AU2001253749A1 - 2-fluorobenzenesulfonyl compounds for the treatment of inflammation - Google Patents
2-fluorobenzenesulfonyl compounds for the treatment of inflammationInfo
- Publication number
- AU2001253749A1 AU2001253749A1 AU2001253749A AU5374901A AU2001253749A1 AU 2001253749 A1 AU2001253749 A1 AU 2001253749A1 AU 2001253749 A AU2001253749 A AU 2001253749A AU 5374901 A AU5374901 A AU 5374901A AU 2001253749 A1 AU2001253749 A1 AU 2001253749A1
- Authority
- AU
- Australia
- Prior art keywords
- fluorobenzenesulfonyl
- inflammation
- compounds
- treatment
- fluorobenzenesulfonyl compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/16—Halogen atoms or nitro radicals
-
- 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
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/46—Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/18—Radicals substituted by singly bound hetero atoms other than halogen by sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19953300P | 2000-04-25 | 2000-04-25 | |
US60199533 | 2000-04-25 | ||
US25338000P | 2000-11-27 | 2000-11-27 | |
US60253380 | 2000-11-27 | ||
PCT/US2001/012983 WO2001081332A2 (en) | 2000-04-25 | 2001-04-20 | 2-fluorobenzenesulfonyl compounds for the treatment of inflammation |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001253749A1 true AU2001253749A1 (en) | 2001-11-07 |
Family
ID=26894867
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001253749A Abandoned AU2001253749A1 (en) | 2000-04-25 | 2001-04-20 | 2-fluorobenzenesulfonyl compounds for the treatment of inflammation |
AU2001255600A Abandoned AU2001255600A1 (en) | 2000-04-25 | 2001-04-20 | Regioselective synthesis of 3,4-di(carbocyclyl or heterocyclyl)thiophenes |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001255600A Abandoned AU2001255600A1 (en) | 2000-04-25 | 2001-04-20 | Regioselective synthesis of 3,4-di(carbocyclyl or heterocyclyl)thiophenes |
Country Status (5)
Country | Link |
---|---|
US (2) | US20020183362A1 (en) |
EP (2) | EP1276736A2 (en) |
JP (2) | JP2003531202A (en) |
AU (2) | AU2001253749A1 (en) |
WO (2) | WO2001081332A2 (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2002119574A (en) | 1999-12-23 | 2004-01-10 | Нитромед, Инк. (Us) | Nitrosated and nitrosylated cyclooxygenase-2 inhibitors, compositions based on them and methods for their use |
US20040092552A1 (en) * | 2000-04-25 | 2004-05-13 | Brown David L | 2-Fluorobenzenesulfonyl compounds for the treatment of inflammation |
US20020183362A1 (en) * | 2000-04-25 | 2002-12-05 | Pharmacia Corporation | 2-Fluorobenzenesulfonyl compounds for the treatment of inflammation |
US20030232996A1 (en) * | 2001-04-20 | 2003-12-18 | Brown David L | Regioselective synthesis of 3,4-di{(carboclyl or heterocyclyl)thiophenes |
RU2004132721A (en) | 2002-04-08 | 2005-06-27 | Глэксо Груп Лимитед (GB) | (2-Alcoxy) phenyl) Cyclopent-1-Enyl) Aromatic Carboxylic acid and Heterocyclic Carbonic Acid and its derivatives |
GB0221443D0 (en) * | 2002-09-16 | 2002-10-23 | Glaxo Group Ltd | Pyridine derivates |
CA2505945A1 (en) * | 2002-12-02 | 2004-06-17 | Fujisawa Pharmaceutical Co., Ltd. | Pyrazole derivatives useful as cox-i inhibitors |
EP2067776A1 (en) | 2003-07-24 | 2009-06-10 | Euro-Celtique S.A. | Piperidine compounds and pharmaceutical compositions containing them |
ITMI20040019A1 (en) * | 2004-01-12 | 2004-04-12 | Univ Bari | ISOSSAZOLIC DERIVATIVES AND THEIR USE AS CYCLOSXYGENASE INHIBITORS |
CA2584317A1 (en) * | 2004-10-15 | 2006-04-27 | Memory Pharmaceuticals Corporation | Pyrazole derivatives as phosphodiesterase 4 inhibitors |
WO2007076039A2 (en) * | 2005-12-20 | 2007-07-05 | Massachusetts Institute Of Technology | Communications and power harvesting system for in-pipe wireless sensor networks |
NL2000351C2 (en) | 2005-12-22 | 2007-09-11 | Pfizer Prod Inc | Estrogen modulators. |
AU2007292436A1 (en) * | 2006-09-07 | 2008-03-13 | Allergan, Inc. | Heteroaromatic compounds having sphingosine-1-phosphate (S1P) receptor agonist biological activity |
CA2685266C (en) | 2007-04-27 | 2014-01-28 | Purdue Pharma L.P. | Trpv1 antagonists and uses thereof for the treatment of prevention of pain, ui and ulcer, ibd, or ibs in an animal |
US7989450B2 (en) | 2008-01-11 | 2011-08-02 | Universita' Degli Studi Di Bari | Functionalized diarylisoxazoles inhibitors of ciclooxygenase |
CA2894399A1 (en) | 2012-12-06 | 2014-06-12 | Quanticel Pharmaceuticals, Inc. | Histone demethylase inhibitors |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4820827A (en) | 1982-03-03 | 1989-04-11 | E. I. Du Pont De Nemours And Company | 2,3-diaryl-5-bromothiophene compounds of use for the treatment of inflammaton and dysmenorrhea |
US5663180A (en) * | 1983-10-29 | 1997-09-02 | G.D. Searle & Co. | Substituted cyclopentenes for the treatment of inflammation |
US5571810A (en) | 1990-06-11 | 1996-11-05 | Fujisawa Pharmaceutical Co., Ltd. | Thiophene derivatives |
GB9012936D0 (en) | 1990-06-11 | 1990-08-01 | Fujisawa Pharmaceutical Co | Thiophene derivatives,processes for preparation thereof and pharmaceutical composition comprising the same |
DK0679157T3 (en) | 1993-01-15 | 1998-07-27 | Searle & Co | Novel 3,4-diarylthiophenes and analogs thereof for use as anti-inflammatory agents |
AU6718494A (en) * | 1993-05-13 | 1994-12-12 | Merck Frosst Canada Inc. | 2-substituted-3,4-diarylthiophene derivatives as inhibitors of cyclooxygenase |
US5380738A (en) * | 1993-05-21 | 1995-01-10 | Monsanto Company | 2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents |
GB9602877D0 (en) | 1996-02-13 | 1996-04-10 | Merck Frosst Canada Inc | 3,4-Diaryl-2-hydroxy-2,5- dihydrofurans as prodrugs to cox-2 inhibitors |
US5474995A (en) | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
DE10075033I2 (en) * | 1993-11-30 | 2001-08-02 | Searle & Co | substituted pyrazolyl-benzenesulfonamides for the treatment of inflammation. |
US5401765A (en) * | 1993-11-30 | 1995-03-28 | G. D. Searle | 1,4,5-triphenyl pyrazolyl compounds for the treatment of inflammation and inflammation-related disorders |
US5393790A (en) * | 1994-02-10 | 1995-02-28 | G.D. Searle & Co. | Substituted spiro compounds for the treatment of inflammation |
AU2424895A (en) * | 1994-05-04 | 1995-11-29 | G.D. Searle & Co. | Substituted spirodienes for the treatment of inflammation |
JPH10504542A (en) * | 1994-07-27 | 1998-05-06 | ジー.ディー.サール アンド カンパニー | Substituted thiazole compounds for treating inflammation |
US5521213A (en) | 1994-08-29 | 1996-05-28 | Merck Frosst Canada, Inc. | Diaryl bicyclic heterocycles as inhibitors of cyclooxygenase-2 |
US5908852A (en) * | 1994-11-14 | 1999-06-01 | G. D. Searle & Co. | 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation |
US5739166A (en) * | 1994-11-29 | 1998-04-14 | G.D. Searle & Co. | Substituted terphenyl compounds for the treatment of inflammation |
JP2636819B2 (en) * | 1994-12-20 | 1997-07-30 | 日本たばこ産業株式会社 | Oxazole-based heterocyclic aromatic compounds |
US5686470A (en) * | 1995-02-10 | 1997-11-11 | Weier; Richard M. | 2, 3-substituted pyridines for the treatment of inflammation |
CN1107058C (en) * | 1995-02-13 | 2003-04-30 | G·D·瑟尔公司 | Substituted isoxazoles for the treatment of inflammation |
US5886016A (en) * | 1995-09-15 | 1999-03-23 | G.D. Searle & Co. | Benzopyranopyrazolyl derivatives for the treatment of inflammation |
US5756529A (en) * | 1995-09-29 | 1998-05-26 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies |
US5981576A (en) | 1995-10-13 | 1999-11-09 | Merck Frosst Canada, Inc. | (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors |
KR100387658B1 (en) * | 1996-04-12 | 2003-08-19 | 지.디. 썰 엘엘씨 | Substituted benzenesulfonamide derivatives as prodrugs of cox-2 inhibitors |
AU5377698A (en) * | 1996-12-10 | 1998-07-03 | G.D. Searle & Co. | Substituted pyrrolyl compounds for the treatment of inflammation |
JPH11180871A (en) * | 1997-09-26 | 1999-07-06 | Sankyo Co Ltd | Medicine containing 1,2-diphenylpyrrole derivative |
FR2769311B1 (en) * | 1997-10-07 | 1999-12-24 | Union Pharma Scient Appl | NOVEL 3,4-DIARYLTHIAZOLIN-2-ONE OR -2-THIONE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND THERAPEUTIC USES |
NZ333399A (en) * | 1997-12-24 | 2000-05-26 | Sankyo Co | Cyclooxygenase-2 inhibitors (COX-2) for the prevention and treatment of tumors, cachexia and tumor-metastasis |
TNSN99111A1 (en) * | 1998-06-11 | 2005-11-10 | Pfizer | NOVEL SULFONYLBENZENE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
US6294558B1 (en) * | 1999-05-31 | 2001-09-25 | Pfizer Inc. | Sulfonylbenzene compounds as anti-inflammatory/analgesic agents |
US20020183362A1 (en) * | 2000-04-25 | 2002-12-05 | Pharmacia Corporation | 2-Fluorobenzenesulfonyl compounds for the treatment of inflammation |
US6673818B2 (en) * | 2001-04-20 | 2004-01-06 | Pharmacia Corporation | Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation |
-
2001
- 2001-04-20 US US09/839,424 patent/US20020183362A1/en not_active Abandoned
- 2001-04-20 AU AU2001253749A patent/AU2001253749A1/en not_active Abandoned
- 2001-04-20 WO PCT/US2001/012983 patent/WO2001081332A2/en not_active Application Discontinuation
- 2001-04-20 JP JP2001578424A patent/JP2003531202A/en not_active Withdrawn
- 2001-04-20 JP JP2001578423A patent/JP2003531201A/en not_active Withdrawn
- 2001-04-20 EP EP01928781A patent/EP1276736A2/en not_active Withdrawn
- 2001-04-20 WO PCT/US2001/013092 patent/WO2001081333A2/en not_active Application Discontinuation
- 2001-04-20 AU AU2001255600A patent/AU2001255600A1/en not_active Abandoned
- 2001-04-20 US US09/838,986 patent/US6600052B1/en not_active Expired - Fee Related
- 2001-04-20 EP EP01927279A patent/EP1296971A2/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
US6600052B1 (en) | 2003-07-29 |
WO2001081332A2 (en) | 2001-11-01 |
WO2001081332A3 (en) | 2002-04-04 |
EP1276736A2 (en) | 2003-01-22 |
JP2003531202A (en) | 2003-10-21 |
WO2001081333A2 (en) | 2001-11-01 |
JP2003531201A (en) | 2003-10-21 |
EP1296971A2 (en) | 2003-04-02 |
WO2001081333A3 (en) | 2002-04-25 |
US20020183362A1 (en) | 2002-12-05 |
AU2001255600A1 (en) | 2001-11-07 |
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