AR111419A1 - Compuestos fusionados de indazol piridona como antivirales - Google Patents
Compuestos fusionados de indazol piridona como antiviralesInfo
- Publication number
- AR111419A1 AR111419A1 ARP180101043A ARP180101043A AR111419A1 AR 111419 A1 AR111419 A1 AR 111419A1 AR P180101043 A ARP180101043 A AR P180101043A AR P180101043 A ARP180101043 A AR P180101043A AR 111419 A1 AR111419 A1 AR 111419A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halo
- optionally substituted
- ring
- cycloalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title 1
- 239000003443 antiviral agent Substances 0.000 title 1
- 229940121357 antivirals Drugs 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract 11
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 8
- -1 -OH Chemical group 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 3
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 3
- 125000000520 N-substituted aminocarbonyl group Chemical group [*]NC(=O)* 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 150000004292 cyclic ethers Chemical class 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
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- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/12—Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/02—Heterocyclic 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 two hetero rings
- C07D405/12—Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four 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
- C07D491/12—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 three hetero rings
- C07D491/16—Peri-condensed systems
-
- 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
- C07D491/22—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 four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1), caracterizado porque: R¹ es H o halo; R² se selecciona independientemente en cada aparición entre halo, CN, haloalquilo C₁₋₃, haloalcoxi C₁₋₃, -OR³, -N(R)R³, y alquilo C₁₋₃ opcionalmente sustituido con hasta tres grupos seleccionados entre R³, -N(R)R³, CN, -OH, -CONR₂, -COOR, y -OR³; R³ es un alquilo C₁₋₄ que está opcionalmente sustituido con uno a tres grupos seleccionados de halo, haloalquilo C₁₋₃, -OH, alcoxi C₁₋₃, haloalcoxi C₁₋₃, oxo, CN, -NH₂, -NH(alquilo C₁₋₃), -N(alquilo C₁₋₃)₂, -COOR, -CONR₂, cicloalquilo C₃₋₅, y un éter cíclico de 4 - 6 miembros, en el que el cicloalquilo C₃₋₅ y el éter cíclico de 4 - 6 miembros están cada uno opcionalmente sustituidos con uno o dos grupos seleccionados de halo, -OH, alcoxi C₁₋₃, y alquilo C₁₋₃; o R³ es un anillo cicloalquilo C₃₋₅ o éter cíclico de 4 - 6 miembros, en el que el anillo cicloalquilo C₃₋₅ o éter cíclico de 4 - 6 miembros están cada uno opcionalmente sustituidos con uno a tres grupos seleccionados de halo, alquilo C₁₋₃, -OH, alcoxi C₁₋₃, haloalcoxi C₁₋₃, haloalquilo C₁₋₃, -NH₂, -NH(alquilo C₁₋₃), y -N(alquilo C₁₋₃)₂; n es 0, 1, ó 2; W es -COOR⁴, -C(O)NH-SO₂R⁵, -C(O)NH-SO₂NR₂, 5-tetrazolilo, o 1,2,4-oxadiazol-3-il-5(4H)-ona; R⁴ es H o alquilo C₁₋₆ que está opcionalmente sustituido con uno a tres grupos seleccionados de halo, -OR, oxo, CN, y -NR₂; R⁵ es alquilo C₁₋₆ que está opcionalmente sustituido con uno a tres grupos seleccionados de halo, -OR, oxo, CN, y-NR₂; R⁶ es H o alquilo C₁₋₆; R⁷ es H o alquilo C₁₋₆, o R⁷ tomado junto con R⁹ y los átomos que los unen R⁷ con R⁹ forman un anillo como se describe a continuación; R⁸ es H o alquilo C₁₋₆; R⁹ se selecciona entre: (i) H; (ii) alquilo C₁₋₆ opcionalmente sustituido con hasta tres grupos seleccionados entre cicloalquilo C₃₋₆, -OR, -NR₂, halo, CN, COOR, CONR₂, y oxo; y (iii) un anillo seleccionado de (a) cicloalquilo C₃₋₆, (b) fenilo, (c) heterociclilo de 5 - 6 miembros que contiene uno o dos heteroátomos seleccionados de N, O y S como miembros del anillo, y (d) heteroarilo de 5 - 6 miembros que contiene uno o dos heteroátomos seleccionados de N, o y S como miembros del anillo, en el que cada uno de los anillos (a) a (d) está opcionalmente sustituido con hasta tres grupos seleccionados de alquilo C₁₋₂, (CH₂)₀₋₂-OR, -NR₂, halo, CN, COOR, y CONR₂; o R⁹ tomado junto con R⁷ y los átomos que los unen R⁹ con R⁷ forma un anillo cicloalquilo de 3 - 7 miembros, o un anillo heterocíclico de 3 - 7 miembros que contiene N, O ó S como miembro de anillo; en donde el anillo cicloalquilo o heterocíclico está opcionalmente sustituido con hasta tres grupos seleccionados de entre R, -OR, -NR₂, halo, CN, COOR, CONR₂, y oxo; R se selecciona independientemente en cada caso de H y alquilo C₁₋₃ opcionalmente sustituido con uno a tres grupos seleccionados de halo, -OH, alcoxi C₁₋₃, oxo, CN, -NH₂, -NH(alquilo C₁₋₃), -N(alquilo C₁₋₃)₂, y ciclopropilo; y dos grupos R unidos directamente al mismo átomo pueden tomarse opcionalmente junto con el átomo al que ambos están unidos para formar un anillo de 3 - 6 miembros que puede contener opcionalmente un heteroátomo seleccionado de N, O y S como miembro del anillo, y puede estar sustituido con hasta dos grupos seleccionados de -OH, oxo, alquilo C₁₋₃ y alcoxi C₁₋₃; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762490890P | 2017-04-27 | 2017-04-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR111419A1 true AR111419A1 (es) | 2019-07-10 |
Family
ID=62148437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180101043A AR111419A1 (es) | 2017-04-27 | 2018-04-24 | Compuestos fusionados de indazol piridona como antivirales |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US10301312B2 (es) |
| EP (2) | EP3615533B1 (es) |
| JP (1) | JP7290573B2 (es) |
| CN (1) | CN110831942B (es) |
| AR (1) | AR111419A1 (es) |
| ES (1) | ES2899922T3 (es) |
| TW (1) | TWI810182B (es) |
| UY (1) | UY37699A (es) |
| WO (1) | WO2018198079A1 (es) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016183266A1 (en) | 2015-05-13 | 2016-11-17 | Enanta Pharmaceuticals, Inc. | Ehpatitis b antiviral agents |
| CN109069488B (zh) | 2016-03-07 | 2021-09-07 | 英安塔制药有限公司 | 乙型肝炎抗病毒剂 |
| AR111419A1 (es) | 2017-04-27 | 2019-07-10 | Novartis Ag | Compuestos fusionados de indazol piridona como antivirales |
| CN110066278B (zh) | 2017-06-01 | 2021-06-08 | 广东东阳光药业有限公司 | 稠合三环类化合物及其在药物中的应用 |
| IL272941B2 (en) | 2017-08-28 | 2023-03-01 | Enanta Pharm Inc | Antiviral agents for viral hepatitis b |
| CN111433210A (zh) * | 2017-12-20 | 2020-07-17 | 诺华股份有限公司 | 作为抗病毒药的稠合三环吡唑并-二氢吡嗪基-吡啶酮化合物 |
| US11058678B2 (en) | 2018-01-22 | 2021-07-13 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2019177937A1 (en) | 2018-03-12 | 2019-09-19 | Arbutus Biopharma, Inc. | Substituted 2-pyridone tricyclic compounds, analogues thereof, and methods using same |
| WO2019191166A1 (en) | 2018-03-29 | 2019-10-03 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| WO2020043080A1 (en) | 2018-08-28 | 2020-03-05 | Sunshine Lake Pharma Co., Ltd. | Fused tricyclic compounds and uses thereof in medicine |
| KR20210065965A (ko) | 2018-09-21 | 2021-06-04 | 이난타 파마슈티칼스, 인코포레이티드 | 항바이러스제로서 작용화된 헤테로사이클 |
| KR20210069680A (ko) | 2018-09-30 | 2021-06-11 | 선샤인 레이크 파르마 컴퍼니 리미티드 | 융합된 사환형 화합물 및 약물에서의 이의 용도 |
| US11198693B2 (en) | 2018-11-21 | 2021-12-14 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| TW202033523A (zh) * | 2019-01-17 | 2020-09-16 | 美商愛彼特生物製藥股份有限公司 | 經取代的多環羧酸、其類似物及使用其之方法 |
| US11236111B2 (en) | 2019-06-03 | 2022-02-01 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| WO2020247575A1 (en) | 2019-06-04 | 2020-12-10 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| US11760755B2 (en) | 2019-06-04 | 2023-09-19 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| US11738019B2 (en) | 2019-07-11 | 2023-08-29 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2021018207A1 (zh) * | 2019-07-30 | 2021-02-04 | 上海挚盟医药科技有限公司 | 一类用于治疗和/或预防乙型肝炎病毒感染的化合物及其制备方法和应用 |
| US11236108B2 (en) | 2019-09-17 | 2022-02-01 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| WO2021188414A1 (en) | 2020-03-16 | 2021-09-23 | Enanta Pharmaceuticals, Inc. | Functionalized heterocyclic compounds as antiviral agents |
| CN120051281A (zh) * | 2022-10-04 | 2025-05-27 | 蓝樫鸟医药公司 | 吲唑吡啶酮化合物及其用途 |
| WO2024263770A1 (en) * | 2023-06-21 | 2024-12-26 | The Trustees Of The University Of Pennsylvania | Toll-like receptor (tlr) agonist lipidoid compounds, lipid nanoparticles (lnps) comprising the same, and methods of use thereof |
Family Cites Families (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0090505B1 (en) | 1982-03-03 | 1990-08-08 | Genentech, Inc. | Human antithrombin iii, dna sequences therefor, expression vehicles and cloning vectors containing such sequences and cell cultures transformed thereby, a process for expressing human antithrombin iii, and pharmaceutical compositions comprising it |
| AU4055697A (en) | 1996-08-16 | 1998-03-06 | Schering Corporation | Mammalian cell surface antigens; related reagents |
| US6111090A (en) | 1996-08-16 | 2000-08-29 | Schering Corporation | Mammalian cell surface antigens; related reagents |
| WO1999020758A1 (en) | 1997-10-21 | 1999-04-29 | Human Genome Sciences, Inc. | Human tumor necrosis factor receptor-like proteins tr11, tr11sv1, and tr11sv2 |
| AU2591599A (en) | 1998-02-09 | 1999-08-23 | Genentech Inc. | Novel tumor necrosis factor receptor homolog and nucleic acids encoding the same |
| CA2378179A1 (en) | 1999-07-12 | 2001-01-18 | Genentech, Inc. | Promotion or inhibition of angiogenesis and cardiovascularization by tumor necrosis factor ligand/receptor homologs |
| AU2003218989A1 (en) | 2002-02-19 | 2003-09-09 | Pharmacia Italia S.P.A. | Tricyclic pyrazole derivatives, process for their preparation and their use as antitumor agents |
| CN101899114A (zh) | 2002-12-23 | 2010-12-01 | 惠氏公司 | 抗pd-1抗体及其用途 |
| EP1631260A2 (en) | 2003-02-28 | 2006-03-08 | Transform Pharmaceuticals, Inc. | Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen |
| NZ543654A (en) | 2003-05-23 | 2009-05-31 | Wyeth Corp | GITR ligand and GITR ligand-related molecules and antibodies and uses thereof |
| US20050048054A1 (en) | 2003-07-11 | 2005-03-03 | Shino Hanabuchi | Lymphocytes; methods |
| EP1692318A4 (en) | 2003-12-02 | 2008-04-02 | Genzyme Corp | COMPOSITIONS AND METHODS FOR DIAGNOSIS AND TREATMENT OF LUNG CANCER |
| GB0409799D0 (en) | 2004-04-30 | 2004-06-09 | Isis Innovation | Method of generating improved immune response |
| WO2006083289A2 (en) | 2004-06-04 | 2006-08-10 | Duke University | Methods and compositions for enhancement of immunity by in vivo depletion of immunosuppressive cell activity |
| AU2006230099B2 (en) | 2005-03-25 | 2012-04-19 | Gitr, Inc. | GITR binding molecules and uses therefor |
| AU2006244885B2 (en) | 2005-05-09 | 2011-03-31 | E. R. Squibb & Sons, L.L.C. | Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics |
| CN101248089A (zh) | 2005-07-01 | 2008-08-20 | 米德列斯公司 | 抗程序性死亡配体1(pd-l1)的人单克隆抗体 |
| US20110212086A1 (en) | 2006-01-19 | 2011-09-01 | Genzyme Corporation | GITR Antibodies For The Treatment of Cancer |
| CA2691357C (en) | 2007-06-18 | 2014-09-23 | N.V. Organon | Antibodies to human programmed death receptor pd-1 |
| CN101801413A (zh) | 2007-07-12 | 2010-08-11 | 托勒克斯股份有限公司 | 采用gitr结合分子的联合疗法 |
| JP2011512332A (ja) | 2008-02-11 | 2011-04-21 | キュアー テック リミテッド | 腫瘍治療のためのモノクローナル抗体 |
| US8168757B2 (en) | 2008-03-12 | 2012-05-01 | Merck Sharp & Dohme Corp. | PD-1 binding proteins |
| AU2009266873A1 (en) | 2008-07-02 | 2010-01-07 | Emergent Product Development Seattle, Llc | TGF-beta antagonist multi-target binding proteins |
| AR072999A1 (es) | 2008-08-11 | 2010-10-06 | Medarex Inc | Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos |
| US20110159023A1 (en) | 2008-08-25 | 2011-06-30 | Solomon Langermann | Pd-1 antagonists and methods for treating infectious disease |
| JP5798919B2 (ja) | 2008-08-25 | 2015-10-21 | アンプリミューン、インコーポレーテッドAmplimmune, Inc. | Pd−1アンタゴニストの組成物および使用方法 |
| JPWO2010030002A1 (ja) | 2008-09-12 | 2012-02-02 | 国立大学法人三重大学 | 外来性gitrリガンド発現細胞 |
| HUE034832T2 (hu) | 2008-12-09 | 2021-12-28 | Hoffmann La Roche | Anti-PD-L1 antitestek és alkalmazásuk T-sejt-funkció fokozására |
| EP2393835B1 (en) | 2009-02-09 | 2017-04-05 | Université d'Aix-Marseille | Pd-1 antibodies and pd-l1 antibodies and uses thereof |
| JP2012518598A (ja) * | 2009-02-25 | 2012-08-16 | Msd株式会社 | ピリミドピリミドインダゾール誘導体 |
| AU2010289677B2 (en) | 2009-09-03 | 2014-07-31 | Merck Sharp & Dohme Llc | Anti-GITR antibodies |
| GB0919054D0 (en) | 2009-10-30 | 2009-12-16 | Isis Innovation | Treatment of obesity |
| WO2011066342A2 (en) | 2009-11-24 | 2011-06-03 | Amplimmune, Inc. | Simultaneous inhibition of pd-l1/pd-l2 |
| CN105693861A (zh) | 2009-12-29 | 2016-06-22 | 新兴产品开发西雅图有限公司 | 异二聚体结合蛋白及其应用 |
| WO2013039954A1 (en) | 2011-09-14 | 2013-03-21 | Sanofi | Anti-gitr antibodies |
| BR112014012819B1 (pt) | 2011-11-28 | 2022-08-16 | Merck Patent Gmbh | Anticorpo anti-pd-l1 ou fragmento de ligação ao antígeno do mesmo e composição |
| CA2857344C (en) | 2011-12-21 | 2019-02-12 | Novira Therapeutics, Inc. | Hepatitis b antiviral agents |
| UY34887A (es) | 2012-07-02 | 2013-12-31 | Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware | Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos |
| EP3099685B1 (en) | 2014-01-30 | 2018-04-18 | F.Hoffmann-La Roche Ag | Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis b virus infection |
| SI3114128T1 (sl) | 2014-03-07 | 2019-04-30 | F. Hoffmann-La Roche Ag | Novi 6-spojeni heteroarildihidropirimidini za zdravljenje in preprečevanje okužbe z virusom hepatitisa B |
| KR20160148715A (ko) * | 2014-05-13 | 2016-12-26 | 에프. 호프만-라 로슈 아게 | B형 간염 바이러스 감염의 치료 또는 예방을 위한 신규한 다이하이드로퀴놀리진온 |
| RU2664329C1 (ru) | 2014-08-14 | 2018-08-16 | Ф. Хоффманн-Ля Рош Аг | Новые пиридазоны и триазиноны для лечения и профилактики заражения вирусом гепатита b |
| US9637485B2 (en) | 2014-11-03 | 2017-05-02 | Hoffmann-La Roche Inc. | 6,7-dihydrobenzo[a]quinolizin-2-one derivatives for the treatment and prophylaxis of hepatitis B virus infection |
| WO2016128335A1 (en) | 2015-02-11 | 2016-08-18 | F. Hoffmann-La Roche Ag | Novel 2-oxo-6,7-dihydrobenzo[a]quinolizine-3-carboxylic acid derivatives for the treatment and prophylaxis of hepatitis b virus infection |
| WO2017016960A1 (en) | 2015-07-24 | 2017-02-02 | F. Hoffmann-La Roche Ag | Process for the preparation of (6s)-6-alkyl-10-alkoxy-9-(substituted alkoxy)-2-oxo-6,7-dihydrobenzo[a]quinolizine-3-carboxylic acid analogues |
| WO2017016921A1 (en) | 2015-07-24 | 2017-02-02 | F. Hoffmann-La Roche Ag | New crystalline forms of (6s)-10-methoxy-6-isopropyl-9-(3-methoxypropoxy)-2-oxo-6,7-dihydrobenzo[a]quinolizine-3-carboxylic acid |
| EP3328855B1 (en) | 2015-07-27 | 2019-05-15 | H. Hoffnabb-La Roche Ag | Novel tetracyclic 4-oxo-pyridine-3-carboxylic acid derivatives for the treatment and prophylaxis of hepatitis b virus infection |
| WO2017102648A1 (en) | 2015-12-15 | 2017-06-22 | F. Hoffmann-La Roche Ag | Combination therapy of an hbsag inhibitor and a nucleos(t)ide analogue |
| WO2017108630A1 (en) | 2015-12-21 | 2017-06-29 | F. Hoffmann-La Roche Ag | Combination therapy of an hbsag inhibitor and an hbv capsid assembly inhibitor |
| WO2017114812A1 (en) | 2015-12-29 | 2017-07-06 | F. Hoffmann-La Roche Ag | Combination therapy of an hbsag inhibitor and an interferon |
| UY37128A (es) | 2016-02-19 | 2017-09-29 | Novartis Ag | Compuestos tetracíclicos de piridona como antivirales |
| WO2017216686A1 (en) | 2016-06-16 | 2017-12-21 | Novartis Ag | 8,9-fused 2-oxo-6,7-dihydropyrido-isoquinoline compounds as antivirals |
| WO2017216685A1 (en) | 2016-06-16 | 2017-12-21 | Novartis Ag | Pentacyclic pyridone compounds as antivirals |
| TW201811788A (zh) | 2016-09-09 | 2018-04-01 | 瑞士商諾華公司 | 作為抗病毒劑之多環吡啶酮化合物 |
| TW201819380A (zh) * | 2016-10-18 | 2018-06-01 | 瑞士商諾華公司 | 作為抗病毒劑之稠合四環吡啶酮化合物 |
| CN106928215B (zh) | 2017-03-06 | 2019-03-22 | 河南春风医药科技有限公司 | 一种喹嗪酮类化合物的制备方法 |
| CN106928245B (zh) | 2017-03-06 | 2019-06-11 | 河南春风医药科技有限公司 | 一种喹嗪酮类化合物及其制备方法和应用 |
| AR111419A1 (es) * | 2017-04-27 | 2019-07-10 | Novartis Ag | Compuestos fusionados de indazol piridona como antivirales |
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2018
- 2018-04-24 AR ARP180101043A patent/AR111419A1/es unknown
- 2018-04-25 UY UY0001037699A patent/UY37699A/es not_active Application Discontinuation
- 2018-04-26 TW TW107114191A patent/TWI810182B/zh active
- 2018-04-27 CN CN201880042367.6A patent/CN110831942B/zh active Active
- 2018-04-27 WO PCT/IB2018/052921 patent/WO2018198079A1/en not_active Ceased
- 2018-04-27 EP EP18723982.7A patent/EP3615533B1/en active Active
- 2018-04-27 US US15/965,172 patent/US10301312B2/en active Active
- 2018-04-27 ES ES18723982T patent/ES2899922T3/es active Active
- 2018-04-27 EP EP21194883.1A patent/EP3998269A1/en active Pending
- 2018-04-27 JP JP2019557564A patent/JP7290573B2/ja active Active
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2019
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2020
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| JP2020517667A (ja) | 2020-06-18 |
| EP3615533B1 (en) | 2021-09-08 |
| TWI810182B (zh) | 2023-08-01 |
| TW201841919A (zh) | 2018-12-01 |
| EP3998269A1 (en) | 2022-05-18 |
| UY37699A (es) | 2018-11-30 |
| US20180312507A1 (en) | 2018-11-01 |
| US10975078B2 (en) | 2021-04-13 |
| US20200270252A1 (en) | 2020-08-27 |
| WO2018198079A1 (en) | 2018-11-01 |
| US10301312B2 (en) | 2019-05-28 |
| US20190300530A1 (en) | 2019-10-03 |
| JP7290573B2 (ja) | 2023-06-13 |
| ES2899922T3 (es) | 2022-03-15 |
| CN110831942B (zh) | 2023-04-04 |
| CN110831942A (zh) | 2020-02-21 |
| EP3615533A1 (en) | 2020-03-04 |
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