PL409463A1 - Kryształy (R) lub (S)-2-[[[3-metylo-4(2,2,2-trifluoroetoksy)-2-pirydynylo] metylo] sulfinylo]-1H-benzimidazolu, kompozycja farmaceutyczna zawierająca te kryształy i ich zastosowanie oraz sposób ich stabilizacji - Google Patents
Kryształy (R) lub (S)-2-[[[3-metylo-4(2,2,2-trifluoroetoksy)-2-pirydynylo] metylo] sulfinylo]-1H-benzimidazolu, kompozycja farmaceutyczna zawierająca te kryształy i ich zastosowanie oraz sposób ich stabilizacjiInfo
- Publication number
- PL409463A1 PL409463A1 PL409463A PL40946301A PL409463A1 PL 409463 A1 PL409463 A1 PL 409463A1 PL 409463 A PL409463 A PL 409463A PL 40946301 A PL40946301 A PL 40946301A PL 409463 A1 PL409463 A1 PL 409463A1
- Authority
- PL
- Poland
- Prior art keywords
- methyl
- crystals
- trifluoroethoxy
- sulfinyl
- benzimidazole
- Prior art date
Links
- 239000013078 crystal Substances 0.000 title abstract 6
- MJIHNNLFOKEZEW-VWLOTQADSA-N 2-[(s)-[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl]-1h-benzimidazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1C[S@](=O)C1=NC2=CC=CC=C2N1 MJIHNNLFOKEZEW-VWLOTQADSA-N 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
- MJIHNNLFOKEZEW-RUZDIDTESA-N dexlansoprazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1C[S@@](=O)C1=NC2=CC=CC=C2N1 MJIHNNLFOKEZEW-RUZDIDTESA-N 0.000 abstract 3
- -1 alkyl acetate Chemical compound 0.000 abstract 2
- 201000006549 dyspepsia Diseases 0.000 abstract 2
- 208000007882 Gastritis Diseases 0.000 abstract 1
- 206010061459 Gastrointestinal ulcer Diseases 0.000 abstract 1
- 241000590002 Helicobacter pylori Species 0.000 abstract 1
- 208000032843 Hemorrhage Diseases 0.000 abstract 1
- 206010020601 Hyperchlorhydria Diseases 0.000 abstract 1
- 206010025323 Lymphomas Diseases 0.000 abstract 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 abstract 1
- 208000005718 Stomach Neoplasms Diseases 0.000 abstract 1
- 208000013200 Stress disease Diseases 0.000 abstract 1
- 206010042220 Stress ulcer Diseases 0.000 abstract 1
- 208000025865 Ulcer Diseases 0.000 abstract 1
- 208000000718 duodenal ulcer Diseases 0.000 abstract 1
- 206010017758 gastric cancer Diseases 0.000 abstract 1
- 201000011587 gastric lymphoma Diseases 0.000 abstract 1
- 208000021302 gastroesophageal reflux disease Diseases 0.000 abstract 1
- 210000001035 gastrointestinal tract Anatomy 0.000 abstract 1
- 229940037467 helicobacter pylori Drugs 0.000 abstract 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 abstract 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 abstract 1
- 230000002980 postoperative effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 201000011549 stomach cancer Diseases 0.000 abstract 1
- 231100000397 ulcer Toxicity 0.000 abstract 1
Classifications
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- 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
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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
- A61K31/435—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
- A61K9/5078—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings with drug-free core
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P31/04—Antibacterial agents
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5026—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Przedmiotem wynalazku są kryształy (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu, które wytwarza się zgodnie ze sposobem, w którym krystalizuje się je w temperaturze od 0°C do 35°C z roztworu octanu C1-4-alkilu zawierającego (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazol o stężeniu od 0,1 g/ml do 0,5 g/ml. Przedmiotem wynalazku jest również kompozycja farmaceutyczna, zawierająca określone powyżej kryształy, która służy do zapobiegania lub leczenia wrzodów przewodu pokarmowego, zapalenia błony śluzowej żołądka, zapalenia przełyku z zarzucania treści żołądkowej, NUD (niestrawności niewrzodowej), raka żołądka, żołądkowego chłoniaka MALT, krwotoku z górnej części przewodu pokarmowego, wrzodu spowodowanego niesterydowym środkiem przeciwzapalnym, nadkwasoty i wrzodu spowodowanego stresem pooperacyjnym lub choroby spowodowanej Helicobacter pylori. Ponadto, przedmiotem wynalazku jest zastosowanie określonych powyżej kryształów do wytwarzania wspomnianej powyżej kompozycji farmaceutycznej. Przedmiotem wynalazku jest również sposób stabilizowania kryształów (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu, w którym krystalizuje się je w temperaturze od około 0°C do około 35°C z roztworu octanu C1-4-alkilu zawierającego (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazol w stężeniu od około 0,1 g/ml do około 0,5 g/ml.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000367757 | 2000-12-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL409463A1 true PL409463A1 (pl) | 2016-02-15 |
Family
ID=18838123
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL399787A PL399787A1 (pl) | 2000-12-01 | 2001-11-30 | Krysztaly (R)- lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu, kompozycja farmaceutyczna zawierajaca te krysztaly i ich zastosowanie |
| PL409463A PL409463A1 (pl) | 2000-12-01 | 2001-11-30 | Kryształy (R) lub (S)-2-[[[3-metylo-4(2,2,2-trifluoroetoksy)-2-pirydynylo] metylo] sulfinylo]-1H-benzimidazolu, kompozycja farmaceutyczna zawierająca te kryształy i ich zastosowanie oraz sposób ich stabilizacji |
| PL362801A PL214684B1 (pl) | 2000-12-01 | 2001-11-30 | Sposób wytwarzania krysztalów (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL399787A PL399787A1 (pl) | 2000-12-01 | 2001-11-30 | Krysztaly (R)- lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu, kompozycja farmaceutyczna zawierajaca te krysztaly i ich zastosowanie |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL362801A PL214684B1 (pl) | 2000-12-01 | 2001-11-30 | Sposób wytwarzania krysztalów (R) lub (S)-2-[[[3-metylo-4-(2,2,2-trifluoroetoksy)-2-pirydynylo]metylo]sulfinylo]-1H-benzimidazolu |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7285668B2 (pl) |
| EP (2) | EP1337525B8 (pl) |
| KR (3) | KR20100002278A (pl) |
| CN (1) | CN1254473C (pl) |
| AT (1) | ATE511508T1 (pl) |
| AU (1) | AU2002218506A1 (pl) |
| CA (1) | CA2436825C (pl) |
| CY (1) | CY1112347T1 (pl) |
| DK (1) | DK1337525T3 (pl) |
| ES (1) | ES2367419T3 (pl) |
| HK (1) | HK1054380B (pl) |
| HU (1) | HU229356B1 (pl) |
| NO (1) | NO326019B1 (pl) |
| PL (3) | PL399787A1 (pl) |
| PT (1) | PT1337525E (pl) |
| TW (1) | TWI290922B (pl) |
| WO (1) | WO2002044167A1 (pl) |
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| AU2004207720A1 (en) * | 2003-01-31 | 2004-08-12 | Teijin Pharma Limited | Crystal of (23S)-1alpha-hydroxy-27-nor-25-methylenevitamin D3-26,23-lactone and process for producing the same |
| US20050220870A1 (en) * | 2003-02-20 | 2005-10-06 | Bonnie Hepburn | Novel formulation, omeprazole antacid complex-immediate release for rapid and sustained suppression of gastric acid |
| MXPA06000524A (es) * | 2003-07-18 | 2006-08-11 | Santarus Inc | Formulacion farmaceutica y metodo para tratar desordenes gastrointestinales provocados por acido. |
| US8993599B2 (en) * | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| TWI398273B (zh) * | 2003-07-18 | 2013-06-11 | Santarus Inc | 用於抑制酸分泌之醫藥調配物及其製備及使用之方法 |
| US20070292498A1 (en) * | 2003-11-05 | 2007-12-20 | Warren Hall | Combinations of proton pump inhibitors, sleep aids, buffers and pain relievers |
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| EP1681056A1 (en) * | 2005-01-14 | 2006-07-19 | Krka Tovarna Zdravil, D.D., Novo Mesto | Process for preparing lansoprazole |
| CA2624179A1 (en) * | 2005-10-06 | 2007-04-12 | Auspex Pharmaceuticals, Inc. | Deuterated inhibitors of gastric h+, k+-atpase with enhanced therapeutic properties |
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| IT1391776B1 (it) * | 2008-11-18 | 2012-01-27 | Dipharma Francis Srl | Procedimento per la preparazione di dexlansoprazolo |
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| CN103254174B (zh) * | 2013-06-05 | 2014-06-11 | 湖北济生医药有限公司 | 一种兰索拉唑化合物及其药物组合物 |
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| CN104958276A (zh) * | 2015-07-30 | 2015-10-07 | 青岛蓝盛洋医药生物科技有限责任公司 | 一种治疗胃溃疡的药物兰索拉唑组合物胶囊 |
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| JPS6150978A (ja) | 1984-08-16 | 1986-03-13 | Takeda Chem Ind Ltd | ピリジン誘導体およびその製造法 |
| DK171989B1 (da) | 1987-08-04 | 1997-09-08 | Takeda Chemical Industries Ltd | Fremgangsmåde til fremstilling af 2-(2-pyridylmethylsulfinyl)-benzimidazoler |
| SE504459C2 (sv) * | 1994-07-15 | 1997-02-17 | Astra Ab | Förfarande för framställning av substituerade sulfoxider |
| HRP960232A2 (en) | 1995-07-03 | 1998-02-28 | Astra Ab | A process for the optical purification of compounds |
| JPH1085502A (ja) * | 1996-09-19 | 1998-04-07 | Konica Corp | 晶析方法 |
| TW385306B (en) | 1996-11-14 | 2000-03-21 | Takeda Chemical Industries Ltd | Method for producing crystals of benzimidazole derivatives |
| JP3828648B2 (ja) | 1996-11-14 | 2006-10-04 | 武田薬品工業株式会社 | 2−(2−ピリジルメチルスルフィニル)ベンズイミダゾール系化合物の結晶およびその製造法 |
| HUP9904073A3 (en) * | 1996-11-22 | 2000-04-28 | Procter & Gamble | Compositions for the treatment of gastrointestinal disorders containing bismuth and nsaid |
| AU2481899A (en) * | 1998-01-30 | 1999-08-16 | Sepracor, Inc. | S-lansoprazole compositions and methods |
| JP4536905B2 (ja) * | 1999-06-17 | 2010-09-01 | 武田薬品工業株式会社 | ベンズイミダゾール化合物の結晶 |
| JP3283252B2 (ja) * | 1999-06-17 | 2002-05-20 | 武田薬品工業株式会社 | ベンズイミダゾール化合物の結晶 |
| TWI275587B (en) * | 1999-06-17 | 2007-03-11 | Takeda Chemical Industries Ltd | A crystal of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole |
| WO2001002389A1 (en) * | 1999-06-30 | 2001-01-11 | Takeda Chemical Industries, Ltd. | Crystals of benzimidazole compounds |
| JP2001039975A (ja) * | 1999-07-26 | 2001-02-13 | Eisai Co Ltd | スルホキシド誘導体の結晶およびその製造法 |
| AU6727700A (en) | 1999-08-25 | 2001-03-19 | Takeda Chemical Industries Ltd. | Process for the preparation of optically active sulfoxide derivatives |
| KR100775802B1 (ko) | 2000-04-28 | 2007-11-12 | 다케다 야쿠힌 고교 가부시키가이샤 | 광학 활성 술폭시드 유도체의 제조 방법 |
| EP1897877B1 (en) | 2000-05-15 | 2014-09-24 | Takeda Pharmaceutical Company Limited | Crystalline forms of (R)-lanzoprazole |
| CN1117747C (zh) * | 2000-06-19 | 2003-08-13 | 中国科学院成都有机化学研究所 | 光学纯兰索拉唑的制备方法 |
-
2001
- 2001-11-30 CA CA2436825A patent/CA2436825C/en not_active Expired - Lifetime
- 2001-11-30 AU AU2002218506A patent/AU2002218506A1/en not_active Abandoned
- 2001-11-30 EP EP01998545A patent/EP1337525B8/en not_active Expired - Lifetime
- 2001-11-30 HK HK03106568.6A patent/HK1054380B/en not_active IP Right Cessation
- 2001-11-30 HU HU0400781A patent/HU229356B1/hu unknown
- 2001-11-30 PL PL399787A patent/PL399787A1/pl unknown
- 2001-11-30 EP EP10177469A patent/EP2345650A1/en not_active Ceased
- 2001-11-30 KR KR1020097023619A patent/KR20100002278A/ko not_active Ceased
- 2001-11-30 AT AT01998545T patent/ATE511508T1/de active
- 2001-11-30 KR KR1020087028441A patent/KR100939948B1/ko not_active Expired - Lifetime
- 2001-11-30 KR KR1020037007334A patent/KR100887912B1/ko not_active Expired - Lifetime
- 2001-11-30 CN CNB018198163A patent/CN1254473C/zh not_active Expired - Lifetime
- 2001-11-30 PL PL409463A patent/PL409463A1/pl unknown
- 2001-11-30 ES ES01998545T patent/ES2367419T3/es not_active Expired - Lifetime
- 2001-11-30 US US10/432,798 patent/US7285668B2/en not_active Expired - Lifetime
- 2001-11-30 DK DK01998545.6T patent/DK1337525T3/da active
- 2001-11-30 PT PT01998545T patent/PT1337525E/pt unknown
- 2001-11-30 TW TW090129629A patent/TWI290922B/zh not_active IP Right Cessation
- 2001-11-30 PL PL362801A patent/PL214684B1/pl unknown
- 2001-11-30 WO PCT/JP2001/010462 patent/WO2002044167A1/en not_active Ceased
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2003
- 2003-05-28 NO NO20032437A patent/NO326019B1/no not_active IP Right Cessation
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2007
- 2007-09-07 US US11/899,918 patent/US20080306118A1/en not_active Abandoned
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2011
- 2011-08-24 CY CY20111100809T patent/CY1112347T1/el unknown
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