JP2015508102A5 - - Google Patents

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Publication number
JP2015508102A5
JP2015508102A5 JP2014558836A JP2014558836A JP2015508102A5 JP 2015508102 A5 JP2015508102 A5 JP 2015508102A5 JP 2014558836 A JP2014558836 A JP 2014558836A JP 2014558836 A JP2014558836 A JP 2014558836A JP 2015508102 A5 JP2015508102 A5 JP 2015508102A5
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JP
Japan
Prior art keywords
optionally substituted
hydrogen
pharmaceutically acceptable
acceptable salt
calcification
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JP2014558836A
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English (en)
Japanese (ja)
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JP6302846B2 (ja
JP2015508102A (ja
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Priority claimed from PCT/US2013/027191 external-priority patent/WO2013126608A1/en
Publication of JP2015508102A publication Critical patent/JP2015508102A/ja
Publication of JP2015508102A5 publication Critical patent/JP2015508102A5/ja
Application granted granted Critical
Publication of JP6302846B2 publication Critical patent/JP6302846B2/ja
Active legal-status Critical Current
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JP2014558836A 2012-02-22 2013-02-21 Tnap阻害剤としてのスルホンアミド化合物およびその使用 Active JP6302846B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261601957P 2012-02-22 2012-02-22
US61/601,957 2012-02-22
PCT/US2013/027191 WO2013126608A1 (en) 2012-02-22 2013-02-21 Sulfonamide compounds and uses as tnap inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2018002991A Division JP6544545B2 (ja) 2012-02-22 2018-01-11 Tnap阻害剤としてのスルホンアミド化合物およびその使用

Publications (3)

Publication Number Publication Date
JP2015508102A JP2015508102A (ja) 2015-03-16
JP2015508102A5 true JP2015508102A5 (enExample) 2016-03-24
JP6302846B2 JP6302846B2 (ja) 2018-03-28

Family

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Family Applications (2)

Application Number Title Priority Date Filing Date
JP2014558836A Active JP6302846B2 (ja) 2012-02-22 2013-02-21 Tnap阻害剤としてのスルホンアミド化合物およびその使用
JP2018002991A Active JP6544545B2 (ja) 2012-02-22 2018-01-11 Tnap阻害剤としてのスルホンアミド化合物およびその使用

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2018002991A Active JP6544545B2 (ja) 2012-02-22 2018-01-11 Tnap阻害剤としてのスルホンアミド化合物およびその使用

Country Status (10)

Country Link
US (3) US9458147B2 (enExample)
EP (1) EP2817292B1 (enExample)
JP (2) JP6302846B2 (enExample)
KR (1) KR102083041B1 (enExample)
CN (1) CN104334527B (enExample)
AU (1) AU2013222345B2 (enExample)
BR (1) BR112014020773A2 (enExample)
CA (1) CA2865071C (enExample)
RU (1) RU2627701C2 (enExample)
WO (1) WO2013126608A1 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5986570B2 (ja) 2010-09-01 2016-09-06 トーマス・ジェファーソン・ユニバーシティThomas Jefferson University 筋修復および再生のための組成物および方法
BR112014020773A2 (pt) 2012-02-22 2020-10-27 Sanford-Burnham Medical Research Institute compostos de sulfonamida e seus usos como inibidores tnap
JP2017502092A (ja) 2014-01-14 2017-01-19 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Millennium Pharmaceuticals, Inc. ヘテロアリール及びその使用
TN2016000270A1 (en) 2014-01-14 2017-10-06 Millennium Pharm Inc Heteroaryls and uses thereof.
CN103755628B (zh) * 2014-01-27 2015-07-29 河北科技大学 2-氨基-3-碘-5-溴吡啶的合成方法
WO2016054056A1 (en) * 2014-10-01 2016-04-07 The Usa, As Represented By The Secretary, Dept. Of Health And Human Services Methods of treating pxe with tnap inhibitors
CN107207527B (zh) 2015-07-08 2019-10-01 第一三共株式会社 作为tnap抑制剂的吡啶并噁嗪酮化合物
ITUA20161994A1 (it) * 2016-03-24 2017-09-24 Azienda Ospedaliera Univ Senese Uso degli inibitori ddx3 come agenti anti-iperproliferativi
MY200642A (en) * 2016-06-08 2024-01-08 Clementia Pharmaceuticals Inc Method for treating heterotopic ossification
TW201829417A (zh) 2016-12-23 2018-08-16 日商第一三共股份有限公司 氧氮呯化合物
EP3559007B1 (en) * 2016-12-23 2023-08-16 Daiichi Sankyo Company, Limited Sulfonamide compounds having tnap inhibitory activity
WO2020014330A1 (en) * 2018-07-10 2020-01-16 Academia Sinica A biomarker and target for diagnosis, prognosis and treatment of ankylosing spondylitis
KR102880470B1 (ko) 2018-10-23 2025-11-03 다이이찌 산쿄 가부시키가이샤 바이아릴 유도체
AU2020239048B2 (en) 2019-03-12 2025-10-16 Arcus Biosciences, Inc. Treatment of oncogene-driven cancers
KR20210144821A (ko) 2019-03-29 2021-11-30 아르커스 바이오사이언시즈 인코포레이티드 규명된 아데노신 지문을 이용한 암의 치료방법
WO2021113512A1 (en) 2019-12-04 2021-06-10 The Board Of Trustees Of The Leland Stanford Junior University Enhancing blood-brain barrier drug transport by targeting endogenous regulators
CN113683563B (zh) * 2021-08-31 2024-01-30 合肥工业大学 一种多取代3-磺酰胺喹啉化合物的合成方法
CN115837023B (zh) * 2023-02-20 2023-05-16 中山大学附属第八医院(深圳福田) 1-甲基烟酰胺在制备抗血管钙化药物中的应用
KR102790313B1 (ko) * 2023-11-07 2025-04-04 주식회사 레드엔비아 Tnap 저해 화합물 및 이의 용도

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW352384B (en) * 1992-03-24 1999-02-11 Hoechst Ag Sulfonamido- or sulfonamidocarbonylpyridine-2-carboxamides, process for their preparation and their use as pharmaceuticals
JP2000247949A (ja) 1999-02-26 2000-09-12 Eisai Co Ltd スルホンアミド含有インドール化合物
ES2341843T3 (es) * 2000-02-03 2010-06-29 EISAI R&D MANAGEMENT CO., LTD. Inhibidores de la expresion de integrina.
CA2468745A1 (en) * 2001-11-30 2003-06-12 The Burnham Institute Induction of apoptosis in cancer cells
GB0206219D0 (en) * 2002-03-15 2002-05-01 Ferring Bv Non-Peptide GnRH antagonists
US20040110802A1 (en) * 2002-08-23 2004-06-10 Atli Thorarensen Antibacterial benzoic acid derivatives
AU2003265382A1 (en) * 2002-08-23 2004-03-11 Pharmacia & Upjohn Company Llc Antibacterial benzoic acid derivatives
ATE363470T1 (de) 2002-11-18 2007-06-15 Chemocentryx Inc Arylsulfonamide
CN100589803C (zh) * 2004-07-28 2010-02-17 霍夫曼-拉罗奇有限公司 芳基-吡啶衍生物
US20090142347A1 (en) * 2004-09-29 2009-06-04 The Burnham Institute For Medical Research Tissue-Nonspecific Alkaline Phosphatase (TNAP): a Therapeutic Target for Arterial Calcification
SE0402735D0 (sv) * 2004-11-09 2004-11-09 Astrazeneca Ab Novel compounds
GB0425026D0 (en) * 2004-11-12 2004-12-15 Biofocus Discovery Ltd Compounds which bind to the active site of protein kinase enzymes
JP2008519814A (ja) * 2004-11-12 2008-06-12 ガラパゴス・ナムローゼ・フェンノートシャップ プロテインキナーゼ酵素の活性部位と結合する窒素複素環式芳香族化合物
PT1860941E (pt) * 2005-03-16 2008-12-22 Basf Se Bifenil-n-(4-piridil)metilsulfonamidas
WO2007014008A2 (en) * 2005-07-22 2007-02-01 Glaxo Group Limted Benzenesulfonamide inhibitor of ccr2 chemokine receptor
KR20080104310A (ko) * 2006-02-14 2008-12-02 바스프 에스이 해충 방제를 위한 피리딘-4-일메틸아미드
CN101484438A (zh) * 2006-05-03 2009-07-15 阿斯利康(瑞典)有限公司 吡唑衍生物及其作为p13k抑制剂的用途
EP2016075A1 (en) * 2006-05-03 2009-01-21 AstraZeneca AB Thiazole derivatives and their use as anti-tumour agents
AU2007293653B2 (en) * 2006-09-08 2011-02-17 Novartis Ag N-biaryl (hetero) arylsulphonamide derivatives useful in the treatment of diseases mediated by lymphocytes interactions
WO2008042867A2 (en) * 2006-09-29 2008-04-10 Emiliem Inc. Modulators of multiple kinases
EP2433496A1 (en) * 2007-05-08 2012-03-28 Burnham Institute for Medical Research Tissue non-specific alkaline phosphatase inhibitors and uses thereof for treating vascular calcification
EP2190466A4 (en) * 2007-08-10 2011-12-21 Burnham Inst Medical Research Tissue-specific alkaline phosphatase (TNAP) activators and their use
US8039493B2 (en) * 2007-09-27 2011-10-18 Hoffmann-La Roche Inc. Biaryl sulfonamide derivatives
WO2009055418A1 (en) * 2007-10-22 2009-04-30 Smithkline Beecham Corporation Pyridosulfonamide derivatives as pi3 kinase inhibitors
US8268834B2 (en) * 2008-03-19 2012-09-18 Novartis Ag Pyrazine derivatives that inhibit phosphatidylinositol 3-kinase enzyme
CA2723424A1 (en) * 2008-05-19 2009-11-26 Burnham Institute For Medical Research Intestinal alkaline phosphatase modulators and uses thereof
UA104147C2 (uk) * 2008-09-10 2014-01-10 Новартис Аг Похідна піролідиндикарбонової кислоти та її застосування у лікуванні проліферативних захворювань
TW201016676A (en) * 2008-10-03 2010-05-01 Astrazeneca Ab Heterocyclic derivatives and methods of use thereof
WO2010130638A1 (en) * 2009-05-14 2010-11-18 Evotec Ag Sulfonamide compounds, pharmaceutical compositions and uses thereof
SG175925A1 (en) * 2009-05-15 2011-12-29 Novartis Ag Aryl pyridine as aldosterone synthase inhibitors
CA2944788C (en) * 2009-06-29 2023-08-22 Agios Pharmaceuticals, Inc. Compounds, and compositions thereof, which modulate pyruvate kinase m2, and methods of making same
FR2970967B1 (fr) * 2011-01-27 2013-02-15 Pf Medicament Derives de type azaindazole ou diazaindazole comme medicament
BR112014020773A2 (pt) 2012-02-22 2020-10-27 Sanford-Burnham Medical Research Institute compostos de sulfonamida e seus usos como inibidores tnap
WO2016054056A1 (en) * 2014-10-01 2016-04-07 The Usa, As Represented By The Secretary, Dept. Of Health And Human Services Methods of treating pxe with tnap inhibitors

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