IL161576A0 - Benzimidazoles and analogues and their use as protein kinases inhibitors - Google Patents
Benzimidazoles and analogues and their use as protein kinases inhibitorsInfo
- Publication number
- IL161576A0 IL161576A0 IL16157602A IL16157602A IL161576A0 IL 161576 A0 IL161576 A0 IL 161576A0 IL 16157602 A IL16157602 A IL 16157602A IL 16157602 A IL16157602 A IL 16157602A IL 161576 A0 IL161576 A0 IL 161576A0
- Authority
- IL
- Israel
- Prior art keywords
- benzimidazoles
- analogues
- protein kinases
- kinases inhibitors
- inhibitors
- Prior art date
Links
- 102000001253 Protein Kinase Human genes 0.000 title 1
- 150000001556 benzimidazoles Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 108060006633 protein kinase Proteins 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- 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
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- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- 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
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- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- 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
- C07D403/14—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 three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07—ORGANIC CHEMISTRY
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- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Toxicology (AREA)
- Urology & Nephrology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Child & Adolescent Psychology (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0113868A FR2831537B1 (en) | 2001-10-26 | 2001-10-26 | NOVEL BENZIMIDAZOLE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF, THEIR USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND THE USE THEREOF |
| GB0206895A GB0206895D0 (en) | 2002-03-22 | 2002-03-22 | Chemical compounds |
| GB0206893A GB0206893D0 (en) | 2002-03-22 | 2002-03-22 | Chemical compounds |
| US39515102P | 2002-07-11 | 2002-07-11 | |
| US39506002P | 2002-07-11 | 2002-07-11 | |
| PCT/GB2002/004763 WO2003035065A1 (en) | 2001-10-26 | 2002-10-24 | Benzimidazoles and analogues and their use as protein kinases inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL161576A0 true IL161576A0 (en) | 2004-09-27 |
Family
ID=27515325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL16157602A IL161576A0 (en) | 2001-10-26 | 2002-10-24 | Benzimidazoles and analogues and their use as protein kinases inhibitors |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1441725A1 (en) |
| JP (1) | JP5039268B2 (en) |
| AU (1) | AU2002334217B2 (en) |
| BR (1) | BR0213562A (en) |
| CA (1) | CA2465247C (en) |
| IL (1) | IL161576A0 (en) |
| MX (1) | MXPA04003954A (en) |
| UY (1) | UY27516A1 (en) |
| WO (1) | WO2003035065A1 (en) |
Families Citing this family (174)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7524635B2 (en) | 2003-04-17 | 2009-04-28 | Biosite Incorporated | Methods and compositions for measuring natriuretic peptides and uses thereof |
| CA2475633C (en) * | 2002-02-06 | 2013-04-02 | Vertex Pharmaceuticals Incorporated | Heteroaryl compounds useful as inhibitors of gsk-3 |
| DE10227668A1 (en) * | 2002-06-20 | 2004-01-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Medicines for the treatment of systemic inflammatory response syndrome |
| BR0313078A (en) | 2002-08-06 | 2005-07-12 | Astrazeneca Ab | A compound or a pharmaceutically acceptable salt thereof, a pharmaceutical composition, and use of the compound or a pharmaceutically acceptable salt thereof. |
| US7462613B2 (en) | 2002-11-19 | 2008-12-09 | Sanofi-Aventis Deutschland Gmbh | Pyridazinone derivatives as pharmaceuticals and pharmaceutical compositions containing them |
| US7309701B2 (en) | 2002-11-19 | 2007-12-18 | Sanofi-Aventis Deutschland Gmbh | Pyridazinone derivatives as pharmaceuticals and pharmaceutical compositions containing them |
| JP2004189738A (en) * | 2002-11-29 | 2004-07-08 | Nippon Nohyaku Co Ltd | Substituted anilide derivatives, intermediates thereof, agricultural and horticultural agents, and methods of using the same |
| TWI372050B (en) | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| KR101190964B1 (en) * | 2003-07-03 | 2012-10-12 | 아스텍스 테라퓨틱스 리미티드 | Benzimidazole derivatives and their use as protein kinases inhibitors |
| GB0315657D0 (en) * | 2003-07-03 | 2003-08-13 | Astex Technology Ltd | Pharmaceutical compounds |
| AR045037A1 (en) * | 2003-07-10 | 2005-10-12 | Aventis Pharma Sa | TETRAHIDRO-1H-PIRAZOLO [3,4-C] SUBSTITUTED PYRIDINS, COMPOSITIONS THAT CONTAIN THEM AND ITS USE. |
| OA13252A (en) * | 2003-09-08 | 2007-01-31 | Aventis Pharma Inc | Thienopyrazoles. |
| MXPA06003150A (en) * | 2003-09-17 | 2006-08-31 | Johnson & Johnson | Fused heterocyclic compounds. |
| AU2004297235A1 (en) | 2003-12-04 | 2005-06-23 | Vertex Pharmaceuticals Incorporated | Quinoxalines useful as inhibitors of protein kinases |
| WO2005065686A1 (en) * | 2004-01-07 | 2005-07-21 | Adipogen Pharmaceuticals Pty Limited | Differentiation modulating agents and uses therefor |
| US20050209284A1 (en) * | 2004-02-12 | 2005-09-22 | Boehringer Ingelheim Pharmaceuticals, Inc. | Tec kinase inhibitors |
| ITTO20040125A1 (en) * | 2004-03-01 | 2004-06-01 | Rotta Research Lab | NEW HETEROCYCLIC AMIDINS INHIBITIVE THE PRODUCTION OF NITROGEN OXIDE (NO) FOR ANTI-INFLAMMATORY AND ANALGESIC ACTIVITY |
| DE102004010207A1 (en) * | 2004-03-02 | 2005-09-15 | Aventis Pharma S.A. | New 4-benzimidazolyl-3(2H)-pyridazinone derivatives are kinase inhibitors, especially useful for treatment of cancer |
| DE102004010194A1 (en) * | 2004-03-02 | 2005-10-13 | Aventis Pharma Deutschland Gmbh | 4-Benzimidazol-2-yl-pyridazin-3-one derivatives, their preparation and use in medicaments |
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| WO2021233454A1 (en) * | 2020-05-22 | 2021-11-25 | 上海长森药业有限公司 | Novel tricyclic aromatic heterocyclic compound and preparation method therefor, pharmaceutical composition and use thereof |
| WO2022066938A1 (en) * | 2020-09-24 | 2022-03-31 | Forkhead Biotherapeutics, Inc. | Agents for the treatment of diseases by inhibition of foxo1 |
| CN112239452B (en) * | 2020-10-14 | 2022-05-10 | 武汉尚赛光电科技有限公司 | Electron transport type heteroanthracene derivative and organic electroluminescent device thereof |
| JP2023552862A (en) * | 2020-12-15 | 2023-12-19 | ファイザー・インク | Pyrido[2,3-D]imidazole derivatives and their use as inhibitors of ITK for the treatment of skin diseases |
| CA3228627A1 (en) | 2021-08-11 | 2023-02-16 | Thomas Butler | Covalent inhibitors of menin-mll interaction for diabetes mellitus |
| AU2022331496A1 (en) | 2021-08-20 | 2024-02-29 | Biomea Fusion, Inc. | Crystalline form of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(r)-[(1-oxo -2-propen-1-yl)amino]-1-piperidinyl]methyl]-2-pyridinecarboxamide, an irreversible menin-mll inhibitor for the treatment of cancer |
| CN114478511B (en) * | 2022-02-24 | 2023-06-20 | 中国药科大学 | Benzoxazole compound and its preparation method, pharmaceutical composition and application |
| EP4531838A1 (en) * | 2022-06-01 | 2025-04-09 | Kuda Therapeutics, Inc. | Imidazopyridine and oxazolopyridine derivatives and analogs thereof, methods of preparation thereof, methods of hif-1/2a pathway inhibition, and induction of ferroptosis |
| WO2024155710A1 (en) | 2023-01-18 | 2024-07-25 | Biomea Fusion, Inc. | Crystalline forms of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6- yl]phenyl]-4-[[3(r)-[(l-oxo-2-propen-l-yl)amino]-l-piperidinyl]methyl]-2-pyridinecarboxamide as a covalent inhibitor of menin-mll interaction |
| WO2025040140A1 (en) * | 2023-08-22 | 2025-02-27 | National Institute Of Biological Sciences, Beijing | Substituted pyrazol-4-yl urea as kinase inhibitors |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2130030A1 (en) * | 1971-06-18 | 1972-12-21 | Bayer Ag | Fungicidal and bactericidal agents |
| DE2130029A1 (en) * | 1971-06-18 | 1972-12-21 | Bayer Ag | Anthelmintic 2-pyrazolyl-benzimidazoles prodn - from 2-hydroxy -benzimidazoles and pyrazoles with phosphorus halides |
| BE793501A (en) * | 1971-12-31 | 1973-06-29 | Ciba Geigy | HETEROCYCLIC COMPOUNDS AND PHYTOPHARMACEUTICAL PRODUCTS WHICH CONTAIN IT |
| ES2219670T3 (en) * | 1994-11-10 | 2004-12-01 | Millennium Pharmaceuticals, Inc. | USE OF PIRAZOLA COMPOUNDS FOR THE TREATMENT OF GLOMERULONEFRITIS, CANCER, ATEROSCLEROSIS OR RESTENOSIS. |
| EP1006114B1 (en) * | 1997-04-11 | 2003-01-22 | Grelan Pharmaceutical Co., Ltd. | Pyrazole derivatives and cox inhibitors containing them |
| DE50010931D1 (en) * | 1999-06-23 | 2005-09-15 | Aventis Pharma Gmbh | SUBSTITUTED BENZIMIDAZOLE |
| PE20010306A1 (en) * | 1999-07-02 | 2001-03-29 | Agouron Pharma | INDAZOLE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM USEFUL FOR THE INHIBITION OF PROTEIN KINASE |
| YU54202A (en) * | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Indazole compounds,pharmaceutical compositions,and methods for mediating or inhibiting cell proliferation |
| JP2004536113A (en) * | 2001-07-03 | 2004-12-02 | カイロン コーポレイション | Indazole benzimidazole compounds as inhibitors of tyrosine kinase and serine / threonine kinase |
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2002
- 2002-10-24 IL IL16157602A patent/IL161576A0/en unknown
- 2002-10-24 EP EP02801954A patent/EP1441725A1/en not_active Withdrawn
- 2002-10-24 BR BR0213562-0A patent/BR0213562A/en not_active Application Discontinuation
- 2002-10-24 MX MXPA04003954A patent/MXPA04003954A/en active IP Right Grant
- 2002-10-24 WO PCT/GB2002/004763 patent/WO2003035065A1/en not_active Ceased
- 2002-10-24 AU AU2002334217A patent/AU2002334217B2/en not_active Ceased
- 2002-10-24 CA CA2465247A patent/CA2465247C/en not_active Expired - Fee Related
- 2002-10-24 JP JP2003537632A patent/JP5039268B2/en not_active Expired - Fee Related
- 2002-10-25 UY UY27516A patent/UY27516A1/en unknown
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| WO2003035065A1 (en) | 2003-05-01 |
| JP5039268B2 (en) | 2012-10-03 |
| CA2465247A1 (en) | 2003-05-01 |
| EP1441725A1 (en) | 2004-08-04 |
| BR0213562A (en) | 2004-08-31 |
| JP2005509633A (en) | 2005-04-14 |
| MXPA04003954A (en) | 2004-11-29 |
| AU2002334217B2 (en) | 2008-07-03 |
| CA2465247C (en) | 2010-05-18 |
| UY27516A1 (en) | 2003-04-30 |
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