NO971672L - Benzofuran og benzokondenserte forbindelser, deres fremstilling og deres anvendelse som leukotrien B4(LTB4)antagonister - Google Patents
Benzofuran og benzokondenserte forbindelser, deres fremstilling og deres anvendelse som leukotrien B4(LTB4)antagonisterInfo
- Publication number
- NO971672L NO971672L NO971672A NO971672A NO971672L NO 971672 L NO971672 L NO 971672L NO 971672 A NO971672 A NO 971672A NO 971672 A NO971672 A NO 971672A NO 971672 L NO971672 L NO 971672L
- Authority
- NO
- Norway
- Prior art keywords
- ltb4
- antagonists
- compounds
- benzo
- heteroatoms
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/42—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4
- C07D311/56—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 without hydrogen atoms in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/14—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with at least one hydroxy group on a condensed ring system containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32287694A | 1994-10-13 | 1994-10-13 | |
PCT/IB1995/000401 WO1996011920A1 (en) | 1994-10-13 | 1995-05-26 | Benzopyran and benzo-fused compounds, their preparation and their use as leukotriene b4 (ltb4) antagonists |
Publications (2)
Publication Number | Publication Date |
---|---|
NO971672D0 NO971672D0 (no) | 1997-04-11 |
NO971672L true NO971672L (no) | 1997-06-11 |
Family
ID=23256829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO971672A NO971672L (no) | 1994-10-13 | 1997-04-11 | Benzofuran og benzokondenserte forbindelser, deres fremstilling og deres anvendelse som leukotrien B4(LTB4)antagonister |
Country Status (23)
Country | Link |
---|---|
US (2) | US6051601A (sh) |
EP (1) | EP0785930A1 (sh) |
JP (1) | JP2983295B2 (sh) |
KR (1) | KR100232341B1 (sh) |
CN (1) | CN1160399A (sh) |
AU (1) | AU696890B2 (sh) |
BR (1) | BR9504385A (sh) |
CA (1) | CA2201742A1 (sh) |
CO (1) | CO4480024A1 (sh) |
CZ (1) | CZ111797A3 (sh) |
FI (1) | FI971524A0 (sh) |
HU (1) | HUT77515A (sh) |
IL (1) | IL115529A0 (sh) |
MX (1) | MX9702731A (sh) |
NO (1) | NO971672L (sh) |
NZ (1) | NZ285156A (sh) |
PE (1) | PE10897A1 (sh) |
PL (1) | PL319688A1 (sh) |
RU (1) | RU2128655C1 (sh) |
TR (1) | TR199501270A2 (sh) |
TW (1) | TW304941B (sh) |
WO (1) | WO1996011920A1 (sh) |
ZA (1) | ZA958597B (sh) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SK31399A3 (en) * | 1996-09-16 | 2000-05-16 | Pfizer | Processes and intermediates for preparing substituted chromanol derivatives |
CA2274908A1 (en) * | 1996-12-13 | 1998-06-18 | Eli Lilly And Company | Leukotriene antagonists for cerebral focal stroke |
IL128731A0 (en) * | 1998-03-12 | 2000-01-31 | Pfizer Prod Inc | Method of preventing allograft rejection |
EP0963755A3 (en) * | 1998-04-16 | 2001-03-14 | Pfizer Products Inc. | Use of benzopyranes for preventing allograft rejection |
SE0004245D0 (sv) | 2000-11-20 | 2000-11-20 | Pharmacia Ab | Novel compounds and their use |
CA2433516A1 (en) * | 2001-01-30 | 2002-08-08 | Keith Michael Devries | Processes for preparing chromanylbenzoic acids |
AU4239302A (en) * | 2001-06-28 | 2003-01-02 | Pfizer Products Inc. | Benzoic acid substituted benzopyrans for the treatment of atherosclerosis |
WO2004000830A1 (en) | 2002-06-19 | 2003-12-31 | Biovitrum Ab | Novel compounds, their use and preparation |
CA2574627A1 (en) * | 2004-07-22 | 2006-02-02 | Pharmacia Corporation | Compositions for treatment of inflammation and pain using a combination of a cox-2 selective inhibitor and a ltb4 receptor antagonist |
US7674822B2 (en) | 2004-11-24 | 2010-03-09 | Wyeth | PTP1b inhibitors |
BRPI0519013A2 (pt) | 2004-12-13 | 2009-11-03 | Lilly Co Eli | composto ou esteroisÈmeros únicos, misturas de esteroisÈmeros, sais, tautÈmeros ou pró-drogas destes farmaceuticamente aceitáveis, composição farmacêutica, e, uso de um composto |
CA2600004A1 (en) | 2005-02-25 | 2006-09-08 | Eli Lilly And Company | Spiro-heterocyclic chromans, thiochromans and dihydroquinolines |
US7842713B2 (en) * | 2006-04-20 | 2010-11-30 | Pfizer Inc | Fused phenyl amido heterocyclic compounds |
US7928238B2 (en) | 2006-05-11 | 2011-04-19 | Janssen Pharmaceutica Nv | 1,2,3,4-tetrahydro-quinoline derivatives as CETP inhibitors |
JP2009536954A (ja) | 2006-05-11 | 2009-10-22 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Cetp阻害剤としての3,4−ジヒドロ−2h−ベンゾ[1,4]オキサジンおよびチアジン誘導体 |
PE20110303A1 (es) | 2008-09-11 | 2011-05-21 | Pfizer | Derivados de heteroaril acetamidas como activadores de glucoquinasa |
EP2406253B1 (en) | 2009-03-11 | 2013-07-03 | Pfizer Inc. | Benzofuranyl derivatives used as glucokinase inhibitors |
US9453022B2 (en) | 2012-02-14 | 2016-09-27 | Children's Hospital Medical Center | Use of small molecule inhibitors targeting the interaction between Rac GTPase and p67 (phox) |
CN102920692A (zh) * | 2012-10-25 | 2013-02-13 | 中国人民解放军第二军医大学 | (e)-2-(1-羟基-4-环己酮)乙基咖啡酸酯在制备防治类风湿关节炎的药物中的应用 |
SG11201707418WA (en) | 2015-03-13 | 2017-10-30 | Forma Therapeutics Inc | Alpha-cinnamide compounds and compositions as hdac8 inhibitors |
WO2017040963A1 (en) | 2015-09-03 | 2017-03-09 | Forma Therapeutics, Inc. | [6,6] fused bicyclic hdac8 inhibitors |
US10450309B2 (en) | 2015-11-30 | 2019-10-22 | Merch Sharp & Dohme Corp. | Aryl sulfonamides as BLT1 antagonists |
US10336733B2 (en) | 2015-11-30 | 2019-07-02 | Merk Sharp & Dohme Corp. | Aryl acylsulfonamides as BLT1 antagonists |
US20190382363A1 (en) * | 2015-11-30 | 2019-12-19 | Merck Sharp & Dohme Corp. | Aryl sulfonamides as blt1 antagonists |
EP3383389B1 (en) | 2015-11-30 | 2021-04-28 | Merck Sharp & Dohme Corp. | Aryl acylsulfonamides as blt1 antagonists |
WO2018071687A1 (en) * | 2016-10-13 | 2018-04-19 | The Regents Of The University Of California | Methods of treating pruritis |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4565882A (en) * | 1984-01-06 | 1986-01-21 | G. D. Searle & Co. | Substituted dihydrobenzopyran-2-carboxylates |
CA1320490C (en) * | 1987-01-12 | 1993-07-20 | Darrel M. Gapinski | Anti-inflammatory agents |
US4889871A (en) * | 1987-05-29 | 1989-12-26 | G. D. Searle & Co. | Alkoxy-substituted dihydrobenzopyran-2-carboxylate derivatives |
CA2019335C (en) * | 1989-06-27 | 2000-08-01 | Mitoshi Konno | Phenylalkan (en)oic acids |
US4996230A (en) * | 1990-02-16 | 1991-02-26 | Eli Lilly And Company | Leukotriene antagonists |
US5073562A (en) * | 1990-05-10 | 1991-12-17 | G. D. Searle & Co. | Alkoxy-substituted dihydrobenzopyran-2-carboxylic acids and derivatives thereof |
US5051438A (en) * | 1990-05-16 | 1991-09-24 | G. D. Searle & Co. | Alkoxy-substituted dihydrobenzopyran-2-carboxylic acids and derivatives thereof, compositions and use |
US5124350A (en) * | 1990-06-28 | 1992-06-23 | G. D. Searle & Co. | Leukotriene b4 antagonists |
MX9300312A (es) * | 1992-01-23 | 1993-07-31 | Pfizer | Antagonistas benzopiranicos y relacionado de ltb. |
WO1993015066A1 (en) * | 1992-01-23 | 1993-08-05 | Pfizer Inc. | Benzopyran and related ltb4 antagonists |
-
1995
- 1995-05-26 MX MX9702731A patent/MX9702731A/es unknown
- 1995-05-26 RU RU97105834A patent/RU2128655C1/ru active
- 1995-05-26 WO PCT/IB1995/000401 patent/WO1996011920A1/en not_active Application Discontinuation
- 1995-05-26 CA CA002201742A patent/CA2201742A1/en not_active Abandoned
- 1995-05-26 PL PL95319688A patent/PL319688A1/xx unknown
- 1995-05-26 CZ CZ971117A patent/CZ111797A3/cs unknown
- 1995-05-26 HU HU9702048A patent/HUT77515A/hu unknown
- 1995-05-26 CN CN95195608A patent/CN1160399A/zh active Pending
- 1995-05-26 JP JP8513057A patent/JP2983295B2/ja not_active Expired - Lifetime
- 1995-05-26 NZ NZ285156A patent/NZ285156A/xx unknown
- 1995-05-26 EP EP95918114A patent/EP0785930A1/en not_active Withdrawn
- 1995-05-26 US US08/809,728 patent/US6051601A/en not_active Expired - Fee Related
- 1995-05-26 AU AU24167/95A patent/AU696890B2/en not_active Ceased
- 1995-05-26 KR KR1019970702392A patent/KR100232341B1/ko not_active IP Right Cessation
- 1995-10-04 CO CO95046243A patent/CO4480024A1/es unknown
- 1995-10-06 IL IL11552995A patent/IL115529A0/xx unknown
- 1995-10-10 PE PE1995281391A patent/PE10897A1/es not_active Application Discontinuation
- 1995-10-11 BR BR9504385A patent/BR9504385A/pt not_active Application Discontinuation
- 1995-10-12 ZA ZA958597A patent/ZA958597B/xx unknown
- 1995-10-13 TW TW084110874A patent/TW304941B/zh active
- 1995-10-13 TR TR95/01270A patent/TR199501270A2/xx unknown
-
1997
- 1997-04-11 NO NO971672A patent/NO971672L/no not_active Application Discontinuation
- 1997-04-11 FI FI971524A patent/FI971524A0/fi unknown
-
2000
- 2000-01-28 US US09/493,707 patent/US6133286A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
IL115529A0 (en) | 1996-01-19 |
PL319688A1 (en) | 1997-08-18 |
CO4480024A1 (es) | 1997-07-09 |
FI971524A (fi) | 1997-04-11 |
CN1160399A (zh) | 1997-09-24 |
RU2128655C1 (ru) | 1999-04-10 |
EP0785930A1 (en) | 1997-07-30 |
HUT77515A (hu) | 1998-05-28 |
MX9702731A (es) | 1997-06-28 |
FI971524A0 (fi) | 1997-04-11 |
AU696890B2 (en) | 1998-09-24 |
US6051601A (en) | 2000-04-18 |
CA2201742A1 (en) | 1996-04-25 |
PE10897A1 (es) | 1997-04-21 |
JP2983295B2 (ja) | 1999-11-29 |
TR199501270A2 (tr) | 1996-06-21 |
BR9504385A (pt) | 1997-05-27 |
NO971672D0 (no) | 1997-04-11 |
WO1996011920A1 (en) | 1996-04-25 |
AU2416795A (en) | 1996-05-06 |
CZ111797A3 (cs) | 1998-07-15 |
ZA958597B (en) | 1997-04-14 |
JPH09512035A (ja) | 1997-12-02 |
US6133286A (en) | 2000-10-17 |
KR100232341B1 (ko) | 2000-07-01 |
NZ285156A (en) | 1999-01-28 |
TW304941B (sh) | 1997-05-11 |
KR970706270A (ko) | 1997-11-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO971672L (no) | Benzofuran og benzokondenserte forbindelser, deres fremstilling og deres anvendelse som leukotrien B4(LTB4)antagonister | |
DE60214996T2 (de) | Antagonisten der mcp-1-funktion und verfahren zu deren verwendung | |
DE60208159T2 (de) | Antagonisten von mcp-1 tätigkeit und deren verwendungsmethoden | |
NO971673L (no) | Benzopyran og benzokondenserte forbindelser, deres fremstiling og anvendelse som leukotrien B4 (LTB4) antagonister | |
DE69915508T2 (de) | Benzofuranderivate, verfahren zu ihrer herstellung und deren verwendungen | |
CN102227417B (zh) | 作为沉默调节蛋白调节剂的色烯酮类似物 | |
CN101248041A (zh) | 鞘氨醇激酶抑制剂 | |
JP2004532227A (ja) | ベータ−3アデノレセプタ作動薬として有用な2,6−置換クロマン誘導体 | |
AU2020354138B2 (en) | Heteroarylamidopyridinol derivative and pharmaceutical composition comprising same as active ingredient for prevention or treatment of autoimmune disease | |
HU211171A9 (en) | N-(3-hydroxy-4-piperidinyl)(dihydrobenzofuran, dihydro- 2h-benzopyran or dihydrobenzodioxin) carboxamide derivatives | |
DE69318238T2 (de) | Benzopyran-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Zellenschutzmittel | |
US20040167171A1 (en) | Benzo-fused 5-membered hetrocycle compounds, process for preparation of the same, and use thereof | |
JP2007520539A (ja) | カンナビノイド受容体モジュレーターとしてのピリジン誘導体 | |
CN115397412A (zh) | Mas相关g蛋白受体x4的调节剂及相关产物和方法 | |
NZ323543A (en) | Substituted 4-(1h-benzimidazol-2-yl-amino)piperidine derivatives useful for the treatment of allergic diseases | |
RU2154064C2 (ru) | N-замещенные пиперидинилбензоаты, их n-оксидные формы, фармацевтически приемлемые соли присоединения кислот и стереохимически изомерные формы, способы их получения, фармацевтическая композиция на их основе и промежуточный продукт | |
DE69330283T2 (de) | Neue 4-(3-benzofuranyl) piperidinyl und 4-(3-benzothienyl) piperidinyl-derivate und diese enthaltende pharmazeutische zusammenstellungen | |
JPS60184074A (ja) | 上昇した眼内圧の治療用の2‐スルフアモイルベンゾ〔b〕フラン誘導体 | |
JPH072850A (ja) | 新規(アリール(アルキル)カルボニル)ヘテロ環状 化合物 | |
KR20070012407A (ko) | 2-아미노피리미딘 유도체 | |
EP0699197B1 (en) | 4-p-fluorobenzoyl-1-piperidinyl-propoxy-chromen-4-one derivatives, their preparation and their use in the treatment of psychosis and schizophrenia | |
RU2004126953A (ru) | Производное пиперидина и фармацевтическая композиция, включающая его в качестве активного ингредиента | |
BR9707643A (pt) | Novas N-metil-n-(4-(piperidin-1-il)-2-(aril)butil)benzamidas substituídas úteis para o tratamento de doenças alérgicas | |
WO2012081570A1 (ja) | ラクタム化合物又はその塩及びppar活性化剤 | |
JP2022505401A (ja) | ムスカリンm1受容体陽性アロステリックモジュレーターとしてのピロロ-ピリダジン誘導体 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC2A | Withdrawal, rejection or dismissal of laid open patent application |