AU2002221080A1 - Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparingthe same and use thereof - Google Patents
Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparingthe same and use thereofInfo
- Publication number
- AU2002221080A1 AU2002221080A1 AU2002221080A AU2108002A AU2002221080A1 AU 2002221080 A1 AU2002221080 A1 AU 2002221080A1 AU 2002221080 A AU2002221080 A AU 2002221080A AU 2108002 A AU2108002 A AU 2108002A AU 2002221080 A1 AU2002221080 A1 AU 2002221080A1
- Authority
- AU
- Australia
- Prior art keywords
- substituents
- group optionally
- pyridyl groups
- thiazole derivatives
- hydrocarbon group
- 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
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/28—Antiandrogens
-
- 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
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/32—Antioestrogens
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cephalosporin Compounds (AREA)
Abstract
The present invention provides a pharmaceutical composition having a steroid C17,20-lyase inhibitory activity, which is useful as a prophylactic or therapeutic agent of prostatism, tumor such as breast cancer and the like, more particularly, a steroid C17,20-lyase inhibitor containing a compound represented by the formula: <CHEM> wherein A<1> is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, one of A<2> and A<3> is a hydrogen atom, a halogen atom, a C1-4 aliphatic hydrocarbon group optionally having substituents or an optionally esterified carboxyl group, the other of A<2> and A<3> is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, and at least one of A<1>, A<2> and A<3> is a 3-pyridyl group optionally having substituents, or a salt thereof or a prodrug thereof.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000373868 | 2000-12-08 | ||
JP2000-373868 | 2000-12-08 | ||
PCT/JP2001/010723 WO2002046186A1 (en) | 2000-12-08 | 2001-12-07 | Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparing the same and use thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2002221080A1 true AU2002221080A1 (en) | 2002-06-18 |
Family
ID=18843165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002221080A Abandoned AU2002221080A1 (en) | 2000-12-08 | 2001-12-07 | Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparingthe same and use thereof |
Country Status (8)
Country | Link |
---|---|
US (1) | US7067537B2 (en) |
EP (1) | EP1348706B1 (en) |
JP (1) | JP2008266349A (en) |
AT (1) | ATE440096T1 (en) |
AU (1) | AU2002221080A1 (en) |
CA (1) | CA2431171A1 (en) |
DE (1) | DE60139639D1 (en) |
WO (1) | WO2002046186A1 (en) |
Families Citing this family (25)
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ES2569919T3 (en) | 1999-04-09 | 2016-05-13 | Kyowa Hakko Kirin Co., Ltd. | Procedure to control the activity of an immunofunctional molecule |
US6946292B2 (en) | 2000-10-06 | 2005-09-20 | Kyowa Hakko Kogyo Co., Ltd. | Cells producing antibody compositions with increased antibody dependent cytotoxic activity |
MXPA05002082A (en) * | 2002-08-23 | 2005-06-08 | Rigel Pharmaceuticals Inc | Pyridyl substituted heterocycles useful for treating or preventing hcv infection. |
US7071223B1 (en) * | 2002-12-31 | 2006-07-04 | Pfizer, Inc. | Benzamide inhibitors of the P2X7 receptor |
EP1620412A2 (en) | 2003-05-02 | 2006-02-01 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds and hydro isomers thereof |
ES2281801T3 (en) * | 2003-05-12 | 2007-10-01 | Pfizer Products Inc. | BENZAMIDE INHIBITORS OF THE P2X7 RECEIVER. |
WO2005049065A2 (en) | 2003-11-19 | 2005-06-02 | Rigel Pharmaceuticals, Inc. | Synergistic combinations of dihaloacetamide with interferon or ribavirin for treatment hcv infections |
ATE396718T1 (en) * | 2003-12-19 | 2008-06-15 | Rigel Pharmaceuticals Inc | COMPOSITIONS AND METHODS FOR TREATING HEPATITIS C VIRUS (HCV) INFECTION |
US7514434B2 (en) | 2004-02-23 | 2009-04-07 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds having an oxadiazole moiety and hydro isomers thereof |
JP2008504363A (en) * | 2004-06-29 | 2008-02-14 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | Combination therapy using benzamide inhibitor of P2X7 receptor |
CN1980902A (en) * | 2004-06-29 | 2007-06-13 | 辉瑞产品有限公司 | Method for preparing 5-'4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h'1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers |
WO2007027230A2 (en) | 2005-05-02 | 2007-03-08 | Rigel Pharmaceuticals, Inc. | Heterocyclic anti-viral compounds comprising metabolizable moieties and their uses |
US9233941B2 (en) | 2007-02-02 | 2016-01-12 | Baylor College Of Medicine | Methods and compositions for the treatment of body weight related disorders |
EP2120580B1 (en) * | 2007-02-02 | 2017-12-27 | Baylor College Of Medicine | Compositions and methods for the treatment of metabolic disorders |
US9085566B2 (en) | 2007-02-02 | 2015-07-21 | Baylor College Of Medicine | Compositions and methods for the treatment of metabolic and related disorders |
US9212179B2 (en) | 2007-02-02 | 2015-12-15 | Baylor College Of Medicine | Compositions and methods for the treatment of metabolic disorders |
US9187485B2 (en) | 2007-02-02 | 2015-11-17 | Baylor College Of Medicine | Methods and compositions for the treatment of cancer and related hyperproliferative disorders |
CL2008003158A1 (en) | 2007-10-26 | 2009-05-29 | Univ California | Compounds derived from diarylthiohydantoin with strong antagonistic activity and with minimal agonist activity on the androgen receptor (ar); preparation procedure; pharmaceutical composition comprising them; use in the treatment of a proliferative disorder such as prostate cancer. |
JP2011513203A (en) * | 2008-03-14 | 2011-04-28 | 大塚製薬株式会社 | MMP-2 and / or MMP-9 inhibitor |
GB0818241D0 (en) | 2008-10-06 | 2008-11-12 | Cancer Res Technology | Compounds and their use |
EA031153B1 (en) | 2011-06-10 | 2018-11-30 | Мерк Патент Гмбх | Use of pyrimidine compounds with btk inhibitory activity |
US20130184280A1 (en) * | 2011-12-21 | 2013-07-18 | Telik, Inc. | Substituted thiazoles as vegfr2 kinase inhibitors |
AU2013346882B2 (en) * | 2012-11-16 | 2017-05-04 | F. Hoffmann-La Roche Ag | Process for the preparation of 2-trifluoromethyl isonicotinic acid and esters |
WO2019014315A1 (en) * | 2017-07-11 | 2019-01-17 | Cyteir Therapeutics, Inc. | Rad51 inhibitors |
MX2022010693A (en) * | 2020-02-28 | 2022-09-26 | Univ Texas | Inhibitors of receptor interacting protein kinase i for the treatment of disease. |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
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US3821384A (en) * | 1972-10-06 | 1974-06-28 | Uniroyal Inc | Pharmaceutical compositions containing a4-aryl-2-(3-pyridyl)thiazole and methods of using same |
US4153703A (en) | 1977-06-30 | 1979-05-08 | Uniroyal, Inc. | Method of controlling insects and acarids with certain aryl-substituted thiazoles |
EP0149884B1 (en) | 1983-09-09 | 1992-12-16 | Takeda Chemical Industries, Ltd. | 5-pyridyl-1,3-thiazole derivatives, their production and use |
NZ221729A (en) | 1986-09-15 | 1989-07-27 | Janssen Pharmaceutica Nv | Imidazolyl methyl-substituted benzimidazole derivatives and pharmaceutical compositions |
NZ224288A (en) | 1987-04-22 | 1989-12-21 | Merrell Dow Pharma | 17b-(cyclopropylamino)androst-5-en-3b-ol and related compounds and methods using these for treatment of non-humans |
US4966898A (en) | 1989-08-15 | 1990-10-30 | Merrell Dow Pharmaceuticals Inc. | 4-substituted 17β-(cyclopropylamino)androst-5-en-3β-ol and related compounds useful as C17-20 lyase inhibitors |
DE69227986T2 (en) | 1991-03-01 | 1999-06-17 | Electrostatic Technology, Inc., Branford, Conn. | POWDER COATING METHOD FOR THE PRODUCTION OF CIRCUIT BOARDS AND SIMILAR |
US5457102A (en) | 1994-07-07 | 1995-10-10 | Janssen Pharmaceutica, N.V. | Pyrroloimidazolyl and imidazopyridinyl substituted 1H-benzimidazole derivatives |
CA2132449C (en) | 1992-03-31 | 2002-09-10 | Susan E. Barrie | 17 - substituted steroids useful in cancer treatment |
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EP0721943A4 (en) | 1993-09-30 | 1996-09-04 | Yamanouchi Pharma Co Ltd | Azole derivative and pharmaceutical composition thereof |
AU3846395A (en) | 1994-11-07 | 1996-05-31 | Janssen Pharmaceutica N.V. | Compositions comprising carbazoles and cyclodextrins |
PL322028A1 (en) | 1995-03-01 | 1998-01-05 | Yamanouchi Pharma Co Ltd | Derivatives of imidazoles and pharmaceutic composition containing them |
WO1997000257A1 (en) | 1995-06-14 | 1997-01-03 | Yamanouchi Pharmaceutical Co., Ltd. | Fused imidazole derivatives and medicinal composition thereof |
EP0880540B1 (en) | 1996-02-14 | 2002-06-12 | Aventis Pharmaceuticals Inc. | 17-beta-cyclopropyl(amino/oxy) 4-aza steroids as active inhibitors of testosterone 5-alpha-reductase and c17-20-lyase |
EP0906115A1 (en) * | 1996-04-30 | 1999-04-07 | Takeda Chemical Industries, Ltd. | COMBINED USE OF GnRH AGONIST AND ANTAGONIST |
AU4298997A (en) | 1996-08-26 | 1998-03-19 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Thiazole derivatives useful as selective inhibitors of pde-iv |
AU4015497A (en) | 1996-08-26 | 1998-03-19 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Thiazole derivatives useful as selective inhibitors of pde-iv |
JPH10195056A (en) | 1996-11-12 | 1998-07-28 | Takeda Chem Ind Ltd | Condensed benzene derivative, its production and agent |
TR199902442T2 (en) | 1997-01-28 | 2000-07-21 | Merck & Co.,Inc. | Thiazole benzenesulfonamides as β3 agonists in the treatment of sugar and obesity. |
ATE231128T1 (en) * | 1997-02-21 | 2003-02-15 | Takeda Chemical Industries Ltd | JOINTS WITH CONDENSED RINGS, METHOD FOR THEIR PRODUCTION AND THEIR APPLICATION |
JPH1179993A (en) * | 1997-09-05 | 1999-03-23 | Sumitomo Pharmaceut Co Ltd | Immunosuppressant |
HUP0004037A3 (en) | 1997-10-02 | 2002-03-28 | Daiichi Seiyaku Co | Novel dihydronaphthalene compounds and process for producing the same |
ATE257703T1 (en) | 1997-10-27 | 2004-01-15 | Takeda Chemical Industries Ltd | 1,3-THIAZOLES AS ADENOSINE A3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF ASTHMA, ALLERGIES AND DIABETES |
ATE293102T1 (en) * | 1998-04-23 | 2005-04-15 | Takeda Pharmaceutical | NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE |
CA2368122A1 (en) | 1999-03-15 | 2000-09-21 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
JP2000302680A (en) | 1999-04-23 | 2000-10-31 | Takeda Chem Ind Ltd | Brain protective agent |
AU765473B2 (en) | 1999-04-23 | 2003-09-18 | Takeda Pharmaceutical Company Limited | 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof |
WO2001010865A1 (en) | 1999-08-06 | 2001-02-15 | Takeda Chemical Industries, Ltd. | p38MAP KINASE INHIBITORS |
AU7950100A (en) | 1999-10-22 | 2001-05-08 | Takeda Chemical Industries Ltd. | 1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof |
WO2001068645A2 (en) | 2000-03-15 | 2001-09-20 | Axys Pharmaceuticals, Inc. | N-cyanomethylcarboxamides and their use as protease inhibitors |
AU2001248820A1 (en) * | 2000-04-28 | 2001-11-12 | Shionogi And Co., Ltd. | Thiazole and oxazole derivatives |
EP1432698A2 (en) * | 2001-09-26 | 2004-06-30 | Bayer Pharmaceuticals Corporation | Substituted 3-pyridyl indoles and indazoles as c17,20 lyase inhibitors |
-
2001
- 2001-12-07 AU AU2002221080A patent/AU2002221080A1/en not_active Abandoned
- 2001-12-07 CA CA002431171A patent/CA2431171A1/en not_active Abandoned
- 2001-12-07 US US10/433,910 patent/US7067537B2/en not_active Expired - Fee Related
- 2001-12-07 WO PCT/JP2001/010723 patent/WO2002046186A1/en active Application Filing
- 2001-12-07 DE DE60139639T patent/DE60139639D1/en not_active Expired - Lifetime
- 2001-12-07 AT AT01999258T patent/ATE440096T1/en not_active IP Right Cessation
- 2001-12-07 EP EP01999258A patent/EP1348706B1/en not_active Expired - Lifetime
-
2008
- 2008-06-12 JP JP2008154723A patent/JP2008266349A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
ATE440096T1 (en) | 2009-09-15 |
EP1348706A4 (en) | 2005-08-10 |
US7067537B2 (en) | 2006-06-27 |
WO2002046186A1 (en) | 2002-06-13 |
DE60139639D1 (en) | 2009-10-01 |
JP2008266349A (en) | 2008-11-06 |
EP1348706B1 (en) | 2009-08-19 |
EP1348706A1 (en) | 2003-10-01 |
CA2431171A1 (en) | 2002-06-13 |
US20040072876A1 (en) | 2004-04-15 |
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