CL2020002317A1 - Compuesto inhibidor de tirosina quinasa c-abl: modalidades y métodos de fabricación y uso - Google Patents
Compuesto inhibidor de tirosina quinasa c-abl: modalidades y métodos de fabricación y usoInfo
- Publication number
- CL2020002317A1 CL2020002317A1 CL2020002317A CL2020002317A CL2020002317A1 CL 2020002317 A1 CL2020002317 A1 CL 2020002317A1 CL 2020002317 A CL2020002317 A CL 2020002317A CL 2020002317 A CL2020002317 A CL 2020002317A CL 2020002317 A1 CL2020002317 A1 CL 2020002317A1
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- CL
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- Prior art keywords
- abl
- tyrosine kinase
- compound
- modalities
- manufacture
- Prior art date
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/38—[b, e]- or [b, f]-condensed with six-membered rings
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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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
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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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
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- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/22—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from lactams, cyclic ketones or cyclic oximes, e.g. by reactions involving Beckmann rearrangement
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- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
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- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D267/18—[b, e]-condensed
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- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D267/20—[b, f]-condensed
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- C—CHEMISTRY; METALLURGY
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- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
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- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D281/16—[b, f]-condensed
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- C07D285/36—Seven-membered rings
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- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- C07D403/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- 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
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- C07D471/02—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 two hetero rings
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
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- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
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Abstract
En el presente documento, se divulgan modalidades de un compuesto que inhibe la tirosina quinasa c-Abl (también denominada en el presente documento “c-Abl”). Las modalidades de compuesto descritas en el presente documento corresponden a novedosos inhibidores de la tirosina quinasa c-Abl, que se pueden unir a un sitio alostérico en c-Abl e inhibir su actividad a través de diferentes vías. Las modalidades de compuesto son capaces de pasar a través de la barrera hematoencefálica, por lo que permiten inhibir la actividad de la tirosina quinasa c-Abl y su efecto sobre vías y/o proteínas cerebrales. Las modalidades de compuesto descritas en el presente documento corresponden a efectivos agentes terapéuticos para tratar enfermedades en las que existe actividad de la tirosina quinasa c-Abl, como distintos tipos de cáncer, enfermedades de las neuronas motrices y enfermedades neurodegenerativas. Además, en el presente documento se divulgan modalidades de métodos de fabricación y uso de las modalidades de compuesto inhibidor de c-Abl.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862641126P | 2018-03-09 | 2018-03-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2020002317A1 true CL2020002317A1 (es) | 2021-01-08 |
Family
ID=65904559
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2020002317A CL2020002317A1 (es) | 2018-03-09 | 2020-09-07 | Compuesto inhibidor de tirosina quinasa c-abl: modalidades y métodos de fabricación y uso |
Country Status (3)
| Country | Link |
|---|---|
| US (3) | US11649218B2 (es) |
| CL (1) | CL2020002317A1 (es) |
| WO (1) | WO2019173761A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ773110A (en) | 2018-09-18 | 2024-11-29 | Terns Inc | Compounds for treating certain leukemias |
| WO2021119183A1 (en) | 2019-12-13 | 2021-06-17 | 712 North, Inc. | Tricyclic compounds with oma1/opa1 modulatory properties |
| EP4410779A4 (en) * | 2021-09-30 | 2025-07-30 | Jiangsu Hansoh Pharmaceutical Group Co Ltd | FOUR-MEMBERED FUSED RING COMPOUND, PREPARATION METHOD AND USE THEREOF |
| EP4177246A1 (en) * | 2021-11-04 | 2023-05-10 | Centro Atlántico del Medicamento, SA | Fused oxazepines as inhibitors of peroxiredoxins |
| JP2024540522A (ja) | 2021-11-19 | 2024-10-31 | ザ・ブロード・インスティテュート・インコーポレイテッド | キナーゼを標的結合部分で標識するための二官能性キメラ分子及びその使用方法 |
| CN114702454A (zh) * | 2022-03-29 | 2022-07-05 | 江西师范大学 | 5-烷基-11-芳基-5H-二苯并[b,e][1,4]二氮杂卓衍生物的制备方法 |
| TW202502333A (zh) * | 2023-03-30 | 2025-01-16 | 大陸商江蘇豪森藥業集團有限公司 | 四元稠環類化合物鹽晶型及其製備方法和應用 |
| CN116617393A (zh) * | 2023-05-16 | 2023-08-22 | 中国人民解放军军事科学院军事医学研究院 | c-Abl激酶激活剂DPH在阿尔兹海默病治疗中的应用 |
| CN116987040B (zh) * | 2023-06-21 | 2025-09-23 | 中国中医科学院中药研究所 | 二苯并二氮杂卓衍生物及其制备方法和应用 |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3845074A (en) | 1969-06-20 | 1974-10-29 | En Nom Collectif Science Union | Dibenzo(b,f)thiazepin(1,4)-11-yl amino alkanoic acids |
| US3773768A (en) * | 1970-10-26 | 1973-11-20 | American Cyanamid Co | 7-amino-2-chloro-11-(4-methyl-1-piperazinyl)dibenz(b,f)(1,4)oxazepine and salts thereof |
| JPS5576869A (en) | 1978-12-06 | 1980-06-10 | Chugai Pharmaceut Co Ltd | Dibenzoxazepine derivative and its preparation |
| JPS56166179A (en) * | 1980-05-28 | 1981-12-21 | Chugai Pharmaceut Co Ltd | Dibenzoxazepine derivative and its preparation |
| JPS56166180A (en) * | 1980-05-28 | 1981-12-21 | Chugai Pharmaceut Co Ltd | Dibenzoxazepine derivative and its preparation |
| JPS572279A (en) * | 1980-06-04 | 1982-01-07 | Chugai Pharmaceut Co Ltd | Dibenzoxazepin derivative |
| JPS57120580A (en) * | 1981-01-20 | 1982-07-27 | Chugai Pharmaceut Co Ltd | Dibenzoxazepinone derivative |
| JPS58206520A (ja) * | 1982-05-27 | 1983-12-01 | Chugai Pharmaceut Co Ltd | 悪性腫瘍の転移抑制剤 |
| JPS58225073A (ja) * | 1982-06-25 | 1983-12-27 | Chugai Pharmaceut Co Ltd | ジベンゾオキサゼピノン誘導体 |
| JPS58225074A (ja) * | 1982-06-25 | 1983-12-27 | Chugai Pharmaceut Co Ltd | ジベンゾオキサゼピン誘導体 |
| US4610819A (en) | 1984-09-19 | 1986-09-09 | A. H. Robins Company, Inc. | Process for the preparation of aromatic-1,4-oxazepinones and thiones |
| US4704386A (en) | 1985-08-29 | 1987-11-03 | G. D. Searle & Co. | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(phenylsulfinyl-, and phenylsulfonyl)alkanoyl]hydrazides |
| EP0240721A3 (en) * | 1986-03-12 | 1991-01-02 | Chugai Seiyaku Kabushiki Kaisha | Therapeutic agent for the treatment of peripheral circulatory disorders |
| DK0419861T3 (da) | 1989-08-29 | 1996-03-04 | Boehringer Ingelheim Pharma | Anvendelse af dibenz(b,f) (1,4)oxazepin (og thiazepin)-11(10H)-oner og -thioner til fremstilling af farmaceutisk præparat til forebyggelse eller behandling af AIDS |
| US5180720A (en) * | 1991-05-03 | 1993-01-19 | G. D. Searle & Co. | 2- and 3-alkoxy or hydroxy-8-substituted-dibenz[b,f]-[1,4]oxazepine-10(11H)-carboxylic acid, substituted hydrazides and methods for treating pain |
| US5173486A (en) | 1991-08-26 | 1992-12-22 | Bristol-Myers Squibb Company | Dibenz[b,f][1,4]oxazepin-11(10H)-ones for multidrug resistance reversing agents |
| US7186713B2 (en) * | 2003-01-21 | 2007-03-06 | Ecopia Biosciences, Inc. | Farnesyl dibenzodiazepinones and methods of treating cancer using same |
| AU2004206046B2 (en) * | 2003-01-21 | 2009-12-17 | Thallion Pharmaceuticals Inc. | Farnesyl dibenzodiazepinones, processes for their production and their use as pharmaceuticals |
| US7655646B2 (en) * | 2003-01-21 | 2010-02-02 | Thallion Pharmaceuticals, Inc. | Dibenzodiazepinone analogues, processes for their production and their use as pharmaceuticals |
| US7297524B2 (en) * | 2003-01-21 | 2007-11-20 | Thallion Pharmceuticals Inc. | Polynucleotides for production of farnesyl dibenzodiazepinones |
| US7456169B2 (en) * | 2003-02-27 | 2008-11-25 | Abbott Laboratories Inc. | Heterocyclic kinase inhibitors |
| CA2515790C (en) | 2003-02-27 | 2012-11-27 | Abbott Laboratories | Heterocyclic kinase inhibitors |
| US7060698B2 (en) | 2003-05-19 | 2006-06-13 | Hoffmann-La Roche Inc. | Benzoxazepinone derivatives |
| US20090029972A1 (en) * | 2004-09-27 | 2009-01-29 | Ecopia Biosciences Inc | Dibenzodiazepinone Analogues, Processes for Their Production and Their Use as Pharmaceuticals |
| US7763604B2 (en) * | 2005-05-16 | 2010-07-27 | Thallion Pharma Ceuticals, Inc. | Methods for administration of a farnesyl dibenzodiazepinone |
| US7384935B2 (en) * | 2005-09-27 | 2008-06-10 | Thallion Pharmaceuticals, Inc. | Phosphate prodrugs of a farnesyl dibenzodiazepinone, processes for their production and their use as pharmaceuticals |
| CN105481788A (zh) | 2006-10-28 | 2016-04-13 | 梅特希尔基因公司 | 组蛋白脱乙酰酶抑制剂 |
| AU2008225014B2 (en) | 2007-03-15 | 2014-12-11 | Protocell Therapeutics, Inc. | Dibenzo(b,f)(1,4)oxazapine compounds |
| US8063037B2 (en) * | 2007-05-07 | 2011-11-22 | N. V. Organon | Progesterone receptor modulators |
| US8158623B2 (en) * | 2007-05-29 | 2012-04-17 | Shanghai Institute Of Materia Medica Chinese Academy Of Sciences | Heptacyclic compounds and the pharmaceutical uses thereof for preventing and treating diabetes and metabolic syndrome |
| BRPI0813356A2 (pt) | 2007-06-15 | 2014-12-30 | Irm Llc | Inibidores de proteína quinase e métodos para uso dos mesmos |
| US20090062255A1 (en) * | 2007-08-17 | 2009-03-05 | Thallion Pharmaceuticals Inc. | Tumor-targeting evaluation methodology and compounds related thereto |
| US20090170837A1 (en) * | 2007-08-17 | 2009-07-02 | Thallion Pharmaceuticals Inc. | Methods for treating ras driven cancer in a subject |
| WO2009137462A2 (en) | 2008-05-05 | 2009-11-12 | Envivo Pharmaceuticals, Inc. | Methods for treating cognitive disorders using inhibitors of histone deacetylase |
| UY34171A (es) | 2011-07-01 | 2013-01-31 | Gilead Sciences Inc | Compuestos heterocíclicos fusionados como moduladores del canal iónico |
| AU2015224425B2 (en) | 2011-07-01 | 2017-02-09 | Gilead Sciences, Inc. | Fused benzoxazepinones as ion channel modulators |
| US9695144B2 (en) | 2013-12-23 | 2017-07-04 | Purdue Pharma L.P. | Dibenzazepine derivatives and use thereof |
| WO2016027790A1 (ja) | 2014-08-19 | 2016-02-25 | 日本農薬株式会社 | オキサゼピン化合物及び該化合物を有効成分として含有する農園芸用殺虫剤並びにその使用方法 |
| CN105384792B (zh) * | 2014-08-23 | 2020-12-22 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的化合物及其在药物中的应用 |
| CN105949143B (zh) * | 2016-06-01 | 2018-03-20 | 洛阳师范学院 | 二芳基并氧氮杂卓酮类化合物的合成方法 |
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| US20210101872A1 (en) | 2021-04-08 |
| US20250340521A1 (en) | 2025-11-06 |
| US12435047B2 (en) | 2025-10-07 |
| WO2019173761A1 (en) | 2019-09-12 |
| US20230303501A1 (en) | 2023-09-28 |
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