AU2002340010A1 - Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitors - Google Patents
Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitorsInfo
- Publication number
- AU2002340010A1 AU2002340010A1 AU2002340010A AU2002340010A AU2002340010A1 AU 2002340010 A1 AU2002340010 A1 AU 2002340010A1 AU 2002340010 A AU2002340010 A AU 2002340010A AU 2002340010 A AU2002340010 A AU 2002340010A AU 2002340010 A1 AU2002340010 A1 AU 2002340010A1
- Authority
- AU
- Australia
- Prior art keywords
- indazoles
- substituted
- lyase inhibitors
- pyridyl indoles
- indoles
- 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
- KDWAJWXWMMNKHA-UHFFFAOYSA-N 2-pyridin-3-yl-1h-indole Chemical class N1C2=CC=CC=C2C=C1C1=CC=CN=C1 KDWAJWXWMMNKHA-UHFFFAOYSA-N 0.000 title 1
- 150000002473 indoazoles Chemical class 0.000 title 1
- 239000002697 lyase inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
-
- 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
- A61P9/12—Antihypertensives
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32499301P | 2001-09-26 | 2001-09-26 | |
| US60/324,993 | 2001-09-26 | ||
| PCT/US2002/030482 WO2003027094A2 (en) | 2001-09-26 | 2002-09-26 | Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2002340010A1 true AU2002340010A1 (en) | 2003-04-07 |
Family
ID=23265979
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2002362603A Abandoned AU2002362603A1 (en) | 2001-09-26 | 2002-09-26 | 3-pyridyl or 4-isoquinolinyl thiazoles as c17,20 lyase inhibitors |
| AU2002340010A Abandoned AU2002340010A1 (en) | 2001-09-26 | 2002-09-26 | Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitors |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2002362603A Abandoned AU2002362603A1 (en) | 2001-09-26 | 2002-09-26 | 3-pyridyl or 4-isoquinolinyl thiazoles as c17,20 lyase inhibitors |
Country Status (5)
| Country | Link |
|---|---|
| EP (2) | EP1432698A2 (en) |
| JP (2) | JP2005532983A (en) |
| AU (2) | AU2002362603A1 (en) |
| CA (2) | CA2461360A1 (en) |
| WO (8) | WO2003027105A1 (en) |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4160295B2 (en) * | 2000-12-08 | 2008-10-01 | 武田薬品工業株式会社 | Substituted thiazole derivatives having a 3-pyridyl group, method for producing the same, and use thereof |
| DE60139639D1 (en) * | 2000-12-08 | 2009-10-01 | Takeda Pharmaceutical | SUBSTITUTED THIAZONE DERIVATIVES WITH 3-PYRIDYL GROUPS, PROCESS FOR THEIR PREPARATION AND THEIR USE |
| US20040147561A1 (en) * | 2002-12-27 | 2004-07-29 | Wenge Zhong | Pyrid-2-one derivatives and methods of use |
| EP1628666B1 (en) * | 2003-05-14 | 2015-09-23 | NeuroGenetic Pharmaceuticals, Inc. | Compouds and uses thereof in modulating amyloid beta |
| ES2222827B1 (en) * | 2003-07-30 | 2006-03-01 | Laboratorios Del Dr. Esteve, S.A. | DERIVATIVES OF 5-INDOLILSULFONAMIDS, ITS PREPARATION AND ITS APPLICATION AS MEDICINES. |
| WO2005049018A1 (en) * | 2003-11-14 | 2005-06-02 | Vertex Pharmaceuticals Incorporated | Thiazoles and oxazoles useful as modulators of atp-binding cassette transporters |
| JP2007532669A (en) * | 2004-04-13 | 2007-11-15 | イカジェン インコーポレイテッド | Polycyclic pyrimidines as potassium ion channel modulators |
| JP4602686B2 (en) * | 2004-04-15 | 2010-12-22 | 広栄化学工業株式会社 | Process for producing 2,6-dihalogeno-4-arylpyridines |
| EP3067053A1 (en) | 2004-10-13 | 2016-09-14 | PTC Therapeutics, Inc. | Compounds for nonsense suppression, and methods for their use |
| CN101065358B (en) * | 2004-10-20 | 2015-03-11 | 默克雪兰诺有限公司 | 3-Arylaminopyridine Derivatives |
| WO2006051723A1 (en) * | 2004-11-09 | 2006-05-18 | Kaneka Corporation | Method for producing 1-halo-3-aryl-2-propanone |
| GB0428514D0 (en) * | 2004-12-31 | 2005-02-09 | Prosidion Ltd | Compounds |
| AU2005325497A1 (en) * | 2005-01-19 | 2006-07-27 | Biolipox Ab | Indoles useful in the treatment of inflammation |
| WO2006122011A2 (en) | 2005-05-09 | 2006-11-16 | Achillion Pharmaceuticals, Inc. | Thiazole compounds and methods of use |
| UA97348C2 (en) * | 2005-07-29 | 2012-02-10 | 4Сц Аг | HETEROCYCLIC NF-kB INHIBITORS |
| FR2889526B1 (en) * | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | SUBSTITUTED 7-AZA-INDAZOLES, COMPOSITIONS CONTAINING SAME, PROCESS FOR PRODUCTION AND USE |
| KR20080066938A (en) * | 2005-10-07 | 2008-07-17 | 깃세이 야쿠힌 고교 가부시키가이샤 | Nitrogen containing heterocyclic compound and pharmaceutical composition containing it |
| TWI385169B (en) | 2005-10-31 | 2013-02-11 | Eisai R&D Man Co Ltd | Heterocyclic substituted pyridine derivatives and antifungal agent containing same |
| EP1971596A2 (en) * | 2005-12-28 | 2008-09-24 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compounds and their use as mineralocorticoid receptor ligands |
| WO2007082808A2 (en) * | 2006-01-18 | 2007-07-26 | F. Hoffmann-La Roche Ag | Thiazoles as 11 beta-hsd1 inhibitors |
| JP4912414B2 (en) * | 2006-01-24 | 2012-04-11 | イーライ リリー アンド カンパニー | Indolesulfonamide-based progesterone receptor modulators |
| EP2001849B1 (en) * | 2006-03-29 | 2014-11-26 | F. Hoffmann-La Roche AG | Pyridine and pyrimidine derivatives as mglur2 antagonists |
| US7652018B2 (en) | 2006-08-15 | 2010-01-26 | Wyeth Llc | Imidazolidin-2-one derivatives useful as PR modulators |
| US7649007B2 (en) | 2006-08-15 | 2010-01-19 | Wyeth Llc | Oxazolidine derivatives as PR modulators |
| WO2008021338A2 (en) | 2006-08-15 | 2008-02-21 | Wyeth | Tricyclic oxazolidone derivatives useful as pr modulators |
| WO2008021337A1 (en) | 2006-08-15 | 2008-02-21 | Wyeth | Oxazinan-2-one derivatives useful as pr modulators |
| ATE534642T1 (en) * | 2006-09-21 | 2011-12-15 | Eisai R&D Man Co Ltd | PYRIDINE DERIVATIVE SUBSTITUTED BY A HETEROARYL RING AND ANTIFUNGAL AGENT CONTAINING SAME |
| EP2065377B1 (en) | 2006-09-21 | 2011-11-23 | Eisai R&D Management Co., Ltd. | Pyridine derivative substituted by heteroaryl ring, and antifungal agent comprising the same |
| ZA200902127B (en) | 2006-10-02 | 2010-07-28 | Cortendo Invest Ab | Ketoconazole enantiomer in humans |
| US8466154B2 (en) | 2006-10-27 | 2013-06-18 | The Board Of Regents Of The University Of Texas System | Methods and compositions related to wrapping of dehydrons |
| US9187485B2 (en) | 2007-02-02 | 2015-11-17 | Baylor College Of Medicine | Methods and compositions for the treatment of cancer and related hyperproliferative disorders |
| BRPI0811939A2 (en) | 2007-05-22 | 2014-11-25 | Achillion Pharmaceuticals Inc | HETEROARILY REPLACED THIAZOIS |
| AU2008286879B2 (en) | 2007-08-13 | 2013-08-22 | Monsanto Technology Llc | Compositions and methods for controlling nematodes |
| AU2008310097B2 (en) | 2007-10-09 | 2013-05-16 | Merck Patent Gmbh | Pyridine derivatives useful as glucokinase activators |
| US8513287B2 (en) | 2007-12-27 | 2013-08-20 | Eisai R&D Management Co., Ltd. | Heterocyclic ring and phosphonoxymethyl group substituted pyridine derivatives and antifungal agent containing same |
| MX2010007604A (en) * | 2008-01-11 | 2010-08-02 | Novartis Ag | Pyrimidines as kinase inhibitors. |
| WO2009094224A1 (en) | 2008-01-25 | 2009-07-30 | Millennium Pharmaceuticals, Inc. | Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors |
| CN101965176B (en) | 2008-02-08 | 2012-06-20 | 株式会社资生堂 | Whitening agents and skin external preparations |
| US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
| UA105005C2 (en) | 2008-06-16 | 2014-04-10 | Юніверсіті Оф Теннессі Рісерч Фаундейшн | Compounds for the treatment of cancer |
| US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
| US9029408B2 (en) | 2008-06-16 | 2015-05-12 | Gtx, Inc. | Compounds for treatment of cancer |
| AU2009282567B2 (en) * | 2008-08-20 | 2014-10-02 | Merck Sharp & Dohme Corp. | Substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
| BRPI0919004A2 (en) | 2008-09-22 | 2019-09-24 | Cayman Chem Co | multiheteroaryl compound as h-pgds inhibitors and their use for the treatment of prostaglandin d2 mediated diseases |
| US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| CN102395585A (en) | 2009-01-30 | 2012-03-28 | 米伦纽姆医药公司 | Heteroaryls and their use as pi3k inhibitors |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| CA2755660A1 (en) * | 2009-03-19 | 2010-09-23 | Sanofi | Hsp90 inhibiting indazole derivatives, compositions containing same and use thereof |
| JP5728487B2 (en) * | 2009-10-29 | 2015-06-03 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Tricyclic heterocyclic compounds |
| WO2011051198A2 (en) * | 2009-10-30 | 2011-05-05 | Bayer Cropscience Ag | Pyridine derivatives as agricultural pesticides |
| DE102009058280A1 (en) * | 2009-12-14 | 2011-06-16 | Merck Patent Gmbh | thiazole |
| MX377405B (en) | 2010-03-01 | 2025-03-07 | Gtx Inc | COMPOUNDS FOR THE TREATMENT OF CANCER. |
| EP2593453B1 (en) | 2010-07-15 | 2014-09-17 | Bristol-Myers Squibb Company | Azaindazole compounds |
| CA2807149C (en) | 2010-08-04 | 2017-05-02 | Pellficure Pharmaceuticals, Inc. | Novel treatment of prostate carcinoma |
| US8859768B2 (en) | 2010-08-11 | 2014-10-14 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9062038B2 (en) | 2010-08-11 | 2015-06-23 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| TW201217365A (en) | 2010-08-11 | 2012-05-01 | Millennium Pharm Inc | Heteroaryls and uses thereof |
| JP2013542941A (en) | 2010-10-13 | 2013-11-28 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | Heteroaryl and uses thereof |
| CN103270029B (en) | 2010-10-22 | 2016-01-20 | 拜耳知识产权有限责任公司 | As the heterogeneous ring compound of agricultural chemicals |
| EP2632903A4 (en) * | 2010-10-28 | 2014-11-26 | Viamet Pharmaceuticals Inc | Metalloenzyme inhibitor compounds |
| CN103328473A (en) | 2010-11-12 | 2013-09-25 | 百时美施贵宝公司 | Substituted azaindazole compounds |
| GB2485404A (en) * | 2010-11-15 | 2012-05-16 | Nat Univ Ireland | Metal-complexed pyridyl-substituted tetrazole compounds and their use in treating cancer |
| CN102675286B (en) * | 2011-03-07 | 2015-08-19 | 中国科学院上海药物研究所 | Indazole compounds, preparation method, application and pharmaceutical composition thereof |
| AU2012249421B9 (en) * | 2011-04-28 | 2015-10-22 | Novartis Ag | 17alpha-hydroxylase/C17,20-lyase inhibitors |
| US20120302573A1 (en) * | 2011-05-25 | 2012-11-29 | Paul Francis Jackson | Methods of inhibiting pro matrix metalloproteinase activation |
| WO2013049263A1 (en) | 2011-09-27 | 2013-04-04 | Bristol-Myers Squibb Company | Substituted bicyclic heteroaryl compounds |
| CA2886117C (en) | 2012-10-05 | 2022-05-31 | Merck Sharp & Dohme Corp. | Indoline compounds and their use as aldosterone synthase inhibitors |
| WO2014099833A1 (en) * | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Indazole compounds as aldosterone synthase inhibitors |
| KR102246652B1 (en) | 2013-03-05 | 2021-04-29 | 유니버시티 오브 테네시 리서치 파운데이션 | Compounds for treatment of cancer |
| US20160022606A1 (en) | 2013-03-14 | 2016-01-28 | Pellficure Pharmaceuticals Inc. | Novel therapy for prostate carcinoma |
| WO2016040896A1 (en) | 2014-09-12 | 2016-03-17 | Pellficure Pharmaceuticals, Inc. | Compositions and methods for treatment of prostate carcinoma |
| EP3528799A1 (en) | 2016-10-24 | 2019-08-28 | Pellficure Pharmaceuticals, Inc. | Pharmaceutical compositions of 5-hydroxy-2-methylnaphthalene-1, 4-dione |
| JP7193071B2 (en) * | 2017-02-08 | 2022-12-20 | 国立大学法人東海国立大学機構 | Fluorescent materials and UV absorbers |
| CN120025336A (en) * | 2019-12-18 | 2025-05-23 | 加利福尼亚大学董事会 | LIN28 inhibitors and methods of use thereof |
| US20210246109A1 (en) * | 2020-02-11 | 2021-08-12 | University Of Kentucky Research Foundation | Potent and selective inhibitors of cytochrome p450 |
| WO2023049199A1 (en) * | 2021-09-24 | 2023-03-30 | Zeno Management, Inc. | Azole compounds |
| CN117551029A (en) * | 2023-11-22 | 2024-02-13 | 河南大学 | A kind of synthetic method of 4-bromo-3-cyanopyridine |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK150068C (en) * | 1978-06-02 | 1987-06-29 | Pfizer | METHOD OF ANALOGUE FOR THE PREPARATION OF AMINOTHIAZOLES |
| JPS55133366A (en) * | 1979-04-05 | 1980-10-17 | Otsuka Pharmaceut Factory Inc | Thiazole derivative |
| US4536505A (en) * | 1983-05-17 | 1985-08-20 | Ciba-Geigy Corporation | Certain N-(pyridyl) indoles |
| DE3940476A1 (en) * | 1989-12-07 | 1991-06-13 | Bayer Ag | PYRIDINYLPYRIMIDINE DERIVATIVES |
| DE3940477A1 (en) * | 1989-12-07 | 1991-06-13 | Bayer Ag | HETARYL-SUBSTITUTED PYRIDINYLPYRIMIDINE DERIVATIVES |
| JPH04154773A (en) * | 1990-10-15 | 1992-05-27 | Green Cross Corp:The | Thiazole derivative |
| DE4117560A1 (en) * | 1991-05-29 | 1992-12-03 | Bayer Ag | USE OF PYRIDINYLPYRIMIDINE DERIVATIVES TO PROTECT TECHNICAL MATERIALS |
| TW223004B (en) * | 1991-11-25 | 1994-05-01 | Sumitomo Chemical Co | |
| US5395817A (en) * | 1992-01-22 | 1995-03-07 | Imperial Chemical Industries Plc | N-arylindoles and their use as herbicides |
| US5599774A (en) * | 1992-01-22 | 1997-02-04 | Imperial Chemical Industries Plc | N-arylindoles and their use as herbicides |
| CA2131625A1 (en) * | 1992-03-09 | 1993-09-16 | Donald R. James | Novel arylindazoles and their use as herbicides |
| US5444038A (en) * | 1992-03-09 | 1995-08-22 | Zeneca Limited | Arylindazoles and their use as herbicides |
| CA2206315A1 (en) * | 1994-11-29 | 1996-06-06 | Hisamitsu Pharmaceutical Co., Inc. | Antibacterial preparation or bactericide comprising 2-aminothiazole derivative and/or salt thereof |
| US6046136A (en) * | 1997-06-24 | 2000-04-04 | Zeneca Limited | Herbicidal heterocyclic N-oxides compounds |
| US5840721A (en) * | 1997-07-09 | 1998-11-24 | Ontogen Corporation | Imidazole derivatives as MDR modulators |
| JP3409029B2 (en) * | 1997-10-03 | 2003-05-19 | メルク フロスト カナダ アンド カンパニー | Arylthiophene derivatives as PDEIV inhibitors |
| CA2331118A1 (en) * | 1998-05-12 | 1999-11-18 | Wyeth | Oxazole-aryl-carboxylic acids useful in the treatment of insulin resistance and hyperglycemia |
| WO2000006556A1 (en) * | 1998-07-27 | 2000-02-10 | Abbott Laboratories | Substituted oxazolines as antiproliferative agents |
| ES2317889T3 (en) * | 2000-03-01 | 2009-05-01 | Janssen Pharmaceutica Nv | DERIVATIVES OF TIAZOLIL 2,4-DISPOSED. |
-
2002
- 2002-09-26 AU AU2002362603A patent/AU2002362603A1/en not_active Abandoned
- 2002-09-26 WO PCT/US2002/030981 patent/WO2003027105A1/en not_active Ceased
- 2002-09-26 WO PCT/US2002/030483 patent/WO2003027085A2/en not_active Ceased
- 2002-09-26 CA CA002461360A patent/CA2461360A1/en not_active Abandoned
- 2002-09-26 WO PCT/US2002/030834 patent/WO2003027107A1/en not_active Ceased
- 2002-09-26 CA CA002461363A patent/CA2461363A1/en not_active Abandoned
- 2002-09-26 JP JP2003530675A patent/JP2005532983A/en not_active Withdrawn
- 2002-09-26 EP EP02778338A patent/EP1432698A2/en not_active Withdrawn
- 2002-09-26 WO PCT/US2002/030979 patent/WO2003027101A1/en not_active Ceased
- 2002-09-26 EP EP02799636A patent/EP1432706A2/en not_active Withdrawn
- 2002-09-26 WO PCT/US2002/030924 patent/WO2003027100A1/en not_active Ceased
- 2002-09-26 WO PCT/US2002/030482 patent/WO2003027094A2/en not_active Ceased
- 2002-09-26 WO PCT/US2002/030983 patent/WO2003027096A1/en not_active Ceased
- 2002-09-26 AU AU2002340010A patent/AU2002340010A1/en not_active Abandoned
- 2002-09-26 WO PCT/US2002/030982 patent/WO2003027095A1/en not_active Ceased
- 2002-09-26 JP JP2003530682A patent/JP2005528325A/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002362603A1 (en) | 2003-04-07 |
| CA2461363A1 (en) | 2003-04-03 |
| WO2003027094A2 (en) | 2003-04-03 |
| WO2003027095A1 (en) | 2003-04-03 |
| WO2003027107A1 (en) | 2003-04-03 |
| WO2003027085A2 (en) | 2003-04-03 |
| EP1432706A2 (en) | 2004-06-30 |
| WO2003027085A3 (en) | 2003-12-04 |
| WO2003027105A1 (en) | 2003-04-03 |
| WO2003027096A1 (en) | 2003-04-03 |
| EP1432698A2 (en) | 2004-06-30 |
| WO2003027094A3 (en) | 2003-10-23 |
| CA2461360A1 (en) | 2003-04-03 |
| JP2005532983A (en) | 2005-11-04 |
| JP2005528325A (en) | 2005-09-22 |
| WO2003027101A1 (en) | 2003-04-03 |
| WO2003027100A1 (en) | 2003-04-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2002340010A1 (en) | Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitors | |
| AU2002362895A1 (en) | 5-carbamoyl-1,1-biphenyl-4-carboxamide derivatives and their use as p38 kinase inhibitors | |
| AU2002346929A1 (en) | 5-acylamino-1,1-biphenyl-4-carboxamide derivatives and their use as p38 kinase inhibitors | |
| AP2003002857A0 (en) | New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors. | |
| AU2001251063A1 (en) | 3-cyanoquinolines,3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors | |
| AU2002303892A1 (en) | 5-aralkylsulfonyl-3- (pyrrol-2-ylmethylidene)-2-indolinone derivatives as kinase inhibitors | |
| MXPA03006260A (en) | Substituted amine derivatives and methods of use. | |
| AP2003002836A0 (en) | 3-(4-Amidopyrrol-2-ylmethlidene)-2-indolinone derivatives as protein kinase inhibitors. | |
| AU2002213336A1 (en) | Substituted heterocyclic compounds for treating multidrug resistance | |
| AU2001274009A1 (en) | Substituted indoles as parp inhibitors | |
| AU2001269939A1 (en) | Methods for eliminating the formation of biofilm | |
| AU2002357003A1 (en) | Indoles as naaladase inhibitors | |
| AU2002226911A1 (en) | Indol derivative and their use as inhibitors of p38 kinase | |
| HUP0500111A3 (en) | Indolinone derivatives useful as protein kinase inhibitors | |
| AU2002361861A1 (en) | SELECTIVE 11Beta-HSD INHIBITORS AND METHODS FOR USE THEREOF | |
| PL369850A1 (en) | Substituted indoles, method for production and use thereof for the inhibition of pain | |
| ZA200307306B (en) | Indolines, substituted in portion 6, and their use as kinase inhibitors. | |
| AU2001266648A1 (en) | Kits and methods for optimizing the efficacy of chondroprotective compositions | |
| AU2002230056A1 (en) | Indole derivatives and their uses as heparanase inhibitors | |
| AU2002334728A1 (en) | Substituted 3-pyridyl pyrroles and 3-pyridyl pyrazoles as c17,20 lyase inhibitors | |
| AU2002213830A1 (en) | The use of selective noradrenaline reuptake inhibitors for the treatment of tension-type headache | |
| AU2002334730A1 (en) | Substituted 3-pyridyl imidazoles as c17,20 lyase inhibitors | |
| AU2002327756A1 (en) | Substituted 3-pyridyl oxazoles as c17,20 lyase inhibitors | |
| AU2002337751A1 (en) | Substituted 3-pyridyl pyrimidines as c17,20 lyase inhibitors | |
| AU2002355325A1 (en) | Substituted amine derivatives and their use as monoamine neurotransmitter re-uptake inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |