CR10787A - Substituted pyrazole and triazole compounds as ksp inhibitors - Google Patents
Substituted pyrazole and triazole compounds as ksp inhibitorsInfo
- Publication number
- CR10787A CR10787A CR10787A CR10787A CR10787A CR 10787 A CR10787 A CR 10787A CR 10787 A CR10787 A CR 10787A CR 10787 A CR10787 A CR 10787A CR 10787 A CR10787 A CR 10787A
- Authority
- CR
- Costa Rica
- Prior art keywords
- triazole compounds
- substituted pyrazole
- ksp inhibitors
- ksp
- inhibitors
- 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 1
- -1 TRIAZOLE COMPOUNDS Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 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 |
---|---|
CR10787A true CR10787A (es) | 2009-07-02 |
Family
ID=39144618
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CR10787A CR10787A (es) | 2006-11-13 | 2009-05-08 | Substituted pyrazole and triazole compounds as ksp inhibitors |
Country Status (32)
Country | Link |
---|---|
US (2) | US7902240B2 (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 |
---|---|---|---|---|
US7902240B2 (en) * | 2006-11-13 | 2011-03-08 | Novartis Ag | Substituted pyrazole and triazole compounds as KSP inhibitors |
WO2008086122A2 (en) * | 2007-01-05 | 2008-07-17 | Novartis Ag | Imidazole derivatives as kinesin spindle protein inhibitors (eg-5) |
WO2011128388A2 (en) * | 2010-04-15 | 2011-10-20 | Novartis Ag | Oxazole and thiazole compounds as ksp inhibitors |
AU2011239977B2 (en) * | 2010-04-15 | 2014-11-27 | Novartis Ag | Triazole compounds as KSP inhibitors |
WO2014089140A1 (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 |
WO2014151030A1 (en) * | 2013-03-15 | 2014-09-25 | Novartis Ag | Cell proliferation inhibitors and conjugates thereof |
EP3077376B1 (en) | 2013-12-04 | 2019-10-16 | Merck Sharp & Dohme Corp. | Process for making reverse transcriptase inhibitors |
WO2016020791A1 (en) | 2014-08-05 | 2016-02-11 | Novartis Ag | Ckit antibody drug conjugates |
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 |
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 |
JP2002541146A (ja) | 1999-04-02 | 2002-12-03 | ニューロゲン コーポレイション | アリールおよびヘテロアリール融合のアミノアルキル−イミダゾール誘導体および糖尿病薬としてのその使用 |
US6545004B1 (en) | 1999-10-27 | 2003-04-08 | Cytokinetics, Inc. | Methods and compositions utilizing quinazolinones |
KR20020062930A (ko) | 1999-10-27 | 2002-07-31 | 싸이토키네틱스, 인코포레이티드 | 퀴나졸리논을 사용하는 방법 및 조성물 |
CA2425185A1 (en) | 2000-10-06 | 2002-04-11 | Stephane De Lombaert | Benzimidazole and indole derivatives as crf receptor modulators |
EP1360180A1 (en) | 2001-01-19 | 2003-11-12 | Cytokinetics, Inc. | Phenothiazine kinesin inhibitors |
EP1351671A1 (en) | 2001-01-19 | 2003-10-15 | Cytokinetics, Inc. | Triphenylmethane kinesin inhibitors |
CA2465491A1 (en) | 2001-11-07 | 2003-05-15 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
CA2466033A1 (en) | 2001-11-08 | 2003-05-15 | The University Of Chicago | Method of treating disorder related to high cholesterol concentration |
US6753428B2 (en) | 2001-11-20 | 2004-06-22 | Cytokinetics, Inc. | Process for the racemization of chiral quinazolinones |
US7262186B2 (en) | 2001-12-06 | 2007-08-28 | Merck & Co., Inc. | Substituted pyrazolo[3,4-d] pyrimidinones as a mitotic kinesin inhibitor |
ATE447577T1 (de) | 2001-12-06 | 2009-11-15 | Merck & Co Inc | Mitotische kinesin-hemmer |
ATE424388T1 (de) | 2001-12-06 | 2009-03-15 | Merck & Co Inc | Mitotische kinesinhemmer |
AU2002364128B2 (en) | 2001-12-06 | 2008-03-06 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
DE60222302T2 (de) | 2001-12-06 | 2008-05-29 | Merck & Co., Inc. | Inhibitoren von mitotischem kinesin |
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 |
EP1465888A2 (en) | 2002-01-10 | 2004-10-13 | Neurogen Corporation | Melanin concentrating hormone receptor ligands: substituted benzoimidazole analogues |
US7009049B2 (en) | 2002-02-15 | 2006-03-07 | Cytokinetics, Inc. | Syntheses of quinazolinones |
JP4399269B2 (ja) | 2002-03-08 | 2010-01-13 | 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薬 |
WO2003097053A1 (en) | 2002-05-09 | 2003-11-27 | Cytokinetics, Inc. | Compounds, compositions, and methods |
JP2006508030A (ja) | 2002-05-09 | 2006-03-09 | サイトキネティクス・インコーポレーテッド | ピリミジノン化合物、組成物および方法 |
US20040053948A1 (en) | 2002-05-10 | 2004-03-18 | Cytokinetics, Inc. | Compounds, compositions and methods |
WO2003103575A2 (en) | 2002-05-23 | 2003-12-18 | Cytokinetics, Inc. | Compounds, compositions, and methods |
CA2483627A1 (en) | 2002-05-23 | 2003-12-04 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
MXPA04012642A (es) | 2002-06-14 | 2005-03-23 | Merck & Co Inc | Inhibidores de la cinesina mitotica. |
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 |
JP2005537257A (ja) | 2002-07-08 | 2005-12-08 | メルク エンド カムパニー インコーポレーテッド | 有糸分裂キネシン結合部位 |
EP1539727B1 (en) | 2002-07-17 | 2009-02-18 | Cytokinetics, Inc. | Compounds, compositions, and methods for treating cellular proliferative diseases |
EP1537089A4 (en) | 2002-07-23 | 2008-04-16 | Cytokinetics Inc | CONNECTIONS, COMPOSITIONS AND PROCEDURES |
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 |
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 |
CA2561904A1 (en) | 2004-04-06 | 2005-10-27 | Chiron Corporation | Mitotic kinesin inhibitors |
DK1753723T3 (da) * | 2004-05-21 | 2008-10-20 | Novartis Vaccines & Diagnostic | Substituerede quinolinderivater som mitotiske kinesininhibitorer |
MXPA06014909A (es) * | 2004-06-18 | 2007-02-28 | Chiron Corp | Derivados de n-(1-(1-bencil -4-fenil-1h -imidazol -2-il)-2, 2-dimetilpropil) benzamida y compuestos relacionados como inhibidores de proteina de huso de cinesina (ksp) para el tratamiento del cancer. |
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 |
MY147188A (en) * | 2005-08-09 | 2012-11-14 | Novartis Ag | Substituted imidazole compounds as ksp inhibitors |
US7902240B2 (en) * | 2006-11-13 | 2011-03-08 | Novartis Ag | Substituted pyrazole and triazole compounds as KSP inhibitors |
-
2007
- 2007-11-08 US US11/937,426 patent/US7902240B2/en 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 MX MX2009005071A patent/MX2009005071A/es active IP Right Grant
- 2007-11-08 EP EP07844993.1A patent/EP2091926B1/en active Active
- 2007-11-08 JP JP2009536490A patent/JP5264755B2/ja not_active Expired - Fee Related
- 2007-11-08 US US12/312,389 patent/US8129358B2/en not_active Expired - Fee Related
- 2007-11-08 GE GEAP200711253A patent/GEP20125389B/en unknown
- 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 AU AU2007323998A patent/AU2007323998B2/en not_active Ceased
- 2007-11-08 CA CA002668661A patent/CA2668661A1/en not_active Abandoned
- 2007-11-08 CN CN2007800456741A patent/CN101558049B/zh not_active Expired - Fee Related
- 2007-11-08 WO PCT/US2007/084154 patent/WO2008063912A1/en active Application Filing
- 2007-11-08 KR KR1020097012214A patent/KR20090081020A/ko not_active Application Discontinuation
- 2007-11-08 BR BRPI0719002-6A patent/BRPI0719002A2/pt not_active IP Right Cessation
- 2007-11-12 TW TW096142719A patent/TW200831480A/zh unknown
- 2007-11-13 PE PE2007001561A patent/PE20081169A1/es not_active Application Discontinuation
- 2007-11-13 CL CL200703272A patent/CL2007003272A1/es unknown
- 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 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 EC EC2009009326A patent/ECSP099326A/es unknown
- 2009-05-13 HN HN2009000968A patent/HN2009000968A/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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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal (granting procedure) |