BR0312798A - Derivados de isotiazol úteis como agentes anticancerìgenos - Google Patents
Derivados de isotiazol úteis como agentes anticancerìgenosInfo
- Publication number
- BR0312798A BR0312798A BR0312798-2A BR0312798A BR0312798A BR 0312798 A BR0312798 A BR 0312798A BR 0312798 A BR0312798 A BR 0312798A BR 0312798 A BR0312798 A BR 0312798A
- Authority
- BR
- Brazil
- Prior art keywords
- anticancer agents
- derivatives useful
- formula
- compounds
- isothiazole derivatives
- Prior art date
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
- C07D417/12—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
"DERIVADOS DE ISOTIAZOL úTEIS COMO AGENTES ANTICANCERìGENOS". A presente invenção refere-se a compostos de fórmula 1 ou aos seus sais, pró-drogas, solvatos ou hidratos farmaceuticamente aceitáveis em que X, R^ 1^, e R^ 2^ são tal como aqui definidos. A invenção também refere-se a composições farmacêuticas contendo os compostos de fórmula 1 e a métodos de tratamento de distúrbios hiperproliferativos em um mamífero pela administração de compostos de fórmula 1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39838602P | 2002-07-25 | 2002-07-25 | |
PCT/IB2003/003161 WO2004011461A1 (en) | 2002-07-25 | 2003-07-14 | Isothiazole derivatives useful as anticancer agents |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0312798A true BR0312798A (pt) | 2005-05-03 |
Family
ID=31188391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0312798-2A BR0312798A (pt) | 2002-07-25 | 2003-07-14 | Derivados de isotiazol úteis como agentes anticancerìgenos |
Country Status (8)
Country | Link |
---|---|
US (1) | US7276602B2 (pt) |
EP (1) | EP1527071A1 (pt) |
JP (1) | JP4511352B2 (pt) |
AU (1) | AU2003281664A1 (pt) |
BR (1) | BR0312798A (pt) |
CA (1) | CA2493701A1 (pt) |
MX (1) | MXPA05000950A (pt) |
WO (1) | WO2004011461A1 (pt) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2349588C2 (ru) | 2004-08-26 | 2009-03-20 | Пфайзер Продактс Инк. | Способы получения производных изотиазола |
US7429667B2 (en) | 2005-01-20 | 2008-09-30 | Ardea Biosciences, Inc. | Phenylamino isothiazole carboxamidines as MEK inhibitors |
US7842836B2 (en) | 2006-04-11 | 2010-11-30 | Ardea Biosciences | N-aryl-N'alkyl sulfamides as MEK inhibitors |
CN101454004B (zh) * | 2006-04-18 | 2013-12-04 | 阿迪亚生命科学公司 | 作为mek抑制剂的吡啶酮磺酰胺类和吡啶酮硫酰胺类 |
US8509487B2 (en) * | 2007-04-19 | 2013-08-13 | Avago Technologies General Ip (Singapore) Pte. Ltd. | System and method for optically measuring a parameter of an object |
WO2010011375A2 (en) | 2008-04-21 | 2010-01-28 | Merck & Co., Inc. | Inhibitors of janus kinases |
EP2791139B1 (en) | 2011-12-12 | 2017-11-08 | Dr. Reddy's Laboratories Ltd. | Substituted heterocyclic compounds as tropomyosin receptor kinase a (trka) inhibitors |
CN102944674B (zh) * | 2012-11-05 | 2014-10-22 | 武汉远征世纪制药有限公司 | 一种检测TrkB受体pan-Tyr位点活性的ELISA试剂盒及其使用方法 |
BR112015021334B1 (pt) | 2013-03-14 | 2020-04-07 | Panoptica Inc | formulação ocular tópica em suspenão e uso da mesma para tratamento e/ou melhora de uma doença do segmento posterior do olho |
US9394305B2 (en) | 2014-06-23 | 2016-07-19 | Dr. Reddy's Laboratories Ltd. | Substituted imidazo[1,2-a]pyridine compounds as tropomyosin receptor kinase a (TrkA) inhibitors |
EP3942045A1 (en) | 2019-03-21 | 2022-01-26 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
WO2020245208A1 (en) | 2019-06-04 | 2020-12-10 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Use of cd9 as a biomarker and as a biotarget in glomerulonephritis or glomerulosclerosis |
EP4054579A1 (en) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
WO2023193809A1 (zh) * | 2022-04-08 | 2023-10-12 | 深圳众格生物科技有限公司 | Sarm1抑制剂化合物、包含其的药物组合物及其制备方法和用途 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69222637T2 (de) | 1991-05-10 | 1998-02-26 | Rhone Poulenc Rorer Int | Bis mono- und bicyclische aryl- und heteroarylderivate mit inhibierender wirkung auf die egf und/oder pdgf-rezeptor tyrosinkinase |
IL112721A0 (en) * | 1994-03-10 | 1995-05-26 | Zeneca Ltd | Azole derivatives |
GEP20032896B (en) | 1997-10-27 | 2003-02-25 | Agouron Pharma | 4-Aminothiazole Derivatives, Containing Them Pharmaceutical Compositions Inhibiting Cyclin-Dependent Kinases and Methods for Treatment |
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 |
HN2000000051A (es) | 1999-05-19 | 2001-02-02 | Pfizer Prod Inc | Derivados heterociclicos utiles como agentes anticancerosos |
ES2271086T3 (es) * | 2000-11-28 | 2007-04-16 | Pfizer Products Inc. | Sales de una isotiazol-4-carboxamida y su uso como agentes de antihiperproliferacion. |
-
2003
- 2003-07-14 JP JP2004524014A patent/JP4511352B2/ja not_active Expired - Fee Related
- 2003-07-14 AU AU2003281664A patent/AU2003281664A1/en not_active Abandoned
- 2003-07-14 BR BR0312798-2A patent/BR0312798A/pt not_active IP Right Cessation
- 2003-07-14 EP EP03741009A patent/EP1527071A1/en not_active Withdrawn
- 2003-07-14 CA CA002493701A patent/CA2493701A1/en not_active Abandoned
- 2003-07-14 MX MXPA05000950A patent/MXPA05000950A/es not_active Application Discontinuation
- 2003-07-14 WO PCT/IB2003/003161 patent/WO2004011461A1/en active Application Filing
- 2003-07-24 US US10/626,406 patent/US7276602B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
WO2004011461A1 (en) | 2004-02-05 |
MXPA05000950A (es) | 2005-05-16 |
JP4511352B2 (ja) | 2010-07-28 |
US7276602B2 (en) | 2007-10-02 |
AU2003281664A1 (en) | 2004-02-16 |
JP2005536523A (ja) | 2005-12-02 |
CA2493701A1 (en) | 2004-02-05 |
US20040152691A1 (en) | 2004-08-05 |
EP1527071A1 (en) | 2005-05-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE 6A. E 7A. ANUIDADES. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2064 DE 27/07/2010. |