07
CR20150183A (es) 2015-08-10
DK3656384T3 (da) 2022-04-19
DK2903977T3 (en) 2017-12-04
PL2903977T3 (pl) 2018-01-31
DK3295942T3 (da) 2020-02-10
EP3656384B1 (fr) 2022-02-23
TWI538907B (zh) 2016-06-21
DOP2015000082A (es) 2015-08-16
ECSP15018618A (es) 2019-06-30
HK1207369A1 (en) 2016-01-29
CY1125202T1 (el) 2024-02-16
EP3295942B1 (fr) 2019-11-20

Similar Documents

Publication Publication Date Title
MA37959A2 (fr) Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih
CL2019000588A1 (es) Compuestos y composiciones como inhibidores de los receptores endosomales tlr.
MX2019001096A (es) Antagonistas del receptor 7/8 tipo toll (tlr7/8) y uso de los mismos.
EP2931730A4 (fr) Dérivés 4-pyridinonetriazines en tant qu'inhibiteurs de l'intégrase du vih
MA39172A1 (fr) Dérivés bicycliques hétérocycliques comme inhibiteurs de bromodomaines
EA201691070A1 (ru) Новые трициклические соединения в качестве противораковых средств
MA35926B1 (fr) Pyrrolidine-2-carboxamides substitués
MA38922A2 (fr) Dérivés de quinolizine substitués utiles en tant qu'inhibiteurs de l'integrase du vih
EA201070988A1 (ru) Противовирусные терапевтические средства
MX2015005015A (es) Inhibidores heteroarilo de pde4.
EP2871957A4 (fr) Composés macrocycliques en tant qu'inhibiteurs de l'intégrase du vih
EA201891378A1 (ru) Полициклические соединения в качестве ингибиторов тирозинкиназы брутона
CL2012001821A1 (es) Compuestos derivados de 5-alquinil-pirimidinas, inhibidores de quinasas; composiciones farmaceuticas que los contienen; y su uso para el tratamiento y/o prevencion de cancer, infecciones, enfermedades inflamatorias y autoinmunitarias.
MA38645A1 (fr) Nouveaux inhibiteurs de cyp17/antiandrogènes
MA39193A1 (fr) Modulateurs du gpr6 à base de tétrahydropyridopyrazines
CR20140135A (es) Nuevos derivados de aril-quinolina
CO7350620A2 (es) Nuevos derivados de piridina
EA201490037A1 (ru) Антагонисты trpv4
CR20140071A (es) Nuevos compuestos de 4-piperidinilo para uso como inhibidores de la tankirasa
MA39152A1 (fr) Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine
MA38982A1 (fr) Nouvel octahydro-cyclobuta [1,2-c; 3,4-c'] dipyrrol-2-yl
EA201891379A1 (ru) Ингибиторы тирозинкиназы брутона и способы их применения
EP2986291A4 (fr) Composés dérivés de 4-pyridone et leurs utilisations en tant qu'inhibiteurs de la vih intégrase
EA201270253A1 (ru) Производные n1-ацил-5-фторпиримидинона
EP2877469A4 (fr) Dérivés de naphthyridinedione substitués en tant qu'inhibiteurs de l'intégrase du vih