SG10201804868PA - Compounds for the inhibition of indoleamine-2,3-dioxygenase - Google Patents
Compounds for the inhibition of indoleamine-2,3-dioxygenaseInfo
- Publication number
- SG10201804868PA SG10201804868PA SG10201804868PA SG10201804868PA SG10201804868PA SG 10201804868P A SG10201804868P A SG 10201804868PA SG 10201804868P A SG10201804868P A SG 10201804868PA SG 10201804868P A SG10201804868P A SG 10201804868PA SG 10201804868P A SG10201804868P A SG 10201804868PA
- Authority
- SG
- Singapore
- Prior art keywords
- compounds
- dioxygenase
- ido
- indoleamine
- inhibition
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 102000006639 indoleamine 2,3-dioxygenase Human genes 0.000 title 1
- 108020004201 indoleamine 2,3-dioxygenase Proteins 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
- 239000005557 antagonist Substances 0.000 abstract 2
- IHWDSEPNZDYMNF-UHFFFAOYSA-N 1H-indol-2-amine Chemical compound C1=CC=C2NC(N)=CC2=C1 IHWDSEPNZDYMNF-UHFFFAOYSA-N 0.000 abstract 1
- -1 CYCLOHEXYL-ETHYL Chemical group 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000203 mixture Substances 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
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- 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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-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
CYCLOHEXYL-ETHYL SUBSTITUTED DIAZA- AND TRIAZA-TRICYCLIC COMPOUNDS AS INDOLE-AMINE-,3-DIOXYGENASE (IDO) ANTAGONISTS FOR THE TREATMENT OF CANCER The present invention relates to compounds, and pharmaceutically acceptable compositions thereof, useful as antagonists of IDO, and for the treatment of IDO-related disorders. (No suitable figure)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462046242P | 2014-09-05 | 2014-09-05 | |
| US201562151011P | 2015-04-22 | 2015-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG10201804868PA true SG10201804868PA (en) | 2018-07-30 |
Family
ID=54147306
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201700579XA SG11201700579XA (en) | 2014-09-05 | 2015-09-04 | Cyclohexyl-ethyl substituted diaza- and triaza-tricyclic compounds as indole-amine-2,3-dioxygenase (ido) antagonists for the treatment of cancer |
| SG10201804868PA SG10201804868PA (en) | 2014-09-05 | 2015-09-04 | Compounds for the inhibition of indoleamine-2,3-dioxygenase |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201700579XA SG11201700579XA (en) | 2014-09-05 | 2015-09-04 | Cyclohexyl-ethyl substituted diaza- and triaza-tricyclic compounds as indole-amine-2,3-dioxygenase (ido) antagonists for the treatment of cancer |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US9771370B2 (en) |
| EP (1) | EP3189054B1 (en) |
| JP (1) | JP6680766B2 (en) |
| KR (1) | KR20170044144A (en) |
| CN (1) | CN107074859B (en) |
| AU (1) | AU2015311826B2 (en) |
| BR (1) | BR112017003764A2 (en) |
| CA (1) | CA2956465A1 (en) |
| CL (1) | CL2017000420A1 (en) |
| ES (1) | ES2751602T3 (en) |
| IL (1) | IL250890B (en) |
| MX (1) | MX2017002365A (en) |
| PH (1) | PH12017500196A1 (en) |
| RU (1) | RU2017111200A (en) |
| SG (2) | SG11201700579XA (en) |
| WO (1) | WO2016037026A1 (en) |
| ZA (1) | ZA201700737B (en) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201311891D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compound |
| GB201311888D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| US20180228907A1 (en) | 2014-04-14 | 2018-08-16 | Arvinas, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
| SG11201700579XA (en) * | 2014-09-05 | 2017-02-27 | Merck Patent Gmbh | Cyclohexyl-ethyl substituted diaza- and triaza-tricyclic compounds as indole-amine-2,3-dioxygenase (ido) antagonists for the treatment of cancer |
| CN105884828A (en) * | 2015-02-16 | 2016-08-24 | 上海迪诺医药科技有限公司 | Polycyclic compound, pharmaceutical composition and application thereof |
| WO2016165613A1 (en) | 2015-04-12 | 2016-10-20 | Hangzhou Innogate Pharma Co., Ltd. | Heterocycles useful as ido and tdo inhibitors |
| GB201506872D0 (en) | 2015-04-22 | 2015-06-03 | Ge Oil & Gas Uk Ltd | Novel compounds |
| US10308647B2 (en) * | 2015-10-29 | 2019-06-04 | Scifluor Life Sciences, Inc. | Fused imidazole derivatives as IDO/TDO inhibitors |
| WO2017134555A1 (en) | 2016-02-02 | 2017-08-10 | Emcure Pharmaceuticals Limited | Derivatives of pyrroloimidazole or analogues thereof which are useful for the treatment of inter alia cancer |
| WO2017149469A1 (en) | 2016-03-03 | 2017-09-08 | Emcure Pharmaceuticals Limited | Heterocyclic compounds useful as ido and/or tdo modulators |
| CN105732643A (en) * | 2016-04-18 | 2016-07-06 | 苏州大学 | Conjugate and preparation method thereof and application to preparation of IDO enzyme inhibitor and non-steroidal anti-inflammatory drugs |
| CN107312005B (en) * | 2016-04-27 | 2021-12-17 | 上海翰森生物医药科技有限公司 | Fused imidazole derivative with IDO/TDO inhibitory activity and preparation method and application thereof |
| WO2017198159A1 (en) * | 2016-05-16 | 2017-11-23 | 鲁南制药集团股份有限公司 | Imidazole derivative containing bridge ring |
| CN107556316B (en) * | 2016-06-30 | 2021-11-12 | 鲁南制药集团股份有限公司 | Bridged ring-containing imidazole derivatives |
| CN107383012B (en) * | 2016-05-16 | 2021-09-28 | 鲁南制药集团股份有限公司 | Bicyclic imidazole alcohol derivatives |
| CN105902542A (en) * | 2016-05-16 | 2016-08-31 | 张阳 | Application of conjugate in preparation of medicine for treating cardiovascular diseases |
| CN107488179B (en) * | 2016-06-11 | 2024-06-07 | 鲁南制药集团股份有限公司 | Imidazole alcohol derivative containing bridged ring |
| WO2018028491A1 (en) * | 2016-08-09 | 2018-02-15 | 苏州国匡医药科技有限公司 | Indoleamine2,3-dioxygenase inhibitors and uses thereof in pharmacy |
| EP3505517A4 (en) | 2016-08-23 | 2020-01-15 | Beijing InnoCare Pharma Tech Co., Ltd. | FUSED HETEROCYCLIC DERIVATIVE, ITS PREPARATION METHOD AND ITS MEDICAL USE |
| WO2018045966A1 (en) * | 2016-09-12 | 2018-03-15 | 广州必贝特医药技术有限公司 | Imidazole-containing fused tricyclic compounds and applications thereof |
| EP3515914A4 (en) | 2016-09-24 | 2020-04-15 | BeiGene, Ltd. | INNOVATIVE 5- OR 8-SUBSTITUTED IMIDAZO [1,5-A] PYRIDINE AS SELECTIVE INHIBITORS OF INDOLEAMINE AND / OR TRYPTOPHANE-2,3-DIOXYGENASES |
| EP3560928B1 (en) * | 2016-12-20 | 2021-10-20 | Shenzhen Chipscreen Biosciences Co., Ltd. | Fused imidazole compound having indoleamine 2,3-dioxygenase inhibitory activity |
| SG10201911243WA (en) | 2016-12-22 | 2020-02-27 | Calithera Biosciences Inc | Compositions and methods for inhibiting arginase activity |
| CN110191709A (en) | 2017-01-17 | 2019-08-30 | 德州大学系统董事会 | It can be used as the compound of indole amine 2,3-dioxygenase and/or tryptophan dioxygenase inhibitor |
| WO2018175954A1 (en) * | 2017-03-23 | 2018-09-27 | F. Hoffmann-La Roche Ag | Synthesis of imidazo[5,1-a]isoindole derivative useful as ido inhibitors |
| EP3606528B1 (en) * | 2017-04-05 | 2023-10-18 | The Broad Institute, Inc. | Tricyclic compounds as glycogen synthase kinase 3 (gsk3) inhibitors and uses thereof |
| EP3645533B1 (en) * | 2017-06-28 | 2025-03-26 | Genentech, Inc. | Tdo2 and ido1 inhibitors |
| CN109384791B (en) * | 2017-08-09 | 2020-09-11 | 江苏恒瑞医药股份有限公司 | Crystal form of imidazo isoindole derivative free alkali and preparation method thereof |
| CN107501272B (en) * | 2017-09-05 | 2020-03-31 | 中国药科大学 | Imidazoisoindole IDO1 inhibitor, and preparation method and application thereof |
| CN108424414A (en) * | 2017-12-08 | 2018-08-21 | 苏州国匡医药科技有限公司 | Indoleamine 2,3-dioxygenase modulating compound of the one kind containing heterocycle and its purposes in pharmacy |
| EP3727374A4 (en) * | 2017-12-21 | 2021-11-10 | Merck Patent GmbH | COMBINATION OF AN ANTI-PD-L1 ANTIBODY AND AN IDO1 INHIBITOR FOR THE TREATMENT OF CANCER |
| CN111587116A (en) | 2018-01-05 | 2020-08-25 | 迪克纳制药公司 | Decrease β-catenin and IDO expression to enhance immunotherapy |
| US11046649B2 (en) | 2018-07-17 | 2021-06-29 | Board Of Regents, The University Of Texas System | Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase |
| PL237893B1 (en) | 2018-11-30 | 2021-06-14 | Univ Medyczny W Bialymstoku | New L-proline sulfonamide derivatives containing the pyrazolo [4,3-e] tetrazolo [4,5-b] [1,2,4] triazine system, the method of their preparation, their application and the pharmaceutical composition containing them |
| EP4052705A1 (en) | 2021-03-05 | 2022-09-07 | Universität Basel Vizerektorat Forschung | Compositions for the treatment of ebv associated diseases or conditions |
| MX2023010371A (en) | 2021-03-05 | 2024-02-12 | Univ Basel | Compositions for the treatment of ebv associated diseases or conditions. |
| CN113816965B (en) * | 2021-11-23 | 2022-03-08 | 北京鑫开元医药科技有限公司 | Compound with IDO (indomethacin diphosphate) inhibitory activity and preparation method thereof |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1307193A1 (en) | 2000-07-27 | 2003-05-07 | Affymax Research Institute | Agonists of follicle stimulating hormone activity |
| WO2010056567A1 (en) * | 2008-11-13 | 2010-05-20 | Merck Sharp & Dohme Corp. | Imidazoisoindole neuropeptide s receptor antagonists |
| NO2694640T3 (en) * | 2011-04-15 | 2018-03-17 | ||
| SG10201707545XA (en) | 2013-03-14 | 2017-10-30 | Newlink Genetics Corp | Tricyclic compounds as inhibitors of immunosuppression mediated by tryptophan metabolization |
| SG11201700579XA (en) * | 2014-09-05 | 2017-02-27 | Merck Patent Gmbh | Cyclohexyl-ethyl substituted diaza- and triaza-tricyclic compounds as indole-amine-2,3-dioxygenase (ido) antagonists for the treatment of cancer |
| GB201418300D0 (en) * | 2014-10-15 | 2014-11-26 | Redx Pharma Ltd | Compounds |
-
2015
- 2015-09-04 SG SG11201700579XA patent/SG11201700579XA/en unknown
- 2015-09-04 KR KR1020177007060A patent/KR20170044144A/en not_active Withdrawn
- 2015-09-04 BR BR112017003764A patent/BR112017003764A2/en not_active IP Right Cessation
- 2015-09-04 US US14/845,428 patent/US9771370B2/en not_active Expired - Fee Related
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| US20170355703A1 (en) | 2017-12-14 |
| ZA201700737B (en) | 2019-04-24 |
| US9771370B2 (en) | 2017-09-26 |
| KR20170044144A (en) | 2017-04-24 |
| RU2017111200A3 (en) | 2019-03-12 |
| MX2017002365A (en) | 2017-05-17 |
| JP2017525742A (en) | 2017-09-07 |
| AU2015311826B2 (en) | 2019-05-23 |
| EP3189054B1 (en) | 2019-07-24 |
| US10329297B2 (en) | 2019-06-25 |
| US20160075711A1 (en) | 2016-03-17 |
| CN107074859B (en) | 2021-08-06 |
| EP3189054A1 (en) | 2017-07-12 |
| JP6680766B2 (en) | 2020-04-15 |
| IL250890B (en) | 2019-12-31 |
| CA2956465A1 (en) | 2016-03-10 |
| CL2017000420A1 (en) | 2017-10-06 |
| BR112017003764A2 (en) | 2017-12-05 |
| SG11201700579XA (en) | 2017-02-27 |
| ES2751602T3 (en) | 2020-04-01 |
| RU2017111200A (en) | 2018-10-05 |
| IL250890A0 (en) | 2017-04-30 |
| CN107074859A (en) | 2017-08-18 |
| WO2016037026A1 (en) | 2016-03-10 |
| PH12017500196A1 (en) | 2017-07-10 |
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