KR950032111A - 당 알콜의 신규한 황산 에스테르 - Google Patents
당 알콜의 신규한 황산 에스테르 Download PDFInfo
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- KR950032111A KR950032111A KR1019950000506A KR19950000506A KR950032111A KR 950032111 A KR950032111 A KR 950032111A KR 1019950000506 A KR1019950000506 A KR 1019950000506A KR 19950000506 A KR19950000506 A KR 19950000506A KR 950032111 A KR950032111 A KR 950032111A
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Abstract
본 발명은 하기 일반식 ( I ) 의 당 알콜 및 당 알콜-유사 화합물 및 그의 염의 신규한 황산 에스테르에 관한 것이다.
상기식에서, A는 하나 이상의 하이드록시 그룹이 황산으로 에스테르화된, 1-하이드록시 그룹이 없는 당 알콜 또는 이들의 유도체의 잔기이거나 또는 트리스-(하이드록시메틸)메틸 잔기이고; X는 -NR1CO-, -NHCONH-, -NHCSNH-, -NHSO2-, -NR1또는 -O-이고; m 및 p는 각각 독립적으로 O 또는 1이고; R1은 수소, 저급-알킬 또는 하이드록시-저급-알킬이며; B는 공액화된 다중 결합 시스템이다.
또한 본 발명은 일반식 (I)의 화합물 또는 그의 염을 함유하는 약학 제제; 특히 혈관 벽에서의 동맥경화성변화의 치료 및/또는 예방(예 : 관상 또는 말단 혈관성형술 또는 보조 수술 후의 재발협착증의 예방)을 위한 약제로서의 일반식 (I)의 화합물 및 그의 염의 용도; 일반식 (I )의 화합물 및 그의 염의 제조 방법 뿐만 아니라 상기 징후를 위한 약제의 제조에 관한 것이다.
Description
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Claims (10)
- 하기 일반식 (I)의 화합물 및 그의 염 :상기식에서, A는 하나 이상의 하이드록시 그룹이 황산으로 에스테르화된, 1-하이드록시 그룹이 없는 당 알콜 또는 이들의 유도체의 잔기이거나 또는 트리스-(하이드록시메틸)메틸 잔기이고; X는 -NR1CO-, -NHCONH-, -NHCSNH-, -NHSO2-, -NR1또는 -O-이고; m 및 p는 각각 독립적으로 0 또는 1이고; R1은 수소, 저급-알킬 또는 하이드록시-저급-알킬이며; B는 공액화된 다중 결합 시스템이다.
- 제1항에 있어서, X가 -NR1CO-, -NHCONH-, -NHCSNH-, -NHSO2-또는 -O-이고; B가 공액화된 이중 결합 시스템인 화합물 및 그의 염.
- 제1항에 있어서, A가 -(CHR2)nCH2R2이고, n은 1 내지 5의 정수이고, R2는 H, -OSO3H 또는 OZ이고, Z가 보호그룹이고, 적어도 하나의 잔기 R2가 -OSO3H인 화합물.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 공액화된 다중 결합 시스템 B가 2 내지 8개의 공액화된 다중 결합을 지닌 폴리엔 또는 폴리린 탄화수소 잔기인 화합물.
- 제1항 내지 제4항 중 어느 한 항에 있어서, 상기 공액화된 다중 결합 시스템 B가 공액화된 이중 결합의 시스템인 화합물.
- 제5항에 있어서, 상기 공액화된 이중 결합 시스템이 방향족 고리 시스템인 화합물.
- 제6항에 있어서, 상기 방향족 고리 시스템이 페닐렌; 저급-알킬 치환된 페닐렌; 나프틸렌, 플루오레닐렌; 또는 하기 일반식 (a) 내지 (s)중 하나의 잔기인 화합물 :상기식에서, Y는 탄소-탄소 결합, -O-, -CO-, -CH2-, -CH2-CH2-, -C≡C-, -CH(O)CH-, -CH=CH-, -SO2-, -C(CF3)2-, -CONR1-, -NHC0NH-, -NHCOCONH-, 페닐렌 또는 페닐렌디옥시이고; R1은 수소, 저급-알킬 또는 하이드록시-저급-알킬이고; R3및 R4는 수소, 저급-알킬, 저급-알콕시, 할로겐 또는 -SO3H이고; R5는 저급-알콕시-저급-알콕시, 페녹시 또는 할로겐에 의해 치환된 페녹시이고; R6은 수소 또는 SO5H이고; D는 -CH2CH2- 또는 -CH=CH-이며; V는 -CH=CH-, -CH2CH2- 또는 단일 결합을 의미한다.
- (Z)-부텐디오산(Z)-〔3-비페닐-4-일옥시메틸-5-〔3-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일카바모일)-아크릴로일아미노〕-페닐아미드〕-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)-아미드 10나트륨 염, (E)-2-클로로스틸벤-4,4′-디카복실산 비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 10나트륨 염, (Z)-스틸벤-4,4′-디카복실산 비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 10나트륨 염,(2E,4E,6E,8E,1OE,12E,14E)-2,6,11,15-테트라메틸-헥사데카-2,4,6,8,10,12,14-헵타엔디카복실산 비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 1O나트륨 염,4,4′-에틸렌-디벤조산 비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 1O 나트륨 염, 3,3′-비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)-1,1′-톨루엔-2,6-디일)-디우레아 1O 나트륨 염, 4,4′-비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미노)-3,3′-디니트로-N,N′-(4,4′-메틸렌-디페닐)-디벤즈아미드 10나트륨 염. N,N′-비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-l-일)-2,2′-디니트로-4,4′-설포닐디아닐린 10나트륨 염, (Z)-스틸벤-4,4′-디카복실산 비스-(2,3,4,5,6-펜타-O-설포-L-람니트-1-일아미드) 8나트륨 염, 나프탈렌-1,5-디설폰산 비스-(2,3,4,5, 6-펜타-0-설포-D-글루시트-1-일아미드) 1O 나트륨 염, N,N′-비스-〔4-(2,3,4,5-테트라-O-설포-D-아라비니트-1-일옥시)-페닐〕-이소프탈아미드 8나트륨 염, 1,3-비스- 〔4-〔2,3,4,5,6-펜타-O-설포-D-갈락티트-6-일옥시)-페닐〕-우레아 10나트륨 염, N,N′-비스-〔4-〔3-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)-우레이도〕-페닐〕-이소프탈아미드 10나트륨 염, 9-옥소-9H-플루오렌-2,7-디카복실산 비스-〔메틸-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)아미드〕 10나트륨 염, 4,4′-메틸렌-디벤조산 비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 10나트륨 염, 나프탈렌-2,6-디카복실산 비스-(2,3.4,5,6-펜타-O-설포-D-글루시트-1-일아미드) 10나트륨 염, N.N′-비스-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)-이소프탈아미드 10나트륨 염, N,N′-비스-〔4-〔3-(2,3,4,5,6-펜타-O-설포-D-글루시트-1-일)-우레이도〕-페닐〕-푸마르아미드 1O나트륨 염, 4,4′-설포닐-디벤조산 비스-(2,3,4,5,6-펜타 -O-설포-D-글루시트-1-일아미드) 10나트륨 염.
- 특히 혈관벽중 동맥경화성 변화의 치료 및/또는 예방을 위한, 제1항 내지 제8항 중 어느 한 항에 따른 화합물, 및 치료적으로 불활성인 담체를 함유하는 약제.
- 제1항 내지 제8항 중 어느 한 항에 따른 화합물의 상응하는 비-황산화된 화합물을 황산화제와 반응시킴을 포함하는 제1항 내지 제8항 중 어느 한 항에 따른 화합물의 제조 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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CH114/94 | 1994-01-14 | ||
CH11494 | 1994-01-14 | ||
CH3315/94 | 1994-11-07 | ||
CH331594 | 1994-11-07 |
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KR950032111A true KR950032111A (ko) | 1995-12-20 |
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KR1019950000506A KR950032111A (ko) | 1994-01-14 | 1995-01-13 | 당 알콜의 신규한 황산 에스테르 |
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US (1) | US5521160A (ko) |
EP (1) | EP0663391B1 (ko) |
JP (1) | JP2862489B2 (ko) |
KR (1) | KR950032111A (ko) |
CN (1) | CN1043349C (ko) |
AT (1) | ATE151416T1 (ko) |
AU (1) | AU685196B2 (ko) |
CA (1) | CA2139720A1 (ko) |
CZ (1) | CZ8395A3 (ko) |
DE (1) | DE59500162D1 (ko) |
DK (1) | DK0663391T3 (ko) |
ES (1) | ES2101583T3 (ko) |
FI (1) | FI950127A (ko) |
GR (1) | GR3024012T3 (ko) |
HU (1) | HUT72412A (ko) |
IL (1) | IL112284A (ko) |
NO (1) | NO302817B1 (ko) |
NZ (1) | NZ270316A (ko) |
RU (1) | RU2139854C1 (ko) |
TW (1) | TW308598B (ko) |
UA (1) | UA42696C2 (ko) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2174582A1 (en) * | 1995-05-05 | 1996-11-06 | Alexander Chucholowski | Sulphuric acid esters of amino-sugars |
CA2174583A1 (en) * | 1995-05-05 | 1996-11-06 | Alexander Chucholowski | Sulfuric acid esters of sugar alcohols |
US7105552B2 (en) * | 1998-05-08 | 2006-09-12 | Theracos, Inc. | Heterocyclic analogs of diphenylethylene compounds |
US6245814B1 (en) | 1998-05-08 | 2001-06-12 | Calyx Therapeutics, Inc. | Diphenylethylene compounds |
US6331633B1 (en) | 1998-05-08 | 2001-12-18 | Calyx Therapeutics Inc. | Heterocyclic analogs of diphenylethylene compounds |
US6624197B1 (en) | 1998-05-08 | 2003-09-23 | Calyx Therapeutics, Inc. | Diphenylethylene compounds |
AU769489B2 (en) * | 1998-09-11 | 2004-01-29 | Ilexus Pty Limited | Fc receptor modulators and uses thereof |
US7407978B2 (en) * | 1999-04-06 | 2008-08-05 | Theracos, Inc. | Heterocyclic analogs of diphenylethylene compounds |
US20020002200A1 (en) * | 2000-02-04 | 2002-01-03 | Bishwagit Nag | Novel diphenylethylene compounds |
US20080108825A1 (en) * | 1999-11-08 | 2008-05-08 | Theracos, Inc. | Compounds for treatment of inflammation, diabetes and related disorders |
US7323496B2 (en) * | 1999-11-08 | 2008-01-29 | Theracos, Inc. | Compounds for treatment of inflammation, diabetes and related disorders |
US6525093B1 (en) * | 1999-11-08 | 2003-02-25 | Calyx Therapeutics Inc. | Compounds to treat diabetes and associated conditions |
US20080103302A1 (en) * | 2000-02-04 | 2008-05-01 | Theracos, Inc. | Compounds for treatment of inflammation, diabetes and related disorders |
US6635786B2 (en) * | 2001-01-16 | 2003-10-21 | Guilford Pharmaceuticals, Inc. | Symmetrically disubstituted aromatic compounds and pharmaceutical compositions for inhibiting poly (ADP-ribose) glycohydrolase, and methods for their use |
GB0228410D0 (en) | 2002-12-05 | 2003-01-08 | Glaxo Group Ltd | Novel Compounds |
CN1318479C (zh) * | 2002-12-11 | 2007-05-30 | 日产化学工业株式会社 | 新颖的二氨基苯衍生物、使用了该衍生物的聚酰亚胺前体和聚酰亚胺及液晶定向处理剂 |
JP6051998B2 (ja) | 2012-03-30 | 2016-12-27 | 日油株式会社 | マルチアーム型ポリエチレングリコール誘導体、その中間体及び製造方法 |
CN104768549A (zh) * | 2012-05-22 | 2015-07-08 | 耶路撒冷希伯来大学的益生研究开发有限公司 | 未分化细胞的选择性抑制剂 |
CN110092737B (zh) * | 2018-01-31 | 2022-06-17 | 海思美域(深圳)科技有限公司 | 一种抗静电化合物、材料的表面处理方法及改性材料 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3734815A1 (de) * | 1987-10-14 | 1989-04-27 | Luitpold Werk Chem Pharm | Polyschwefelsaeureester von bis-aldonsaeureamiden und deren derivaten, verfahren zu ihrer herstellung und arzneimittel |
DE3734853A1 (de) * | 1987-10-14 | 1989-04-27 | Luitpold Werk Chem Pharm | Bis-aldonsaeureamide und verfahren zu ihrer herstellung |
US5298616A (en) * | 1990-10-03 | 1994-03-29 | Hoffmann-La Roche Inc. | Sulfated O-polysaccharide-trehaloses |
CA2061370A1 (en) * | 1991-03-13 | 1992-09-14 | Markus Hosang | Pharmaceutical preparations |
-
1994
- 1994-12-20 TW TW083111951A patent/TW308598B/zh active
-
1995
- 1995-01-04 US US08/368,519 patent/US5521160A/en not_active Expired - Fee Related
- 1995-01-06 CA CA002139720A patent/CA2139720A1/en not_active Abandoned
- 1995-01-09 ES ES95100180T patent/ES2101583T3/es not_active Expired - Lifetime
- 1995-01-09 AT AT95100180T patent/ATE151416T1/de not_active IP Right Cessation
- 1995-01-09 IL IL11228495A patent/IL112284A/en not_active IP Right Cessation
- 1995-01-09 DK DK95100180.9T patent/DK0663391T3/da active
- 1995-01-09 EP EP95100180A patent/EP0663391B1/de not_active Expired - Lifetime
- 1995-01-09 HU HU9500052A patent/HUT72412A/hu unknown
- 1995-01-09 DE DE59500162T patent/DE59500162D1/de not_active Expired - Fee Related
- 1995-01-09 AU AU10106/95A patent/AU685196B2/en not_active Ceased
- 1995-01-10 NZ NZ270316A patent/NZ270316A/en unknown
- 1995-01-11 RU RU95100773A patent/RU2139854C1/ru active
- 1995-01-11 CN CN95101166A patent/CN1043349C/zh not_active Expired - Fee Related
- 1995-01-11 FI FI950127A patent/FI950127A/fi unknown
- 1995-01-12 CZ CZ9583A patent/CZ8395A3/cs unknown
- 1995-01-13 NO NO950137A patent/NO302817B1/no not_active IP Right Cessation
- 1995-01-13 UA UA95018035A patent/UA42696C2/uk unknown
- 1995-01-13 KR KR1019950000506A patent/KR950032111A/ko not_active Application Discontinuation
- 1995-01-13 JP JP7003729A patent/JP2862489B2/ja not_active Expired - Lifetime
-
1997
- 1997-07-08 GR GR970401667T patent/GR3024012T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
NO950137D0 (no) | 1995-01-13 |
US5521160A (en) | 1996-05-28 |
CZ8395A3 (en) | 1995-11-15 |
FI950127A0 (fi) | 1995-01-11 |
IL112284A (en) | 1998-10-30 |
TW308598B (ko) | 1997-06-21 |
EP0663391B1 (de) | 1997-04-09 |
JP2862489B2 (ja) | 1999-03-03 |
NO950137L (no) | 1995-07-17 |
CA2139720A1 (en) | 1995-07-15 |
CN1043349C (zh) | 1999-05-12 |
RU95100773A (ru) | 1996-10-27 |
DK0663391T3 (da) | 1997-10-20 |
RU2139854C1 (ru) | 1999-10-20 |
GR3024012T3 (en) | 1997-10-31 |
FI950127A (fi) | 1995-07-15 |
AU1010695A (en) | 1995-07-27 |
ATE151416T1 (de) | 1997-04-15 |
UA42696C2 (uk) | 2001-11-15 |
EP0663391A1 (de) | 1995-07-19 |
HUT72412A (en) | 1996-04-29 |
AU685196B2 (en) | 1998-01-15 |
ES2101583T3 (es) | 1997-07-01 |
NZ270316A (en) | 1996-08-27 |
NO302817B1 (no) | 1998-04-27 |
DE59500162D1 (de) | 1997-05-15 |
JPH07206803A (ja) | 1995-08-08 |
CN1109889A (zh) | 1995-10-11 |
IL112284A0 (en) | 1995-03-30 |
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