ES2141137T3 - Agentes terapeuticos para la enfermedad de parkinson. - Google Patents
Agentes terapeuticos para la enfermedad de parkinson.Info
- Publication number
- ES2141137T3 ES2141137T3 ES93307654T ES93307654T ES2141137T3 ES 2141137 T3 ES2141137 T3 ES 2141137T3 ES 93307654 T ES93307654 T ES 93307654T ES 93307654 T ES93307654 T ES 93307654T ES 2141137 T3 ES2141137 T3 ES 2141137T3
- Authority
- ES
- Spain
- Prior art keywords
- straight
- alkoxy
- branched chain
- naphthyl
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- 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
-
- A—HUMAN NECESSITIES
- 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
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- A—HUMAN NECESSITIES
- 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
-
- 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
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
- C07D473/08—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
- C07D473/12—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1, 3, and 7, e.g. caffeine
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Radar Systems Or Details Thereof (AREA)
Abstract
SE PRESENTAN DERIVADOS DE LA XANTINA COMO AGENTES TERAPEUTICOS PARA LA ENFERMEDAD DE PARKINSON, QUE TIENEN LA FORMULA: EN QUE: R1 Y R2 REPRESENTAN CADA UNO METILO O ETILO; R3 REPRESENTA HIDROGENO, ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA O ALKINILO O ALKELINO C2-C6 DE CADENA RECTA O RAMIFICADA; R4 REPRESENTA CICLOALKILO C3-C8; UN GRUPO -(CH2)N-R5 DONDE N ES 0 O UN ENTERO DE 1 A 4 Y R5 REPRESENTA FENILO, NAFTILO O UN GRUPO HETEROCICLICO O UN GRUPO FENILO, NAFTILO O HETEROCICLICO SUSTITUIDO QUE CONTIENE DE 1 A 4 SUSTITUYENTES SELECCIONADOS DEL ALKILO C1-C6, ALCOXI C1-C6, HIDROXI, HALOGENO, NITRO, AMINO, MONO O DIALKILAMINO C1-C6, TIFLUOROMETILO, BENCILOXI, FENILO, FENOXI O ALCOXI C1-C6 SUSTITUIDO POR HIDROXI, ALCOXI C1-C6, HALOGENO, NITRO, AZIDA, CARBOXI O (C1-C6 ALCOXI)CARBONILO; O UN GRUPO DONDE Y1 E Y2 REPRESENTAN CADA UNO HIDROGENO, HALOGENO O ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA; Y Z REPRESENTA UN GRUPO EN QUE R6 REPRESENTA HIDROGENO, HIDROXI, ALKILO C1-C6 DE CADENA RECTA O RAMIFICADA, ALCOXI C1-C6 DE CADENA RECTA O RAMIFICADA, HALOGENO, NITRO O AMINO Y M REPRESENTA UN ENTERO DE 1 A 4; UN GRUPO FENILO, NAFTILO O HETEROCICLICO O UN GRUPO FENILO, NAFTILO O HETEROCICLICO SUSTITUIDO IGUAL A COMO SE HA DEFINIDO EN R5; Y X1 Y X2 REPRESENTA CADA UNO O O S; O UNA SAL FARMACEUTICAMENTE ACEPTABLE DE LOS MISMOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25783492 | 1992-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2141137T3 true ES2141137T3 (es) | 2000-03-16 |
Family
ID=17311787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES93307654T Expired - Lifetime ES2141137T3 (es) | 1992-09-28 | 1993-09-28 | Agentes terapeuticos para la enfermedad de parkinson. |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0590919B1 (es) |
| JP (1) | JP2613355B2 (es) |
| AT (1) | ATE188216T1 (es) |
| CA (1) | CA2107014C (es) |
| DE (1) | DE69327438T2 (es) |
| DK (1) | DK0590919T3 (es) |
| ES (1) | ES2141137T3 (es) |
| GR (1) | GR3032972T3 (es) |
| NO (1) | NO304946B1 (es) |
| PT (1) | PT590919E (es) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU6781194A (en) * | 1993-05-03 | 1994-11-21 | United States Of America, Represented By The Secretary, Department Of Health And Human Services, The | 8-substituted 1,3,7-trialkyl-xanthine derivatives as a2-selective adenosine receptor antagonists |
| GB9312853D0 (en) | 1993-06-22 | 1993-08-04 | Euro Celtique Sa | Chemical compounds |
| WO1995023148A1 (en) * | 1994-02-23 | 1995-08-31 | Kyowa Hakko Kogyo Co., Ltd. | Xanthine derivative |
| US5620676A (en) * | 1994-03-08 | 1997-04-15 | The United States Of America As Represented By The Department Of Health And Human Services | Biologically active ATP analogs |
| US5591776A (en) | 1994-06-24 | 1997-01-07 | Euro-Celtique, S.A. | Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV |
| US5922751A (en) | 1994-06-24 | 1999-07-13 | Euro-Celtique, S.A. | Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same |
| GB9415529D0 (en) | 1994-08-01 | 1994-09-21 | Wellcome Found | Phenyl xanthine derivatives |
| JPH10508032A (ja) * | 1994-12-13 | 1998-08-04 | ユーロ−セルティーク,エス.エイ. | アリールチオキサンチン類 |
| EP0799040B1 (en) | 1994-12-13 | 2003-08-20 | Euroceltique S.A. | Trisubstituted thioxanthines |
| US6166041A (en) | 1995-10-11 | 2000-12-26 | Euro-Celtique, S.A. | 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma |
| US6075016A (en) | 1996-04-10 | 2000-06-13 | Euro-Celtique S.A. | 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity |
| US5864037A (en) | 1996-06-06 | 1999-01-26 | Euro-Celtique, S.A. | Methods for the synthesis of chemical compounds having PDE-IV inhibitory activity |
| GB9703044D0 (en) | 1997-02-14 | 1997-04-02 | Glaxo Group Ltd | Phenyl xanthine esters and amides |
| ES2264210T3 (es) * | 1997-09-05 | 2006-12-16 | Kyowa Hakko Kogyo Co., Ltd. | Derivados de xantina para el tratamiento de la isquemia cerebral. |
| WO1999030715A1 (en) * | 1997-12-15 | 1999-06-24 | Kyowa Hakko Kogyo Co., Ltd. | Preventives/remedies for sleep disturbance |
| GB9817623D0 (en) | 1998-08-13 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
| AR023966A1 (es) * | 1999-05-12 | 2002-09-04 | Fujisawa Pharmaceutical Co | Una composicion farmaceutica para la prevencion y/o el tratamiento de la enfermedad de parkinson y los sintomas concomitantes de la misma, y el uso de unantagonista dual receptor de adenosina a1 a2a para preparar dicha composicion |
| AU7962000A (en) * | 1999-10-29 | 2001-05-14 | Kyowa Hakko Kogyo Co. Ltd. | Us0027324for eating disorders |
| SI1953162T1 (sl) * | 2001-02-24 | 2012-09-28 | Boehringer Ingelheim Pharma | Ksantinski derivati, njihova priprava in njihova uporaba kot zdravila |
| TWI330183B (es) | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
| US20060106040A1 (en) * | 2002-12-19 | 2006-05-18 | Michael Grzelak | Adenosine A2a receptor antagonists for the treatment of extra-pyramidal syndrome and other movement disorders |
| AU2004236101B2 (en) * | 2003-05-09 | 2010-11-11 | Kyowa Kirin Co., Ltd. | Microcrystal |
| TW200507882A (en) * | 2003-07-17 | 2005-03-01 | Kyowa Hakko Kogyo Kk | Solid formulations |
| TWI346114B (en) | 2003-09-29 | 2011-08-01 | Method for stabilization of diarylvinylene compounds | |
| WO2005072739A1 (ja) * | 2004-01-28 | 2005-08-11 | Kyowa Hakko Kogyo Co., Ltd. | 片頭痛の治療剤 |
| WO2006059713A1 (ja) * | 2004-12-03 | 2006-06-08 | Kyowa Hakko Kogyo Co., Ltd. | 薬物依存症の予防および/または治療剤 |
| KR20090094465A (ko) * | 2006-12-22 | 2009-09-07 | 슈바르츠 파르마 악티엔게젤샤프트 | 선택적 a2a 수용체 안타고니스토로서의 8-알키닐잔틴 유도체 |
| US8871751B2 (en) | 2008-01-18 | 2014-10-28 | The Board Of Trustees Of The University Of Illinois | Compositions and methods relating to nuclear hormone and steroid hormone receptors including inhibitors of estrogen receptor alpha-mediated gene expression and inhibition of breast cancer |
| WO2012070601A1 (ja) * | 2010-11-24 | 2012-05-31 | ヤマサ醤油株式会社 | 新規な2-アルキニル-n9-プロパギルアデニンおよびその医薬用途 |
| RU2477726C1 (ru) * | 2011-10-18 | 2013-03-20 | Общество С Ограниченной Ответственностью "Ньювак" (Ооо "Ньювак") | Замещенные феноксиуксусные кислоты, их эфиры и амиды, включающие 2,6-диоксо-2,3,6,7-тетрагидро-1н-пурин-8-иловый фрагмент, - антагонисты аденозинового a2a рецептора и их применение |
| RU2480469C1 (ru) * | 2012-02-03 | 2013-04-27 | Общество С Ограниченной Ответственностью "Ньювак" (Ооо "Ньювак") | Замещенные 1,3-диэтил-8-винил-7-метил-3,7-дигидро-пурин-2,6-дионы-антагонисты аденозинового a2a рецептора и их применение |
| CN103554109A (zh) * | 2013-11-15 | 2014-02-05 | 南京华威医药科技开发有限公司 | 伊曲茶碱多晶型 |
| CN105884776A (zh) * | 2014-11-05 | 2016-08-24 | 南京瑞天医药科技有限公司 | 一种伊曲茶碱的新晶型及其制备方法 |
| WO2016148260A1 (ja) * | 2015-03-17 | 2016-09-22 | 協和発酵キリン株式会社 | 医薬組成物 |
| CN107427518A (zh) * | 2015-03-19 | 2017-12-01 | 协和发酵麒麟株式会社 | 治疗及/或预防路易小体病的药剂 |
| WO2020125779A1 (en) * | 2018-12-21 | 2020-06-25 | Sunshine Lake Pharma Co., Ltd. | 8-substituted styryl xanthine derivatives and uses thereof |
| WO2020216152A1 (en) * | 2019-04-24 | 2020-10-29 | Dongguan Hec New Drug R&D Co., Ltd. | 8-substituted aryl vinyl xanthine derivatives and uses thereof |
| CN110041331B (zh) * | 2019-05-17 | 2020-08-07 | 广东东阳光药业有限公司 | 苯乙烯基黄嘌呤衍生物及其用途 |
| WO2021093701A1 (en) * | 2019-11-11 | 2021-05-20 | Sunshine Lake Pharma Co., Ltd. | 8-substituted styryl xanthine derivatives and uses thereof |
| CN111018856B (zh) * | 2019-12-12 | 2021-10-01 | 广东东阳光药业有限公司 | 8-取代的苯乙烯基黄嘌呤衍生物及其用途 |
| CN111072663B (zh) * | 2019-12-12 | 2021-10-01 | 广东东阳光药业有限公司 | 8-取代的苯乙烯基黄嘌呤衍生物及其用途 |
| JP7801234B2 (ja) * | 2020-03-10 | 2026-01-16 | マーベル・バイオテクノロジー | 障害を処置するためのプリン化合物 |
| CN111548351B (zh) * | 2020-06-22 | 2021-03-12 | 连云港贵科药业有限公司 | 一种伊曲茶碱的合成方法 |
| CN113248505B (zh) * | 2021-06-09 | 2021-09-21 | 南京安杰新生物医药有限公司 | 伊曲茶碱去甲基杂质的制备方法 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2729642A (en) * | 1954-08-13 | 1956-01-03 | Chattanooga Medicine Co | Water soluble salts of 8-(para-aminobenzyl) caffeine and method for their preparation |
| AT297021B (de) * | 1969-07-30 | 1972-03-10 | Parke Davis & Co | Verfahren zur Herstellung neuer Xanthinverbindungen |
| US3624216A (en) * | 1970-06-25 | 1971-11-30 | Abbott Lab | 8-substituted theophyllines as anti-inflammatory agents |
| US3624215A (en) * | 1970-06-25 | 1971-11-30 | Abbott Lab | 8-substituted theophyllines as anti-anxiety agents |
| US3900474A (en) * | 1973-05-14 | 1975-08-19 | Kendall & Co | Trifluoroalkyl, fluorobenzyl, pentafluorobenzyl, fluorobenzenesulfonyl, and pentafluorobenzenesulfonyl theophyllines |
| ES8303412A1 (es) * | 1981-10-06 | 1983-02-01 | Invest Tecnica Aplicada | Procedimiento de obtencion de nuevas xantinas con actividad farmacologica |
| US4452788A (en) * | 1982-04-21 | 1984-06-05 | Warner-Lambert Company | Substituted 8-phenylxanthines |
| FR2531085A1 (fr) * | 1982-07-28 | 1984-02-03 | Adir | Nouveaux derives de la xanthine, leur procede de preparation et les compositions pharmaceutiques les renfermant |
| US4593095A (en) * | 1983-02-18 | 1986-06-03 | The Johns Hopkins University | Xanthine derivatives |
| US4696932A (en) * | 1984-10-26 | 1987-09-29 | The United States Of America As Represented By The Department Of Health And Human Services | Biologically-active xanthine derivatives |
| GB8510758D0 (en) * | 1985-04-27 | 1985-06-05 | Wellcome Found | Compounds |
| HU197746B (en) * | 1985-09-05 | 1989-05-29 | Sandoz Ag | Process for producing xantin derivatives and pharmaceutical compositions containing them |
| US4755517A (en) * | 1986-07-31 | 1988-07-05 | Warner-Lambert Company | Derivatives of xanthine, pharmaceutical compositions and methods of use therefor |
| US4783530A (en) * | 1986-11-13 | 1988-11-08 | Marion Laboratories, Inc. | 8-arylxanthines |
| US4968672A (en) * | 1987-01-02 | 1990-11-06 | The United States Of America As Represented By The Department Of Health And Human Services | Adenosine receptor prodrugs |
| DE3843117A1 (de) * | 1988-12-22 | 1990-06-28 | Boehringer Ingelheim Kg | Neue xanthinderivate mit adenosin-antagonistischer wirkung |
| JPH06102662B2 (ja) * | 1989-09-01 | 1994-12-14 | 協和醗酵工業株式会社 | キサンチン誘導体 |
| FR2665636B1 (fr) * | 1990-08-10 | 1994-10-07 | Adir | Utilisation d'un derive de la trimethyl-1,3,7 xanthine pour le traitement des troubles de la memoire, des troubles intellectuels de la senescence et de la maladie d'alzheimer. |
| WO1992006976A1 (en) * | 1990-10-18 | 1992-04-30 | Kyowa Hakko Kogyo Co., Ltd. | Xanthine derivative |
| CA2093403C (en) * | 1992-04-08 | 1999-08-10 | Fumio Suzuki | Therapeutic agent for parkinson's disease |
-
1993
- 1993-09-22 JP JP5236176A patent/JP2613355B2/ja not_active Expired - Lifetime
- 1993-09-27 CA CA002107014A patent/CA2107014C/en not_active Expired - Lifetime
- 1993-09-27 NO NO933452A patent/NO304946B1/no not_active IP Right Cessation
- 1993-09-28 DK DK93307654T patent/DK0590919T3/da active
- 1993-09-28 DE DE69327438T patent/DE69327438T2/de not_active Expired - Lifetime
- 1993-09-28 EP EP93307654A patent/EP0590919B1/en not_active Expired - Lifetime
- 1993-09-28 PT PT93307654T patent/PT590919E/pt unknown
- 1993-09-28 AT AT93307654T patent/ATE188216T1/de not_active IP Right Cessation
- 1993-09-28 ES ES93307654T patent/ES2141137T3/es not_active Expired - Lifetime
-
2000
- 2000-03-16 GR GR20000400672T patent/GR3032972T3/el not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69327438T2 (de) | 2000-06-21 |
| NO933452L (no) | 1994-03-29 |
| NO933452D0 (no) | 1993-09-27 |
| CA2107014A1 (en) | 1994-03-29 |
| EP0590919A1 (en) | 1994-04-06 |
| DK0590919T3 (da) | 2000-04-17 |
| DE69327438D1 (de) | 2000-02-03 |
| CA2107014C (en) | 2000-06-13 |
| JPH06211856A (ja) | 1994-08-02 |
| JP2613355B2 (ja) | 1997-05-28 |
| GR3032972T3 (en) | 2000-07-31 |
| NO304946B1 (no) | 1999-03-08 |
| PT590919E (pt) | 2000-04-28 |
| EP0590919B1 (en) | 1999-12-29 |
| ATE188216T1 (de) | 2000-01-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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