KR930700468A - 신규의 약학적 활성을 지닌 카테콜 유도체 - Google Patents
신규의 약학적 활성을 지닌 카테콜 유도체Info
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- KR930700468A KR930700468A KR1019920702604A KR920702604A KR930700468A KR 930700468 A KR930700468 A KR 930700468A KR 1019920702604 A KR1019920702604 A KR 1019920702604A KR 920702604 A KR920702604 A KR 920702604A KR 930700468 A KR930700468 A KR 930700468A
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- compound
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- dihydroxy
- methylidene
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- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
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- C07D233/96—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
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Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (43)
- 일반식(I)의 화합물 또는 약학적으로 적용가능한 그이 염 또는 에스테르.
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- 상기식중, R1은 니트로, 할로겐 또는 시아노기와 같은 전기적으로 음성인 치환체이며, R2는
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- [상기식중, X1,X2,Y 및 Z는 독립적으로 산소, 황 또는 NR(식중, R은 수소알킬, 시클로알킬, 아랄킬 또는 아릴기이다)을 나타낸다.]로 부터 선택된 그룹이다.
- 제1항에 있어서, R1이 시아노기인 화합물.
- 제1항에 있어서, R1이 니트로기인 화합물.
- 제1항에 있어서, R1이 할로겐인 화합물.
- 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식(Ia)그룹인 화합물.
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- 상기식중, X1및 X2는 모두 NR(식중, R은 수소 또는 알킬이다.)을 나타내며, Y는 산소 또는 황을 나타내며 Z도 산소 또는 황이다.
- 제5항에 있어서, 구조식(I)의 화합물이 4-〔(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2-티옥소이미다졸리딘-5-온, 4-〔(3,4-디히드록시-5-클로로페닐)메틸리덴]-2-티옥소이미다졸리딘-5-온 및 4-〔(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2,5-이미다졸리딘디온 중에서 선택된 화합물.
- 4-〔(3,4-디히드록시-5-시아노페닐)메틸리덴〕-2-티옥소이미다졸리딘-5-온 또는 약학적으로 적용 가능한 그의 염 또는 에스테르.
- 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식 (Ia)인 화합물.
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- 상기식중, X1,Y 및 Z는 각각 독립적으로 산소 또는 황을 NR(식중, R은 수소 또는알킬이다.)을 나타낸다.
- 제8항에 있어서, 구조식(I)의 화합물이 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2-티옥소티아졸리딘-4-온, 5-〔(3,4-디히드록시-5-니트로페닐)메틸리덴]-3-메틸-2-티옥소티아졸리딘-4-온, 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-티아졸리딘-2,4-디온, 5-[(3,4-디히드록시-5-클로로페닐)메틸리덴]-티아졸리딘-2,4-디온, 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-4-티옥소-2-옥사졸리딘 및 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-4-티옥소티아졸리딘-2-온 중에서 선택
- 5-[(3,4-디히드록시-5-시아노페닐)메틸리덴]-2-티옥소티아졸리딘-4-온 또는약학적으로 적용 가능한 그의 염 또는 에스테르.
- 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식(Ia)그룹인 화합물.
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- 상기식중, X, 및 Z는 독립적으로 산소 또는 황이며 Y 및 X2는 NR(식중, 은 수소이다.)을 나타낸다.
- 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-2-아미노티아졸리딘-4-온 또는 약학적으로 적용가능한 그의 염 또는 에스테르.
- 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 (Ia) 그룹이며, 그중 R2가
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- [상기식중, Y는 산소 또는 황이며, X1은 NR(식중, R은 수소 또는 알킬이다.)을 나타낸다.]인 화합물.
- 제13항에 있어서, Y가 산소인 화합물.
- 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-2,4,6(1H,3H,5h)-피리미딘트리온 또는 약학적으로 적용가능한 그의 염 또는 에스테르.
- 5-[(3,4,-디히드록시-5-니트로페닐)메틸]-(1H,3H,5H)-피리미딘-2,4,6-트리온 또는 약학적으로 적용가능한 그이 염 또는 에스테르.
- 제1항 낸지 16항에 있어서, 외과적 수술, 치료, 진단등의 의학적 방법에 사용되는 화합물.
- 제1항 내지 16항의 화합물과 약학적으로 적용가능한 담체 또는 희석제를 함유하는 약학적 조성물.
- 본 발명에서 사용하는 약제의 제조 및 지방 과산화에 의한 조직 손상의 치료를 위한 제1항 내지 16항의 화합물의 용도.
- 제19항에 있어서, 치료 또는 예방을 해야할 조직 손상의 상태가, 심장 질환, 류마티스 관절염, 종양, 염증 질환, 이식 부작용, 저혈, 노화인 화합물의 용도.
- 제1-16항의 화합물의 효과적인 양을 그 대상에 복용시키는 지방 과산화에 의한 조직 손상의 예방 및 치료방법.
- 구조식(Ⅱ) 화합물의 알데히드기를 활성 메틸렌기를 가진 구조식 (Ⅲ)또는 (Ⅳ)화합물과 축합시켜, R2가 구조식(Ia) 기인 구조식(Ⅰ)화합물을 얻은후, 구조식(Ⅰa) 기의 탄소 -탄소 이중결합을 환원시켜 R2가 본 발명의 구조식(Ib)기 인 구조식(Ⅰ) 화합물을 생성시키는 공정으로 행해지는 구조식(Ⅰ)화합물의 제조방법.
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- 상기식중, R1은 니트로, 할로겐, 시아노기와 같은 전기적으로 음성인 치환체이며, R2는
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- 상기식중,X1,X2,및 Z는 각각 독립적으로 산소, 황 또는 NR(식중,R은 수소, 알킬,시클로알킬, 아랄킬 또는 아릴기이다.)을 나타낸다.
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- 상기식중, R1은 상기한바와 같다.
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- 상기식중,X1,X2,Y및 Z는 상기한 바와 같다.
- ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909009565A GB9009565D0 (en) | 1990-04-27 | 1990-04-27 | New pharmacologically active catechol derivatives |
GB9101563.6 | 1991-01-24 | ||
GB919101563A GB9101563D0 (en) | 1991-01-24 | 1991-01-24 | New pharmacologically active catechol derivatives |
GB9009565.4 | 1991-01-24 | ||
PCT/FI1991/000124 WO1991017151A1 (en) | 1990-04-27 | 1991-04-26 | New pharmacologically active catechol derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
KR930700468A true KR930700468A (ko) | 1993-03-15 |
KR100207144B1 KR100207144B1 (en) | 1999-07-15 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920702604A KR100207144B1 (en) | 1990-04-27 | 1992-10-21 | New pharmacologically active catechol derivatives |
Country Status (17)
Country | Link |
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US (3) | US5362733A (ko) |
EP (1) | EP0526598B1 (ko) |
JP (1) | JP2972377B2 (ko) |
KR (1) | KR100207144B1 (ko) |
AT (1) | ATE146462T1 (ko) |
AU (1) | AU646464B2 (ko) |
CA (1) | CA2080917C (ko) |
DE (1) | DE69123738T2 (ko) |
FI (1) | FI95129C (ko) |
HU (1) | HU214872B (ko) |
IE (1) | IE911430A1 (ko) |
LT (1) | LT3137B (ko) |
LV (1) | LV10097B (ko) |
NO (1) | NO301928B1 (ko) |
PL (1) | PL166269B1 (ko) |
PT (1) | PT97507B (ko) |
WO (1) | WO1991017151A1 (ko) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1996022772A1 (en) * | 1995-01-23 | 1996-08-01 | Eli Lilly And Company | Method for treating multiple sclerosis |
AU5577498A (en) * | 1997-01-31 | 1998-08-25 | Shionogi & Co., Ltd. | Compounds having metalloprotease inhibitory activity |
EP1006794B1 (en) * | 1997-03-12 | 2007-11-28 | Robert W. Esmond | A method for treating or preventing alzheimer's disease |
US20040058873A1 (en) * | 1998-03-12 | 2004-03-25 | Esmond Robert W. | Method for treating or preventing Alzheimer's disease |
US6191154B1 (en) | 1998-11-27 | 2001-02-20 | Case Western Reserve University | Compositions and methods for the treatment of Alzheimer's disease, central nervous system injury, and inflammatory diseases |
WO2001030771A1 (fr) * | 1999-10-28 | 2001-05-03 | Kyowa Hakko Kogyo Co., Ltd. | Derives de thiazolidinedione |
WO2002053155A1 (en) * | 2000-12-30 | 2002-07-11 | Geron Corporation | Telomerase inhibitor |
MXPA04000695A (es) * | 2001-07-23 | 2005-08-26 | Galileo Pharmaceuticals Inc | Compuestos citoprotectores, formulaciones farmaceuticas y cosmeticas y metodos. |
US6679051B1 (en) * | 2002-07-31 | 2004-01-20 | Ford Global Technologies, Llc | Diesel engine system for use with emission control device |
RU2379299C2 (ru) | 2003-11-21 | 2010-01-20 | Актелион Фармасьютиклз Лтд | Производные 5-(бенз-(z)-илиден)тиазолидин-4-она и их применение в качестве иммуносупрессорных агентов |
USRE43833E1 (en) | 2003-11-21 | 2012-11-27 | Actelion Pharmaceuticals Ltd. | Thiazolidin-4-one derivatives |
US7872027B2 (en) * | 2006-02-17 | 2011-01-18 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Low molecular weight Myc-max inhibitors |
DK2094676T3 (da) * | 2006-11-23 | 2013-06-10 | Actelion Pharmaceuticals Ltd | Ny fremgangsmåde til fremstillingen af 2-iminothiazolidin-4-on-derivater |
US8912340B2 (en) | 2006-11-23 | 2014-12-16 | Actelion Pharmaceuticals Ltd. | Process for the preparation of 2-imino-thiazolidin-4-one derivatives |
FR2919608B1 (fr) * | 2007-08-01 | 2012-10-05 | Univ Rennes | Derives d'imidazolones,procede de preparation et applications biologiques |
US20100075926A1 (en) * | 2008-07-23 | 2010-03-25 | Li-Huei Tsai | Activation of histone deacetylase 1 (hdac1) protects against dna damage and increases neuronal survival |
KR101411838B1 (ko) * | 2011-02-09 | 2014-06-27 | 부산대학교 산학협력단 | 피부미백, 항산화 및 ppar 활성을 갖는 신규 화합물 및 이의 의학적 용도 |
DK2734510T3 (en) | 2011-07-22 | 2019-03-04 | Massachusetts Inst Technology | CLASS I-HISTONDEACETYLASES (HDAC) ACTIVATORS AND APPLICATIONS THEREOF |
PT2885266T (pt) | 2012-08-17 | 2020-05-29 | Actelion Pharmaceuticals Ltd | Processo para a preparação de (2z,5z)-5-(3-cloro-4-((r)-2,3-di-hidropropoxi)benzilideno)-2-(propilimino)-3-(o-tolil)tiazolidin-4-ona e intermediário utilizado no referido processo |
WO2017176812A1 (en) * | 2016-04-05 | 2017-10-12 | Immune Sensor, Llc | cGAS ANTAGONIST COMPOUNDS |
JPWO2022163843A1 (ko) * | 2021-02-01 | 2022-08-04 |
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DE1038050B (de) * | 1955-11-17 | 1958-09-04 | Farmaceutici Italia S A Soc | Verfahren zur Herstellung von 5-(3', 4'-Dioxybenzyliden)-Derivaten heterocyclischer Verbindungen |
US4013770A (en) * | 1972-06-16 | 1977-03-22 | Canada Packers Limited | Antiviral 5-(substituted benzal) hydantoins |
GB1434074A (en) * | 1972-06-16 | 1976-04-28 | Canada Packers Ltd | Antiviral compositions comprising hydantoin derivatives |
US4264617A (en) * | 1972-06-16 | 1981-04-28 | Canada Packers, Limited | Antiviral 5-(substituted benzal) hydantoins |
GB1601310A (en) * | 1978-05-23 | 1981-10-28 | Lilly Industries Ltd | Aryl hydantoins |
JPS5697277A (en) * | 1980-01-07 | 1981-08-05 | Takeda Chem Ind Ltd | Thiazolidine derivative |
DE3013626C2 (de) * | 1980-04-09 | 1985-06-27 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von 5-Arylidenhydantoinen (A) |
DE3013647C2 (de) * | 1980-04-09 | 1985-07-11 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von 5-Arylidenhydantoinen (B) |
JPS60233063A (ja) * | 1984-05-02 | 1985-11-19 | Showa Denko Kk | 5−ベンジリデンヒダントインの製造法 |
US4582903A (en) * | 1984-08-17 | 1986-04-15 | Stauffer Chemical Company | Synthesis of unsaturated hydantoins with an inexpensive catalyst |
US4650876A (en) * | 1984-08-17 | 1987-03-17 | Stauffer Chemical Company | Hydrogenation of substituted, unsaturated hydantoins to substituted, saturated hydantoins |
PT83152B (pt) * | 1985-08-09 | 1989-03-30 | Lilly Co Eli | Processo para a preparacao de compostos di-t-butilfenoicos |
US5208250A (en) * | 1988-05-25 | 1993-05-04 | Warner-Lambert Company | Known and selected novel arylmethylenyl derivatives of thiazolidinones, imidazolidinones and oxazolidinones useful as antiallergy agents and anti-inflammatory agents |
US5306822A (en) * | 1988-05-25 | 1994-04-26 | Warner-Lambert Company | Arylmethylenyl derivatives of oxazolidinone |
IE940525L (en) * | 1988-05-25 | 1989-11-25 | Warner Lambert Co | Known and selected novel arylmethylenyl derivatives of¹thiazolidinones, imidazolidinones and oxazolidinones useful¹as antiallergy agents and antiinflammatory agents |
GB8911073D0 (en) * | 1989-05-15 | 1989-06-28 | Fujisawa Pharmaceutical Co | New benzofuran derivatives,a process for the preparation thereof and pharmaceutical composition comprising the same |
JPH1052765A (ja) | 1996-08-09 | 1998-02-24 | Sukematsu Iwashita | 鉄筋材の圧接装置 |
-
1991
- 1991-04-26 WO PCT/FI1991/000124 patent/WO1991017151A1/en active IP Right Grant
- 1991-04-26 PL PL91296620A patent/PL166269B1/pl unknown
- 1991-04-26 DE DE69123738T patent/DE69123738T2/de not_active Expired - Fee Related
- 1991-04-26 AU AU77618/91A patent/AU646464B2/en not_active Ceased
- 1991-04-26 EP EP91920959A patent/EP0526598B1/en not_active Expired - Lifetime
- 1991-04-26 AT AT91920959T patent/ATE146462T1/de not_active IP Right Cessation
- 1991-04-26 US US07/949,477 patent/US5362733A/en not_active Expired - Fee Related
- 1991-04-26 HU HU9203369A patent/HU214872B/hu not_active IP Right Cessation
- 1991-04-26 CA CA002080917A patent/CA2080917C/en not_active Expired - Fee Related
- 1991-04-26 PT PT97507A patent/PT97507B/pt not_active IP Right Cessation
- 1991-04-26 JP JP3096814A patent/JP2972377B2/ja not_active Expired - Fee Related
- 1991-04-29 IE IE143091A patent/IE911430A1/en not_active IP Right Cessation
-
1992
- 1992-10-21 KR KR1019920702604A patent/KR100207144B1/ko not_active IP Right Cessation
- 1992-10-23 FI FI924838A patent/FI95129C/fi active
- 1992-10-26 LV LVP-92-185A patent/LV10097B/en unknown
- 1992-10-26 NO NO924132A patent/NO301928B1/no not_active IP Right Cessation
- 1992-11-17 LT LTIP227A patent/LT3137B/lt not_active IP Right Cessation
-
1994
- 1994-10-18 US US08/325,024 patent/US5614541A/en not_active Expired - Fee Related
-
1995
- 1995-06-07 US US08/472,658 patent/US5889037A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
HUT65662A (en) | 1994-07-28 |
FI95129C (fi) | 1995-12-27 |
LV10097A (lv) | 1994-05-10 |
PT97507A (pt) | 1992-01-31 |
LT3137B (en) | 1995-01-31 |
PL166269B1 (pl) | 1995-04-28 |
NO301928B1 (no) | 1997-12-29 |
KR100207144B1 (en) | 1999-07-15 |
IE911430A1 (en) | 1991-11-06 |
JP2972377B2 (ja) | 1999-11-08 |
EP0526598A1 (en) | 1993-02-10 |
PT97507B (pt) | 1998-08-31 |
HU214872B (hu) | 1998-07-28 |
US5362733A (en) | 1994-11-08 |
NO924132L (no) | 1992-12-23 |
LTIP227A (lt) | 1994-08-25 |
FI924838A (fi) | 1992-10-23 |
NO924132D0 (no) | 1992-10-26 |
AU646464B2 (en) | 1994-02-24 |
LV10097B (en) | 1995-02-20 |
US5614541A (en) | 1997-03-25 |
US5889037A (en) | 1999-03-30 |
WO1991017151A1 (en) | 1991-11-14 |
FI95129B (fi) | 1995-09-15 |
CA2080917A1 (en) | 1991-10-28 |
HU9203369D0 (en) | 1993-01-28 |
CA2080917C (en) | 2001-06-12 |
DE69123738T2 (de) | 1997-07-03 |
EP0526598B1 (en) | 1996-12-18 |
DE69123738D1 (en) | 1997-01-30 |
ATE146462T1 (de) | 1997-01-15 |
JPH05331148A (ja) | 1993-12-14 |
FI924838A0 (fi) | 1992-10-23 |
AU7761891A (en) | 1991-11-27 |
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