JP2018503631A5 - - Google Patents

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JP2018503631A5
JP2018503631A5 JP2017535439A JP2017535439A JP2018503631A5 JP 2018503631 A5 JP2018503631 A5 JP 2018503631A5 JP 2017535439 A JP2017535439 A JP 2017535439A JP 2017535439 A JP2017535439 A JP 2017535439A JP 2018503631 A5 JP2018503631 A5 JP 2018503631A5
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hydrocarbyl
alkyl
cycloalkyl
alkoxy
substituted
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JP6903580B2 (ja
JP2018503631A (ja
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Priority to JP2021103894A priority Critical patent/JP7337883B2/ja
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Priority to JP2023135162A priority patent/JP7771139B2/ja
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JP2017535439A 2014-12-29 2015-12-29 乳酸脱水素酵素の小分子阻害剤及びその使用方法 Active JP6903580B2 (ja)

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Application Number Priority Date Filing Date Title
JP2021103894A JP7337883B2 (ja) 2014-12-29 2021-06-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法
JP2023135162A JP7771139B2 (ja) 2014-12-29 2023-08-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法

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US201462097226P 2014-12-29 2014-12-29
US62/097,226 2014-12-29
PCT/US2015/067895 WO2016109559A2 (en) 2014-12-29 2015-12-29 Small molecule inhibitors of lactate dehydrogenase and methods of use thereof

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JP2018503631A JP2018503631A (ja) 2018-02-08
JP2018503631A5 true JP2018503631A5 (cg-RX-API-DMAC10.html) 2021-02-12
JP6903580B2 JP6903580B2 (ja) 2021-07-14

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JP2017535439A Active JP6903580B2 (ja) 2014-12-29 2015-12-29 乳酸脱水素酵素の小分子阻害剤及びその使用方法
JP2021103894A Active JP7337883B2 (ja) 2014-12-29 2021-06-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法
JP2023135162A Active JP7771139B2 (ja) 2014-12-29 2023-08-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法

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JP2021103894A Active JP7337883B2 (ja) 2014-12-29 2021-06-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法
JP2023135162A Active JP7771139B2 (ja) 2014-12-29 2023-08-23 乳酸脱水素酵素の小分子阻害剤及びその使用方法

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US (5) US10351532B2 (cg-RX-API-DMAC10.html)
EP (2) EP3954685B1 (cg-RX-API-DMAC10.html)
JP (3) JP6903580B2 (cg-RX-API-DMAC10.html)
CN (1) CN107624112B (cg-RX-API-DMAC10.html)
AU (2) AU2015374118B2 (cg-RX-API-DMAC10.html)
CA (2) CA2978823C (cg-RX-API-DMAC10.html)
DK (1) DK3240785T3 (cg-RX-API-DMAC10.html)
ES (2) ES3042832T3 (cg-RX-API-DMAC10.html)
HU (1) HUE055662T2 (cg-RX-API-DMAC10.html)
PL (1) PL3240785T3 (cg-RX-API-DMAC10.html)
SI (1) SI3240785T1 (cg-RX-API-DMAC10.html)
WO (1) WO2016109559A2 (cg-RX-API-DMAC10.html)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2978823C (en) * 2014-12-29 2023-10-10 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Small molecule inhibitors of lactate dehydrogenase and methods of use thereof
AU2017208998B2 (en) * 2016-01-21 2021-07-15 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Bruton's tyrosine kinase inhibitors
US10954228B2 (en) 2016-06-29 2021-03-23 The Trustees Of The University Of Pennsylvania 1 H-pyrazol-1-yl-thiazoles as inhibitors of lactate dehydrogenase and methods of use thereof
TW201837026A (zh) 2017-01-10 2018-10-16 德商拜耳廠股份有限公司 作為除害劑之雜環衍生物(二)
AU2018346597B2 (en) 2017-10-06 2023-07-13 Forma Therapeutics, Inc. Inhibiting Ubiquitin Specific Peptidase 30
IL278291B2 (en) 2018-05-17 2023-10-01 Forma Therapeutics Inc Condensed bicyclic compounds are useful as ubiquitin-specific peptidase 30 inhibitors
WO2020030613A1 (en) 2018-08-07 2020-02-13 Kemijski Institut Small molecule-inhibitors of 6-phosphofructo-1-kinase for reducing lactate generation by cancer cells
EP3632908A1 (en) 2018-10-02 2020-04-08 Inventiva Inhibitors of the yap/taz-tead interaction and their use in the treatment of cancer
EP4218934B1 (en) 2018-10-05 2025-06-18 Forma Therapeutics, Inc. Inhibiting ubiquitin-specific protease 30 (usp30)
TWI820231B (zh) 2018-10-11 2023-11-01 德商拜耳廠股份有限公司 用於製備經取代咪唑衍生物之方法
EA202191432A1 (ru) 2018-11-22 2021-10-14 Цилу Регор Терапьютикс Инк. Агонисты glp-1r и их применения
AU2019387370A1 (en) 2018-11-30 2021-06-10 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
AU2020256647B2 (en) 2019-04-12 2025-07-31 Qilu Regor Therapeutics Inc. GLP-1R agonists and uses thereof
WO2020221899A1 (en) * 2019-05-02 2020-11-05 Université Catholique de Louvain Lactate dehydrogenase inhibitor polypeptides for use in the treatment of cancer
US11725026B2 (en) * 2019-06-28 2023-08-15 The Research Foundation For The State University Of New York Compositions and methods for inhibiting lactate dehydrogenase a activity
WO2021026290A1 (en) 2019-08-07 2021-02-11 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services T cells having enhanced anti-tumor activity
US11752138B2 (en) 2020-05-18 2023-09-12 Vanderbilt University Treating primary or idiopathic hyperoxaluria with small molecule inhibitors of lactate dehydrogenase
MX2022014130A (es) * 2020-05-18 2023-02-16 Chinook Therapeutics Canada Inc Compuestos de pirazolilo sustituido y metodos de uso de estos.
WO2021234543A1 (en) * 2020-05-18 2021-11-25 Chinook Therapeutics Canada, Inc. Substituted pyrazolyl compounds and methods of use thereof
WO2021251842A1 (en) * 2020-06-08 2021-12-16 Qatar Foundation For Education, Science And Community Development Targeting of lactate dehydrogenase c, methods of preparing same, and methods of using same in combination with anti-cancer treatments
BR112022026904A2 (pt) 2020-07-02 2023-01-24 Bayer Ag Derivados de heterocicleno como agentes de controle de pragas
US20240066027A1 (en) * 2020-12-03 2024-02-29 Domain Therapeutics Novel par-2 inhibitors
WO2024212024A1 (en) * 2023-04-09 2024-10-17 Meta Pharmaceuticals (Hk) Limited Novel substituted pyrrole compounds, compositions comprising the substituted pyrrole compound, and methods of use thereof
WO2025011479A1 (en) * 2023-07-13 2025-01-16 Meta Pharmaceuticals (Hk) Limited Pyrazole based inhibitors of LDH and their use in immune and inflammatory diseases
WO2025026738A1 (en) 2023-07-31 2025-02-06 Bayer Aktiengesellschaft 6-[5-(ethylsulfonyl)-1-methyl-1h-imidazol-4-yl]-7-methyl-3-(pentafluoroethyl)-7h-imidazo[4,5-c]pyridazine derivatives as pesticides
WO2025241048A1 (en) * 2024-05-20 2025-11-27 Meta Pharmaceuticals (Hk) Limited Inhibitors of lactate dehydrogenase, compositions comprising the inhibitor, and methods of use thereof
WO2025241047A1 (en) * 2024-05-20 2025-11-27 Meta Pharmaceuticals (Hk) Limited Inhibitors of lactate dehydrogenase, compositions comprising the inhibitor, and methods of use thereof
WO2025241049A1 (en) * 2024-05-20 2025-11-27 Meta Pharmaceuticals (Hk) Limited Inhibitors of lactate dehydrogenase, compositions comprising the inhibitor, and methods of use thereof
CN118772058B (zh) * 2024-06-14 2026-03-17 济南尚博医药股份有限公司 一种2-氯-4-(1h-吡唑-3-基)苯甲腈的合成方法及应用

Family Cites Families (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5182289A (en) 1988-06-14 1993-01-26 Schering Corporation Heterobicyclic compounds having antiinflammatory activity
WO1990008146A1 (en) * 1989-01-10 1990-07-26 Pfizer Inc. Anti-inflammatory 1-heteroaryl-oxindole-3-carboxamides
US5602113A (en) 1991-02-07 1997-02-11 Boehringer Ingelheim Pharmaceuticals, Inc. Pyridobenzo- and pyridiothieno-diazepines useful for the treatment of HIV infection
CN1071924A (zh) 1991-10-29 1993-05-12 纳幕尔杜邦公司 除草的三唑羧酸酰胺
JPH0680569A (ja) 1992-09-03 1994-03-22 Asahi Chem Ind Co Ltd 血小板凝集阻害剤
US5342851A (en) 1992-10-07 1994-08-30 Mcneil-Ppc, Inc. Substituted thiazole derivatives useful as platelet aggregation inhibitors
DE4405207A1 (de) 1994-02-18 1995-08-24 Bayer Ag N-Pyrazolylaniline und N-Pyrazolylaminopyridine
US20020028936A1 (en) * 1999-04-12 2002-03-07 Gerhard Sperl 1,3-disubstituted indolin-2-ones for neoplasia
US6136079A (en) 1999-04-30 2000-10-24 Eastman Kodak Company Dye for ink jet ink
WO2001005758A2 (en) 1999-07-15 2001-01-25 Nps Allelix Corp. Indoles and indazoles for the treatment of migraine
US6407238B1 (en) 1999-10-29 2002-06-18 Boehringer Ingelheim Pharmaceuticals, Inc. Process of making substituted pyrazoles
US6436965B1 (en) 2000-03-02 2002-08-20 Merck Frosst Canada & Co. PDE IV inhibiting amides, compositions and methods of treatment
JP2002167531A (ja) 2000-11-29 2002-06-11 Fuji Photo Film Co Ltd インクジェット記録用インク組成物及び画像形成方法
PA8535601A1 (es) 2000-12-21 2002-11-28 Pfizer Derivados benzimidazol y piridilimidazol como ligandos para gabaa
TWI311133B (en) 2001-04-20 2009-06-21 Eisai R&D Man Co Ltd Carboxylic acid derivativeand the salt thereof
WO2003002062A2 (en) 2001-06-29 2003-01-09 Tularik Inc. Bis-aryl thiazole derivatives
IL159811A0 (en) 2001-07-13 2004-06-20 Neurogen Corp Heteroaryl substituted fused bicyclic heteroaryl compounds as gabaa receptor ligands
EP1314733A1 (en) 2001-11-22 2003-05-28 Aventis Pharma Deutschland GmbH Indole-2-carboxamides as factor Xa inhibitors
AU2003256297A1 (en) 2002-08-09 2004-02-25 Eli Lilly And Company Benzimidazoles and benzothiazoles as inhibitors of map kinase
WO2004016592A1 (en) 2002-08-14 2004-02-26 Ppd Discovery, Inc. Prenylation inhibitors and methods of their synthesis and use
US20040166137A1 (en) 2002-11-08 2004-08-26 Lackey John William Hetero-substituted benzimidazole compounds and antiviral uses thereof
CA2520804A1 (en) 2003-04-03 2004-10-28 Merck & Co., Inc. Biaryl substituted pyrazoles as sodium channel blockers
GB0323845D0 (en) 2003-10-10 2003-11-12 Angeletti P Ist Richerche Bio Chemical compounds,compositions and uses
US7387980B2 (en) 2004-09-22 2008-06-17 Symyx Technologies, Inc. Methods of using heterocycle-amine ligands, compositions, complexes, and catalysts
EP1807417A2 (en) 2004-11-04 2007-07-18 Neurogen Corporation Pyrazolylmethyl heteroaryl derivatives
WO2006077366A1 (en) 2005-01-19 2006-07-27 Biolipox Ab Indoles useful in the treatment of inflammation
JP2008527028A (ja) 2005-01-19 2008-07-24 バイオリポックス エービー 炎症の治療に有用なインドール類
WO2006077367A1 (en) 2005-01-19 2006-07-27 Biolipox Ab Indoles useful in the treatment of inflamation
WO2006077364A1 (en) 2005-01-19 2006-07-27 Biolipox Ab Indoles useful in the treatment of inflammation
US20090048285A1 (en) 2005-01-19 2009-02-19 Benjamin Pelcman Pyrrolopyridines Useful in the Treatment of Inflammation
WO2006078891A2 (en) 2005-01-21 2006-07-27 Neurogen Corporation Imidazolylmethyl and pyrazolylmethyl heteroaryl derivatives
GB0507198D0 (en) 2005-04-08 2005-05-18 Sb Pharmco Inc Process for preparing bicyclic compounds
US7456292B2 (en) 2005-06-30 2008-11-25 Bexel Pharmaceuticals, Inc. Hydroxamic acid-containing amino acid derivatives
WO2007018508A1 (en) 2005-07-28 2007-02-15 Glaxo Group Limited Novel m3 muscarinic acetycholine receptor antagonists
WO2007018514A1 (en) 2005-07-28 2007-02-15 Glaxo Group Limited Novel m3 muscarinic acetylcholine receptor antagonists
WO2007021941A2 (en) 2005-08-16 2007-02-22 Icagen, Inc. Inhibitors of voltage-gated sodium channels
WO2007038571A2 (en) 2005-09-26 2007-04-05 Smithkline Beecham Corporation Prolyl hydroxylase antagonists
US20090306169A1 (en) 2005-10-06 2009-12-10 Brandish Philip E Use of Fused Pyrrole Carboxylic Acids for the Treatment of Neurodegenerative and Psychiatric Diseases and D-Amino Acid Oxidase Inhibitors
AU2006303545B2 (en) 2005-10-17 2012-09-06 Isagro Ricerca S.R.L. Compounds and relative use for the control of phytopathogens
WO2007048732A1 (de) 2005-10-28 2007-05-03 Basf Aktiengesellschaft Verwendung von 5-amino-pyrazolen zur bekämpfung pflanzenpathogener schadpilze, neue 5-amino-pyrazole, verfahren zu ihrer herstellung und sie enthaltende mittel
US7960544B2 (en) 2005-12-16 2011-06-14 Ironwood Pharmaceuticals, Inc. Useful indole compounds
ITMI20052459A1 (it) 2005-12-22 2007-06-23 Isagro Spa Sali quaternari e relativo uso per il controllo di fitopatogeni
US20080090834A1 (en) 2006-07-06 2008-04-17 Pfizer Inc Selective azole pde10a inhibitor compounds
GB0614068D0 (en) * 2006-07-14 2006-08-23 Glaxo Group Ltd Compounds
WO2008009924A2 (en) 2006-07-18 2008-01-24 Biolipox Ab Indoles useful in the treatment of inflammation
EP2053920B1 (en) 2007-01-26 2014-04-30 North Carolina State University Inhibition of bacterial biofilms with imidazole derivatives
WO2008121861A2 (en) 2007-03-28 2008-10-09 Xenon Pharmaceuticals Inc. Pyrazole and pyrrole compounds useful in treating iron disorders
ES2423932T3 (es) 2007-08-27 2013-09-25 Basf Se Compuestos de pirazol para controlar plagas de invertebrados
WO2009076454A2 (en) 2007-12-12 2009-06-18 Calcimedica, Inc. Compounds that modulate intracellular calcium
WO2009108551A2 (en) 2008-02-25 2009-09-03 H. Lundbeck A/S Heteroaryl amide analogues
CA2719234A1 (en) 2008-05-08 2009-11-12 Joan M. Fletcher Spiroazaindoles
US9029408B2 (en) 2008-06-16 2015-05-12 Gtx, Inc. Compounds for treatment of cancer
RU2011105810A (ru) * 2008-07-17 2012-08-27 Асахи Касеи Фарма Корпорейшн (Jp) Азотсодержащие бициклические гетероциклические соединения
KR20100122513A (ko) * 2008-07-17 2010-11-22 아사히 가세이 파마 가부시키가이샤 질소 함유 복소환 화합물
WO2010010186A1 (en) 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases
TWI607996B (zh) 2008-09-24 2017-12-11 巴地斯顏料化工廠 控制無脊椎害蟲之吡唑化合物
US10167263B2 (en) * 2008-11-20 2019-01-01 Northwestern University Treatment of amyotrophic lateral sclerosis
WO2010065067A1 (en) * 2008-11-20 2010-06-10 Bodymedia, Inc. Method and apparatus for determining critical care parameters
CN101747276B (zh) 2008-11-28 2011-09-07 中国中化股份有限公司 具有含氮五元杂环的醚类化合物及其应用
CN102239162B (zh) 2008-12-04 2014-05-28 弗·哈夫曼-拉罗切有限公司 哒嗪酮衍生物
CN102264737A (zh) 2008-12-23 2011-11-30 雅培制药有限公司 抗病毒化合物
JP2012521429A (ja) 2009-03-23 2012-09-13 メルク・シャープ・エンド・ドーム・コーポレイション 疼痛治療用のp2x3受容体アンタゴニスト
JP5756457B2 (ja) 2009-04-06 2015-07-29 アジオス ファーマシューティカルズ, インコーポレイテッド ピルビン酸キナーゼm2調節剤、治療組成物および関連する使用方法
WO2011057942A1 (en) 2009-11-12 2011-05-19 Basf Se Insecticidal methods using pyridine compounds
ES2460915T3 (es) 2009-12-21 2014-05-16 Novartis Ag Piridinas fusionadas con heteroarilo disustituido
WO2011091410A1 (en) 2010-01-25 2011-07-28 Glaxos Smithkline Llc Trpv4 antagonists
EP2638012A1 (en) 2010-11-10 2013-09-18 Boehringer Ingelheim International GmbH Pyridyl ureas as mineralocorticoid receptor antagonists
WO2012074022A1 (ja) 2010-12-01 2012-06-07 旭硝子株式会社 イリジウムカチオン錯体および発光組成物
AR084515A1 (es) 2010-12-22 2013-05-22 Merz Pharma Gmbh & Co Kgaa Derivados heterociclicos nitrogenados, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades asociadas al sistema nervioso central tales como parkinson y alzheimer, entre otras
JP2014506915A (ja) 2011-03-04 2014-03-20 ノバルティス アーゲー キナーゼ阻害剤としての四置換シクロヘキシル化合物
EP2704701B1 (en) 2011-05-03 2018-01-03 PRCL Research Inc. Compounds for inflammation and immune-related uses
WO2012151440A1 (en) 2011-05-03 2012-11-08 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use for increasing lifetime of the red blood cells and treating anemia
WO2012154880A1 (en) 2011-05-09 2012-11-15 Proteostasis Therapeutics, Inc. Proteostasis regulators for treating cystic fibrosis and other protein misfolding diseases
JP2013040240A (ja) 2011-08-11 2013-02-28 Fujifilm Corp アゾ化合物、アゾ顔料、顔料分散物、着色組成物、カラーフィルター用着色組成物、カラーフィルター、カラーフィルター用着色組成物の調製方法、インクジェット記録用インク、印刷インク、塗料、染料、及び、レジストインク
KR20140060535A (ko) 2011-08-24 2014-05-20 깃세이 야쿠힌 고교 가부시키가이샤 축합 헤테로환 유도체 및 그 의약용도
ITPI20110143A1 (it) * 2011-12-20 2013-06-21 Univ Pisa Agenti terapeutici in grado di ridurre la produzione cellulare di acido lattico e composizioni farmaceutiche che comprendono tali composti
CA2863517C (en) 2012-01-20 2019-11-05 Genosco Substituted pyrimidine compounds and their use as syk inhibitors
KR102018409B1 (ko) 2012-07-30 2019-09-04 다이쇼 세이야꾸 가부시끼가이샤 부분적으로 포화된 질소 함유 복소환 화합물
WO2014062938A1 (en) 2012-10-19 2014-04-24 Bristol-Myers Squibb Company Rory modulators
EP2934527A4 (en) 2012-12-20 2016-07-13 Merck Sharp & Dohme 2-pyridyloxy-4-ESTER-orexin receptor antagonists
WO2014099697A1 (en) 2012-12-20 2014-06-26 Merck Sharp & Dohme Corp. 3-ester-4-substituted orexin receptor antagonists
US9643955B2 (en) 2012-12-20 2017-05-09 Merck Sharp & Dohme Corp. 2-pyridyloxy-3-nitrile-4-substituted orexin receptor antagonists
FR3001219A1 (fr) 2013-01-22 2014-07-25 Centre Nat Rech Scient Inhibiteurs de kinases
HK1220626A1 (zh) 2013-03-15 2017-05-12 The Centre For Drug Research And Development 具细胞毒性和抗有丝分裂的化合物以及其使用方法
WO2014156922A1 (ja) 2013-03-29 2014-10-02 コニカミノルタ株式会社 異性体混合金属錯体組成物、有機エレクトロルミネッセンス素子、照明装置及び表示装置
WO2014173880A1 (en) 2013-04-22 2014-10-30 Syngenta Participations Ag Novel microbiocides
WO2014176475A2 (en) 2013-04-26 2014-10-30 The Regents Of The University Of Michigan Egfr inhibitors and uses thereof
US9169221B2 (en) 2013-04-29 2015-10-27 Comsats Institute Of Information Technology Dihydro 1,4-benzoxazines and method of synthesizing the same using sulfonium salts
CA2978823C (en) 2014-12-29 2023-10-10 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Small molecule inhibitors of lactate dehydrogenase and methods of use thereof

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