KR970707108A - 항염증제로 유용한, 복소환부를 갖는 디-t-부틸페놀 화합물(DI-TERT-BUTYLPHENOL COMPOUNDS WITH HETEROCYCLIC MOIETY, USEFUL AS ANTI-INFLAMMATORY AGENTS) - Google Patents
항염증제로 유용한, 복소환부를 갖는 디-t-부틸페놀 화합물(DI-TERT-BUTYLPHENOL COMPOUNDS WITH HETEROCYCLIC MOIETY, USEFUL AS ANTI-INFLAMMATORY AGENTS)Info
- Publication number
- KR970707108A KR970707108A KR1019970702584A KR19970702584A KR970707108A KR 970707108 A KR970707108 A KR 970707108A KR 1019970702584 A KR1019970702584 A KR 1019970702584A KR 19970702584 A KR19970702584 A KR 19970702584A KR 970707108 A KR970707108 A KR 970707108A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- hydrogen
- unsubstituted
- methyl
- group
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D231/08—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with oxygen or sulfur atoms directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
본 발명은 하기 화학식(Ⅰ)의 구조를 갖는 화합물에 관한 것이다:
[식 중, a) 각각의 R은 독립적으로 탄소수 1 내지 7의 알킬이고; b) Z는 0 또는 N-X이고; c) X는 수소, 탄소수 1 내지 7의 알킬; C(O)Y, C(S)Y, 및 SO2Y이고;d) Y는 R', OR' 및 NR'2로부터 선택되고; e) 각각의 R'은 수소, 탄소수 1 내지 7의 알킬, 및 페닐로부터 선택된다].
또한 본 발명의 목적은 상기 화합물을 이용하여 염증 및/또는 통증을 치료하는 방법에 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (14)
- 하기 화학식(Ⅰ)의 화합물:[식 중, a) 각각의 R은 독립적으로 탄소수 1 내지 7의 알킬이고; b) Z는 0 또는 N-X이고; c) X는 수소, 탄소수 1 내지 7의 알킬, C(O)Y, C(S)Y, 및 SO2Y로 구성된 군으로부터 선택되고; d) Y는 R', OR' 및 NR'2구성된 군으로부터 선택되고; e) R'은 수소, 탄소수 1 내지 7의 알킬, 및 페닐로 구성된 군으로부터 선택된다].
- 제1항에 있어서, Z가 산소인 화합물.
- 제1항에 있어서, 각각의 R이 비치환된 C1-C3알카닐인 화합물.
- 제3항에 있어서, Z가 산소인 화합물.
- 제3항에 있어서, 양 R이 동일부인 화합물.
- 제5항에 있어서, 양 R이 메틸이고, Z가 산소인 화합물.
- 제3항에 있어서, Z가 N-X인 화합물.
- 제7항에 있어서, X가 수소 또는 비치환된 C1-C3알카닐이고, 양 R이 동일부인 화합물.
- 제7항에 있어서, X가 C(O)Y, C(S)Y, 및 SO2Y로 구성된 군으로부터 선택되고; R'은 수소 또는 비치환된 C1-C3알카닐이고; 양 R이 동일부인 화합물.
- 제9항에 있어서, X가 SO2Y이고 Y가 비치환된 C1-C3알카닐인 화합물.
- 제10항에 있어서, Y가 메틸이고, 양 R이 메틸인 화합물.
- 제8항에 있어서, 양 R이 메틸인 화합물.
- 하기를 함유하는 약제학적 조성물: (a) 안전 및 유효량의 청구항 1, 4, 6, 8 또는 9의 화합물; 및 (b) 약제학적으로 허용가능한 담체.
- 청구항 1, 4, 6, 8 또는 9의 화합물의 안전 및 유효량을 경구 투여하는 것으로 이루어진, 염증 및 통증의 치료방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8/326619 | 1994-10-20 | ||
US08/326,619 US5510361A (en) | 1994-10-20 | 1994-10-20 | Di-tert-butylphenol compounds with heterocyclic moiety, useful as anti-inflammatory agents |
US08/326619 | 1994-10-20 | ||
PCT/US1995/012878 WO1996012710A1 (en) | 1994-10-20 | 1995-10-18 | Di-tert-butylphenol compounds with heterocyclic moiety, useful as anti-inflammatory agents |
Publications (2)
Publication Number | Publication Date |
---|---|
KR970707108A true KR970707108A (ko) | 1997-12-01 |
KR100226509B1 KR100226509B1 (ko) | 1999-10-15 |
Family
ID=23272988
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019970702584A KR100226509B1 (ko) | 1994-10-20 | 1995-10-18 | 항염증제로 유용한, 복소환부를 갖는 디-t-부틸페놀 화합물 |
Country Status (8)
Country | Link |
---|---|
US (1) | US5510361A (ko) |
EP (1) | EP0787130A1 (ko) |
JP (1) | JPH10507754A (ko) |
KR (1) | KR100226509B1 (ko) |
AU (1) | AU705645B2 (ko) |
FI (1) | FI971674A0 (ko) |
NO (1) | NO971789L (ko) |
WO (1) | WO1996012710A1 (ko) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4408084A1 (de) * | 1994-03-10 | 1995-09-14 | Hoechst Ag | 3,5-Disubstituierte und 3,4,5-trisubstituierte 2-Isoxazoline und Isoxazole, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
JP3588734B2 (ja) * | 1996-07-26 | 2004-11-17 | コニカミノルタホールディングス株式会社 | 電子写真感光体 |
US5985930A (en) * | 1996-11-21 | 1999-11-16 | Pasinetti; Giulio M. | Treatment of neurodegenerative conditions with nimesulide |
DE60234057D1 (de) | 2001-07-25 | 2009-11-26 | Raptor Pharmaceutical Inc | Zusammensetzungen und verfahren zur modulation des transports durch die blut-hirn-schranke |
US6815555B2 (en) | 2001-09-26 | 2004-11-09 | Theravance, Inc. | Substituted phenol compounds useful for anesthesia and sedation |
US6555563B1 (en) | 2001-11-16 | 2003-04-29 | Medinox, Inc. | Heteroaryl substituted amidinyl and imidazolyl compounds and methods employing same for the treatment of inflammation |
US7479507B2 (en) * | 2003-01-14 | 2009-01-20 | Adam Heller | Anti-inflammatory substituted phenols and elastomeric compositions for oral delivery of drugs |
US20050003024A1 (en) * | 2003-03-04 | 2005-01-06 | The Procter & Gamble Company | Regulation of mammalian hair growth |
US20050255060A1 (en) * | 2004-05-10 | 2005-11-17 | Oblong John E | Personal care compositions and methods regulating mammalian hair growth |
US20050255059A1 (en) * | 2004-05-10 | 2005-11-17 | Oblong John E | Personal care compositions and methods regulating mammalian hair growth |
EP1889198B1 (en) | 2005-04-28 | 2014-11-26 | Proteus Digital Health, Inc. | Pharma-informatics system |
US20070203240A1 (en) * | 2006-02-27 | 2007-08-30 | The Procter & Gamble Company | Personal care compositions and methods for regulating mammalian hair growth |
WO2008036682A2 (en) | 2006-09-18 | 2008-03-27 | Raptor Pharmaceutical Inc. | Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates |
DK3395372T3 (da) | 2009-02-20 | 2022-04-19 | Enhanx Biopharm Inc | System til afgivelse af glutathion-baseret medikament |
EP2427178B1 (en) | 2009-05-06 | 2023-01-04 | Laboratory Skin Care, Inc. | Dermal delivery compositions comprising active agent-calcium phosphate particle complexes and methods of using the same |
US20120077778A1 (en) | 2010-09-29 | 2012-03-29 | Andrea Bourdelais | Ladder-Frame Polyether Conjugates |
EP2970125B1 (en) | 2013-03-14 | 2018-07-18 | Dart Neuroscience (Cayman) Ltd. | Substituted naphthyridine and quinoline compounds as mao inhibitors |
US9550754B2 (en) | 2014-09-11 | 2017-01-24 | AbbVie Deutschland GmbH & Co. KG | 4,5-dihydropyrazole derivatives, pharmaceutical compositions containing them, and their use in therapy |
Family Cites Families (14)
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GR61620B (en) * | 1976-10-14 | 1978-12-04 | Byk Gulden Lomberg Chem Fab | Preparation process of pyrazol-1-yl-phenyloxic acids |
US4535165A (en) * | 1981-11-23 | 1985-08-13 | Riker Laboratories, Inc. | Substituted diazoles and thiazoles |
JPS58148858A (ja) * | 1982-02-26 | 1983-09-05 | Yamanouchi Pharmaceut Co Ltd | 3,5−ジ−tert−ブチル−4−ヒドロキシフエニル置換複素環化合物 |
IE59813B1 (en) * | 1986-05-09 | 1994-04-06 | Warner Lambert Co | Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them |
JPH0615542B2 (ja) * | 1986-07-22 | 1994-03-02 | 吉富製薬株式会社 | ピラゾロピリジン化合物 |
US4724246A (en) * | 1986-12-10 | 1988-02-09 | Ciba-Geigy Corporation | Substituted 1,3,4-oxathiazol-2-one stabilizers |
DE3702757A1 (de) * | 1987-01-30 | 1988-08-11 | Hoechst Ag | Neue imidazo- und triazolo-thiadiazine, verfahren zu ihrer herstellung, die sie enthaltenden arzneimittel und ihre verwendung, sowie einige bei der herstellung der genannten verbindungen gebildete zwischenprodukte |
DE3702758A1 (de) * | 1987-01-30 | 1988-09-29 | Hoechst Ag | Substituierte 3-phenyl-7h-thiazolo (3,2-b) (1,2,4) triazin-7-one, verfahren zu ihrer herstellung, die sie enthaltenden arzneimittel und ihre verwendung, sowie einige bei der herstellung der genannten verbindungen gebildete zwischenprodukte |
DE3702756A1 (de) * | 1987-01-30 | 1988-08-11 | Hoechst Ag | 5-(3-alkyl-5-tert.butyl-4-hydroxyphenyl)-2- amino-6h-1,3,4-thiadiazine, verfahren zu ihrer herstellung, die sie enthaltenden arzneimittel und ihre verwendung |
JPH01180878A (ja) * | 1988-01-11 | 1989-07-18 | Yoshitomi Pharmaceut Ind Ltd | 縮合ピラゾール化合物 |
US5155122A (en) * | 1988-11-29 | 1992-10-13 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxyphenyl-1,3,4-thiadiazoles, and oxadiazoles and 3,5-di-tertiary-butyl-4-hydroxy-phenyl-1,2,4-thiadazoles, oxadiazoles and triazoles as antiinflammatory agents |
JPH02229169A (ja) * | 1989-03-01 | 1990-09-11 | Takeda Chem Ind Ltd | ピラゾロン誘導体 |
DE3918979A1 (de) * | 1989-06-10 | 1990-12-13 | Basf Ag | Verfahren zur herstellung von pyrazol und dessen derivaten |
DE4408084A1 (de) * | 1994-03-10 | 1995-09-14 | Hoechst Ag | 3,5-Disubstituierte und 3,4,5-trisubstituierte 2-Isoxazoline und Isoxazole, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
-
1994
- 1994-10-20 US US08/326,619 patent/US5510361A/en not_active Expired - Fee Related
-
1995
- 1995-10-18 EP EP95936860A patent/EP0787130A1/en not_active Withdrawn
- 1995-10-18 AU AU38598/95A patent/AU705645B2/en not_active Ceased
- 1995-10-18 KR KR1019970702584A patent/KR100226509B1/ko not_active IP Right Cessation
- 1995-10-18 WO PCT/US1995/012878 patent/WO1996012710A1/en not_active Application Discontinuation
- 1995-10-18 JP JP8513964A patent/JPH10507754A/ja active Pending
-
1997
- 1997-04-18 NO NO971789A patent/NO971789L/no unknown
- 1997-04-18 FI FI971674A patent/FI971674A0/fi unknown
Also Published As
Publication number | Publication date |
---|---|
NO971789D0 (no) | 1997-04-18 |
AU705645B2 (en) | 1999-05-27 |
MX9702941A (es) | 1997-07-31 |
US5510361A (en) | 1996-04-23 |
AU3859895A (en) | 1996-05-15 |
KR100226509B1 (ko) | 1999-10-15 |
FI971674A (fi) | 1997-04-18 |
EP0787130A1 (en) | 1997-08-06 |
JPH10507754A (ja) | 1998-07-28 |
NO971789L (no) | 1997-06-19 |
FI971674A0 (fi) | 1997-04-18 |
WO1996012710A1 (en) | 1996-05-02 |
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