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
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 |
---|---|---|---|---|
EP2091926B1 (fr) * | 2006-11-13 | 2015-10-21 | Novartis AG | Composés de pyrazole et de triazole substitués comme inhibiteurs de ksp |
JP2010515687A (ja) * | 2007-01-05 | 2010-05-13 | ノバルティス アーゲー | キネシンスピンドルタンパク質阻害剤(eg−5)としてのイミダゾール誘導体 |
CA2794406A1 (fr) * | 2010-04-15 | 2011-10-20 | Novartis Ag | Composes de triazole comme inhibiteurs de la ksp |
JP2013525290A (ja) * | 2010-04-15 | 2013-06-20 | ノバルティス アーゲー | Ksp阻害剤としてのオキサゾールおよびチアゾール化合物 |
WO2014089140A1 (fr) * | 2012-12-05 | 2014-06-12 | Merck Sharp & Dohme Corp. | Procédé de préparation d'inhibiteurs de transcriptase inverse |
CN105451773A (zh) * | 2013-03-15 | 2016-03-30 | 诺华股份有限公司 | 细胞增殖抑制剂及其缀合物 |
US9498540B2 (en) | 2013-03-15 | 2016-11-22 | Novartis Ag | Cell proliferation inhibitors and conjugates thereof |
KR101803671B1 (ko) | 2013-12-04 | 2017-11-30 | 머크 샤프 앤드 돔 코포레이션 | 역전사효소 억제제의 제조 방법 |
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 |
CA3166630A1 (fr) | 2020-01-03 | 2021-07-08 | Berg Llc | Amides polycycliques utilises en tant que modulateurs d'ube2k pour le traitement du cancer |
Family Cites Families (47)
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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 |
MXPA02004162A (es) | 1999-10-27 | 2003-08-20 | Cytokinetics Inc | Metodo y composiciones que utilizan quinazolinonas. |
KR20030060904A (ko) | 2000-10-06 | 2003-07-16 | 뉴로젠 코포레이션 | Crf 수용체 조절자로서 벤즈이미다졸 및 인돌 유도체 |
US6992082B2 (en) | 2001-01-19 | 2006-01-31 | Cytokinetics, Inc. | Phenothiazine kinesin inhibitors |
US20040132830A1 (en) | 2001-01-19 | 2004-07-08 | Finer Jeffrey T | Triphenylmethane kinesin inhibitors |
AU2002363429B2 (en) | 2001-11-07 | 2008-05-08 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
EP1450816A4 (fr) | 2001-11-08 | 2008-02-13 | Univ Chicago | Methode de traitement de troubles lies a un taux de cholesterol eleve |
AU2002346471A1 (en) | 2001-11-20 | 2003-06-10 | Cytokinetics, Inc. | Process for the racemization of chiral quinazolinones |
WO2003050122A2 (fr) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Inhibiteurs mitotiques de la kinesine |
EP1458726B1 (fr) | 2001-12-06 | 2009-07-15 | Merck & Co., Inc. | Inhibiteurs miotitiques de la kinesine |
WO2003049678A2 (fr) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Inhibiteurs mitotiques de la kinesine |
WO2003049679A2 (fr) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Inhibiteurs mitotiques de la kinésine |
US7378411B2 (en) | 2001-12-06 | 2008-05-27 | Merck & Co., Inc. | Substituted thienopyrimidinones as a mitotic kinesin inhibitor |
JP2005516004A (ja) * | 2001-12-07 | 2005-06-02 | ヴァージニア コモンウェルス ユニバーシティ | 新形成の治療 |
JP2005526709A (ja) | 2002-01-10 | 2005-09-08 | ニューロジェン・コーポレーション | メラニン凝集ホルモン受容体リガンド:置換ベンゾイミダゾールアナログ |
AU2003213092A1 (en) | 2002-02-15 | 2003-09-09 | Smithkline Beecham Corporation | Syntheses of quinazolinones |
AU2003249597B2 (en) | 2002-03-08 | 2007-06-28 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
US7214800B2 (en) | 2002-05-09 | 2007-05-08 | Cytokinetics, Inc. | Compounds, compositions, and methods |
RU2004135554A (ru) | 2002-05-09 | 2006-01-20 | Цитокинетикс, Инк. (Us) | Пиримидиноны, композиции на их основе и способы их использования |
AU2003290507A1 (en) | 2002-05-10 | 2004-04-08 | Cytokinetics, Inc. | Compounds, compositions and methods |
AU2003265242A1 (en) | 2002-05-23 | 2003-12-22 | Cytokinetics, Inc. | Compounds, compositions, and methods |
AU2003231799A1 (en) | 2002-05-23 | 2003-12-12 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
ES2282647T3 (es) | 2002-06-14 | 2007-10-16 | MERCK & CO., INC. | Inhibidores de cinesina mitotica. |
ATE446094T1 (de) | 2002-06-14 | 2009-11-15 | Merck & Co Inc | Mitotische kinesin-hemmer |
GB0214139D0 (en) * | 2002-06-19 | 2002-07-31 | Glaxo Group Ltd | Chemical compounds |
CA2489562A1 (fr) | 2002-07-08 | 2004-01-15 | Merck & Co., Inc. | Site de liaison de la kinesine mitotique |
ATE423110T1 (de) | 2002-07-17 | 2009-03-15 | Cytokinetics Inc | Verbindungen, zusammensetzungen und verfahren zur behandlung von zellulären proliferativen erkrankungen |
WO2004009036A2 (fr) | 2002-07-23 | 2004-01-29 | Cytokinetics, Inc. | Composes, compositions et procedes |
JP2005536553A (ja) | 2002-08-21 | 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 |
EP1554265A4 (fr) | 2002-09-13 | 2008-05-07 | Cytokinetics Inc | Compos s, compositions et m thodes |
WO2004100873A2 (fr) | 2003-05-07 | 2004-11-25 | Cytokinetics, Inc. | Composes, compositions et methodes |
EP1622878A4 (fr) | 2003-05-15 | 2008-04-09 | Cytokinetics Inc | Composes, compositions et procedes |
JP4895220B2 (ja) * | 2004-04-06 | 2012-03-14 | 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 | キネシン有糸分裂インヒビター |
DE602005008953D1 (de) * | 2004-05-21 | 2008-09-25 | Novartis Vaccines & Diagnostic | Substituierte chinolinderivate als inhibitoren von mitotischem kinesin |
KR101170925B1 (ko) * | 2004-06-18 | 2012-08-07 | 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 | 암 치료용 키네신 방추 단백질 (ksp) 억제제로서의n-(1-(1-벤질-4-페닐-1h-이미다졸-2-일)-2,2-디메틸프로필)벤자미드 유도체 및 관련 화합물 |
CN101233115A (zh) * | 2004-10-19 | 2008-07-30 | 诺华疫苗和诊断公司 | 吲哚和苯并咪唑衍生物 |
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 |
EP2091926B1 (fr) * | 2006-11-13 | 2015-10-21 | Novartis AG | Composés de pyrazole et de triazole substitués comme inhibiteurs de ksp |
-
2007
- 2007-11-08 EP EP07844993.1A patent/EP2091926B1/fr active Active
- 2007-11-08 WO PCT/US2007/084154 patent/WO2008063912A1/fr active Application Filing
- 2007-11-08 JP JP2009536490A patent/JP5264755B2/ja not_active Expired - Fee Related
- 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 MX MX2009005071A patent/MX2009005071A/es active IP Right Grant
- 2007-11-08 US US12/312,389 patent/US8129358B2/en not_active Expired - Fee Related
- 2007-11-08 EA EA200900631A patent/EA017748B1/ru not_active IP Right Cessation
- 2007-11-08 US US11/937,426 patent/US7902240B2/en 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 GE GEAP200711253A patent/GEP20125389B/en unknown
- 2007-11-08 NZ NZ576640A patent/NZ576640A/en not_active IP Right Cessation
- 2007-11-08 CA CA002668661A patent/CA2668661A1/fr not_active Abandoned
- 2007-11-08 KR KR1020097012214A patent/KR20090081020A/ko not_active Application Discontinuation
- 2007-11-08 ES ES07844993.1T patent/ES2557478T3/es active Active
- 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 GT GT200900122A patent/GT200900122A/es unknown
- 2009-05-12 CO CO09048059A patent/CO6382171A2/es not_active Application Discontinuation
- 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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