CN101395158A - 可作为激酶抑制剂的吡咯并三嗪苯胺前体药物化合物 - Google Patents
可作为激酶抑制剂的吡咯并三嗪苯胺前体药物化合物 Download PDFInfo
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- CN101395158A CN101395158A CNA2007800079168A CN200780007916A CN101395158A CN 101395158 A CN101395158 A CN 101395158A CN A2007800079168 A CNA2007800079168 A CN A2007800079168A CN 200780007916 A CN200780007916 A CN 200780007916A CN 101395158 A CN101395158 A CN 101395158A
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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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- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Virology (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Molecular Biology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77985106P | 2006-03-07 | 2006-03-07 | |
| US60/779,851 | 2006-03-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101395158A true CN101395158A (zh) | 2009-03-25 |
Family
ID=38475749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2007800079168A Pending CN101395158A (zh) | 2006-03-07 | 2007-03-05 | 可作为激酶抑制剂的吡咯并三嗪苯胺前体药物化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7572795B2 (https=) |
| EP (1) | EP2001886A2 (https=) |
| JP (1) | JP2009535295A (https=) |
| KR (1) | KR20080107408A (https=) |
| CN (1) | CN101395158A (https=) |
| AR (1) | AR059778A1 (https=) |
| AU (1) | AU2007223342A1 (https=) |
| BR (1) | BRPI0708644A2 (https=) |
| CA (1) | CA2645031A1 (https=) |
| EA (1) | EA200801945A1 (https=) |
| IL (1) | IL193653A0 (https=) |
| MX (1) | MX2008011136A (https=) |
| NO (1) | NO20083717L (https=) |
| PE (1) | PE20080139A1 (https=) |
| TW (1) | TW200804390A (https=) |
| WO (1) | WO2007103839A2 (https=) |
| ZA (1) | ZA200807459B (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102153558A (zh) * | 2011-02-23 | 2011-08-17 | 扬州永济医药新技术有限公司 | 多靶点抗肿瘤抑制剂2-氨吡咯-三嗪的衍生物及其合成方法 |
| CN104507941A (zh) * | 2012-07-31 | 2015-04-08 | 百时美施贵宝公司 | 芳基内酰胺激酶抑制剂 |
| CN107001376A (zh) * | 2014-12-09 | 2017-08-01 | 拜耳制药股份公司 | 治疗癌症的化合物 |
| CN110590839A (zh) * | 2018-06-13 | 2019-12-20 | 四川海思科制药有限公司 | 一种乐伐替尼衍生物及制备方法和用途 |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101025675B1 (ko) * | 2002-04-23 | 2011-03-30 | 브리스톨-마이어스 스큅 컴퍼니 | 키나제 억제제로서 유용한 피롤로-트리아진 아닐린 화합물 |
| CN101395158A (zh) * | 2006-03-07 | 2009-03-25 | 百时美施贵宝公司 | 可作为激酶抑制剂的吡咯并三嗪苯胺前体药物化合物 |
| WO2009158450A1 (en) * | 2008-06-25 | 2009-12-30 | Bristol-Myers Squibb Company | Crystalline forms of ((((4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl)carbonyl)(propyl)carbamoyl)oxy)methyl (4-(phosphonooxy)phenyl)acetate, preparation and use thereof |
| WO2009158446A2 (en) * | 2008-06-25 | 2009-12-30 | Bristol-Myers Squibb Company | Crystalline forms of ((((4-((5-(cyclopropylcarbamoyl)-2-methylphenyl)amino)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl)carbonyl)(propyl)carbamoyl)oxy)methyl (4-(phosphonooxy)phenyl)acetate, method of preparation and use thereof |
| HRP20140640T1 (hr) * | 2008-08-19 | 2014-11-21 | Xenoport, Inc. | Prolijekovi monometil estera fumarne kiseline, farmaceutski sastavi iz toga i postupci njihove uporabe |
| ES2539620T3 (es) | 2008-12-19 | 2015-07-02 | Cephalon, Inc. | Pirrolotriazina como inhibidor de ALK y de JAK2 |
| CA2937222C (en) * | 2009-06-25 | 2019-06-04 | Alkermes Pharma Ireland Limited | Prodrugs of nh-acidic compounds |
| CN102596921B (zh) * | 2009-09-29 | 2015-04-29 | 葛兰素集团有限公司 | 新化合物 |
| MX2012003778A (es) * | 2009-09-29 | 2012-06-01 | Glaxo Group Ltd | Compuestos novedosos. |
| CN102918045A (zh) | 2010-03-31 | 2013-02-06 | 百时美施贵宝公司 | 作为蛋白激酶抑制剂的取代的吡咯并三嗪 |
| WO2012031057A1 (en) | 2010-09-01 | 2012-03-08 | Bristol-Myers Squibb Company | Bms- 582949 for the treatment of resistant rheumatic disease |
| AU2013305684B2 (en) | 2012-08-22 | 2016-11-24 | Xenoport, Inc. | Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof |
| US9050345B2 (en) | 2013-03-11 | 2015-06-09 | Bristol-Myers Squibb Company | Pyrrolotriazines as potassium ion channel inhibitors |
| WO2014160633A1 (en) | 2013-03-24 | 2014-10-02 | Xenoport, Inc. | Pharmaceutical compositions of dimethyl fumarate |
| WO2014197860A1 (en) | 2013-06-07 | 2014-12-11 | Xenoport, Inc. | Method of making monomethyl fumarate |
| WO2014205392A1 (en) | 2013-06-21 | 2014-12-24 | Xenoport, Inc. | Cocrystals of dimethyl fumarate |
| EP3041467A1 (en) | 2013-09-06 | 2016-07-13 | XenoPort, Inc. | Crystalline forms of (n,n-diethylcarbamoyl)methyl methyl (2e)but-2-ene-1,4-dioate, methods of synthesis and use |
| US9999672B2 (en) | 2014-03-24 | 2018-06-19 | Xenoport, Inc. | Pharmaceutical compositions of fumaric acid esters |
| WO2017070135A1 (en) * | 2015-10-20 | 2017-04-27 | Bristol-Myers Squibb Company | Prodrugs of 2-(4-(3-((4-amino-7-cyano-imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)piperaz in-1-yl)propanamide derivatives as ck2 inhibitors for the treatment of cancer |
| AU2017246228B2 (en) * | 2016-04-04 | 2021-04-15 | Chemocentryx, Inc. | Soluble C5aR antagonists |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| WO2019071147A1 (en) | 2017-10-05 | 2019-04-11 | Fulcrum Therapeutics, Inc. | INHIBITORS OF KINASE P38 REDUCING EXPRESSION OF DUX4 GENE AND DOWNSTREAM GENES FOR THE TREATMENT OF FSHD |
| EP3761983A1 (en) | 2018-03-05 | 2021-01-13 | Alkermes Pharma Ireland Limited | Aripiprazole dosing strategy |
Family Cites Families (30)
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- 2007-03-05 AU AU2007223342A patent/AU2007223342A1/en not_active Abandoned
- 2007-03-05 WO PCT/US2007/063250 patent/WO2007103839A2/en not_active Ceased
- 2007-03-05 BR BRPI0708644-0A patent/BRPI0708644A2/pt not_active IP Right Cessation
- 2007-03-05 KR KR1020087021851A patent/KR20080107408A/ko not_active Withdrawn
- 2007-03-05 EP EP07757860A patent/EP2001886A2/en not_active Withdrawn
- 2007-03-05 JP JP2008558486A patent/JP2009535295A/ja active Pending
- 2007-03-05 EA EA200801945A patent/EA200801945A1/ru unknown
- 2007-03-06 US US11/682,331 patent/US7572795B2/en active Active
- 2007-03-06 PE PE2007000242A patent/PE20080139A1/es not_active Application Discontinuation
- 2007-03-07 AR ARP070100944A patent/AR059778A1/es unknown
- 2007-03-07 TW TW096107889A patent/TW200804390A/zh unknown
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- 2008-08-29 ZA ZA200807459A patent/ZA200807459B/xx unknown
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2009
- 2009-02-12 US US12/370,081 patent/US20090156555A1/en not_active Abandoned
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102153558A (zh) * | 2011-02-23 | 2011-08-17 | 扬州永济医药新技术有限公司 | 多靶点抗肿瘤抑制剂2-氨吡咯-三嗪的衍生物及其合成方法 |
| CN102153558B (zh) * | 2011-02-23 | 2012-11-21 | 扬州永济医药新技术有限公司 | 多靶点抗肿瘤抑制剂2-氨吡咯-三嗪的衍生物及其合成方法 |
| CN104507941A (zh) * | 2012-07-31 | 2015-04-08 | 百时美施贵宝公司 | 芳基内酰胺激酶抑制剂 |
| CN107001376A (zh) * | 2014-12-09 | 2017-08-01 | 拜耳制药股份公司 | 治疗癌症的化合物 |
| CN110590839A (zh) * | 2018-06-13 | 2019-12-20 | 四川海思科制药有限公司 | 一种乐伐替尼衍生物及制备方法和用途 |
| CN110590839B (zh) * | 2018-06-13 | 2022-04-05 | 四川海思科制药有限公司 | 一种乐伐替尼衍生物及制备方法和用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200807459B (en) | 2009-11-25 |
| US20070213300A1 (en) | 2007-09-13 |
| TW200804390A (en) | 2008-01-16 |
| WO2007103839A2 (en) | 2007-09-13 |
| BRPI0708644A2 (pt) | 2011-06-07 |
| JP2009535295A (ja) | 2009-10-01 |
| KR20080107408A (ko) | 2008-12-10 |
| US20090156555A1 (en) | 2009-06-18 |
| PE20080139A1 (es) | 2008-03-10 |
| AU2007223342A1 (en) | 2007-09-13 |
| US7572795B2 (en) | 2009-08-11 |
| EP2001886A2 (en) | 2008-12-17 |
| WO2007103839A3 (en) | 2008-06-05 |
| CA2645031A1 (en) | 2007-09-13 |
| IL193653A0 (en) | 2009-08-03 |
| AR059778A1 (es) | 2008-04-30 |
| MX2008011136A (es) | 2008-09-08 |
| EA200801945A1 (ru) | 2009-02-27 |
| NO20083717L (no) | 2008-10-06 |
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