JP2025016684A5 - - Google Patents

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Publication number
JP2025016684A5
JP2025016684A5 JP2024193094A JP2024193094A JP2025016684A5 JP 2025016684 A5 JP2025016684 A5 JP 2025016684A5 JP 2024193094 A JP2024193094 A JP 2024193094A JP 2024193094 A JP2024193094 A JP 2024193094A JP 2025016684 A5 JP2025016684 A5 JP 2025016684A5
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JP
Japan
Prior art keywords
thiadiazol
difluoromethyl
indazol
amino
sulfonyl
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.)
Granted
Application number
JP2024193094A
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English (en)
Japanese (ja)
Other versions
JP2025016684A (ja
JP7781244B2 (ja
Filing date
Publication date
Priority claimed from PCT/US2020/051486 external-priority patent/WO2021055744A1/en
Application filed filed Critical
Publication of JP2025016684A publication Critical patent/JP2025016684A/ja
Publication of JP2025016684A5 publication Critical patent/JP2025016684A5/ja
Application granted granted Critical
Publication of JP7781244B2 publication Critical patent/JP7781244B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2024193094A 2019-09-20 2024-11-01 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体 Active JP7781244B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201962903438P 2019-09-20 2019-09-20
US62/903,438 2019-09-20
PCT/US2020/051486 WO2021055744A1 (en) 2019-09-20 2020-09-18 4-substituted indole and indazole sulfonamido derivatives as parg inhibitors
JP2022517374A JP2022548690A (ja) 2019-09-20 2020-09-18 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2022517374A Division JP2022548690A (ja) 2019-09-20 2020-09-18 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体

Publications (3)

Publication Number Publication Date
JP2025016684A JP2025016684A (ja) 2025-02-04
JP2025016684A5 true JP2025016684A5 (OSRAM) 2025-09-08
JP7781244B2 JP7781244B2 (ja) 2025-12-05

Family

ID=72744866

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2022517374A Ceased JP2022548690A (ja) 2019-09-20 2020-09-18 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体
JP2024193094A Active JP7781244B2 (ja) 2019-09-20 2024-11-01 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2022517374A Ceased JP2022548690A (ja) 2019-09-20 2020-09-18 Parg阻害剤としての4-置換インドールおよびインダゾールスルホンアミド誘導体

Country Status (12)

Country Link
US (1) US20220389003A1 (OSRAM)
EP (1) EP4031249A1 (OSRAM)
JP (2) JP2022548690A (OSRAM)
KR (1) KR20220066922A (OSRAM)
CN (1) CN114555593A (OSRAM)
AU (1) AU2020348489A1 (OSRAM)
BR (1) BR112022004624A2 (OSRAM)
CA (1) CA3147493A1 (OSRAM)
IL (1) IL291436A (OSRAM)
MX (1) MX2022003276A (OSRAM)
TW (1) TWI873187B (OSRAM)
WO (1) WO2021055744A1 (OSRAM)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA41179A (fr) 2014-12-19 2017-10-24 Cancer Research Tech Ltd Composés inhibiteurs de parg
EP4413000A1 (en) 2021-10-04 2024-08-14 FoRx Therapeutics AG N,n-dimethyl-4-(7-(n-(1-methylcyclopropyl)sulfamoyl)-imidazo[1,5-a]pyridin-5-yl)piperazine-1-carboxamide derivatives and the corresponding pyrazolo[1,5-a]pyridine derivatives as parg inhibitors for the treatment of cancer
AU2022359801A1 (en) 2021-10-04 2024-02-01 Forx Therapeutics Ag Parg inhibitory compounds
WO2023154913A1 (en) * 2022-02-14 2023-08-17 Arase Therapeutics Inc. Inhibitors of parg
JP2025509180A (ja) * 2022-03-04 2025-04-11 上海瓔黎薬業有限公司 五員ヘテロアリール環構造含有化合物、その医薬組成物及び使用
WO2023175184A1 (en) 2022-03-17 2023-09-21 Forx Therapeutics Ag 2,4-dioxo-1,4-dihydroquinazoline derivatives as parg inhibitors for the treatment of cancer
WO2023175185A1 (en) 2022-03-17 2023-09-21 Forx Therapeutics Ag 2,4-dioxo-1,4-dihydroquinazoline derivatives as parg inhibitors for the treatment of cancer
WO2023183850A1 (en) * 2022-03-23 2023-09-28 Ideaya Biosciences, Inc. Piperazine substituted indazole compounds as inhibitors of parg
CN117157299B (zh) * 2022-04-28 2024-05-28 北京丹擎医药科技有限公司 三环杂环衍生物及其组合物和应用
WO2023224998A1 (en) * 2022-05-17 2023-11-23 858 Therapeutics, Inc. Inhibitors of parg
JP2025522274A (ja) 2022-05-17 2025-07-15 858 セラピューティクス,インコーポレーテッド Pargの阻害剤
WO2024002284A1 (zh) * 2022-06-29 2024-01-04 杭州圣域生物医药科技有限公司 五元并六元含氮化合物、其中间体、制备方法和应用
EP4559912A1 (en) * 2022-07-19 2025-05-28 Evopoint Biosciences Co., Ltd. Sulfur-containing heteroaromatic ring compound, pharmaceutical composition thereof, and use thereof
EP4311829A1 (en) 2022-07-28 2024-01-31 Nodus Oncology Limited Substituted bicyclic heteroaryl sulfonamide derivatives for the treatment of cancer
WO2024074497A1 (en) 2022-10-03 2024-04-11 Forx Therapeutics Ag Parg inhibitory compound
JP2025533274A (ja) * 2022-10-13 2025-10-03 ハンミ ファーマシューティカルズ カンパニー リミテッド Yap-tead相互作用を阻害するための新規なヘテロ二環式化合物及びそれを含む薬学的組成物
WO2024148280A1 (en) 2023-01-06 2024-07-11 Ideaya Biosciences, Inc. Treatment of er+ breast cancer comprising homologous recombination deficiency using parc inhibitor
WO2024173234A1 (en) * 2023-02-13 2024-08-22 Arase Therapeutics Inc. Inhibitors of parg
WO2024173530A1 (en) * 2023-02-14 2024-08-22 Ideaya Biosciences, Inc. Heteroaryl-substituted pyrazolo/imidazo pyridine compounds
WO2024173524A1 (en) * 2023-02-14 2024-08-22 Ideaya Biosciences, Inc. Heteroaryl-substituted benzimidazole compounds
WO2024173453A1 (en) * 2023-02-14 2024-08-22 Ideaya Biosciences, Inc. Heteroaryl-substituted imidazopyridine compounds
WO2024173514A1 (en) * 2023-02-14 2024-08-22 Ideaya Biosciences, Inc. Amide and ester-substituted imidazopyridine compounds
WO2024209035A1 (en) 2023-04-05 2024-10-10 Forx Therapeutics Ag Parg inhibitory compounds
WO2024211506A1 (en) 2023-04-05 2024-10-10 Ideaya Biosciences, Inc. Combination therapy comprising a parg inhibitor and a topoisomerase inhibitor for treating cancer
CN121002021A (zh) * 2023-04-27 2025-11-21 北京丹擎医药科技有限公司 三环杂环衍生物及其组合物和应用
CN119143747A (zh) * 2023-06-16 2024-12-17 上海璎黎药业有限公司 一种杂芳环结构化合物、其药物组合物及应用
WO2025046148A1 (en) 2023-09-01 2025-03-06 Forx Therapeutics Ag Novel parg inhibitors
TW202528308A (zh) * 2023-09-20 2025-07-16 美商愛德亞生物科學公司 Parg抑制劑
WO2025064750A1 (en) 2023-09-20 2025-03-27 Ideaya Biosciences, Inc. Combination therapy with a parg inhibitor
WO2025072544A1 (en) * 2023-09-27 2025-04-03 Ideaya Biosciences, Inc. Sulfonamino indazole compounds as inhibitors of parg
CN119708015A (zh) * 2023-09-28 2025-03-28 杭州圣域生物医药科技有限公司 杂芳基化合物、其中间体、制备方法和应用
WO2025073870A1 (en) 2023-10-03 2025-04-10 Forx Therapeutics Ag Parg inhibitory compound
CN119859145A (zh) * 2023-10-20 2025-04-22 上海璎黎药业有限公司 一种杂芳环磺酰胺结构化合物、其药物组合物及应用
WO2025087941A1 (en) 2023-10-23 2025-05-01 Universite De Geneve Parg inhibitors in combination with parp inhibitors and uses thereof
TW202523299A (zh) * 2023-10-26 2025-06-16 大陸商上海齊魯製藥研究中心有限公司 Parg抑制劑
WO2025093755A1 (en) 2023-11-01 2025-05-08 Forx Therapeutics Ag Novel parc inhibitors
WO2025098445A1 (zh) * 2023-11-07 2025-05-15 南京同诺康医药科技有限公司 Parg抑制剂及其制备方法和用途
WO2025108225A1 (zh) * 2023-11-20 2025-05-30 上海复星医药(集团)股份有限公司 作为parg抑制剂的含氮三环衍生物
WO2025111339A1 (en) * 2023-11-21 2025-05-30 858 Therapeutics, Inc. Treatment of cancer with a parg inhibitor
TW202529739A (zh) * 2023-11-22 2025-08-01 美商858療法股份有限公司 Parg之抑制劑
WO2025133396A1 (en) 2023-12-22 2025-06-26 Forx Therapeutics Ag Novel bicyclo heteroaryl parg inhibitors
WO2025133191A1 (en) * 2023-12-22 2025-06-26 Genecode Novel sulfonamides or sulfones and their use as neuroprotective and/or neurorestorative agents
WO2025229549A1 (en) * 2024-04-30 2025-11-06 Satyarx Pharma Innovations Pvt Ltd Novel heterocyclic compounds as inhibitors of parg
CN118459452B (zh) * 2024-07-10 2024-10-25 苏州国匡医药科技有限公司 一种多聚adp核糖水解酶抑制剂及其应用

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
CA2242425C (en) 1996-02-13 2006-07-18 Zeneca Limited Quinazoline derivatives as vegf inhibitors
DE69709319T2 (de) 1996-03-05 2002-08-14 Astrazeneca Ab, Soedertaelje 4-anilinochinazolin derivate
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
EE05345B1 (et) 1999-02-10 2010-10-15 Astrazeneca Ab Kinasoliini derivaadid angiogeneesi inhibiitoritena
CN1431999A (zh) 2000-05-31 2003-07-23 阿斯特拉曾尼卡有限公司 具有血管损伤活性的吲哚衍生物
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
JP2004502766A (ja) 2000-07-07 2004-01-29 アンギオジェン・ファーマシューティカルズ・リミテッド 血管損傷剤としてのコルヒノール誘導体
RU2003103603A (ru) 2000-07-07 2004-08-20 Энджиоджен Фармасьютикалз Лимитед (Gb) Производные колхинола в качестве ингибиторов ангиогенеза
CA2834101A1 (en) * 2011-01-07 2012-07-12 Taiho Pharmaceutical Co., Ltd. Novel indole or indazole derivative or salt thereof
MA41140A (fr) * 2014-12-12 2017-10-17 Cancer Research Tech Ltd Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg
MA41179A (fr) * 2014-12-19 2017-10-24 Cancer Research Tech Ltd Composés inhibiteurs de parg
EP3697777A1 (en) * 2017-10-19 2020-08-26 eFFECTOR Therapeutics, Inc. Benzimidazole-indole inhibitors of mnk1 and mnk2
EP3870575B1 (en) * 2018-10-25 2023-03-29 ViiV Healthcare UK (No.5) Limited Inhibitors of human immunodeficiency virus replication
WO2023183850A1 (en) * 2022-03-23 2023-09-28 Ideaya Biosciences, Inc. Piperazine substituted indazole compounds as inhibitors of parg

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