JP2020531432A5 - - Google Patents

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JP2020531432A5
JP2020531432A5 JP2020508455A JP2020508455A JP2020531432A5 JP 2020531432 A5 JP2020531432 A5 JP 2020531432A5 JP 2020508455 A JP2020508455 A JP 2020508455A JP 2020508455 A JP2020508455 A JP 2020508455A JP 2020531432 A5 JP2020531432 A5 JP 2020531432A5
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JP7301040B2 (ja
JP2020531432A (ja
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JP2020508455A 2017-08-15 2018-08-15 ピルビン酸キナーゼ調節因子およびその使用 Active JP7301040B2 (ja)

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Application Number Priority Date Filing Date Title
JP2022199462A JP2023027276A (ja) 2017-08-15 2022-12-14 ピルビン酸キナーゼ調節因子およびその使用

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
CNPCT/CN2017/097496 2017-08-15
CN2017097496 2017-08-15
US201862673533P 2018-05-18 2018-05-18
US201862673526P 2018-05-18 2018-05-18
US62/673,526 2018-05-18
US62/673,533 2018-05-18
PCT/US2018/000129 WO2019035865A1 (en) 2017-08-15 2018-08-15 MODULATORS OF PYRUVATE KINASE AND THEIR USE

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JP2022199462A Division JP2023027276A (ja) 2017-08-15 2022-12-14 ピルビン酸キナーゼ調節因子およびその使用

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JP2020531432A JP2020531432A (ja) 2020-11-05
JP2020531432A5 true JP2020531432A5 (enExample) 2021-09-30
JP7301040B2 JP7301040B2 (ja) 2023-06-30

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JP2020508455A Active JP7301040B2 (ja) 2017-08-15 2018-08-15 ピルビン酸キナーゼ調節因子およびその使用
JP2020508498A Active JP7275107B2 (ja) 2017-08-15 2018-08-15 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子
JP2022199462A Pending JP2023027276A (ja) 2017-08-15 2022-12-14 ピルビン酸キナーゼ調節因子およびその使用
JP2023005925A Active JP7530453B2 (ja) 2017-08-15 2023-01-18 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子
JP2024121066A Pending JP2024147805A (ja) 2017-08-15 2024-07-26 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子

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JP2020508498A Active JP7275107B2 (ja) 2017-08-15 2018-08-15 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子
JP2022199462A Pending JP2023027276A (ja) 2017-08-15 2022-12-14 ピルビン酸キナーゼ調節因子およびその使用
JP2023005925A Active JP7530453B2 (ja) 2017-08-15 2023-01-18 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子
JP2024121066A Pending JP2024147805A (ja) 2017-08-15 2024-07-26 血液障害の治療に使用するためのピルビン酸キナーゼ活性化因子

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US (8) US11364240B2 (enExample)
EP (4) EP3668512B1 (enExample)
JP (5) JP7301040B2 (enExample)
KR (3) KR102717594B1 (enExample)
CN (3) CN111032045B (enExample)
AU (4) AU2018316588B2 (enExample)
BR (2) BR112020003254A2 (enExample)
CA (1) CA3072455A1 (enExample)
CL (1) CL2020000375A1 (enExample)
CO (2) CO2020002961A2 (enExample)
CR (1) CR20200123A (enExample)
CY (1) CY1124953T1 (enExample)
DK (2) DK3668512T3 (enExample)
EC (1) ECSP20018487A (enExample)
ES (3) ES2944545T3 (enExample)
FI (1) FI3668512T3 (enExample)
HR (2) HRP20230452T1 (enExample)
HU (2) HUE061910T2 (enExample)
IL (3) IL272599B (enExample)
LT (2) LT3668512T (enExample)
MD (1) MD3668513T2 (enExample)
MX (2) MX2020001832A (enExample)
MY (1) MY204421A (enExample)
PE (1) PE20200724A1 (enExample)
PH (1) PH12020500343B1 (enExample)
PL (2) PL3668512T3 (enExample)
PT (2) PT3668512T (enExample)
RS (2) RS62871B1 (enExample)
SG (2) SG11202001353PA (enExample)
SI (2) SI3668513T1 (enExample)
SM (2) SMT202300146T1 (enExample)
TW (3) TWI796353B (enExample)
UA (1) UA126292C2 (enExample)
WO (3) WO2019035864A1 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TN2019000290A1 (en) 2017-03-20 2021-05-07 Forma Therapeutics Inc Pyrrolopyrrole compositions as pyruvate kinase (pkr) activators
SG11202001353PA (en) 2017-08-15 2020-03-30 Agios Pharmaceuticals Inc Pyruvate kinase modulators and use thereof
EP3697354A4 (en) 2017-10-20 2021-06-30 The Regents of The University of Michigan EYE DISEASE COMPOSITIONS AND METHODS
JP7450610B2 (ja) 2018-09-19 2024-03-15 ノヴォ・ノルディスク・ヘルス・ケア・アーゲー ピルビン酸キナーゼrの活性化
BR112021005188A2 (pt) 2018-09-19 2021-06-08 Forma Therapeutics, Inc. tratamento de anemia falciforme com um composto de ativação de piruvato cinase r
CA3129829A1 (en) * 2019-02-13 2020-08-20 Agios Pharmaceuticals, Inc. Thieno[3,2-b] pyrrole[3,2-d]pyridazinone derivatives and their use as pkm2 derivatives for the treatment of cancer, obesity and diabetes related disorders
CN114008147B (zh) * 2019-06-26 2023-05-02 日产化学株式会社 电荷传输性清漆
BR112022004715A2 (pt) 2019-09-19 2022-06-14 Forma Therapeutics Inc Composições de ativação de piruvato quinase r (pkr)
EP4185293A4 (en) * 2020-07-21 2025-01-15 The Regents of The University of Michigan COMPOSITIONS AND METHODS FOR ACTIVATING PYRUVATE KINASE
CN112490502B (zh) * 2020-12-04 2022-01-21 广州天赐高新材料股份有限公司 一种电解液及锂二次电池
US11566030B2 (en) 2021-02-08 2023-01-31 Global Blood Therapeutics, Inc. Substituted 2,6-dihydropyrrolo[3,4-c]pyrazoles as pyruvate kinase activators
US12128035B2 (en) 2021-03-19 2024-10-29 Novo Nordisk Health Care Ag Activating pyruvate kinase R
US20240409542A1 (en) * 2021-09-30 2024-12-12 Sitryx Therapeutics Limited Novel compounds
EP4433057A1 (en) * 2021-11-16 2024-09-25 Agios Pharmaceuticals, Inc. Compounds for treating mds-associated anemias and other conditions
CN116159061A (zh) * 2023-03-09 2023-05-26 上海市第十人民医院 丙酮酸激酶m2激活剂在制备预防或治疗心力衰竭的药物中的应用
EP4671102A1 (en) 2023-03-28 2025-12-31 Honda Motor Co., Ltd. METHOD FOR PROVIDING INFORMATION, PROGRAM FOR PROVIDING INFORMATION, STORAGE MEDIA AND INFORMATION PROCESSING APPARATUS
WO2024238659A1 (en) 2023-05-15 2024-11-21 Agios Pharmaceuticals, Inc. Crystalline salts or amorphous forms of 2-((1h-pyrazol-3-yl)methyl)-6-((6-aminopyridin-2-yl)methyl)-4-methyl-4,6-dihydro -5h-thiazolo[5',4':4,5]pyrrolo[2,3-d]pyridazin-5-one
WO2025010390A1 (en) * 2023-07-05 2025-01-09 Agios Pharmaceuticals, Inc. Synthesis of pyruvate kinase activators
WO2025207563A1 (en) 2024-03-27 2025-10-02 Agios Pharmaceuticals, Inc. Use of a pk activator in the treatment of sickle cell disease

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4405635A (en) 1979-06-18 1983-09-20 Merrell Dow Pharmaceuticals Inc. 4-Aroylimidazol-2-ones and their use as pharmaceuticals
US4883914A (en) 1987-08-17 1989-11-28 American Cyanamid Company Benzenesulfonyl carboxamide compounds useful as herbicidal agents
HK1049154A1 (zh) 1999-07-30 2003-05-02 Abbott Gmbh & Co. Kg 作为酪氨酸激酶抑制剂的2-吡唑啉-5-酮
CA2381581A1 (en) 1999-09-04 2001-03-15 Astrazeneca Ab Substituted n-phenyl 2-hydroxy-2-methyl-3,3,3-trifluoropropanamide derivatives which elevate pyruvate dehydrogenase activity
EP1972629A1 (en) * 2007-03-23 2008-09-24 Mutabilis SA New imidazolo-heteroaryl derivatives with antibacterial properties
FR2933983B1 (fr) * 2008-07-15 2010-08-27 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
JP2011529066A (ja) * 2008-07-23 2011-12-01 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 三環式ピラゾロピリジンキナーゼ阻害剤
US8420649B2 (en) * 2008-08-29 2013-04-16 Amgen Inc. Pyrido[3,2-d]pyridazine-2(1H)-one compounds as p38 modulators and methods of use thereof
CA3041868C (en) 2008-10-09 2023-03-07 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Bis sulfonamide piperazinyl and piperidinyl activators of human pyruvatekinase
CN102448951B (zh) * 2009-04-06 2017-05-10 安吉奥斯医药品有限公司 丙酮酸激酶m2调节剂、治疗组合物和相关使用方法
NZ597379A (en) 2009-06-29 2014-04-30 Agios Pharmaceuticals Inc Therapeutic compounds and compositions
US20130109672A1 (en) 2010-04-29 2013-05-02 The United States Of America,As Represented By The Secretary, Department Of Health And Human Service Activators of human pyruvate kinase
CA2820408C (en) 2010-12-06 2018-03-06 Glaxo Group Limited Pyrimidinone compounds for use in the treatment of diseases or conditions mediated by lp-pla2
TWI549947B (zh) 2010-12-29 2016-09-21 阿吉歐斯製藥公司 治療化合物及組成物
WO2012151452A1 (en) 2011-05-03 2012-11-08 Agios Pharmaceuticals, Inc Pyruvate kinase activators for use in therapy
WO2012151450A1 (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
PH12017501176B1 (en) 2011-05-03 2023-03-08 Agios Pharmaceuticals Inc Pyruvate kinase activators for use in therapy
WO2012151448A1 (en) * 2011-05-03 2012-11-08 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use in therapy
EP2734520B1 (en) * 2011-07-19 2016-09-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US20140249150A1 (en) * 2011-10-13 2014-09-04 Agios Pharmaceuticals, Inc Activators of pyruvate kinase m2 and methods of treating disease
EP2877214B1 (en) 2012-07-26 2019-04-24 Joslin Diabetes Center, Inc. Predicting diabetic complications
EP2917207A1 (en) 2012-11-08 2015-09-16 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions and their use as pkm2 modulators
CN105008363A (zh) * 2013-01-30 2015-10-28 拜耳医药股份公司 作为mknk-1激酶抑制剂的酰氨基咪唑并哒嗪
HK1220610A1 (zh) 2013-03-13 2017-05-12 弗拉特利发现实验室有限责任公司 哒嗪酮化合物和用於治疗囊肿状纤维化的方法
WO2014139144A1 (en) 2013-03-15 2014-09-18 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
AR097543A1 (es) * 2013-09-06 2016-03-23 Lexicon Pharmaceuticals Inc COMPUESTOS BASADOS EN IMIDAZO[1,2-b]PIRIDAZINA, COMPOSICIONES QUE LOS COMPRENDEN Y SUS MÉTODOS DE USO
PT3661925T (pt) 2017-07-07 2022-01-31 Inflazome Ltd Novos compostos de sulfonamida-carboxamida
AR112690A1 (es) 2017-08-15 2019-11-27 Agios Pharmaceuticals Inc Activadores de piruvato quinasas para usar en el tratamiento de trastornos en la sangre
UY37847A (es) 2017-08-15 2019-03-29 Inflazome Ltd Sulfonilureas y sulfoniltioureas útiles como inhibidores de nlrp3
EP3652184A1 (en) 2017-08-15 2020-05-20 AbbVie Inc. Macrocyclic mcl-1 inhibitors and methods of use
SG11202001353PA (en) 2017-08-15 2020-03-30 Agios Pharmaceuticals Inc Pyruvate kinase modulators and use thereof
CA3129829A1 (en) * 2019-02-13 2020-08-20 Agios Pharmaceuticals, Inc. Thieno[3,2-b] pyrrole[3,2-d]pyridazinone derivatives and their use as pkm2 derivatives for the treatment of cancer, obesity and diabetes related disorders

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