CL2007003272A1 - Compuestos derivados de pirazol y triazol sustituidos; y composicion farmaceutica, util para el tratamiento de una enfermedad proliferativa celular. - Google Patents
Compuestos derivados de pirazol y triazol sustituidos; y composicion farmaceutica, util para el tratamiento de una enfermedad proliferativa celular.Info
- Publication number
- CL2007003272A1 CL2007003272A1 CL200703272A CL2007003272A CL2007003272A1 CL 2007003272 A1 CL2007003272 A1 CL 2007003272A1 CL 200703272 A CL200703272 A CL 200703272A CL 2007003272 A CL2007003272 A CL 2007003272A CL 2007003272 A1 CL2007003272 A1 CL 2007003272A1
- Authority
- CL
- Chile
- Prior art keywords
- pirazol
- triazol
- replaced
- useful
- treatment
- Prior art date
Links
- QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical compound C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 230000002062 proliferating effect Effects 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85896406P | 2006-11-13 | 2006-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2007003272A1 true CL2007003272A1 (es) | 2008-03-24 |
Family
ID=39144618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL200703272A CL2007003272A1 (es) | 2006-11-13 | 2007-11-13 | Compuestos derivados de pirazol y triazol sustituidos; y composicion farmaceutica, util para el tratamiento de una enfermedad proliferativa celular. |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US8129358B2 (es) |
| EP (1) | EP2091926B1 (es) |
| JP (1) | JP5264755B2 (es) |
| KR (1) | KR20090081020A (es) |
| CN (1) | CN101558049B (es) |
| AR (1) | AR063805A1 (es) |
| AU (1) | AU2007323998B2 (es) |
| BR (1) | BRPI0719002A2 (es) |
| CA (1) | CA2668661A1 (es) |
| CL (1) | CL2007003272A1 (es) |
| CO (1) | CO6382171A2 (es) |
| CR (1) | CR10787A (es) |
| DO (1) | DOP2009000106A (es) |
| EA (1) | EA017748B1 (es) |
| EC (1) | ECSP099326A (es) |
| ES (1) | ES2557478T3 (es) |
| GE (1) | GEP20125389B (es) |
| GT (1) | GT200900122A (es) |
| HN (1) | HN2009000968A (es) |
| IL (1) | IL198471A0 (es) |
| MA (1) | MA30959B1 (es) |
| MX (1) | MX2009005071A (es) |
| NI (1) | NI200900084A (es) |
| NO (1) | NO20092226L (es) |
| NZ (1) | NZ576640A (es) |
| PE (1) | PE20081169A1 (es) |
| SM (1) | SMP200900045B (es) |
| TN (1) | TN2009000178A1 (es) |
| TW (1) | TW200831480A (es) |
| UA (1) | UA97256C2 (es) |
| WO (1) | WO2008063912A1 (es) |
| ZA (1) | ZA200902940B (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2557478T3 (es) * | 2006-11-13 | 2016-01-26 | Novartis Ag | Compuestos de pirazol y triazol como inhibidores de KSP |
| NZ577727A (en) * | 2007-01-05 | 2012-03-30 | Novartis Ag | Imidazole derivatives as kinesin spindle protein inhibitors (eg-5) |
| BR112012025879A2 (pt) * | 2010-04-15 | 2017-11-21 | Novartis Ag | compostos de triazol como inibidores de ksp |
| US8748626B2 (en) | 2010-04-15 | 2014-06-10 | Novartis Ag | Oxazole and thiazole compounds as KSP inhibitors |
| CA2892919A1 (en) * | 2012-12-05 | 2014-06-12 | Merck Sharp & Dohme Corp. | Process for making reverse transcriptase inhibitors |
| US9498540B2 (en) | 2013-03-15 | 2016-11-22 | Novartis Ag | Cell proliferation inhibitors and conjugates thereof |
| EP2968591A1 (en) * | 2013-03-15 | 2016-01-20 | Novartis AG | Cell proliferation inhibitors and conjugates thereof |
| CA2930585A1 (en) | 2013-12-04 | 2015-06-11 | Merck Sharp & Dohme Corp. | Process for making reverse transcriptase inhibitors |
| US10786578B2 (en) | 2014-08-05 | 2020-09-29 | Novartis Ag | CKIT antibody drug conjugates |
| WO2017097927A1 (en) * | 2015-12-11 | 2017-06-15 | Syngenta Participations Ag | Pesticidally active 1,2,4-triazole derivatives |
| JP2023509452A (ja) | 2020-01-03 | 2023-03-08 | バーグ エルエルシー | がんを処置するためのｕｂｅ２ｋモジュレータとしての多環式アミド |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| US4501728A (en) | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
| US5023252A (en) * | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| US5011472A (en) * | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| US5185450A (en) * | 1991-02-19 | 1993-02-09 | University Of South Florida | Tetrazolium compounds for cell viability assays |
| AUPP042397A0 (en) * | 1997-11-18 | 1997-12-11 | Fujisawa Pharmaceutical Co., Ltd. | 5-arylpyrazole compounds |
| EP1165519A1 (en) | 1999-04-02 | 2002-01-02 | Neurogen Corporation | Aryl and heteroaryl fused aminoalkyl-imidazole derivatives and their use as antidiabetics |
| US6545004B1 (en) | 1999-10-27 | 2003-04-08 | Cytokinetics, Inc. | Methods and compositions utilizing quinazolinones |
| JP2003512461A (ja) | 1999-10-27 | 2003-04-02 | サイトキネティクス・インコーポレーテッド | キナゾリノンを用いた方法並びに組成 |
| EP1322620A1 (en) | 2000-10-06 | 2003-07-02 | Neurogen Corporation | Benzimidazole and indole derivatives as crf receptor modulators |
| WO2002056880A1 (en) | 2001-01-19 | 2002-07-25 | Cytokinetics, Inc. | Triphenylmethane kinesin inhibitors |
| WO2002057244A1 (en) | 2001-01-19 | 2002-07-25 | Cytokinetics, Inc. | Phenothiazine kinesin inhibitors |
| WO2003039460A2 (en) | 2001-11-07 | 2003-05-15 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| TW200300078A (en) | 2001-11-08 | 2003-05-16 | Univ Chicago | Method of treating disorder related to high cholesterol concentration |
| AU2002346471A1 (en) | 2001-11-20 | 2003-06-10 | Cytokinetics, Inc. | Process for the racemization of chiral quinazolinones |
| EP1481077B1 (en) | 2001-12-06 | 2009-11-04 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| EP1463733B1 (en) | 2001-12-06 | 2007-09-05 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| AU2002364128B2 (en) | 2001-12-06 | 2008-03-06 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
| US7262186B2 (en) | 2001-12-06 | 2007-08-28 | Merck & Co., Inc. | Substituted pyrazolo[3,4-d] pyrimidinones as a mitotic kinesin inhibitor |
| WO2003049678A2 (en) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| AU2002357114B2 (en) * | 2001-12-07 | 2008-07-24 | Virginia Commonwealth University | Treatment of neoplasia |
| CA2472470A1 (en) | 2002-01-10 | 2003-07-24 | Neurogen Corporation | Melanin concentrating hormone receptor ligands: substituted benzoimidazole analogues |
| AU2003213092A1 (en) | 2002-02-15 | 2003-09-09 | Smithkline Beecham Corporation | Syntheses of quinazolinones |
| DE60329990D1 (de) | 2002-03-08 | 2009-12-24 | Merck & Co Inc | Mitotische kinesin-hemmer |
| AU2003223786A1 (en) | 2002-05-09 | 2003-11-11 | Cytokinetics, Inc. | Compounds, methods and compositions |
| US7214800B2 (en) | 2002-05-09 | 2007-05-08 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| WO2004026226A2 (en) | 2002-05-10 | 2004-04-01 | Cytokinetics, Inc. | Compounds, compositions and methods |
| WO2003103575A2 (en) | 2002-05-23 | 2003-12-18 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| AU2003231799A1 (en) | 2002-05-23 | 2003-12-12 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| CA2486215A1 (en) | 2002-06-14 | 2003-12-24 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| AU2003245453B2 (en) | 2002-06-14 | 2008-08-14 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
| GB0214139D0 (en) * | 2002-06-19 | 2002-07-31 | Glaxo Group Ltd | Chemical compounds |
| CA2489562A1 (en) | 2002-07-08 | 2004-01-15 | Merck & Co., Inc. | Mitotic kinesin binding site |
| EP1539727B1 (en) | 2002-07-17 | 2009-02-18 | Cytokinetics, Inc. | Compounds, compositions, and methods for treating cellular proliferative diseases |
| JP2006501201A (ja) | 2002-07-23 | 2006-01-12 | サイトキネティクス・インコーポレーテッド | 化合物、組成物および方法 |
| US20040048853A1 (en) | 2002-08-21 | 2004-03-11 | Gustave Bergnes | Compounds, compositions, and methods |
| JP2005539062A (ja) | 2002-09-13 | 2005-12-22 | サイトキネティクス・インコーポレーテッド | 化合物、組成物および方法 |
| US20080021079A1 (en) | 2003-05-07 | 2008-01-24 | Han-Jie Zhou | Compounds, Compositions, and Methods |
| WO2004103282A2 (en) | 2003-05-15 | 2004-12-02 | Cytokinetics, Inc. | Compounds, compositions and methods |
| CN1984912A (zh) | 2004-04-06 | 2007-06-20 | 希龙公司 | 有丝分裂驱动蛋白抑制剂 |
| MXPA06011958A (es) | 2004-05-21 | 2006-12-15 | Chiron Corp | Derivados de quinolina sustituidos como inhibidores de cinesina mitotica. |
| JP4836280B2 (ja) * | 2004-06-18 | 2011-12-14 | ノバルティス バクシンズ アンド ダイアグノスティックス，インコーポレーテッド | 癌を治療するためのキネシンスピンドルタンパク質（ｋｓｐ）阻害剤としてのｎ−（１−（１−ベンジル−４−フェニル−１ｈ−イミダゾール−２−イル）−２，２−ジメチルプロピル）ベンズアミド誘導体および関連化合物 |
| WO2006049835A2 (en) * | 2004-10-19 | 2006-05-11 | Novartis Vaccines And Diagnostics Inc. | Indole and benzimidazole derivatives |
| US7829589B2 (en) * | 2005-06-10 | 2010-11-09 | Elixir Pharmaceuticals, Inc. | Sulfonamide compounds and uses thereof |
| TW200800951A (en) | 2005-08-09 | 2008-01-01 | Novartis Ag | Substituted imidazole compounds as KSP inhibitors |
| ES2557478T3 (es) * | 2006-11-13 | 2016-01-26 | Novartis Ag | Compuestos de pirazol y triazol como inhibidores de KSP |
-
2007
- 2007-11-08 ES ES07844993.1T patent/ES2557478T3/es active Active
- 2007-11-08 NZ NZ576640A patent/NZ576640A/en not_active IP Right Cessation
- 2007-11-08 WO PCT/US2007/084154 patent/WO2008063912A1/en active Application Filing
- 2007-11-08 CA CA002668661A patent/CA2668661A1/en not_active Abandoned
- 2007-11-08 KR KR1020097012214A patent/KR20090081020A/ko not_active Application Discontinuation
- 2007-11-08 GE GEAP200711253A patent/GEP20125389B/en unknown
- 2007-11-08 JP JP2009536490A patent/JP5264755B2/ja not_active Expired - Fee Related
- 2007-11-08 CN CN2007800456741A patent/CN101558049B/zh not_active Expired - Fee Related
- 2007-11-08 UA UAA200904556A patent/UA97256C2/ru unknown
- 2007-11-08 BR BRPI0719002-6A patent/BRPI0719002A2/pt not_active IP Right Cessation
- 2007-11-08 AU AU2007323998A patent/AU2007323998B2/en not_active Ceased
- 2007-11-08 US US12/312,389 patent/US8129358B2/en not_active Expired - Fee Related
- 2007-11-08 MX MX2009005071A patent/MX2009005071A/es active IP Right Grant
- 2007-11-08 EA EA200900631A patent/EA017748B1/ru not_active IP Right Cessation
- 2007-11-08 EP EP07844993.1A patent/EP2091926B1/en active Active
- 2007-11-08 US US11/937,426 patent/US7902240B2/en not_active Expired - Fee Related
- 2007-11-12 TW TW096142719A patent/TW200831480A/zh unknown
- 2007-11-13 CL CL200703272A patent/CL2007003272A1/es unknown
- 2007-11-13 PE PE2007001561A patent/PE20081169A1/es not_active Application Discontinuation
- 2007-11-13 AR ARP070105052A patent/AR063805A1/es unknown
-
2009
- 2009-04-29 ZA ZA200902940A patent/ZA200902940B/xx unknown
- 2009-04-30 IL IL198471A patent/IL198471A0/en unknown
- 2009-05-08 TN TNP2009000178A patent/TN2009000178A1/fr unknown
- 2009-05-08 CR CR10787A patent/CR10787A/es not_active Application Discontinuation
- 2009-05-11 DO DO2009000106A patent/DOP2009000106A/es unknown
- 2009-05-12 CO CO09048059A patent/CO6382171A2/es not_active Application Discontinuation
- 2009-05-12 GT GT200900122A patent/GT200900122A/es unknown
- 2009-05-13 HN HN2009000968A patent/HN2009000968A/es unknown
- 2009-05-13 EC EC2009009326A patent/ECSP099326A/es unknown
- 2009-05-13 NI NI200900084A patent/NI200900084A/es unknown
- 2009-06-01 MA MA31938A patent/MA30959B1/fr unknown
- 2009-06-09 NO NO20092226A patent/NO20092226L/no not_active Application Discontinuation
- 2009-06-10 SM SM200900045T patent/SMP200900045B/it unknown
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