JP2016509056A5 - - Google Patents

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Publication number
JP2016509056A5
JP2016509056A5 JP2015558892A JP2015558892A JP2016509056A5 JP 2016509056 A5 JP2016509056 A5 JP 2016509056A5 JP 2015558892 A JP2015558892 A JP 2015558892A JP 2015558892 A JP2015558892 A JP 2015558892A JP 2016509056 A5 JP2016509056 A5 JP 2016509056A5
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JP
Japan
Prior art keywords
cycloalkyl
alkylene
alkyl
heterocyclyl
cancer
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JP2015558892A
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English (en)
Japanese (ja)
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JP2016509056A (ja
JP6389829B2 (ja
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Priority claimed from PCT/US2014/016643 external-priority patent/WO2014130375A1/en
Publication of JP2016509056A publication Critical patent/JP2016509056A/ja
Publication of JP2016509056A5 publication Critical patent/JP2016509056A5/ja
Application granted granted Critical
Publication of JP6389829B2 publication Critical patent/JP6389829B2/ja
Active legal-status Critical Current
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JP2015558892A 2013-02-21 2014-02-15 Pi3キナーゼモジュレータとしてのヘテロ芳香族化合物、及びその使用方法 Active JP6389829B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361767721P 2013-02-21 2013-02-21
US61/767,721 2013-02-21
PCT/US2014/016643 WO2014130375A1 (en) 2013-02-21 2014-02-15 Heteroaromatic compounds as pi3 kinase modulators

Publications (3)

Publication Number Publication Date
JP2016509056A JP2016509056A (ja) 2016-03-24
JP2016509056A5 true JP2016509056A5 (OSRAM) 2017-03-16
JP6389829B2 JP6389829B2 (ja) 2018-09-12

Family

ID=51351332

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015558892A Active JP6389829B2 (ja) 2013-02-21 2014-02-15 Pi3キナーゼモジュレータとしてのヘテロ芳香族化合物、及びその使用方法

Country Status (14)

Country Link
US (1) US9573953B2 (OSRAM)
EP (1) EP2958564B1 (OSRAM)
JP (1) JP6389829B2 (OSRAM)
KR (1) KR102148681B1 (OSRAM)
AU (1) AU2014219256B2 (OSRAM)
BR (1) BR112015018318A2 (OSRAM)
CA (1) CA2898294C (OSRAM)
ES (1) ES2674705T3 (OSRAM)
MX (1) MX2015010700A (OSRAM)
MY (1) MY182036A (OSRAM)
RU (1) RU2672910C9 (OSRAM)
SG (1) SG11201505493QA (OSRAM)
TW (1) TWI620749B (OSRAM)
WO (1) WO2014130375A1 (OSRAM)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2016311426B2 (en) 2015-08-26 2021-05-20 Blueprint Medicines Corporation Compounds and compositions useful for treating disorders related to NTRK
EP3377497A1 (en) 2015-11-19 2018-09-26 Blueprint Medicines Corporation Compounds and compositions useful for treating disorders related to ntrk
JP7193460B2 (ja) * 2016-12-23 2022-12-20 プレキシコン インコーポレーテッド Cdk8調節およびその適応症のための化合物および方法
US11040027B2 (en) 2017-01-17 2021-06-22 Heparegenix Gmbh Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death
WO2018169700A1 (en) * 2017-03-14 2018-09-20 Sunshine Lake Pharma Co., Ltd. Substituted heteroaryl compounds and methods of use
CN109867670B (zh) * 2017-12-02 2020-07-07 广东东阳光药业有限公司 一种吡唑[1,5-a]吡啶化合物的单钠盐及其医药用途
CN109867671B (zh) * 2017-12-02 2020-07-07 广东东阳光药业有限公司 一种吡唑[1,5-a]吡啶化合物的晶型及其药物组合物和用途
CN109867672B (zh) * 2017-12-02 2020-07-07 广东东阳光药业有限公司 吡唑[1,5-a]吡啶衍生物的盐及其用途
CN109867669B (zh) * 2017-12-02 2021-02-26 广东东阳光药业有限公司 一种吡唑[1,5-a]吡啶化合物的晶型及其药物组合物和用途
CN109867668B (zh) * 2017-12-02 2021-03-26 广东东阳光药业有限公司 一种吡唑[1,5-a]吡啶化合物的晶型及其药物组合物和用途
WO2019125967A1 (en) * 2017-12-20 2019-06-27 Sunshine Lake Pharma Co., Ltd. Salts of pyrazolo[1,5-a]pyridine derivative and use thereof
WO2020078445A1 (zh) * 2018-10-19 2020-04-23 广东东阳光药业有限公司 一种治疗纤维化疾病的药物组合或药物组合物

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304121A (en) 1990-12-28 1994-04-19 Boston Scientific Corporation Drug delivery system making use of a hydrogel polymer coating
US5886026A (en) 1993-07-19 1999-03-23 Angiotech Pharmaceuticals Inc. Anti-angiogenic compositions and methods of use
WO1995015373A2 (en) 1993-11-30 1995-06-08 Mcgill University Inhibition of dna methyltransferase
US5578716A (en) 1993-12-01 1996-11-26 Mcgill University DNA methyltransferase antisense oligonucleotides
US6099562A (en) 1996-06-13 2000-08-08 Schneider (Usa) Inc. Drug coating with topcoat
US6268137B1 (en) 1996-05-22 2001-07-31 Methylgene, Inc. Specific inhibitors of DNA methyl transferase
US6020318A (en) 1997-05-30 2000-02-01 Methylgene, Inc. DNA methyltransferase genomic sequences and antisense oligonucleotides
AU8125098A (en) 1997-05-30 1998-12-30 Mcgill University Dna methyltransferase genomic sequences and antisense oligonucleotides
US6066625A (en) 1998-02-03 2000-05-23 Methylgene, Inc. Optimized antisense oligonucleotides complementary to DNA methyltransferase sequences
US6953783B1 (en) 1998-10-19 2005-10-11 Methylgene, Inc. Modulation of gene expression by combination therapy
JP2003500052A (ja) 1999-05-03 2003-01-07 メチルジーン インコーポレイテッド ヒストン脱アセチル酵素の抑制
DK1233958T3 (da) 1999-11-23 2011-10-17 Methylgene Inc Hæmmere af histondeacetylase
JP2004533850A (ja) 2000-03-24 2004-11-11 メチルジーン・インコーポレーテッド 特異的なヒストン脱アセチル化酵素アイソフォームの阻害
WO2001070675A2 (en) 2000-03-24 2001-09-27 Methylgene, Inc. Inhibitors of histone deacetylase
WO2002088121A1 (en) * 2001-04-27 2002-11-07 Eisai Co., Ltd. Pyrazolo[1,5-a]pyridines and medicines containing the same
US6897220B2 (en) 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
MXPA04002397A (es) 2001-09-14 2004-12-02 Methylgene Inc Inhibidores de histona deacetilasa.
US7868204B2 (en) 2001-09-14 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
US7196078B2 (en) 2002-09-04 2007-03-27 Schering Corpoartion Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors
JP2006503082A (ja) 2002-10-17 2006-01-26 メシルジーン、インコーポレイテッド ヒストンデアセチラーゼの阻害剤
WO2004052315A2 (en) 2002-12-11 2004-06-24 Merck & Co., Inc. Tyrosine kinase inhibitors
ES2222813B1 (es) * 2003-07-24 2005-12-16 Ferrer Internacional, S.A. N-(3-(3-sustituidas-pirazolo(1,5-a)pirimidin-7-il)-fenil)-sulfonamidas y composiciones y metodos relacionados.
CA2539117A1 (en) 2003-09-24 2005-04-07 Methylgene Inc. Inhibitors of histone deacetylase
US7329662B2 (en) 2003-10-03 2008-02-12 Hoffmann-La Roche Inc. Pyrazolo-pyridine
KR101258504B1 (ko) 2004-03-26 2013-04-26 메틸진 인코포레이티드 히스톤 데아세틸라제의 억제제
CA2573538C (en) 2004-07-30 2014-11-25 Methylgene Inc. Inhibitors of vegf receptor and hgf receptor signaling
CN101180299B (zh) 2005-03-23 2010-12-15 弗·哈夫曼-拉罗切有限公司 作为mglur2拮抗剂的乙炔基-吡唑并嘧啶衍生物
JP2011500823A (ja) * 2007-10-22 2011-01-06 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー Pi3キナーゼ阻害物質としてのピリドスルホンアミド誘導体
WO2009085230A1 (en) * 2007-12-19 2009-07-09 Amgen Inc. Inhibitors of pi3 kinase
WO2010118207A1 (en) * 2009-04-09 2010-10-14 Schering Corporation Pyrazolo [1, 5-a] pyrimidine derivatives as mtor inhibitors
CN102573846B (zh) * 2009-08-17 2015-10-07 因特利凯公司 杂环化合物及其用途
US8883801B2 (en) 2010-08-23 2014-11-11 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors
CN102675286B (zh) 2011-03-07 2015-08-19 中国科学院上海药物研究所 一类吲唑类化合物及其制备方法、用途和药物组合物
PT2710018T (pt) 2011-05-19 2022-03-01 Fundacion Del Sector Publico Estatal Centro Nac De Investigaciones Oncologicas Carlos Iii F S P Cnio Compostos macrocíclicos como inibidores de proteína quinases
WO2012174312A2 (en) 2011-06-15 2012-12-20 Glaxosmithkline Llc Benzimidazole derivatives as antiviral agents
KR101274986B1 (ko) 2011-07-27 2013-06-17 한국과학기술원 이미다조피리딘 유도체, 이를 포함하는 PI3K 및/또는 mTOR 저해제용 약학 조성물 및 PI3K 및/또는 mTOR과 연관된 질환 치료용 약학 조성물
GB201205669D0 (en) 2012-03-30 2012-05-16 Agency Science Tech & Res Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
CN102924450A (zh) 2012-11-01 2013-02-13 西安交通大学 6-(5-吡啶基)-1,2,4-三唑并吡啶类化合物及其制备方法和用途

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