JP2013530238A5 - - Google Patents

Download PDF

Info

Publication number
JP2013530238A5
JP2013530238A5 JP2013518692A JP2013518692A JP2013530238A5 JP 2013530238 A5 JP2013530238 A5 JP 2013530238A5 JP 2013518692 A JP2013518692 A JP 2013518692A JP 2013518692 A JP2013518692 A JP 2013518692A JP 2013530238 A5 JP2013530238 A5 JP 2013530238A5
Authority
JP
Japan
Prior art keywords
alkyl
haloalkyl
halo
substituted
cyano
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.)
Withdrawn
Application number
JP2013518692A
Other languages
English (en)
Japanese (ja)
Other versions
JP2013530238A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2011/042525 external-priority patent/WO2012003274A1/en
Publication of JP2013530238A publication Critical patent/JP2013530238A/ja
Publication of JP2013530238A5 publication Critical patent/JP2013530238A5/ja
Withdrawn legal-status Critical Current

Links

JP2013518692A 2010-07-01 2011-06-30 Pi3k活性の阻害剤としての複素環化合物及びその使用 Withdrawn JP2013530238A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US36073110P 2010-07-01 2010-07-01
US61/360,731 2010-07-01
PCT/US2011/042525 WO2012003274A1 (en) 2010-07-01 2011-06-30 Heterocyclic compounds and their use as inhibitors of pi3k activity

Publications (2)

Publication Number Publication Date
JP2013530238A JP2013530238A (ja) 2013-07-25
JP2013530238A5 true JP2013530238A5 (enExample) 2014-08-14

Family

ID=44280219

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013518692A Withdrawn JP2013530238A (ja) 2010-07-01 2011-06-30 Pi3k活性の阻害剤としての複素環化合物及びその使用

Country Status (7)

Country Link
US (1) US20130085131A1 (enExample)
EP (1) EP2588467A1 (enExample)
JP (1) JP2013530238A (enExample)
AU (1) AU2011272853A1 (enExample)
CA (1) CA2803009A1 (enExample)
MX (1) MX2012015135A (enExample)
WO (1) WO2012003274A1 (enExample)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2445900B1 (en) * 2009-06-25 2016-03-02 Amgen, Inc Polycyclic derivatives of pyridine and their use in the treatment of (inter alia) rheumatoid arthritis and similar diseases
MX2011013816A (es) 2009-06-29 2012-04-11 Incyte Corp Pirimidinonas como inhibidores de pi3k.
GB0912778D0 (en) 2009-07-22 2009-08-26 Eisai London Res Lab Ltd Fused aminodihydro-oxazine derivatives
GB0912777D0 (en) 2009-07-22 2009-08-26 Eisai London Res Lab Ltd Fused aminodihydropyrimidone derivatives
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
EP2558463A1 (en) 2010-04-14 2013-02-20 Incyte Corporation Fused derivatives as i3 inhibitors
AU2011255218B2 (en) 2010-05-21 2015-03-12 Infinity Pharmaceuticals, Inc. Chemical compounds, compositions and methods for kinase modulation
WO2011163195A1 (en) 2010-06-21 2011-12-29 Incyte Corporation Fused pyrrole derivatives as pi3k inhibitors
ES2764848T3 (es) 2010-12-20 2020-06-04 Incyte Holdings Corp N-(1-(fenilo sustituido)etilo)-9H-purina-6-aminas como inhibidores de PI3K
GB201100181D0 (en) 2011-01-06 2011-02-23 Eisai Ltd Fused aminodihydrothiazine derivatives
GB201101139D0 (en) 2011-01-21 2011-03-09 Eisai Ltd Fused aminodihydrothiazine derivatives
GB201101140D0 (en) 2011-01-21 2011-03-09 Eisai Ltd Fused aminodihydrothiazine derivatives
SG10201601516QA (en) 2011-01-21 2016-03-30 Eisai R&D Man Co Ltd Methods and compounds useful in the synthesis of fused aminodihydrothiazine derivatives
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
HK1199725A1 (en) 2011-08-29 2015-07-17 无限药品股份有限公司 Heterocyclic compounds and uses thereof
KR20230038593A (ko) 2011-09-02 2023-03-20 인사이트 홀딩스 코포레이션 Pi3k 억제제로서 헤테로시클릴아민
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
WO2014072937A1 (en) 2012-11-08 2014-05-15 Rhizen Pharmaceuticals Sa Pharmaceutical compositions containing a pde4 inhibitor and a pi3 delta or dual pi3 delta-gamma kinase inhibitor
GEP201606598B (en) 2012-11-08 2017-01-10 Pfizer Heteroaromatic compounds as dopamine d1 ligands
AU2013364068B2 (en) 2012-12-21 2016-10-20 Gilead Calistoga Llc Substituted pyrimidine aminoalkyl-quinazolones as phosphatidylinositol 3-kinase inhibitors
US9029384B2 (en) 2012-12-21 2015-05-12 Gilead Calistoga, LLC. Phosphatidylinositol 3-kinase inhibitors
US9481667B2 (en) 2013-03-15 2016-11-01 Infinity Pharmaceuticals, Inc. Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
BR112015031475A2 (pt) 2013-06-14 2017-07-25 Gilead Sciences Inc composto, composição farmacêutica, método para tratamento de uma doença ou condição, kit, e, uso de composto.
SG11201608943VA (en) * 2014-04-30 2016-11-29 Univ Columbia Substituted 4-phenylpiperidines, their preparaiton and use
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
MA40250A (fr) 2014-07-04 2017-05-10 Lupin Ltd Dérivés de quinolizinone utilisés comme inhibiteurs de pi3k
ES2901114T3 (es) 2014-08-29 2022-03-21 Tes Pharma S R L Inhibidores de ácido alfa-amino-beta-carboximucónico semialdehído descarboxilasa
JP6399518B2 (ja) * 2014-12-18 2018-10-03 インターナショナル・ビジネス・マシーンズ・コーポレーションInternational Business Machines Corporation 処理装置、処理方法、およびプログラム
AU2016222556B2 (en) 2015-02-27 2020-08-27 Incyte Holdings Corporation Salts of Pl3K inhibitor and processes for their preparation
CN106008479B (zh) 2015-03-06 2020-01-10 南京圣和药业股份有限公司 作为磷脂酰肌醇3-激酶δ抑制剂的取代嘧啶类化合物及其应用
WO2016183063A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Crystalline forms of a pi3k inhibitor
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
TW201825465A (zh) 2016-09-23 2018-07-16 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
TW201813963A (zh) 2016-09-23 2018-04-16 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
TW201815787A (zh) 2016-09-23 2018-05-01 美商基利科學股份有限公司 磷脂醯肌醇3-激酶抑制劑
MX2020012826A (es) 2018-06-01 2021-03-09 Incyte Corp Regimen de dosificacion para el tratamiento de trastornos relacionados con fosfatidilinositol 3-cinasas (pi3k).
TW202334089A (zh) 2021-11-02 2023-09-01 美商夫雷爾醫療公司 Pparg反向激動劑及其用途

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT72878B (en) 1980-04-24 1983-03-29 Merck & Co Inc Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents
US6043062A (en) 1995-02-17 2000-03-28 The Regents Of The University Of California Constitutively active phosphatidylinositol 3-kinase and uses thereof
GB9611460D0 (en) 1996-06-01 1996-08-07 Ludwig Inst Cancer Res Novel lipid kinase
US5858753A (en) 1996-11-25 1999-01-12 Icos Corporation Lipid kinase
US5822910A (en) 1997-10-02 1998-10-20 Shewmake; I. W. Fishing line tensioning device
US20070015782A1 (en) 2005-04-15 2007-01-18 Eisai Co., Ltd. Benzimidazole compound
TWI573854B (zh) 2007-03-08 2017-03-11 環球展覽公司 磷光材料
HUE028954T2 (en) * 2007-03-23 2017-01-30 Amgen Inc Heterocyclic compounds and their use
PT2139882E (pt) * 2007-03-23 2014-01-30 Amgen Inc Derivados de quinolina ou quinoxalina 3-substituídos e sua utilização como inibidores de fosfatidilinositol 3-cinase (pi3k)
PE20090044A1 (es) 2007-04-06 2009-01-23 Neurocrine Biosciences Inc Antagonistas del receptor de la hormona liberadora de gonadotropina y procedimientos relacionados con los mismos
CA2700088A1 (en) * 2007-09-26 2009-04-02 Astellas Pharma Inc. Quinolone derivative
EP2445900B1 (en) * 2009-06-25 2016-03-02 Amgen, Inc Polycyclic derivatives of pyridine and their use in the treatment of (inter alia) rheumatoid arthritis and similar diseases
WO2011058113A1 (en) * 2009-11-12 2011-05-19 Ucb Pharma S.A. Fused bicyclic pyridine and pyrazine derivatives as kinase inhibitors
WO2011075628A1 (en) * 2009-12-18 2011-06-23 Amgen Inc. Heterocyclic compounds and their uses

Similar Documents

Publication Publication Date Title
JP2013530238A5 (enExample)
JP2013533884A5 (enExample)
JP2013533883A5 (enExample)
JP2013530236A5 (enExample)
ME02754B (me) Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme
JP2017512833A5 (enExample)
JP2024100974A5 (enExample)
JP2016518385A5 (enExample)
HRP20140147T1 (hr) 3-supstituirani derivati hinolina ili hinoksalina i njihova uporaba kao inhibitora fosfatidilinozitol 3-kinaze (pi3k)
JP2017508816A5 (enExample)
JP2011529073A5 (enExample)
JP2010280669A5 (enExample)
JP2015535277A5 (enExample)
JP2014509647A5 (enExample)
JP2014508753A5 (enExample)
JP2019532092A5 (enExample)
JP2013533314A5 (enExample)
JP2013522316A5 (enExample)
RU2016138364A (ru) Амидное производное пирозола
JP2018533593A5 (enExample)
JP2015535832A5 (enExample)
SI2718293T1 (en) SUBSTITUTED PYRIDOPIRAZINS AS NEW INHIBITORS OF VRANIC TYROSIN KINASE (SYK)
JP2020500916A5 (enExample)
JP2014505033A5 (enExample)
JP2012012417A5 (enExample)