KR930700494A - 신규한 옥사디논 유도체 - Google Patents
신규한 옥사디논 유도체Info
- Publication number
- KR930700494A KR930700494A KR1019920703171A KR920703171A KR930700494A KR 930700494 A KR930700494 A KR 930700494A KR 1019920703171 A KR1019920703171 A KR 1019920703171A KR 920703171 A KR920703171 A KR 920703171A KR 930700494 A KR930700494 A KR 930700494A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- alkyl group
- lower alkyl
- hydrogen atom
- atom
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 claims 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 12
- 125000002252 acyl group Chemical group 0.000 claims 11
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 230000008595 infiltration Effects 0.000 claims 2
- 238000001764 infiltration Methods 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 210000000440 neutrophil Anatomy 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 102000012479 Serine Proteases Human genes 0.000 claims 1
- 108010022999 Serine Proteases Proteins 0.000 claims 1
- 229940122055 Serine protease inhibitor Drugs 0.000 claims 1
- 101710102218 Serine protease inhibitor Proteins 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 239000002260 anti-inflammatory agent Substances 0.000 claims 1
- 229940121363 anti-inflammatory agent Drugs 0.000 claims 1
- 230000003110 anti-inflammatory effect Effects 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 239000003001 serine protease inhibitor Substances 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/20—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 4
- C07D265/22—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 하기 일반식[Ⅰ]으로 표시되는 신규한 옥사디논유도체 또는 약학적으로 허용되는 그것 들의 산부가염.
-
- 단, 식 중의 R1∼R4, A, X, Y 및 Z는 각각 다음의 의미를 갖는다. (R1) : 수소원자, 저급알킬기 또는 저급아실기; (R, R2) : 동일 또는 상이하며, 각각 수소원자, 저급알킬기 또는 저급알킬티오저급알킬기이다. 또는 R 및 R2가 함께되어서 알킬사슬로 이루어진 고리를 형성하여도 좋다; (R3) : 수소원자, 불소로 치환되어도 좋은 저급알킬기, 저급알콕시기 또는 할로겐원자; (R4) : 수소원자, 저급알킬기, 수산기, 할로겐원자, 저급알콕시기, 저급알콕시카르보닐기, 카르복실기, 저급알킬티오기, 니트로기, 저급아실록시기 또는 -NR5R6(R5및 R6은 동일 또는 상이하며 수소원자, 저급알킬기 또는 저급아실기이거나 또는 인접하는 질소원자와 함께 되어서 치환기를 갖고 있어서 좋은 헤테고리를 형성하여도 좋다);
-
- 이다. 단, * W는 단일결합, -O-,-S-, -CH=CH- 또는 -NR9-(R9는 수소원자, 저급알킬기 또는 저급아실기)이다; * U는 -CH- 또는 질소원자이다; * V1은 -O-, -S-, -CO-, -CHR10-(R10은 수소원자, 저급알킬기 또는 저급아실기) 또는 -NR11-(R11는 수소원자, 저급알킬기 또는 저급아실기)이다. 여기서 U가 질소원자일때는 V1은 -CO-, -CHR10-(R10은 상기와 같다) 또는 -NR11-(R11은 상기와 같다)이다; * T는 =CH- 또는 =N-이다; * R7및 R8은 동일 또는 상이하며, 각각 수소원자, 불소로 치환되어도 좋은 저급알킬기, 저급아실기, 할로겐원자, 수산기, 저급알콕시기, 저급아시록시기, 카르복실기, 또는 -NR13R14(R13및 R14는 동일 또는 상이하며, 각각 수소원자, 저급알킬기 또는 저급아실기를 의미한다)이다; * m, n은 독립하여 0 내지 2의 정수를 의미한다. (단, m+n<2); * D는 2개 이하의 치환기를 갖고 있어도 좋고, 또 복수의 헤테로원자를 함유하여도 좋은 5 내지 7원의 방향환 또는 치환이다. (Y) : 단일결합, -O-, -S-, -CO- 또는 -NR15-(R15는 수소원자, 저급알킬기 또는 저급아실기이다); (X) : 단일결합, -O-, -CH=CH- 또는 -NR16-(R16는 수소원자, 저급알킬기 또는 저급아실기이다); (Z) : -CH2- 또는 -CO-(단 Z가 -CH2-인 경우는 Y는 단일결합이다); (1) : 0 내지 4의 정수.
- 제1항에 있어서, D가
-
- 단 R17및 R18은 동일, 또는 상이하며, 각각 수소원자, 불소로 치환되어도 좋은 저급알킬기, 저급아실기, 할로겐원자, 수산기, 저급알콕시기, 저급아실록시, 카르복실기 또는 -NR19R20(R19및 R20은 동일 또는 상이하며, 각각 소수원자, 저급알킬기 또는 저급아실기를 의미한다)이다. 인 신규한 옥시디논유도체 또는 약학적으로 허용되는 그것들의 산부가염.
- 의약으로서 적당한 담체와 항염증작용적 유효량의 청구의 범위 제1항 또는 제2항 기재의 화합물을 함유하여 이루어지는 항염증제.
- 의약으로서 적당한 담체와 호중구 침윤억제작용적유효량의 청구의 범위 제1항 또는 제2항 기재의 화합물을 함유하여 이루어지는 호중구침윤억제제.
- 의약으로서 적당한 담체와, 세린프로테아제 저해작용적 유효량의 청구의 범위 제1항 또는 제2항 기재의 화합물을 함유하여 이루어지는 세린프로테아제저해제.
- ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP91-164060 | 1990-04-10 | ||
JP16406091 | 1991-04-10 | ||
PCT/JP1992/000444 WO1992018488A1 (fr) | 1991-04-10 | 1992-04-09 | Nouveau derive d'oxazinone |
Publications (1)
Publication Number | Publication Date |
---|---|
KR930700494A true KR930700494A (ko) | 1993-03-15 |
Family
ID=15786023
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920703171A KR930700494A (ko) | 1990-04-10 | 1992-04-09 | 신규한 옥사디논 유도체 |
Country Status (5)
Country | Link |
---|---|
US (1) | US5332734A (ko) |
EP (1) | EP0533951A4 (ko) |
KR (1) | KR930700494A (ko) |
CA (1) | CA2084997A1 (ko) |
WO (1) | WO1992018488A1 (ko) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05148249A (ja) * | 1991-11-28 | 1993-06-15 | Japan Tobacco Inc | ベンゾオキサジノン誘導体 |
US5985872A (en) * | 1995-05-24 | 1999-11-16 | G.D. Searle & Co. | 2-amino-benzoxazinones for the treatment of viral infections |
WO1997027200A1 (en) * | 1996-01-26 | 1997-07-31 | Smithkline Beecham Plc | Thienoxazinone derivatives useful as antiviral agents |
US8022058B2 (en) | 2000-05-10 | 2011-09-20 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7393652B2 (en) | 2000-05-10 | 2008-07-01 | The Trustees Of Columbia University In The City Of New York | Methods for identifying a chemical compound that directly enhances binding of FKBP12.6 to PKA-phosphorylated type 2 ryanodine receptor (RyR2) |
US7718644B2 (en) | 2004-01-22 | 2010-05-18 | The Trustees Of Columbia University In The City Of New York | Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof |
US7879840B2 (en) | 2005-08-25 | 2011-02-01 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7544678B2 (en) | 2002-11-05 | 2009-06-09 | The Trustees Of Columbia University In The City Of New York | Anti-arrythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) |
JP2007525165A (ja) | 2003-03-07 | 2007-09-06 | トラスティーズ・オブ・コロンビア・ユニバーシティ・イン・ザ・シティ・オブ・ニューヨーク | タイプ1ライアノジン受容体に基づく方法 |
US8710045B2 (en) | 2004-01-22 | 2014-04-29 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the ryanodine receptors |
EP1738176A1 (en) * | 2004-04-08 | 2007-01-03 | Janssen Pharmaceutica N.V. | Immunohistochemical detection method of collagen in a tissue sample |
US7704990B2 (en) | 2005-08-25 | 2010-04-27 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7879846B2 (en) * | 2006-09-21 | 2011-02-01 | Kyorin Pharmaceutical Co.., Ltd. | Serine hydrolase inhibitors |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4013665A (en) * | 1973-10-01 | 1977-03-22 | Bristol-Myers Company | Antiviral, substituted 1,3-dimethyl-1h-pyrazolo(3,4b)quinolines |
JPS5749620A (en) * | 1980-09-11 | 1982-03-23 | Teijin Ltd | Improvement of polyester |
CA1309556C (en) * | 1987-06-09 | 1992-10-27 | Masayuki Kokubo | 4h-3,1-benzoxazin-4-one compounds and pharmaceutical composition thereoffor the inhibition of serine proteases |
JP2765001B2 (ja) * | 1988-02-23 | 1998-06-11 | 武田薬品工業株式会社 | プロテアーゼ阻害剤 |
IL89835A0 (en) * | 1988-04-11 | 1989-12-15 | Merck & Co Inc | Substituted azetidinones,their preparation and pharmaceutical compositions containing them |
US5204462A (en) * | 1990-03-30 | 1993-04-20 | Japan Tobacco, Inc. | 4h-3,1-benzoxazin-4-one derivative |
FR2663633B1 (fr) * | 1990-06-22 | 1994-06-17 | Adir | Nouvelles chalcones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
-
1992
- 1992-04-09 EP EP19920908176 patent/EP0533951A4/en not_active Withdrawn
- 1992-04-09 KR KR1019920703171A patent/KR930700494A/ko not_active IP Right Cessation
- 1992-04-09 WO PCT/JP1992/000444 patent/WO1992018488A1/ja not_active Application Discontinuation
- 1992-04-09 US US07/956,029 patent/US5332734A/en not_active Expired - Fee Related
- 1992-04-09 CA CA002084997A patent/CA2084997A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP0533951A4 (en) | 1993-09-01 |
CA2084997A1 (en) | 1992-10-11 |
US5332734A (en) | 1994-07-26 |
EP0533951A1 (en) | 1993-03-31 |
WO1992018488A1 (fr) | 1992-10-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE174899T1 (de) | Zytotoxische stilben-derivate und diese enthaltende pharmazeutische zusammensetzungen | |
KR930700494A (ko) | 신규한 옥사디논 유도체 | |
KR950000728A (ko) | 포스포네이트 뉴클레오티드 에스테르 유도체 | |
RU95108387A (ru) | Дикетопиперазин, способ его получения, фармацевтическая композиция, применение дикетопиперазина | |
DK0889876T3 (da) | Meta-substituerede phenylensulfonamidderivater | |
KR970704710A (ko) | 트리아졸 화합물 및 도파민 D₃리간드로서의 그의 용도(Triazole Compounds and Their Use as Dopamine-D₃-Ligands) | |
KR910016697A (ko) | 테트라히드로피리딘 유도체 | |
ES8200011A1 (es) | Procedimiento de preparacion de una composicion farmaceuticaen particular psicotropa. | |
ES2051479T3 (es) | Uso de imidazoles substituidos en 4 para disminuir la presion intraocular. | |
KR970707108A (ko) | 항염증제로 유용한, 복소환부를 갖는 디-t-부틸페놀 화합물(DI-TERT-BUTYLPHENOL COMPOUNDS WITH HETEROCYCLIC MOIETY, USEFUL AS ANTI-INFLAMMATORY AGENTS) | |
DE69312567T2 (de) | 2-Formylpyridin-Thiosemicarbazonderivate, ihre Herstellung und ihre Verwendung als Antitumor Mittel | |
DK112688D0 (da) | Heterocykliske forbindelser | |
KR910014119A (ko) | 항-고혈압 활성을 갖는 티아졸리딘 유도체 및 그의 치료용도 | |
YU5199A (sh) | Farmaceutski proizvodi za lečenje i sprečavanje bolesti nastalih od oštećenja vaskularnih endotelialnih ćelija | |
AR007052A1 (es) | Un derivado de carbohidrato, su uso y una composicion farmaceutica que lo comprende | |
DE69330601D1 (de) | Serotoninergische ergolin derivate | |
HUP9601526A2 (hu) | Véralvadásgátló hatású peptidil-arginin-aldehid-származékok és a vegyületeket tartalmazó gyógyszerkészítmények | |
KR950701329A (ko) | 벤조티아졸술폰아미드 유도체, 그의 제조법 및 그 용도(Benzothiazolesulfornamide derivative, method for preparing the same, and use thereof) | |
KR950008515A (ko) | 피리도[1,2,3-d,e][1,3,4] 벤족사디아진 유도체 | |
KR890008121A (ko) | 로다닌 유도체 및 약제학적 조성물 | |
ATE1598T1 (de) | 5(10- 9)abeo-ergolin-derivate, ihre herstellung und sie enthaltende therapeutische zusammensetzungen. | |
WO2000024389A3 (en) | Benzoquinoline derivatives useful as antibacterial agents | |
NZ246598A (en) | Trazodone derivatives; compounds and preparation, pharmaceutical compositions; intermediate compounds | |
DK378087D0 (da) | Tetracycliske indolderivater | |
DK0944628T3 (da) | Hetero-biaryl-pyridoquinazolinonderivater som anti-cancermidler |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
SUBM | Surrender of laid-open application requested |