JP2010526867A5 - - Google Patents

Download PDF

Info

Publication number
JP2010526867A5
JP2010526867A5 JP2010508005A JP2010508005A JP2010526867A5 JP 2010526867 A5 JP2010526867 A5 JP 2010526867A5 JP 2010508005 A JP2010508005 A JP 2010508005A JP 2010508005 A JP2010508005 A JP 2010508005A JP 2010526867 A5 JP2010526867 A5 JP 2010526867A5
Authority
JP
Japan
Prior art keywords
group
alkyl group
hydrogen atom
methyl
dihydro
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2010508005A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010526867A (ja
JP5508257B2 (ja
Filing date
Publication date
Priority claimed from EP07290626A external-priority patent/EP1992625A1/en
Application filed filed Critical
Publication of JP2010526867A publication Critical patent/JP2010526867A/ja
Publication of JP2010526867A5 publication Critical patent/JP2010526867A5/ja
Application granted granted Critical
Publication of JP5508257B2 publication Critical patent/JP5508257B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2010508005A 2007-05-16 2008-05-14 アリールアミドピリミドン化合物 Active JP5508257B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP07290626.6 2007-05-16
EP07290626A EP1992625A1 (en) 2007-05-16 2007-05-16 Arylamide pyrimidone compounds
PCT/IB2008/002458 WO2008155670A2 (en) 2007-05-16 2008-05-14 Arylamide pyrimidone compounds

Publications (3)

Publication Number Publication Date
JP2010526867A JP2010526867A (ja) 2010-08-05
JP2010526867A5 true JP2010526867A5 (enExample) 2011-06-16
JP5508257B2 JP5508257B2 (ja) 2014-05-28

Family

ID=38596326

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010508005A Active JP5508257B2 (ja) 2007-05-16 2008-05-14 アリールアミドピリミドン化合物

Country Status (15)

Country Link
US (1) US8598187B2 (enExample)
EP (2) EP1992625A1 (enExample)
JP (1) JP5508257B2 (enExample)
KR (1) KR20100016511A (enExample)
CN (1) CN101679379A (enExample)
AR (1) AR066604A1 (enExample)
AU (1) AU2008264902A1 (enExample)
BR (1) BRPI0811597A2 (enExample)
CA (1) CA2687156A1 (enExample)
EA (1) EA200971063A1 (enExample)
IL (1) IL201625A0 (enExample)
MX (1) MX2009012377A (enExample)
NZ (1) NZ581164A (enExample)
TW (1) TW200948802A (enExample)
WO (1) WO2008155670A2 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
EP2760862B1 (en) 2011-09-27 2015-10-21 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
AR094929A1 (es) 2013-02-28 2015-09-09 Bristol Myers Squibb Co Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2
CN105102448B (zh) 2013-02-28 2018-03-06 百时美施贵宝公司 作为rock1和rock2抑制剂的苯基吡唑衍生物
WO2015155738A2 (en) 2014-04-09 2015-10-15 Christopher Rudd Use of gsk-3 inhibitors or activators which modulate pd-1 or t-bet expression to modulate t cell immunity

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4145423A (en) 1976-02-10 1979-03-20 Rhone-Poulenc Industries Pyrimidinyl-1,2-dithiole compounds and anti-bilharzia compositions thereof
US5629322A (en) 1994-11-15 1997-05-13 Merck & Co., Inc. Cyclic amidine analogs as inhibitors of nitric oxide synthase
JP4533534B2 (ja) 1998-06-19 2010-09-01 ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド グリコーゲンシンターゼキナーゼ3のインヒビター
AR023052A1 (es) * 1998-09-25 2002-09-04 Mitsuharu Yoshimura Milton Derivados de pirimidona
CN1247586C (zh) 2001-09-21 2006-03-29 赛诺菲安万特 治疗神经退化性疾病的取代的2-嘧啶基-6,7,8,9-四氢嘧啶并[1,2-a]嘧啶-4-酮及7-嘧啶基-2,3-二氢咪唑并[1,2-a]嘧啶-5(1h)酮衍生物
ZA200505258B (en) 2002-12-16 2006-09-27 Mitsubishi Pharma Corp 3-Substituted-4-pyrimidone derivatives
EP1603910B1 (en) 2003-03-07 2009-08-26 Sanofi-Aventis Substituted 2-(diaza-bicyclo-alkyl)-pyrimidone derivatives
EP1454909B1 (en) * 2003-03-07 2008-08-20 Sanofi Aventis 8'-pyridinyl-dihydrospiro (cycloalkyl) -pyrimido (1,2-a) pyrimidin-6-one and 8'-pyrimidinyl-dihydrospiro (cycloalkyl) pyrimido (1,2-a) pyrimidin-6 derivatives -one and their use against neurodegenerative diseases
EP1790649A1 (en) 2005-11-21 2007-05-30 Sanofi-Aventis Substituted bicyclic pyrimidone derivatives

Similar Documents

Publication Publication Date Title
JP2010526867A5 (enExample)
US11401259B2 (en) 1-Pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and compositions thereof for inhibiting the activity of SHP2
AU2014219283C1 (en) Benzothiophene derivatives and compositions thereof as selective estrogen receptor degraders
RU2012148818A (ru) 2,5,6,7-тетрагидро-[1,4]оксазепин-3-илмаины или 2,3,6,7-тетрагидро-[1,4]оксазепин-5-иламины
JP6532607B2 (ja) スルホンアミド化合物又はその塩
RU2001130169A (ru) Производные карбаминовой кислоты и их применение в качестве лигандов метаботропных глутаматных рецепторов
WO2013066833A1 (en) Compounds and methods to inhibit histone deacetylase (hdac) enzymes
RU2011125376A (ru) Способ получения соединений дигидроинденамида, фармацевтические композиции, содержащие данные соединения, и их применение в качестве ингибитора протеинкиназы
WO2013066839A2 (en) Compounds and methods
CA2787018A1 (en) Inhibitors of histone deacetylase (hdac) enzymes
TW200524575A (en) Biaryl linked hydroxamates: preparation and pharmaceutical applications
TW201240970A (en) Pyrazole compounds and thiazole compounds as protein kinases inhibitors
WO2016082713A1 (zh) 2-氨基嘧啶类化合物及其药物组合物和应用
RU2017121044A (ru) Производные амидотиадиазола в качестве ингибиторов надфн-оксидазы
US10577362B2 (en) Substituted 2, 4-diamino-quinoline derivatives for use in the treatment of proliferative diseases
JP2007519695A5 (enExample)
JP2021500340A5 (enExample)
JP2011510972A5 (enExample)
JP2009541404A5 (enExample)
RU2013125338A (ru) Производные триазола в качестве лигандов рецепторов гамк
JP2016525104A5 (enExample)
CN114650986A (zh) 2-氨基喹唑啉酮衍生物
US20240083912A1 (en) Compounds and their uses as mif inhibitors
CN103497179B (zh) 含苯并咪唑结构单元的嘧啶衍生物及其制备方法和用途
Kaur et al. Synthesis of fusidic acid bioisosteres as antiplasmodial agents and molecular docking studies in the binding site of elongation factor-G