EA011287B1 - Производные гетероарилмочевины, пригодные для ингибирования chk1 - Google Patents
Производные гетероарилмочевины, пригодные для ингибирования chk1 Download PDFInfo
- Publication number
- EA011287B1 EA011287B1 EA200702094A EA200702094A EA011287B1 EA 011287 B1 EA011287 B1 EA 011287B1 EA 200702094 A EA200702094 A EA 200702094A EA 200702094 A EA200702094 A EA 200702094A EA 011287 B1 EA011287 B1 EA 011287B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- urea
- ylmethoxy
- phenyl
- methylpyrazin
- chloro
- Prior art date
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- -1 Heteroaryl urea derivatives Chemical class 0.000 title claims description 86
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- DZFHIBKVLIUPKD-UHFFFAOYSA-N 1-(5-cyanopyrazin-2-yl)-3-[5-methyl-2-(morpholin-2-ylmethoxy)phenyl]urea Chemical compound C=1N=C(C#N)C=NC=1NC(=O)NC1=CC(C)=CC=C1OCC1CNCCO1 DZFHIBKVLIUPKD-UHFFFAOYSA-N 0.000 claims description 3
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- 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
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- 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
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- 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
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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
- C07D403/12—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
- C07D413/14—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- General Health & Medical Sciences (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66602605P | 2005-03-29 | 2005-03-29 | |
| PCT/US2006/011584 WO2006105262A1 (en) | 2005-03-29 | 2006-03-29 | HETEROARYL UREA DERIVATIVES USEFUL FOR INHIBITING CHKl |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200702094A1 EA200702094A1 (ru) | 2008-02-28 |
| EA011287B1 true EA011287B1 (ru) | 2009-02-27 |
Family
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| EA200702094A EA011287B1 (ru) | 2005-03-29 | 2006-03-29 | Производные гетероарилмочевины, пригодные для ингибирования chk1 |
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Families Citing this family (14)
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| US5221367A (en) | 1988-08-03 | 1993-06-22 | International Business Machines, Corp. | Strained defect-free epitaxial mismatched heterostructures and method of fabrication |
| CA2673483C (en) * | 2006-10-20 | 2014-04-08 | Icos Corporation | Compositions of chk1 inhibitors |
| CN101200429B (zh) * | 2006-12-13 | 2012-08-22 | 上海睿智化学研究有限公司 | 2-硝基-4,5-二卤代苯酚类和2-氨基-4,5-二卤代苯酚类及其盐及其合成方法 |
| GB201008005D0 (en) | 2010-05-13 | 2010-06-30 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| EP3024456A4 (en) | 2013-07-26 | 2017-04-12 | Update Pharma Inc. | Combinatorial methods to improve the therapeutic benefit of bisantrene |
| CA2950780C (en) | 2014-06-17 | 2023-05-16 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of chk1 and atr inhibitors |
| TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
| WO2017059357A1 (en) | 2015-09-30 | 2017-04-06 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of dna damaging agents and atr inhibitors |
| KR102159442B1 (ko) | 2016-02-04 | 2020-09-24 | 파마엔진 인코포레이티드 | 체크포인트 키나아제 1(chk1) 억제제로서 유용한 3,5-이치환된 피라졸, 및 이의 제조 및 적용 |
| CA3017411C (en) | 2016-03-15 | 2024-06-25 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
| US20200108074A1 (en) * | 2017-03-31 | 2020-04-09 | Seattle Genetics, Inc. | Combinations of chk1- and wee1- inhibitors |
| EP3461480A1 (en) | 2017-09-27 | 2019-04-03 | Onxeo | Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer |
| CN112457306A (zh) | 2019-09-06 | 2021-03-09 | 上海瑛派药业有限公司 | 3,5-二取代吡唑化合物作为激酶抑制剂及其应用 |
| US12404332B2 (en) * | 2020-03-13 | 2025-09-02 | Research Development Foundation | Methods for diagnosing and treating cancers |
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| US20040014765A1 (en) * | 2002-05-29 | 2004-01-22 | Millennium Pharmaceuticals, Inc. | Chk-1 inhibitors |
| US20040259885A1 (en) * | 2002-08-13 | 2004-12-23 | Gaoquan Li | Urea kinase inhibitors |
| WO2006012308A1 (en) * | 2004-06-25 | 2006-02-02 | Icos Corporation | Bisarylurea derivatives useful for inhibiting chk1 |
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| US6174993B1 (en) | 1997-05-21 | 2001-01-16 | The Children's Medical Center Corp. | Short peptides which selectively modulate the activity of serine/threonine kinases |
| US6218109B1 (en) | 1997-09-05 | 2001-04-17 | Baylor College Of Medicine | Mammalian checkpoint genes and proteins |
| GB9718952D0 (en) | 1997-09-05 | 1997-11-12 | Medical Res Council | Mammalian chk1 effector cell cycle checkpoint protein kinase materials and methods |
| JP2001518501A (ja) | 1997-10-06 | 2001-10-16 | ビーエーエスエフ アクチェンゲゼルシャフト | インデノ［１，２−ｃ］−、ナフト［１，２−ｃ］−およびベンゾ［６，７］シクロへプタ［１，２−ｃ］ピラゾール誘導体 |
| WO2000016781A1 (en) | 1998-09-18 | 2000-03-30 | Smithkline Beecham Corporation | Chk1 kinase inhibitors |
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| HN2001000008A (es) | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
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| AU2001243226A1 (en) | 2000-02-25 | 2001-09-03 | The Regents Of The University Of California | Scytonemin and methods of using thereof |
| US6211164B1 (en) | 2000-03-10 | 2001-04-03 | Abbott Laboratories | Antisense oligonucleotides of the human chk1 gene and uses thereof |
| US6534691B2 (en) | 2000-07-18 | 2003-03-18 | E. I. Du Pont De Nemours And Company | Manufacturing process for α-olefins |
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| US20040116497A1 (en) | 2001-01-26 | 2004-06-17 | Gabriella Traquandi | Chromane derivatives, process for their preparation and their use as antitumor agents |
| EP1401831A1 (en) | 2001-07-03 | 2004-03-31 | Chiron Corporation | Indazole benzimidazole compounds as tyrosine and serine/threonine kinase inhibitors |
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| EP1444010A2 (en) | 2001-10-30 | 2004-08-11 | Pharmacia Corporation | Heteroaromatic carboxamide derivatives for the treatment of inflammation |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
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- 2006-03-29 WO PCT/US2006/011584 patent/WO2006105262A1/en not_active Ceased
- 2006-03-29 EP EP10189889A patent/EP2330105A1/en not_active Withdrawn
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- 2006-03-29 SI SI200630870T patent/SI1869020T1/sl unknown
- 2006-03-29 EA EA200702094A patent/EA011287B1/ru not_active IP Right Cessation
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- 2006-03-29 US US11/908,416 patent/US8093244B2/en not_active Expired - Fee Related
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- 2006-03-29 EP EP06748900A patent/EP1869020B1/en active Active
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- 2006-03-29 KR KR1020097002925A patent/KR20090031459A/ko not_active Ceased
- 2006-03-29 KR KR1020077022281A patent/KR100912998B1/ko not_active Expired - Fee Related
- 2006-03-29 DK DK06748900.5T patent/DK1869020T3/da active
- 2006-03-29 CN CN2011101022112A patent/CN102219784A/zh active Pending
- 2006-03-29 PT PT06748900T patent/PT1869020E/pt unknown
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2007
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- 2007-09-26 CR CR9395A patent/CR9395A/es unknown
- 2007-09-28 TN TNP2007000369A patent/TNSN07369A1/en unknown
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- 2007-10-26 MA MA30325A patent/MA29439B1/fr unknown
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2009
- 2009-05-20 JP JP2009122107A patent/JP2009227682A/ja active Pending
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- 2011-02-03 CY CY20111100117T patent/CY1111240T1/el unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002070494A1 (en) * | 2001-03-02 | 2002-09-12 | Icos Corporation | Aryl and heteroaryl urea chk1 inhibitors for use as radiosensitizers and chamosensitizers |
| US20040014765A1 (en) * | 2002-05-29 | 2004-01-22 | Millennium Pharmaceuticals, Inc. | Chk-1 inhibitors |
| US20040259885A1 (en) * | 2002-08-13 | 2004-12-23 | Gaoquan Li | Urea kinase inhibitors |
| WO2006012308A1 (en) * | 2004-06-25 | 2006-02-02 | Icos Corporation | Bisarylurea derivatives useful for inhibiting chk1 |
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| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
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