AU2002221239A1 - Therapeutic benzimidazole compounds - Google Patents
Therapeutic benzimidazole compoundsInfo
- Publication number
- AU2002221239A1 AU2002221239A1 AU2002221239A AU2123902A AU2002221239A1 AU 2002221239 A1 AU2002221239 A1 AU 2002221239A1 AU 2002221239 A AU2002221239 A AU 2002221239A AU 2123902 A AU2123902 A AU 2123902A AU 2002221239 A1 AU2002221239 A1 AU 2002221239A1
- Authority
- AU
- Australia
- Prior art keywords
- therapeutic
- benzimidazole compounds
- benzimidazole
- compounds
- therapeutic benzimidazole
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
-
- 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
-
- 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
Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25177600P | 2000-12-07 | 2000-12-07 | |
US25177300P | 2000-12-07 | 2000-12-07 | |
US60251773 | 2000-12-07 | ||
US60251776 | 2000-12-07 | ||
SE0100009 | 2001-01-02 | ||
SE0100008 | 2001-01-02 | ||
SE0100008A SE0100008D0 (en) | 2001-01-02 | 2001-01-02 | Therapeutic compounds |
SE0100009A SE0100009D0 (en) | 2001-01-02 | 2001-01-02 | Therapeutic compounds |
PCT/SE2001/002725 WO2002046168A1 (en) | 2000-12-07 | 2001-12-07 | Therapeutic benzimidazole compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2002221239A1 true AU2002221239A1 (en) | 2002-06-18 |
Family
ID=27484529
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002221239A Abandoned AU2002221239A1 (en) | 2000-12-07 | 2001-12-07 | Therapeutic benzimidazole compounds |
Country Status (5)
Country | Link |
---|---|
US (1) | US20070004713A1 (en) |
EP (1) | EP1341768A1 (en) |
JP (1) | JP2004515496A (en) |
AU (1) | AU2002221239A1 (en) |
WO (1) | WO2002046168A1 (en) |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6677348B2 (en) | 2000-12-08 | 2004-01-13 | 3M Innovative Properties Company | Aryl ether substituted imidazoquinolines |
UA83620C2 (en) * | 2001-12-05 | 2008-08-11 | Уайт | Substituted benzoxazoles and analogues as estrogenic agents |
ES2335276T3 (en) * | 2002-03-13 | 2010-03-24 | Array Biopharma, Inc. | DERIVATIVES OF BENCIMIDAZOL RENTED N3 AS INHIBITORS OF MEK. |
US20040002524A1 (en) * | 2002-06-24 | 2004-01-01 | Richard Chesworth | Benzimidazole compounds and their use as estrogen agonists/antagonists |
MXPA05002040A (en) | 2002-08-19 | 2005-12-12 | Lorus Therapeutics Inc | 2,4,5-trisubstituted imidazoles and their use as anti-microbial agents. |
DK1587821T3 (en) | 2002-12-19 | 2008-11-10 | Scripps Research Inst | Compositions and Methods for Stabilizing Transthyretin and Inhibiting Transthyretin Failure |
TW200500065A (en) * | 2003-05-21 | 2005-01-01 | Wyeth Corp | Antiarthritic combinations |
SE0302573D0 (en) | 2003-09-26 | 2003-09-26 | Astrazeneca Ab | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof |
US8969372B2 (en) | 2003-11-14 | 2015-03-03 | Aptose Boisciences Inc. | Aryl imidazoles and their use as anti-cancer agents |
JP2007538103A (en) | 2004-05-20 | 2007-12-27 | ザ スクリップス リサーチ インスティテュート | Transthyretin stabilization |
AU2005280178A1 (en) * | 2004-08-26 | 2006-03-09 | Wyeth | Prodrug substituted benzoxazoles as estrogenic agents |
BRPI0514974A (en) | 2004-09-07 | 2008-07-01 | Wyeth Corp | compound, composition, methods of treating or inhibiting a disease or condition, free radical-induced disease states in a mammal, damage to the joint secondary to arthroscopic or surgical procedures in a mammal, infertility in a mammal, lowering cholesterol levels, triglycerides, lp (a), or ldl, to provide cognition or neuroprotection enhancement, contraception in a mammal, and to prepare a compound, and, product |
ATE545644T1 (en) | 2004-09-24 | 2012-03-15 | Astrazeneca Ab | BENZIMIDAZOLE DERIVATIVES, COMPOSITIONS CONTAINING SAME, PRODUCTION THEREOF AND USES THEREOF I |
KR20070072598A (en) * | 2004-10-19 | 2007-07-04 | 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 | Indole and benzimidazole derivatives |
MX2007005290A (en) | 2004-11-02 | 2007-07-09 | Pfizer | Sulfonyl benzimidazole derivatives. |
AU2005316561A1 (en) * | 2004-12-17 | 2006-06-22 | Wyeth | The uses of estrogen beta agonists to treat cognitive diseases |
DE102005012873B4 (en) * | 2005-03-19 | 2007-05-03 | Sanofi-Aventis Deutschland Gmbh | Aminocarbonyl-substituted 8-N-benzimidazoles, process for their preparation and their use as pharmaceuticals |
CA2611032C (en) | 2005-05-25 | 2012-01-17 | Genesense Technologies Inc. | 2-indolyl imidazo[4,5-d]phenanthroline derivatives and their use in the treatment of cancer |
JP2009530274A (en) * | 2006-03-15 | 2009-08-27 | ワイス | N-substituted azacyclylamine compounds as histamine-3 antagonists |
TW200745049A (en) | 2006-03-23 | 2007-12-16 | Astrazeneca Ab | New crystalline forms |
TW200808769A (en) | 2006-04-18 | 2008-02-16 | Astrazeneca Ab | Therapeutic compounds |
PE20081152A1 (en) * | 2006-10-06 | 2008-08-10 | Wyeth Corp | N-SUBSTITUTED AZACYCLYLAMINES AS HISTAMINE-3 ANTAGONISTS |
AR063311A1 (en) | 2006-10-18 | 2009-01-21 | Novartis Ag | ORGANIC COMPOUNDS |
MX2009006706A (en) | 2006-12-22 | 2009-07-02 | Astex Therapeutics Ltd | Bicyclic heterocyclic compounds as fgfr inhibitors. |
JP5442449B2 (en) | 2006-12-22 | 2014-03-12 | アステックス、セラピューティックス、リミテッド | New compounds |
EP2106399A2 (en) | 2007-01-05 | 2009-10-07 | Novartis AG | Imidazole derivatives as kinesin spindle protein inhibitors (eg-5) |
US9623021B2 (en) | 2007-01-22 | 2017-04-18 | Gtx, Inc. | Nuclear receptor binding agents |
US9604931B2 (en) | 2007-01-22 | 2017-03-28 | Gtx, Inc. | Nuclear receptor binding agents |
EA019833B1 (en) | 2007-01-22 | 2014-06-30 | ДЖиТиЭкс, ИНК. | Nuclear receptor binding agents |
GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
CN101990433B (en) | 2008-02-07 | 2014-11-05 | 马萨诸塞眼科耳科诊所 | Compounds that enhance atoh-1 expression |
GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
US8501957B2 (en) * | 2008-12-10 | 2013-08-06 | China Medical University | Benzimidazole compounds and their use as anticancer agents |
GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
GB0906470D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
EP2493310A4 (en) * | 2009-10-27 | 2014-03-12 | Glaxosmithkline Llc | Benzimidazoles as fatty acid synthase inhibitors |
AU2010314891A1 (en) | 2009-11-06 | 2012-06-07 | Vanderbilt University | Aryl and heteroaryl sulfones as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
TWI458714B (en) * | 2009-12-10 | 2014-11-01 | Univ China Medical | Benzimidazole compounds and their use |
JP5782234B2 (en) * | 2010-06-16 | 2015-09-24 | チャイナ メディカル ユニヴァーシティーChina Medical University | Benzimidazole compounds and uses thereof |
EP2397471A1 (en) * | 2010-06-16 | 2011-12-21 | China Medical University | Benzimidazole compounds and their use |
US20130196971A1 (en) * | 2010-09-17 | 2013-08-01 | Christopher Joseph Aquino | Fatty acid synthase inhibitors |
CA2847293C (en) | 2011-09-16 | 2017-03-28 | Richard Frederic Labaudiniere | Solid forms of a transthyretin dissociation inhibitor |
EP2757882B1 (en) | 2011-09-22 | 2020-11-04 | Merck Sharp & Dohme Corp. | Imidazopyridyl compounds as aldosterone synthase inhibitors |
US9351973B2 (en) | 2011-09-22 | 2016-05-31 | Merck Sharp & Dohme Corp. | Pyrazolopyridyl compounds as aldosterone synthase inhibitors |
EP2757883B1 (en) | 2011-09-22 | 2021-01-13 | Merck Sharp & Dohme Corp. | Triazolopyridyl compounds as aldosterone synthase inhibitors |
WO2014055595A1 (en) | 2012-10-05 | 2014-04-10 | Merck Sharp & Dohme Corp. | Indoline compounds as aldosterone synthase inhibitiors related applications |
AU2014235962A1 (en) | 2013-03-20 | 2015-09-10 | Aptose Biosciences Inc. | 2-substituted imidazo[4,5-d]phenanthroline derivatives and their use in the treatment of cancer |
JP6946000B2 (en) | 2013-10-04 | 2021-10-06 | アプトース バイオサイエンシーズ, インコーポレイテッド | Compositions and Methods for the Treatment of Cancer |
CN104072425B (en) * | 2014-07-09 | 2016-12-07 | 大连理工大学 | Benzimidazoles compound and application thereof |
WO2019089511A1 (en) | 2017-10-30 | 2019-05-09 | Aptose Biosciences Inc. | Aryl imidazoles for the treatment of cancer |
CN108456171B (en) * | 2018-03-16 | 2021-07-27 | 中山大学肿瘤防治中心(中山大学附属肿瘤医院、中山大学肿瘤研究所) | FLT3/ITD mutant inhibitor and application thereof in tumor prevention and treatment medicines |
JP2022508648A (en) | 2018-10-05 | 2022-01-19 | アンナプルナ バイオ インコーポレイテッド | Compounds and compositions for treating conditions associated with APJ receptor activity |
WO2021112538A1 (en) * | 2019-12-02 | 2021-06-10 | Hyundai Pharm Co., Ltd. | Glp-1 receptor agonist |
WO2023165523A1 (en) * | 2022-03-01 | 2023-09-07 | 上海璎黎药业有限公司 | Aromatic ring-substituted methoxy derivative and use thereof |
WO2024029819A1 (en) * | 2022-08-01 | 2024-02-08 | 경희대학교 산학협력단 | Pharmaceutical composition containing benzimidazole derivative or pharmaceutically acceptable salt thereof, and method for preparing same |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3152142A (en) * | 1962-05-24 | 1964-10-06 | Dow Chemical Co | Benzimidazole compounds |
US3632397A (en) * | 1966-01-26 | 1972-01-04 | Lilly Co Eli | Method of controlling weeds pre-emergently |
US4093726A (en) * | 1976-12-02 | 1978-06-06 | Abbott Laboratories | N-(2-benzimidazolyl)-piperazines |
GB2053215B (en) * | 1979-06-25 | 1983-04-07 | May & Baker Ltd | Benzimidazole derivatives |
JP2869561B2 (en) * | 1989-05-22 | 1999-03-10 | 大塚製薬株式会社 | Platelet adhesion inhibitor |
FR2677020B1 (en) * | 1991-05-31 | 1993-08-27 | Cird Galderma | COMPOUNDS DERIVED FROM BENZIMIDAZOLE, THEIR PREPARATION PROCESS AND THEIR USE IN THE THERAPEUTIC AND COSMETIC FIELDS. |
US5552426A (en) * | 1994-04-29 | 1996-09-03 | Eli Lilly And Company | Methods for treating a physiological disorder associated with β-amyloid peptide |
IL113472A0 (en) * | 1994-04-29 | 1995-07-31 | Lilly Co Eli | Non-peptidyl tachykinin receptor antogonists |
WO1997012613A1 (en) * | 1995-10-05 | 1997-04-10 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
DE69635135T2 (en) * | 1995-12-28 | 2006-07-06 | Fujisawa Pharmaceutical Co., Ltd. | benzimidazole derivatives |
EP0871442A1 (en) * | 1996-01-09 | 1998-10-21 | Eli Lilly And Company | Benzimidzolyl neuropeptide y receptor antagonists |
JP2000026430A (en) * | 1998-07-02 | 2000-01-25 | Taisho Pharmaceut Co Ltd | 2,5,6-substituted benzimidazole compound derivative |
GB9814620D0 (en) * | 1998-07-06 | 1998-09-02 | Karobio Ab | Vasculoprotector |
JP2000095767A (en) * | 1998-09-28 | 2000-04-04 | Takeda Chem Ind Ltd | Antagonist for gonadotrophic hormone-releasing hormone |
EP1173164A2 (en) * | 1999-04-16 | 2002-01-23 | AstraZeneca AB | Estrogen receptor-beta ligands |
GB9914825D0 (en) * | 1999-06-24 | 1999-08-25 | Smithkline Beecham Spa | Novel compounds |
JP2001192372A (en) * | 2000-01-11 | 2001-07-17 | Teijin Ltd | Benzimidazole derivative |
-
2001
- 2001-12-07 WO PCT/SE2001/002725 patent/WO2002046168A1/en active Application Filing
- 2001-12-07 JP JP2002547907A patent/JP2004515496A/en active Pending
- 2001-12-07 US US10/433,746 patent/US20070004713A1/en not_active Abandoned
- 2001-12-07 AU AU2002221239A patent/AU2002221239A1/en not_active Abandoned
- 2001-12-07 EP EP01999562A patent/EP1341768A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
JP2004515496A (en) | 2004-05-27 |
WO2002046168A1 (en) | 2002-06-13 |
US20070004713A1 (en) | 2007-01-04 |
EP1341768A1 (en) | 2003-09-10 |
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