NO20083717L - Pyrrolotriazin-anilin prodrugforbindelser anvendbare som kinaseinhibitorer - Google Patents
Pyrrolotriazin-anilin prodrugforbindelser anvendbare som kinaseinhibitorerInfo
- Publication number
- NO20083717L NO20083717L NO20083717A NO20083717A NO20083717L NO 20083717 L NO20083717 L NO 20083717L NO 20083717 A NO20083717 A NO 20083717A NO 20083717 A NO20083717 A NO 20083717A NO 20083717 L NO20083717 L NO 20083717L
- Authority
- NO
- Norway
- Prior art keywords
- kinase inhibitors
- pyrrolotriazine
- aniline
- prodrugs useful
- useful
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- UBWMDGGQTGIGMI-UHFFFAOYSA-N NC1=CC=CC=C1.N1N=NC=C2N=CC=C21 Chemical compound NC1=CC=CC=C1.N1N=NC=C2N=CC=C21 UBWMDGGQTGIGMI-UHFFFAOYSA-N 0.000 title 1
- 229940002612 prodrug Drugs 0.000 title 1
- 239000000651 prodrug Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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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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- 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)
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- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
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- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
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Abstract
Forbindelser som har formel (I), omfattende farmasøytisk akseptable salter derav: (I), hvor minst én av X1, X2 eller X3 er (i), og en eventuell gjenværende X1, X2 eller X3 er hydrogen, som er anvendelige som kinasehemmere, hvor R1, R2, R3, R4, R5, R6, A1, A2 og m er som beskrevet her.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77985106P | 2006-03-07 | 2006-03-07 | |
| PCT/US2007/063250 WO2007103839A2 (en) | 2006-03-07 | 2007-03-05 | Pyrrolotriazine aniline prodrug compounds useful as kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20083717L true NO20083717L (no) | 2008-10-06 |
Family
ID=38475749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20083717A NO20083717L (no) | 2006-03-07 | 2008-08-29 | Pyrrolotriazin-anilin prodrugforbindelser anvendbare som kinaseinhibitorer |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7572795B2 (no) |
| EP (1) | EP2001886A2 (no) |
| JP (1) | JP2009535295A (no) |
| KR (1) | KR20080107408A (no) |
| CN (1) | CN101395158A (no) |
| AR (1) | AR059778A1 (no) |
| AU (1) | AU2007223342A1 (no) |
| BR (1) | BRPI0708644A2 (no) |
| CA (1) | CA2645031A1 (no) |
| EA (1) | EA200801945A1 (no) |
| IL (1) | IL193653A0 (no) |
| MX (1) | MX2008011136A (no) |
| NO (1) | NO20083717L (no) |
| PE (1) | PE20080139A1 (no) |
| TW (1) | TW200804390A (no) |
| WO (1) | WO2007103839A2 (no) |
| ZA (1) | ZA200807459B (no) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GEP20074148B (en) * | 2002-04-23 | 2007-07-10 | Bristol Myers Squibb Co | Pyrrolo-triazine aniline compounds useful as kinase inhibitors |
| KR20080107408A (ko) * | 2006-03-07 | 2008-12-10 | 브리스톨-마이어스 스큅 컴퍼니 | 키나제 억제제로서 유용한 피롤로트리아진 아닐린 전구약물화합물 |
| 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 |
| US8148414B2 (en) | 2008-08-19 | 2012-04-03 | Xenoport, Inc. | Prodrugs of methyl hydrogen fumarate, pharmaceutical compositions thereof, and methods of use |
| WO2010071885A1 (en) | 2008-12-19 | 2010-06-24 | Cephalon, Inc. | Pyrrolotriazines as alk and jak2 inhibitors |
| EP2445343B1 (en) | 2009-06-25 | 2021-08-04 | Alkermes Pharma Ireland Limited | Prodrugs of nh-acidic compounds |
| CN104292154A (zh) * | 2009-09-29 | 2015-01-21 | 葛兰素集团有限公司 | 新化合物 |
| JP5752691B2 (ja) * | 2009-09-29 | 2015-07-22 | グラクソ グループ リミテッドGlaxo Group Limited | 新規化合物 |
| 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 |
| 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 |
| US8901305B2 (en) * | 2012-07-31 | 2014-12-02 | Bristol-Myers Squibb Company | Aryl lactam kinase inhibitors |
| 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 |
| US10179118B2 (en) | 2013-03-24 | 2019-01-15 | Arbor Pharmaceuticals, Llc | Pharmaceutical compositions of dimethyl fumarate |
| US9302977B2 (en) | 2013-06-07 | 2016-04-05 | Xenoport, Inc. | Method of making monomethyl fumarate |
| US9421182B2 (en) | 2013-06-21 | 2016-08-23 | 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 |
| MA41136A (fr) * | 2014-12-09 | 2017-10-17 | Bayer Pharma AG | Composés pour le traitement d'un cancer |
| US10550125B2 (en) | 2015-10-20 | 2020-02-04 | Bristol-Myers Squibb Company | Prodrugs of imidazotriazine compounds as CK2 inhibitors |
| KR102395093B1 (ko) | 2016-04-04 | 2022-05-04 | 케모센트릭스, 인크. | 가용성 C5aR 길항제 |
| 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 |
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-
2007
- 2007-03-05 KR KR1020087021851A patent/KR20080107408A/ko not_active Withdrawn
- 2007-03-05 CA CA002645031A patent/CA2645031A1/en not_active Abandoned
- 2007-03-05 BR BRPI0708644-0A patent/BRPI0708644A2/pt not_active IP Right Cessation
- 2007-03-05 EP EP07757860A patent/EP2001886A2/en not_active Withdrawn
- 2007-03-05 AU AU2007223342A patent/AU2007223342A1/en not_active Abandoned
- 2007-03-05 JP JP2008558486A patent/JP2009535295A/ja active Pending
- 2007-03-05 CN CNA2007800079168A patent/CN101395158A/zh active Pending
- 2007-03-05 MX MX2008011136A patent/MX2008011136A/es not_active Application Discontinuation
- 2007-03-05 EA EA200801945A patent/EA200801945A1/ru unknown
- 2007-03-05 WO PCT/US2007/063250 patent/WO2007103839A2/en not_active Ceased
- 2007-03-06 PE PE2007000242A patent/PE20080139A1/es not_active Application Discontinuation
- 2007-03-06 US US11/682,331 patent/US7572795B2/en active Active
- 2007-03-07 TW TW096107889A patent/TW200804390A/zh unknown
- 2007-03-07 AR ARP070100944A patent/AR059778A1/es unknown
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2008
- 2008-08-24 IL IL193653A patent/IL193653A0/en unknown
- 2008-08-29 NO NO20083717A patent/NO20083717L/no not_active Application Discontinuation
- 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
Also Published As
| Publication number | Publication date |
|---|---|
| AR059778A1 (es) | 2008-04-30 |
| CA2645031A1 (en) | 2007-09-13 |
| US7572795B2 (en) | 2009-08-11 |
| WO2007103839A3 (en) | 2008-06-05 |
| WO2007103839A2 (en) | 2007-09-13 |
| EP2001886A2 (en) | 2008-12-17 |
| MX2008011136A (es) | 2008-09-08 |
| CN101395158A (zh) | 2009-03-25 |
| ZA200807459B (en) | 2009-11-25 |
| TW200804390A (en) | 2008-01-16 |
| AU2007223342A1 (en) | 2007-09-13 |
| BRPI0708644A2 (pt) | 2011-06-07 |
| KR20080107408A (ko) | 2008-12-10 |
| US20070213300A1 (en) | 2007-09-13 |
| JP2009535295A (ja) | 2009-10-01 |
| US20090156555A1 (en) | 2009-06-18 |
| IL193653A0 (en) | 2009-08-03 |
| EA200801945A1 (ru) | 2009-02-27 |
| PE20080139A1 (es) | 2008-03-10 |
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