KR970707116A - 테트라히드로이소퀴놀린 유도체 및 그를 함유하는 의약 제제(tetrahydroisoquinoline derivative and medicinal preparation containing the same) - Google Patents
테트라히드로이소퀴놀린 유도체 및 그를 함유하는 의약 제제(tetrahydroisoquinoline derivative and medicinal preparation containing the same) Download PDFInfo
- Publication number
- KR970707116A KR970707116A KR1019970702878A KR19970702878A KR970707116A KR 970707116 A KR970707116 A KR 970707116A KR 1019970702878 A KR1019970702878 A KR 1019970702878A KR 19970702878 A KR19970702878 A KR 19970702878A KR 970707116 A KR970707116 A KR 970707116A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- aryl
- alkoxycarbonyl
- alkoxy
- alkylcarbonyloxy
- Prior art date
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Classifications
-
- 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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
본 발명은 피브리노겐 응집 억제 작용을 갖고, 항혈전제 또는 혈소판응집 저해제로서 유용하게 사용되는 하기 화학식(1)로 나타내는 테트라히드로이소퀴놀린 유도체 및 그를 함유하는 의약 제제에 관한 것이다.
상기 화학식(1)에서, B 및 G는 알킬 등으로 치환될 수 있는 알킬렌을 나타내며; D는 수소, 알킬 등을 나타내며; E는 R1내지 R4에 의해 치환될 수 있는 2위치에서 G와 결합하는 1,2,3,4-테트라히드로퀴놀린을 나타내며; R1내지 R4는 각각 알킬 등을 나타내며; L은 히드록시 등을 나타내며; A는 화학식(2)의 치환기를 나타내며; 그리고 C는 탄소를 나타낸다.
상기 식에서 M 및 R5내지 R8은 수소, 알킬 등을 나타낸다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (2)
- 하기 화학식(1)의 표시된 테트라히드로이소퀴놀린 유도체 :상기 화학식(1)에서, B 및 G는 독립적으로 치환기로 치환될 수 있는 (C : 0-10)알킬렌을 나타내며(상기 치환기는 (C : 0-10)알킬, 아릴(C : 0-8)알킬, (C : 0-10)알킬아미노, 아실아미노, (C : 0-10)알콕시, 아릴(C : 0-8)알콕시, (아릴((C : 0-8)알킬)아미노, 히드록시 또는 할로게노를 나타냄) ; D는 수소, (C : 0-10)알킬, (C : 0-10)알콕시카르보닐 또는 아릴(C : 0-8)알콕시카르보닐, (C : 0-10)아릴카르보닐옥시(C : 0-10)알콕시카르보닐 또는 아릴(C : 0-10)알킬카르보닐옥시(C : 0-10)알콕시카르보닐을 나타내며; E는 치환기 R1, R2, R3및 R4로 치환될 수 있고 2위치에서 G와 결합하는 1,2,3,4-테트라히드로이소퀴놀린을 나타내며 (상기 치환기 R1, R2, R3, 및 R4는 독립적으로 (C : 0-10)알킬, 아릴(C : 0-8)알콕시, (아릴(C : 0-8)알킬)아미노, 히드록시 또는 할로게노를 나타냄); L은 히드록시, (C : 0-10)알킬아미노, 디(C : 0-10)알킬아미노, (아릴(C : 0-10)알킬)아미노, (C : 0-10)알콕시, 아릴(C : 0-8)알콕시, (C : 0-10)알킬카르보닐옥시(C : 0-10)알콕시, 또는 아릴(C : 0-10)알킬카르보닐옥시(C : 0-10)알콕시를 나타내며; 그리고, A는 하기 화학식(2)로 표시된 치환기를 나타내며 C는 탄소를 나타낸다.상기 화학식(2)에서, M은 수소, (C : 0-10)알킬, (C : 0-10)알콕시카르보닐 또는 아릴(C : 0-8)알콕시카르보닐, (C : 0-10)알킬카르보닐옥시(C : 0-10)알콕시카르보닐, 또는 아릴(C : 0-10)알킬카르보닐옥시(C : 0-10)알콕시카르보닐을 나타내며; 그리고, R5, R6, R7, 및 R8은 독립적으로 수소, (C : 0-10)알킬, 아릴(C : 0-8)알킬, (C : 0-10)알킬아미노, 아실아미노, (C : 0-10)알콕시, 아릴(C : 0-8)알콕시, , 히드록시 또는 할로게노를 나타내며; C는 탄소를 나타낸다.
- 제1항의 테트라히드로이소퀴놀린 유도체를 함유하는 의학제제.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP94/269146 | 1994-11-01 | ||
JP26914694 | 1994-11-01 | ||
JP95/109194 | 1995-05-08 | ||
JP10919495 | 1995-05-08 | ||
PCT/JP1995/002201 WO1996013497A1 (fr) | 1994-11-01 | 1995-10-26 | Derive de tetrahydroisoquinoleine et preparation medicinale contenant ce derive |
Publications (1)
Publication Number | Publication Date |
---|---|
KR970707116A true KR970707116A (ko) | 1997-12-01 |
Family
ID=26448987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019970702878A KR970707116A (ko) | 1994-11-01 | 1995-10-26 | 테트라히드로이소퀴놀린 유도체 및 그를 함유하는 의약 제제(tetrahydroisoquinoline derivative and medicinal preparation containing the same) |
Country Status (7)
Country | Link |
---|---|
US (1) | US5789595A (ko) |
EP (1) | EP0790247A4 (ko) |
KR (1) | KR970707116A (ko) |
CN (1) | CN1167485A (ko) |
AU (1) | AU691677B2 (ko) |
CA (1) | CA2204006A1 (ko) |
WO (1) | WO1996013497A1 (ko) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7186855B2 (en) | 2001-06-11 | 2007-03-06 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
US6818787B2 (en) | 2001-06-11 | 2004-11-16 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
US8048917B2 (en) | 2005-04-06 | 2011-11-01 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
CN1874991A (zh) | 2003-08-29 | 2006-12-06 | 小野药品工业株式会社 | 能够结合s1p受体的化合物及其药物用途 |
KR20110140139A (ko) * | 2003-08-29 | 2011-12-30 | 오노 야꾸힝 고교 가부시키가이샤 | S1p 수용체 결합능을 갖는 화합물 및 그 의약 용도 |
CA2591399C (en) | 2004-12-13 | 2014-05-20 | Ono Pharmaceutical Co., Ltd. | Aminocarboxylic acid derivative and medicinal use thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5039805A (en) * | 1988-12-08 | 1991-08-13 | Hoffmann-La Roche Inc. | Novel benzoic and phenylacetic acid derivatives |
CA2037153A1 (en) * | 1990-03-09 | 1991-09-10 | Leo Alig | Acetic acid derivatives |
HUT68769A (en) * | 1991-05-07 | 1995-07-28 | Merck & Co Inc | FIBRINOGéN RECEPTOR ANTAGONIST COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM AS EFFECTIVE SUBSTANCE |
DE69213546T2 (de) * | 1991-05-13 | 1997-02-27 | Fujisawa Pharmaceutical Co | Neue Peptid-Verbindungen und Verfahren zur Herstellung davon |
IL110172A (en) * | 1993-07-22 | 2001-10-31 | Lilly Co Eli | Bicycle compounds and pharmaceuticals containing them |
-
1995
- 1995-10-26 CA CA002204006A patent/CA2204006A1/en not_active Abandoned
- 1995-10-26 US US08/836,521 patent/US5789595A/en not_active Expired - Fee Related
- 1995-10-26 EP EP95935571A patent/EP0790247A4/en not_active Withdrawn
- 1995-10-26 CN CN95196531A patent/CN1167485A/zh active Pending
- 1995-10-26 WO PCT/JP1995/002201 patent/WO1996013497A1/ja not_active Application Discontinuation
- 1995-10-26 AU AU37538/95A patent/AU691677B2/en not_active Ceased
- 1995-10-26 KR KR1019970702878A patent/KR970707116A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0790247A1 (en) | 1997-08-20 |
EP0790247A4 (en) | 2000-07-19 |
US5789595A (en) | 1998-08-04 |
WO1996013497A1 (fr) | 1996-05-09 |
AU691677B2 (en) | 1998-05-21 |
AU3753895A (en) | 1996-05-23 |
CA2204006A1 (en) | 1996-05-09 |
CN1167485A (zh) | 1997-12-10 |
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