MA40523A - 2-(morpholin-4-yl)-1,7-naphthyridines - Google Patents
2-(morpholin-4-yl)-1,7-naphthyridinesInfo
- Publication number
- MA40523A MA40523A MA040523A MA40523A MA40523A MA 40523 A MA40523 A MA 40523A MA 040523 A MA040523 A MA 040523A MA 40523 A MA40523 A MA 40523A MA 40523 A MA40523 A MA 40523A
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- morpholin
- preparation
- naphthyridines
- disease
- Prior art date
Links
- -1 MORPHOLIN-4-YL Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- YJCWMEVTGIOUNH-UHFFFAOYSA-N C1CN(CCO1)C1=CC=C2C=CN=CC2=N1 Chemical class C1CN(CCO1)C1=CC=C2C=CN=CC2=N1 YJCWMEVTGIOUNH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 238000011282 treatment Methods 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
- C07D471/02—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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- C07D491/22—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La présente invention porte sur des composés 2-(morpholin-4-yl)-l,7-naphtyridine substitués représentés par la formule générale (i) ou (ib), sur des procédés de préparation desdits composés, sur des composés intermédiaires utiles pour la préparation desdits composés, sur des combinaisons et des compositions pharmaceutiques comprenant lesdits composés et sur l'utilisation desdits composés pour la fabrication d'une composition pharmaceutique utile pour le traitement ou la prophylaxie d'une maladie, en particulier d'une maladie hyperproliférative en tant qu'agent unique ou en combinaison avec d'autres principes actifs.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14179692 | 2014-08-04 | ||
| EP15159342 | 2015-03-17 | ||
| PCT/EP2015/067804 WO2016020320A1 (fr) | 2014-08-04 | 2015-08-03 | 2- (morpholin -4-yl)-l,7-naphtyridines |
| EP15744596.6A EP3177619B1 (fr) | 2014-08-04 | 2015-08-03 | 2-(morpholin-4-yl)-1,7-naphthyridines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA40523A true MA40523A (fr) | 2017-06-14 |
| MA40523B1 MA40523B1 (fr) | 2018-09-28 |
Family
ID=53762196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA40523A MA40523B1 (fr) | 2014-08-04 | 2015-08-03 | 2-(morpholin-4-yl)-1,7-naphthyridines |
Country Status (42)
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CR20170077A (es) | 2014-08-04 | 2017-06-26 | Nuevolution As | Derivados de heterociclilo opcionalmente condensados de pirimidina útiles para el tratamiento de enfermedades inflamatorias, metabólicas, oncológicas y autoinmunitarias |
| TWI656121B (zh) * | 2014-08-04 | 2019-04-11 | 德商拜耳製藥公司 | 2-(嗎啉-4-基)-1,7-萘啶 |
| CA3011189C (fr) * | 2016-01-14 | 2024-02-20 | Bayer Pharma Aktiengesellschaft | 2-(morpholin-4-yl)-1,7-naphthyridines substituees en 5 |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
| TW201840319A (zh) | 2017-02-24 | 2018-11-16 | 德商拜耳廠股份有限公司 | Atr激酶抑制劑與鐳-223鹽之組合 |
| WO2018153971A1 (fr) | 2017-02-24 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de kinase atr |
| WO2018153970A1 (fr) | 2017-02-24 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Formes solides de 2-[(3r)-3-méthylmorpholin-4-yl]-4-(1-méthyl-1h-pyrazol-5-yl)-8-(1h-pyrazol-5-yl)-1,7-naphtyridine |
| WO2018153975A1 (fr) | 2017-02-24 | 2018-08-30 | Bayer As | Polythérapie comprenant un agent radiopharmaceutique et un inhibiteur de réparation d'adn |
| JOP20190197A1 (ar) | 2017-02-24 | 2019-08-22 | Bayer Pharma AG | مثبط كيناز ايه تي آر للاستخدام في طريقة لعلاج مرض فرط التكاثر |
| WO2018153972A1 (fr) | 2017-02-24 | 2018-08-30 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de kinase atr et d'anti-androgènes |
| US11660301B2 (en) | 2017-02-24 | 2023-05-30 | Bayer Pharma Aktiengesellschaft | Combination of ATR kinase inhibitors with PARP inhibitors |
| WO2018206547A1 (fr) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combinaison d'inhibiteurs de bub1 et d'atr |
| WO2018218197A2 (fr) | 2017-05-26 | 2018-11-29 | Board Of Regents, The University Of Texas System | Inhibiteurs de la kinase atr à base de tétrahydropyrido[4,3-d]pyrimidine |
| US10377591B2 (en) | 2017-07-07 | 2019-08-13 | Zebra Technologies Corporation | Input handling for media processing devices |
| WO2019014618A1 (fr) | 2017-07-13 | 2019-01-17 | Board Of Regents, University Of Texas System | Inhibiteurs hétérocycliques de la kinase atr |
| CA3071795A1 (fr) | 2017-08-04 | 2019-02-07 | Bayer Aktiengesellschaft | Derives de 6-phenyl-4,5-dihydropyridazin-3(2h)-one utilises en tant qu'inhibiteurs de pde3a et pde3b pour le traitement du cancer |
| US11690911B2 (en) | 2017-08-04 | 2023-07-04 | Bayer Aktiengesellschaft | Combination of ATR kinase inhibitors and PD-1/PD-L1 inhibitors |
| JOP20200024A1 (ar) * | 2017-08-04 | 2020-02-02 | Bayer Ag | مركبات ثنائي هيدروكساديازينون |
| JP7290627B2 (ja) | 2017-08-17 | 2023-06-13 | ボード オブ レジェンツ,ザ ユニバーシティ オブ テキサス システム | Atrキナーゼの複素環式阻害剤 |
| WO2019057852A1 (fr) | 2017-09-22 | 2019-03-28 | Bayer Aktiengesellschaft | Utilisation de kap1 en tant que biomarqueur pour la détection ou la surveillance de l'inhibition d'atr chez un sujet |
| EP3461480A1 (fr) | 2017-09-27 | 2019-04-03 | Onxeo | Combinaison d'inhibiteurs de point de contrôle du cycle cellulaire de réponse à un dommage à l'adn et de belinostat pour traiter le cancer |
| EP3720973A1 (fr) | 2017-12-08 | 2020-10-14 | Bayer Aktiengesellschaft | Marqueurs prédictifs pour inhibiteurs d'atr kinase |
| DK3753937T3 (da) * | 2018-02-07 | 2024-02-12 | Wuxi Biocity Biopharmaceutics Co Ltd | Atr-hæmmer og anvendelse deraf |
| JP7341156B2 (ja) * | 2018-03-16 | 2023-09-08 | ボード オブ レジェンツ,ザ ユニバーシティ オブ テキサス システム | Atrキナーゼの複素環式阻害剤 |
| CN112823158B (zh) * | 2018-08-24 | 2023-08-15 | 拜耳股份有限公司 | 制备2-[(3r)-3-甲基吗啉-4-基]-4-(1-甲基-1h-吡唑-5-基)-8-(1h-吡唑-5-基)-1,7-二氮杂萘的方法 |
| WO2020078788A1 (fr) | 2018-10-16 | 2020-04-23 | Bayer Aktiengesellschaft | Combinaison d'inhibiteurs de kinase atr avec des composés de 2,3-dihydro-imidazo[1,2-c]quinazoline |
| AU2019373416A1 (en) * | 2018-10-30 | 2021-06-10 | Repare Therapeutics Inc. | Compounds, pharmaceutical compositions, and methods of preparing compounds and of their use as ATR kinase inhibitors |
| TWI750573B (zh) | 2019-02-01 | 2021-12-21 | 德商拜耳廠股份有限公司 | 1,2,4-三-3(2h)-酮化合物 |
| JP7677897B2 (ja) * | 2019-02-11 | 2025-05-15 | バイエル アクチェンゲゼルシャフト | 過剰増殖性疾患の治療における使用のためのatrキナーゼ阻害剤bay1895344 |
| CN112142744A (zh) * | 2019-06-28 | 2020-12-29 | 上海瑛派药业有限公司 | 取代的稠合杂芳双环化合物作为激酶抑制剂及其应用 |
| KR20220035925A (ko) * | 2019-07-22 | 2022-03-22 | 리페어 세라퓨틱스 인크. | Atr 키나제 억제제로서의 치환된 2-모르폴리노피리딘 유도체 |
| TW202128690A (zh) | 2019-11-21 | 2021-08-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 吡唑并雜芳基類衍生物、其製備方法及其在醫藥上的應用 |
| EP4072551A4 (fr) * | 2019-12-11 | 2023-11-15 | Repare Therapeutics Inc. | Utilisation d'inhibiteurs d'atr en association avec des inhibiteurs de parp |
| MX2022007265A (es) | 2019-12-20 | 2022-09-09 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
| UY38994A (es) | 2019-12-20 | 2021-07-30 | Nuevolution As | Compuestos activos frente a receptores nucleares |
| WO2021198956A1 (fr) | 2020-03-31 | 2021-10-07 | Nuevolution A/S | Composés actifs vis-à-vis des récepteurs nucléaires |
| AU2021245397A1 (en) | 2020-03-31 | 2022-10-20 | Nuevolution A/S | Compounds active towards nuclear receptors |
| TW202216701A (zh) * | 2020-07-03 | 2022-05-01 | 香港商德琪研發有限公司 | Atr抑制劑及其用途 |
| IL299804A (en) * | 2020-07-13 | 2023-03-01 | Beijing Tide Pharmaceutical Co Ltd | Pyrazolopyrimidine compounds for use as ATR kinase inhibitors |
| CN112110934B (zh) * | 2020-09-23 | 2021-12-07 | 上海应用技术大学 | 一种基于azd9291的生物标记物及其制备方法与应用 |
| US20240043419A1 (en) * | 2020-09-27 | 2024-02-08 | Medshine Discovery Inc. | Class of 1,7-naphthyridine compounds and application thereof |
| AU2021360636A1 (en) * | 2020-10-16 | 2023-06-15 | Shanghai De Novo Pharmatech Co., Ltd. | Triheterocyclic derivative, and pharmaceutical composition and application thereof |
| WO2022135560A1 (fr) * | 2020-12-25 | 2022-06-30 | Impact Therapeutics (Shanghai) , Inc | Composés imidazo[1,5-b]pyridazine substitués servant d'inhibiteurs de kinase et leur utilisation |
| AU2022271549A1 (en) * | 2021-05-12 | 2023-11-16 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Sulfoximine-containing atr inhibitor compound |
| KR20240012471A (ko) | 2021-05-21 | 2024-01-29 | 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 | 피라졸로헤테로아릴계 유도체의 약학적으로 허용 가능한 염 및 이의 결정형 |
| TW202321256A (zh) | 2021-07-27 | 2023-06-01 | 大陸商上海輝啟生物醫藥科技有限公司 | 8-氧-3-氮雜雙環[3.2.1]辛烷類化合物或其鹽及其製備方法和用途 |
| WO2023016529A1 (fr) * | 2021-08-11 | 2023-02-16 | 微境生物医药科技(上海)有限公司 | Dérivé de naphtyridine utile comme inhibiteur de l'atr et son procédé de préparation |
| CN116283960A (zh) | 2021-12-21 | 2023-06-23 | 上海安诺达生物科技有限公司 | 取代的稠杂环化合物及其制备方法与应用 |
| CN116731011A (zh) * | 2022-03-01 | 2023-09-12 | 武汉众诚康健生物医药科技有限公司 | 一种萘啶衍生物及其应用 |
| CN116925070B (zh) * | 2022-04-24 | 2026-03-17 | 扬子江药业集团有限公司 | 取代的氮杂稠环化合物及其医药用途 |
| US20250352539A1 (en) | 2022-06-15 | 2025-11-20 | Astrazeneca Ab | Combination therapy for treating cancer |
| WO2024188937A1 (fr) | 2023-03-13 | 2024-09-19 | Bayer Aktiengesellschaft | Associations d'inhibiteurs de kinase atr et d'inhibiteurs de parp pour traiter des affections hyper-prolifératives, par exemple un cancer |
| WO2025015238A2 (fr) * | 2023-07-12 | 2025-01-16 | Kansas State University Research Foundation | N-oxydes de n-méthylmorpholine substitués chiraux et leurs procédés de fabrication et d'utilisation |
| WO2025181153A1 (fr) | 2024-03-01 | 2025-09-04 | F. Hoffmann-La Roche Ag | Utilisation d'inhibiteurs d'atr en combinaison avec des inhibiteurs de pi3k alpha |
| WO2025229051A1 (fr) | 2024-05-03 | 2025-11-06 | F. Hoffmann-La Roche Ag | Utilisation d'inhibiteurs d'atr en combinaison avec un agent anti-androgène |
| WO2025233224A1 (fr) | 2024-05-09 | 2025-11-13 | F. Hoffmann-La Roche Ag | Utilisation d'inhibiteurs d'atr en combinaison avec une thérapie anti-pd(l)1 |
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