CN103052627B - 作为fak抑制剂的嘧啶衍生物 - Google Patents
作为fak抑制剂的嘧啶衍生物 Download PDFInfo
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- CN103052627B CN103052627B CN201180039922.8A CN201180039922A CN103052627B CN 103052627 B CN103052627 B CN 103052627B CN 201180039922 A CN201180039922 A CN 201180039922A CN 103052627 B CN103052627 B CN 103052627B
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- 0 *CCc1nc(Cl)ncc1* Chemical compound *CCc1nc(Cl)ncc1* 0.000 description 3
- JPUYXUBUJJDJNL-UHFFFAOYSA-N Nc(cc1C2)ccc1NC2=O Chemical compound Nc(cc1C2)ccc1NC2=O JPUYXUBUJJDJNL-UHFFFAOYSA-N 0.000 description 2
- AOUABRLHPGCJAI-UHFFFAOYSA-N C#Cc(cc1)c(CC#N)cc1F Chemical compound C#Cc(cc1)c(CC#N)cc1F AOUABRLHPGCJAI-UHFFFAOYSA-N 0.000 description 1
- LWSMKQQPCFVPIB-ARJAWSKDSA-N C/C=C\C(\O)=N/C(O)=C Chemical compound C/C=C\C(\O)=N/C(O)=C LWSMKQQPCFVPIB-ARJAWSKDSA-N 0.000 description 1
- FUBCBZBSAVIJPX-UHFFFAOYSA-N CCCC(C#Cc(c(CC#N)c1)ccc1F)/N=C(\N)/Cl Chemical compound CCCC(C#Cc(c(CC#N)c1)ccc1F)/N=C(\N)/Cl FUBCBZBSAVIJPX-UHFFFAOYSA-N 0.000 description 1
- FVQWGSZTCQGMQE-UHFFFAOYSA-N CC[Si](CC)(CC)C(C(C1(CCC1)C#N)=CC1)=CC1C(F)(F)F Chemical compound CC[Si](CC)(CC)C(C(C1(CCC1)C#N)=CC1)=CC1C(F)(F)F FVQWGSZTCQGMQE-UHFFFAOYSA-N 0.000 description 1
- QUDZZSQTIYRRJY-UHFFFAOYSA-N Cc(c(C(F)(F)F)c1)cc(C2(CCC2)C#N)c1Br Chemical compound Cc(c(C(F)(F)F)c1)cc(C2(CCC2)C#N)c1Br QUDZZSQTIYRRJY-UHFFFAOYSA-N 0.000 description 1
- OLLAAOQRZWWXDA-UHFFFAOYSA-N N#CCc1c(CCc2nc(Cl)ncc2)ccc(F)c1 Chemical compound N#CCc1c(CCc2nc(Cl)ncc2)ccc(F)c1 OLLAAOQRZWWXDA-UHFFFAOYSA-N 0.000 description 1
- ZIMLRDKZPSVXTP-UHFFFAOYSA-N N#CCc1cc(F)ccc1CCc1nc(C2CC2)ncc1 Chemical compound N#CCc1cc(F)ccc1CCc1nc(C2CC2)ncc1 ZIMLRDKZPSVXTP-UHFFFAOYSA-N 0.000 description 1
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
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- C07D233/88—Nitrogen atoms, e.g. allantoin
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- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Transplantation (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102010034699.3 | 2010-08-18 | ||
| DE102010034699A DE102010034699A1 (de) | 2010-08-18 | 2010-08-18 | Pyrimidinderivate |
| PCT/EP2011/003597 WO2012022408A1 (de) | 2010-08-18 | 2011-07-19 | Pyrimidinderivate als fak inhibitoren |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103052627A CN103052627A (zh) | 2013-04-17 |
| CN103052627B true CN103052627B (zh) | 2015-08-19 |
Family
ID=44504442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201180039922.8A Expired - Fee Related CN103052627B (zh) | 2010-08-18 | 2011-07-19 | 作为fak抑制剂的嘧啶衍生物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8906916B2 (https=) |
| EP (1) | EP2606034B1 (https=) |
| JP (2) | JP6049617B2 (https=) |
| CN (1) | CN103052627B (https=) |
| AR (1) | AR082722A1 (https=) |
| AU (1) | AU2011291110B2 (https=) |
| CA (1) | CA2808540C (https=) |
| DE (1) | DE102010034699A1 (https=) |
| DK (1) | DK2606034T3 (https=) |
| ES (1) | ES2572740T3 (https=) |
| HR (1) | HRP20160562T1 (https=) |
| HU (1) | HUE027846T2 (https=) |
| IL (1) | IL224751A (https=) |
| PL (1) | PL2606034T3 (https=) |
| RS (1) | RS54882B1 (https=) |
| SI (1) | SI2606034T1 (https=) |
| WO (1) | WO2012022408A1 (https=) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010034699A1 (de) * | 2010-08-18 | 2012-02-23 | Merck Patent Gmbh | Pyrimidinderivate |
| JP5937112B2 (ja) * | 2011-02-17 | 2016-06-22 | カンサー・セラピューティクス・シーアールシー・プロプライエタリー・リミテッドCancer Therapeutics Crc Pty Limited | 選択的fak阻害剤 |
| EP2675793B1 (en) | 2011-02-17 | 2018-08-08 | Cancer Therapeutics Crc Pty Limited | Fak inhibitors |
| US9013997B2 (en) * | 2012-06-01 | 2015-04-21 | Broadcom Corporation | System for performing distributed data cut-through |
| WO2014027199A1 (en) * | 2012-08-14 | 2014-02-20 | Cancer Therapeutics Crc Pty Ltd | Fak and flt3 inhibitors |
| WO2014026242A1 (en) * | 2012-08-17 | 2014-02-20 | Cancer Therapeutics Crc Pty Limited | Vegfr3 inhibitors |
| CA2882158A1 (en) * | 2012-08-17 | 2014-02-20 | Cancer Therapeutics Crc Pty Limited | Vegfr3 inhibitors |
| TW201412740A (zh) * | 2012-09-20 | 2014-04-01 | Bayer Pharma AG | 經取代之吡咯并嘧啶胺基苯并噻唑酮 |
| WO2014174745A1 (ja) * | 2013-04-26 | 2014-10-30 | 国立大学法人京都大学 | Eg5阻害剤 |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP6441861B2 (ja) | 2018-12-19 |
| JP2017036268A (ja) | 2017-02-16 |
| JP6049617B2 (ja) | 2016-12-21 |
| AU2011291110B2 (en) | 2015-01-22 |
| ES2572740T3 (es) | 2016-06-02 |
| SI2606034T1 (sl) | 2016-07-29 |
| US20130158005A1 (en) | 2013-06-20 |
| HRP20160562T1 (hr) | 2016-06-17 |
| PL2606034T3 (pl) | 2016-07-29 |
| JP2013534227A (ja) | 2013-09-02 |
| US8906916B2 (en) | 2014-12-09 |
| AU2011291110A1 (en) | 2013-04-04 |
| EP2606034A1 (de) | 2013-06-26 |
| WO2012022408A1 (de) | 2012-02-23 |
| CA2808540C (en) | 2018-09-11 |
| CN103052627A (zh) | 2013-04-17 |
| AR082722A1 (es) | 2012-12-26 |
| DK2606034T3 (en) | 2016-05-02 |
| RS54882B1 (sr) | 2016-10-31 |
| DE102010034699A1 (de) | 2012-02-23 |
| CA2808540A1 (en) | 2012-02-23 |
| HUE027846T2 (en) | 2016-11-28 |
| EP2606034B1 (de) | 2016-03-09 |
| IL224751A (en) | 2015-03-31 |
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