MA30959B1 - Composes de pyrazole et de triazole substitues comme inhibiteurs de ksp - Google Patents
Composes de pyrazole et de triazole substitues comme inhibiteurs de kspInfo
- Publication number
- MA30959B1 MA30959B1 MA31938A MA31938A MA30959B1 MA 30959 B1 MA30959 B1 MA 30959B1 MA 31938 A MA31938 A MA 31938A MA 31938 A MA31938 A MA 31938A MA 30959 B1 MA30959 B1 MA 30959B1
- Authority
- MA
- Morocco
- Prior art keywords
- triazole compounds
- substituted pyrazole
- ksp inhibitors
- pharmaceutically acceptable
- ksp
- Prior art date
Links
- NOIXNOMHHWGUTG-UHFFFAOYSA-N 2-[[4-[4-pyridin-4-yl-1-(2,2,2-trifluoroethyl)pyrazol-3-yl]phenoxy]methyl]quinoline Chemical compound C=1C=C(OCC=2N=C3C=CC=CC3=CC=2)C=CC=1C1=NN(CC(F)(F)F)C=C1C1=CC=NC=C1 NOIXNOMHHWGUTG-UHFFFAOYSA-N 0.000 title abstract 2
- -1 TRIAZOLE COMPOUNDS Chemical class 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (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)
Abstract
L'INVENTION CONCERNE DE NOUVEAUX COMPOSÉS DE PYRAZOLE ET DE TRIAZOLE SUBSTITUÉS REPRÉSENTÉS PAR LA FORMULE (I), ET DES SELS, DES ESTERS OU DES PROMÉDICAMENTS PHARMACEUTIQUEMENT ACCEPTABLES DE CEUX-CI, DES COMPOSITIONS DE CES DÉRIVÉS CONTENANT DES EXCIPIENTS PHARMACEUTIQUEMENT ACCEPTABLES AINSI QUE DES UTILISATIONS DE CELLES-CI.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85896406P | 2006-11-13 | 2006-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30959B1 true MA30959B1 (fr) | 2009-12-01 |
Family
ID=39144618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31938A MA30959B1 (fr) | 2006-11-13 | 2009-06-01 | Composes de pyrazole et de triazole substitues comme inhibiteurs de ksp |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US8129358B2 (fr) |
| EP (1) | EP2091926B1 (fr) |
| JP (1) | JP5264755B2 (fr) |
| KR (1) | KR20090081020A (fr) |
| CN (1) | CN101558049B (fr) |
| AR (1) | AR063805A1 (fr) |
| AU (1) | AU2007323998B2 (fr) |
| BR (1) | BRPI0719002A2 (fr) |
| CA (1) | CA2668661A1 (fr) |
| CL (1) | CL2007003272A1 (fr) |
| CO (1) | CO6382171A2 (fr) |
| CR (1) | CR10787A (fr) |
| DO (1) | DOP2009000106A (fr) |
| EA (1) | EA017748B1 (fr) |
| EC (1) | ECSP099326A (fr) |
| ES (1) | ES2557478T3 (fr) |
| GE (1) | GEP20125389B (fr) |
| GT (1) | GT200900122A (fr) |
| HN (1) | HN2009000968A (fr) |
| IL (1) | IL198471A0 (fr) |
| MA (1) | MA30959B1 (fr) |
| MX (1) | MX2009005071A (fr) |
| NI (1) | NI200900084A (fr) |
| NO (1) | NO20092226L (fr) |
| NZ (1) | NZ576640A (fr) |
| PE (1) | PE20081169A1 (fr) |
| SM (1) | SMP200900045B (fr) |
| TN (1) | TN2009000178A1 (fr) |
| TW (1) | TW200831480A (fr) |
| UA (1) | UA97256C2 (fr) |
| WO (1) | WO2008063912A1 (fr) |
| ZA (1) | ZA200902940B (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2009005071A (es) * | 2006-11-13 | 2009-05-25 | Novartis Ag | Compuestos de pirazol y triazol sustituidos como inhibidores de ksp. |
| CA2674318A1 (fr) * | 2007-01-05 | 2008-07-17 | Novartis Ag | Derives cyclises en tant qu'inhibiteurs d'eg-5 |
| EA201201404A1 (ru) * | 2010-04-15 | 2013-04-30 | Новартис Аг | Триазолы как ингибиторы кбв (кинезин-белок веретена) |
| WO2011128388A2 (fr) * | 2010-04-15 | 2011-10-20 | Novartis Ag | Composés d'oxazole et de thiazole comme inhibiteurs de ksp |
| MX355439B (es) * | 2012-12-05 | 2018-04-18 | Merck Sharp & Dohme | Proceso para preparar inhibidores de la transcriptasa inversa. |
| EP2968591A1 (fr) * | 2013-03-15 | 2016-01-20 | Novartis AG | Inhibiteurs de la prolifération cellulaire et leurs conjugués |
| US9498540B2 (en) | 2013-03-15 | 2016-11-22 | Novartis Ag | Cell proliferation inhibitors and conjugates thereof |
| CA2930585A1 (fr) | 2013-12-04 | 2015-06-11 | Merck Sharp & Dohme Corp. | Procede de preparation d'inhibiteurs de transcriptase inverse |
| WO2016020791A1 (fr) | 2014-08-05 | 2016-02-11 | Novartis Ag | Conjugués anticorps ckit-médicament |
| US20190161499A1 (en) * | 2015-12-11 | 2019-05-30 | Syngenta Participations Ag | Pesticidally active 1,2,4-triazole derivatives |
| US11091447B2 (en) | 2020-01-03 | 2021-08-17 | Berg Llc | UBE2K modulators and methods for their use |
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|---|---|---|---|---|
| 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 (fr) | 1999-04-02 | 2002-01-02 | Neurogen Corporation | Derives d'aminoalkyle-imidazole condenses aryles et heteroaryles et leur utilisation comme antidiabetiques |
| US6545004B1 (en) * | 1999-10-27 | 2003-04-08 | Cytokinetics, Inc. | Methods and compositions utilizing quinazolinones |
| BR0015110A (pt) | 1999-10-27 | 2002-07-02 | Cytokinetics Inc | Métodos de tratamento de doenças de proliferação celular, de tratamento de um distúrbio associado com a atividade da cinesina ksp, de inibição da cinesina ksp, de triagem de moduladores da cinesina kps e de triagem de compostos que se ligam na cinesina ksp, e, compostos |
| MXPA03003039A (es) | 2000-10-06 | 2003-10-15 | Neurogen Corp | Derivados de indola y bencimidazola como moduladores del receptor crf. |
| US20040132830A1 (en) | 2001-01-19 | 2004-07-08 | Finer Jeffrey T | Triphenylmethane kinesin inhibitors |
| WO2002057244A1 (fr) | 2001-01-19 | 2002-07-25 | Cytokinetics, Inc. | Inhibiteurs de la kinesine a base de phenothiazine |
| EP1444209A4 (fr) | 2001-11-07 | 2005-02-16 | Merck & Co Inc | Inhibiteurs de la kinesine mitotique |
| EP1450816A4 (fr) | 2001-11-08 | 2008-02-13 | Univ Chicago | Methode de traitement de troubles lies a un taux de cholesterol eleve |
| US6753428B2 (en) | 2001-11-20 | 2004-06-22 | Cytokinetics, Inc. | Process for the racemization of chiral quinazolinones |
| ATE372341T1 (de) | 2001-12-06 | 2007-09-15 | Merck & Co Inc | Inhibitoren von mitotischem kinesin |
| JP4391825B2 (ja) | 2001-12-06 | 2009-12-24 | メルク エンド カムパニー インコーポレーテッド | 有糸分裂キネシン阻害剤 |
| WO2003049527A2 (fr) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Inhibiteurs miotitiques de la kinesine |
| JP2005515208A (ja) | 2001-12-06 | 2005-05-26 | メルク エンド カムパニー インコーポレーテッド | 有糸分裂性キネシン阻害剤 |
| JP4467979B2 (ja) | 2001-12-06 | 2010-05-26 | メルク・シャープ・エンド・ドーム・コーポレイション | 有糸分裂キネシン阻害剤 |
| AU2002357114B2 (en) * | 2001-12-07 | 2008-07-24 | Virginia Commonwealth University | Treatment of neoplasia |
| WO2003059289A2 (fr) | 2002-01-10 | 2003-07-24 | Neurogen Corporation | Ligands recepteurs de l'hormone de concentration de la melanine: analogues de benzoimidazole substitue |
| WO2003070701A2 (fr) | 2002-02-15 | 2003-08-28 | Cytokinetics, Inc. | Syntheses de quinazolinones |
| WO2003079973A2 (fr) | 2002-03-08 | 2003-10-02 | Merck & Co., Inc. | Inhibiteurs de kinesine mitotique |
| AU2003270015A1 (en) | 2002-05-09 | 2003-12-02 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| WO2003094839A2 (fr) | 2002-05-09 | 2003-11-20 | Cytokinetics, Inc. | Composes, compositions et procedes |
| WO2004026226A2 (fr) | 2002-05-10 | 2004-04-01 | Cytokinetics, Inc. | Composes, compositions et procedes |
| JP2005536475A (ja) | 2002-05-23 | 2005-12-02 | 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 |
| US20050234080A1 (en) | 2002-05-23 | 2005-10-20 | Coleman Paul J | Mitotic kinesin inhibitors |
| KR20050010515A (ko) | 2002-06-14 | 2005-01-27 | 머크 앤드 캄파니 인코포레이티드 | 유사분열 키네신 억제제 |
| US7301028B2 (en) | 2002-06-14 | 2007-11-27 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| GB0214139D0 (en) * | 2002-06-19 | 2002-07-31 | Glaxo Group Ltd | Chemical compounds |
| WO2004004652A2 (fr) | 2002-07-08 | 2004-01-15 | Merck & Co., Inc. | Site de liaison de la kinesine mitotique |
| WO2004006865A2 (fr) | 2002-07-17 | 2004-01-22 | Cytokinetics, Inc. | Composes, compositions et methodes |
| EP1537089A4 (fr) | 2002-07-23 | 2008-04-16 | Cytokinetics Inc | Composes, compositions et procedes |
| AU2003262747A1 (en) | 2002-08-21 | 2004-03-11 | Cytokinetics, Inc. | 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 |
| JP2007500746A (ja) | 2003-05-15 | 2007-01-18 | 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 |
| PT1732926E (pt) * | 2004-04-06 | 2009-04-03 | Novartis Vaccines & Diagnostic | Inibidores de cinesinas mitóticas |
| CA2564215A1 (fr) | 2004-05-21 | 2005-12-01 | Chiron Corporation | Derives de quinolinone substituee en tant qu'inhibiteurs de kinesine mitotique |
| 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 |
| KR20070072598A (ko) * | 2004-10-19 | 2007-07-04 | 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 | 인돌 및 벤지미다졸 유도체 |
| 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 |
| MX2009005071A (es) * | 2006-11-13 | 2009-05-25 | Novartis Ag | Compuestos de pirazol y triazol sustituidos como inhibidores de ksp. |
-
2007
- 2007-11-08 MX MX2009005071A patent/MX2009005071A/es active IP Right Grant
- 2007-11-08 KR KR1020097012214A patent/KR20090081020A/ko not_active Ceased
- 2007-11-08 EP EP07844993.1A patent/EP2091926B1/fr active Active
- 2007-11-08 WO PCT/US2007/084154 patent/WO2008063912A1/fr not_active Ceased
- 2007-11-08 US US12/312,389 patent/US8129358B2/en not_active Expired - Fee Related
- 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 EA EA200900631A patent/EA017748B1/ru not_active IP Right Cessation
- 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 US US11/937,426 patent/US7902240B2/en not_active Expired - Fee Related
- 2007-11-08 NZ NZ576640A patent/NZ576640A/en not_active IP Right Cessation
- 2007-11-08 ES ES07844993.1T patent/ES2557478T3/es active Active
- 2007-11-08 AU AU2007323998A patent/AU2007323998B2/en not_active Ceased
- 2007-11-08 CA CA002668661A patent/CA2668661A1/fr not_active Abandoned
- 2007-11-08 GE GEAP200711253A patent/GEP20125389B/en unknown
- 2007-11-12 TW TW096142719A patent/TW200831480A/zh unknown
- 2007-11-13 AR ARP070105052A patent/AR063805A1/es unknown
- 2007-11-13 PE PE2007001561A patent/PE20081169A1/es not_active Application Discontinuation
- 2007-11-13 CL CL200703272A patent/CL2007003272A1/es unknown
-
2009
- 2009-04-29 ZA ZA200902940A patent/ZA200902940B/xx unknown
- 2009-04-30 IL IL198471A patent/IL198471A0/en unknown
- 2009-05-08 CR CR10787A patent/CR10787A/es not_active Application Discontinuation
- 2009-05-08 TN TNP2009000178A patent/TN2009000178A1/fr unknown
- 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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