JP2015503504A5 - - Google Patents

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Publication number
JP2015503504A5
JP2015503504A5 JP2014548896A JP2014548896A JP2015503504A5 JP 2015503504 A5 JP2015503504 A5 JP 2015503504A5 JP 2014548896 A JP2014548896 A JP 2014548896A JP 2014548896 A JP2014548896 A JP 2014548896A JP 2015503504 A5 JP2015503504 A5 JP 2015503504A5
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JP
Japan
Prior art keywords
nitrogen
optionally substituted
membered
oxygen
sulfur
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.)
Pending
Application number
JP2014548896A
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English (en)
Japanese (ja)
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JP2015503504A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/070969 external-priority patent/WO2013096630A1/en
Publication of JP2015503504A publication Critical patent/JP2015503504A/ja
Publication of JP2015503504A5 publication Critical patent/JP2015503504A5/ja
Pending legal-status Critical Current

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JP2014548896A 2011-12-23 2012-12-20 ヘテロアリールおよびその使用 Pending JP2015503504A (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US201161579711P 2011-12-23 2011-12-23
US61/579,711 2011-12-23
US201261672030P 2012-07-16 2012-07-16
US61/672,030 2012-07-16
US201261716172P 2012-10-19 2012-10-19
US61/716,172 2012-10-19
PCT/US2012/070969 WO2013096630A1 (en) 2011-12-23 2012-12-20 Heteroaryls and uses thereof

Publications (2)

Publication Number Publication Date
JP2015503504A JP2015503504A (ja) 2015-02-02
JP2015503504A5 true JP2015503504A5 (enExample) 2016-02-18

Family

ID=48655164

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2014548896A Pending JP2015503504A (ja) 2011-12-23 2012-12-20 ヘテロアリールおよびその使用
JP2014548902A Pending JP2015503505A (ja) 2011-12-23 2012-12-20 ヘテロアリールおよびその使用
JP2014548899A Pending JP2015506347A (ja) 2011-12-23 2012-12-20 ヘテロアリールおよびその使用

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2014548902A Pending JP2015503505A (ja) 2011-12-23 2012-12-20 ヘテロアリールおよびその使用
JP2014548899A Pending JP2015506347A (ja) 2011-12-23 2012-12-20 ヘテロアリールおよびその使用

Country Status (7)

Country Link
US (3) US20130165464A1 (enExample)
EP (3) EP2793879A4 (enExample)
JP (3) JP2015503504A (enExample)
AR (3) AR089445A1 (enExample)
TW (3) TW201332988A (enExample)
UY (3) UY34538A (enExample)
WO (3) WO2013096642A1 (enExample)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009094224A1 (en) 2008-01-25 2009-07-30 Millennium Pharmaceuticals, Inc. Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors
US9090601B2 (en) 2009-01-30 2015-07-28 Millennium Pharmaceuticals, Inc. Thiazole derivatives
US8796314B2 (en) 2009-01-30 2014-08-05 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
CA2750935A1 (en) 2009-01-30 2010-08-12 Millennium Pharmaceuticals, Inc. Heteroaryls and their use as pi3k inhibitors
JP2013533318A (ja) 2010-08-11 2013-08-22 ミレニアム ファーマシューティカルズ, インコーポレイテッド ヘテロアリールおよびその使用
PH12013500274A1 (en) 2010-08-11 2013-03-04 Millennium Pharm Inc Heteroaryls and uses thereof
WO2012021611A1 (en) 2010-08-11 2012-02-16 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
CA2814688A1 (en) 2010-10-13 2012-04-19 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
KR20160067841A (ko) 2013-08-28 2016-06-14 메디베이션 테크놀로지즈, 인크. 헤테로사이클릭 화합물 및 사용 방법
TN2016000270A1 (en) * 2014-01-14 2017-10-06 Millennium Pharm Inc Heteroaryls and uses thereof.
EP3094326A4 (en) 2014-01-14 2017-07-26 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
CN106922146B (zh) * 2014-10-02 2020-05-26 豪夫迈·罗氏有限公司 用于治疗由布鲁顿酪氨酸激酶(btk)介导的疾病的吡唑甲酰胺化合物
CA2978627A1 (en) 2015-03-04 2016-09-09 Medivation Technologies, Inc. Srebp blockers for use in treating liver fibrosis, elevated cholesterol and insulin resistance
CA2977539A1 (en) 2015-03-04 2016-09-09 Medivation Technologies, Inc. Sterol regulatory element-binding proteins (srebps) inhibitors
BR112018068681A2 (pt) 2016-03-16 2019-01-15 Bayer Cropscience Ag derivados de n-(cianobenzil)-6-(ciclopropil-carbonilamino)-4-(fenil)-piridina-2-carboxamida e compostos relacionados como pesticidas e agentes de proteção de plantas
EP3284739A1 (de) 2017-07-19 2018-02-21 Bayer CropScience Aktiengesellschaft Substituierte (het)arylverbindungen als schädlingsbekämpfungsmittel
CN111295381A (zh) 2017-07-28 2020-06-16 株式会社柳韩洋行 可用于合成抗蛋白激酶的选择性抑制剂的中间体及其制备方法
MX393995B (es) 2017-07-28 2025-03-24 Yuhan Corp Proceso mejorado para preparar derivados de aminopirimidina
EP3886854A4 (en) 2018-11-30 2022-07-06 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
CN110041252A (zh) * 2019-05-22 2019-07-23 南京合巨药业有限公司 一种2-氯-4-肼基吡啶的制备方法
CN114867724B (zh) * 2019-05-31 2025-11-07 班塔姆制药有限责任公司 用于制备噻唑基吡唑甲酸及其中间体的方法
WO2021011720A2 (en) * 2019-07-18 2021-01-21 Avidence Therapeutics, Inc. Anti-osteoarthritis compounds and related compositions and methods
US20250171435A1 (en) * 2023-11-27 2025-05-29 Rubedo Life Sciences, Inc. Carbon Linked BCL Inhibitors and Senolytic Compounds and Uses Thereof

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH27357A (en) * 1989-09-22 1993-06-21 Fujisawa Pharmaceutical Co Pyrazole derivatives and pharmaceutical compositions comprising the same
IL104369A0 (en) * 1992-01-13 1993-05-13 Smithkline Beecham Corp Novel compounds and compositions
GB2306108A (en) * 1995-10-13 1997-04-30 Merck & Co Inc Treatment of Raf-mediated cancers with imidazole derivatives
DE69836563T2 (de) * 1997-12-22 2007-05-16 Bayer Pharmaceuticals Corp., West Haven INHIBIERUNG DER p38 KINASE-AKTIVITÄT DURCH DIE VERWENDUNG VON ARYL- UND HETEROARYL-SUBSTITUIERTEN HARNSTOFFEN
JP4316893B2 (ja) * 2001-05-16 2009-08-19 バーテックス ファーマシューティカルズ インコーポレイテッド Srcおよび他のプロテインキナーゼのインヒビター
CA2455181C (en) * 2001-08-01 2010-04-06 Merck & Co., Inc. Benzimidazo[4,5-f]isoquinolinone derivatives
US7582631B2 (en) * 2004-01-14 2009-09-01 Amgen Inc. Substituted heterocyclic compounds and methods of use
US20080045492A1 (en) * 2004-12-21 2008-02-21 Coleman Paul J Mitotic Kinesin Inhibitors
EP1845973B1 (en) * 2005-01-21 2015-08-12 Astex Therapeutics Limited Pharmaceutical compounds
WO2008011557A2 (en) * 2006-07-20 2008-01-24 Borchardt Allen J Heteroaryl inhibitors of rho kinase
UY30892A1 (es) * 2007-02-07 2008-09-02 Smithkline Beckman Corp Inhibidores de la actividad akt
JP2010522770A (ja) * 2007-03-29 2010-07-08 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 Akt活性の阻害物質
GB0709031D0 (en) * 2007-05-10 2007-06-20 Sareum Ltd Pharmaceutical compounds
ES2401557T3 (es) * 2007-08-02 2013-04-22 Amgen, Inc Moduladores de Pl3 cinasas y métodos de uso
EA201001456A1 (ru) * 2008-03-21 2011-06-30 Новартис Аг Новые гетероциклические соединения и их применение
KR20110018451A (ko) * 2008-06-19 2011-02-23 밀레니엄 파머슈티컬스 인코퍼레이티드 티오펜 또는 티아졸 유도체, 그리고 pi3k 저해물질로서 이들의 용도
MX2010014572A (es) * 2008-06-27 2011-03-24 Novartis Ag Compuestos organicos.
CA2750935A1 (en) * 2009-01-30 2010-08-12 Millennium Pharmaceuticals, Inc. Heteroaryls and their use as pi3k inhibitors
WO2010127152A2 (en) * 2009-04-29 2010-11-04 Irm Llc Compounds and compositions as microsomal prostaglandin e synthase-1 inhibitors
WO2010132598A1 (en) * 2009-05-13 2010-11-18 Amgen Inc. Heteroaryl compounds as pikk inhibitors
JO3002B1 (ar) * 2009-08-28 2016-09-05 Irm Llc مركبات و تركيبات كمثبطات كيناز بروتين
EP2627650A2 (en) * 2010-05-26 2013-08-21 Merck Sharp & Dohme Corp. N-phenyl imidazole carboxamide inhibitors of 3-phosphoinositide-dependent protein kinase-1
WO2012084678A1 (en) * 2010-12-23 2012-06-28 Syngenta Participations Ag Novel imidazoles useful as plant fungicides
MX340013B (es) * 2011-03-21 2016-06-22 Hoffmann La Roche Compuestos de benzoxazepina selectivos para fosfatidilinositol 3-cinasa (pi3k) p110 delta y metodos de uso.
CN104136431B (zh) * 2011-12-21 2017-03-15 小野药品工业株式会社 作为凝血因子XIa抑制剂的吡啶酮和嘧啶酮衍生物

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