UY27370A1 - Derivados de benzamida tiazol y composiciones farmacéuticas para inhibir la proliferación de células y métodos para su utilización - Google Patents
Derivados de benzamida tiazol y composiciones farmacéuticas para inhibir la proliferación de células y métodos para su utilizaciónInfo
- Publication number
- UY27370A1 UY27370A1 UY27370A UY27370A UY27370A1 UY 27370 A1 UY27370 A1 UY 27370A1 UY 27370 A UY27370 A UY 27370A UY 27370 A UY27370 A UY 27370A UY 27370 A1 UY27370 A1 UY 27370A1
- Authority
- UY
- Uruguay
- Prior art keywords
- inhibit
- proliferation
- benzamida
- tiazol
- derivatives
- Prior art date
Links
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- 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
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- 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
- C07D417/12—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 chain containing hetero atoms as chain links
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Biotechnology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Psychology (AREA)
Abstract
Los compuestos aminotiazol con benzamida mono-di / sustituidos están representados por la Fórmula (I), y se describen sus sales farmacéuticamente aceptables, metabolitos farmacéuticamente activos, y sales farmacéticamente aceptables de dichos metabolitos. Estos agentes modulan y/o inhiben la proliferación de célula y la actividad de las quinazas de proteína y son útiles como farmacéuticos para tratar malignidades y otros desórdenes.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30367901P | 2001-07-06 | 2001-07-06 | |
US30527401P | 2001-07-13 | 2001-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY27370A1 true UY27370A1 (es) | 2003-04-30 |
Family
ID=26973595
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY27370A UY27370A1 (es) | 2001-07-06 | 2002-07-04 | Derivados de benzamida tiazol y composiciones farmacéuticas para inhibir la proliferación de células y métodos para su utilización |
Country Status (13)
Country | Link |
---|---|
US (1) | US6720346B2 (es) |
EP (1) | EP1438046A4 (es) |
JP (1) | JP2005521631A (es) |
AU (1) | AU2002354801A1 (es) |
BR (1) | BR0210874A (es) |
CA (1) | CA2452609A1 (es) |
HN (1) | HN2002000156A (es) |
MX (1) | MXPA04000069A (es) |
PA (1) | PA8550101A1 (es) |
PE (1) | PE20030269A1 (es) |
SV (1) | SV2003001148A (es) |
UY (1) | UY27370A1 (es) |
WO (1) | WO2003004467A2 (es) |
Families Citing this family (33)
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DE60037321T4 (de) | 1999-08-04 | 2010-01-07 | Icagen, Inc. | Benzanilide als öffner des kaliumkanals |
US6495550B2 (en) * | 1999-08-04 | 2002-12-17 | Icagen, Inc. | Pyridine-substituted benzanilides as potassium ion channel openers |
US7705120B2 (en) | 2001-06-21 | 2010-04-27 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of breast cancer |
AU2003282231A1 (en) * | 2002-08-09 | 2004-02-25 | Pfizer Inc. | Antiproliferative 2-(heteroaryl)-aminothiazole compounds, pharmaceutical compositions and methods for their use |
EP1594854B1 (en) * | 2003-02-06 | 2010-09-01 | Bristol-Myers Squibb Company | Thiazolyl-based compounds useful as kinase inhibitors |
JP2006517234A (ja) | 2003-02-10 | 2006-07-20 | アムジエン・インコーポレーテツド | バニロイド受容体リガンドおよび治療におけるこれらのリガンドの使用 |
EP1594866A1 (en) * | 2003-02-12 | 2005-11-16 | Pfizer Inc. | Antiproliferative 2-(sulfo-phenyl)-aminothiazole derivatives |
AU2004251668B2 (en) * | 2003-06-03 | 2008-03-20 | Triad Therapeutics, Inc | 5-membered heterocycle-based p-38 inhibitors |
PT1641764E (pt) | 2003-06-26 | 2011-10-27 | Novartis Ag | Inibidores de p38 quinase a base de heterociclo de 5 elementos |
US20050026966A1 (en) * | 2003-07-30 | 2005-02-03 | Agouron Pharmaceuticals, Inc. | Process and chiral amine intermediates useful for preparation of antiproliferative 2,4-diaminothiazole amide compounds |
WO2005028624A2 (en) * | 2003-09-15 | 2005-03-31 | Plexxikon, Inc. | Molecular scaffolds for kinase ligand development |
KR20060129413A (ko) * | 2004-01-30 | 2006-12-15 | 에이비 사이언스 | 티로신 키나제 억제제로서의2-(3-치환된-아릴)아미노-4-아릴-티아졸 |
EP1732905A1 (en) * | 2004-03-31 | 2006-12-20 | Lexicon Genetics Incorporated | 2-aminomethylthiazole-5-carboxamides as protein kinase modulators |
WO2005102326A2 (en) * | 2004-04-23 | 2005-11-03 | Ab Science | Use of c-kit inhibitors for treating renal diseases |
US7618981B2 (en) * | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
US7423053B2 (en) * | 2004-07-15 | 2008-09-09 | Hoffmann-La Roche Inc. | 4-Aminothiazole derivatives |
JP4652079B2 (ja) * | 2005-02-15 | 2011-03-16 | 花王株式会社 | 2,2−二置換エチレンジアミン誘導体の製造方法 |
RU2007138584A (ru) * | 2005-03-18 | 2009-04-27 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния (Us) | Соединения, обладающие активностью для коррекции процессинга мутантного cftr, и их применение |
JP2008540537A (ja) * | 2005-05-09 | 2008-11-20 | アキリオン ファーマシューティカルズ,インコーポレーテッド | チアゾール化合物および使用方法 |
JP2009530274A (ja) | 2006-03-15 | 2009-08-27 | ワイス | ヒスタミン−3アンタゴニストとしてのn−置換−アザシクリルアミン化合物 |
MX2008014743A (es) * | 2006-05-19 | 2008-12-01 | Wyeth Corp | N-benzoil- y n-bencilpirrolidin-3-ilaminas como antagonistas de histamina-3. |
PE20081152A1 (es) | 2006-10-06 | 2008-08-10 | Wyeth Corp | Azaciclilaminas n-sustituidas como antagonistas de histamina-3 |
CN101541787B (zh) * | 2006-11-23 | 2015-02-04 | 西巴控股有限公司 | N-烯丙基空间位阻的叔胺的制备方法 |
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GB0705656D0 (en) * | 2007-03-23 | 2007-05-02 | Addex Pharmaceuticals Sa | Novel compounds E1 |
WO2009012252A1 (en) | 2007-07-16 | 2009-01-22 | Wyeth | Aminoalkylazole derivatives as histamine-3 antagonists |
US9066951B2 (en) * | 2008-05-29 | 2015-06-30 | Wisconsin Alumni Research Foundation | Drugs to treat HPV infection |
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JP5212656B2 (ja) * | 2009-09-02 | 2013-06-19 | 日産化学工業株式会社 | イソチオシアナト化合物の製造方法 |
CN103221389B (zh) * | 2010-11-29 | 2016-01-20 | 日产化学工业株式会社 | 异硫氰酸酯化合物的制造方法 |
WO2013089689A1 (en) * | 2011-12-13 | 2013-06-20 | Kneller Bruce W | Constituent of desmodium elegans and methods of use |
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AU700964B2 (en) | 1994-11-10 | 1999-01-14 | Cor Therapeutics, Inc. | Pharmaceutical pyrazole compositions useful as inhibitors of protein kinases |
CN1184478A (zh) | 1995-03-22 | 1998-06-10 | 大正制药株式会社 | 噻唑衍生物 |
WO1997034876A1 (en) | 1996-03-15 | 1997-09-25 | Zeneca Limited | Cinnoline derivatives and use as medicine |
TW513418B (en) | 1996-07-31 | 2002-12-11 | Otsuka Pharma Co Ltd | Thiazole derivatives, their production and use |
HUP0004512A3 (en) * | 1997-10-27 | 2003-01-28 | Agouron Pharmaceuticals Inc La | 4-aminothiazole derivatives, their preparation and their use as inhibitors of cyclin-dependent kinases |
NZ503491A (en) | 1997-11-10 | 2002-08-28 | Bristol Myers Squibb Co | 2-substituted amino-1,3-benzothiazole derivatives useful as protein tyrosine kinase inhibitors |
US6040321A (en) | 1997-11-12 | 2000-03-21 | Bristol-Myers Squibb Company | Aminothiazole inhibitors of cyclin dependent kinases |
UA60365C2 (uk) | 1998-06-04 | 2003-10-15 | Пфайзер Продактс Інк. | Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця |
FR2780058B1 (fr) | 1998-06-17 | 2001-03-09 | Rhodia Chimie Sa | Emulsion aqueuse de silane pour l'hydrofugation de materiaux de construction |
CA2337755C (en) | 1998-09-18 | 2008-07-29 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
GB9823871D0 (en) | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
GB9823873D0 (en) | 1998-10-30 | 1998-12-30 | Pharmacia & Upjohn Spa | 2-ureido-thiazole derivatives,process for their preparation,and their use as antitumour agents |
US6756374B2 (en) | 2001-01-22 | 2004-06-29 | Hoffmann-La Roche Inc. | Diaminothiazoles having antiproliferative activity |
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- 2002-07-02 PE PE2002000595A patent/PE20030269A1/es not_active Application Discontinuation
- 2002-07-04 SV SV2002001148A patent/SV2003001148A/es not_active Application Discontinuation
- 2002-07-04 UY UY27370A patent/UY27370A1/es not_active Application Discontinuation
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- 2002-07-05 CA CA002452609A patent/CA2452609A1/en not_active Abandoned
- 2002-07-05 US US10/190,219 patent/US6720346B2/en not_active Expired - Fee Related
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HN2002000156A (es) | 2003-11-27 |
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PA8550101A1 (es) | 2003-09-05 |
PE20030269A1 (es) | 2003-04-16 |
JP2005521631A (ja) | 2005-07-21 |
US6720346B2 (en) | 2004-04-13 |
CA2452609A1 (en) | 2003-01-16 |
BR0210874A (pt) | 2006-10-24 |
WO2003004467A3 (en) | 2004-05-06 |
EP1438046A2 (en) | 2004-07-21 |
AU2002354801A1 (en) | 2003-01-21 |
SV2003001148A (es) | 2003-03-18 |
MXPA04000069A (es) | 2004-05-21 |
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