JP2023538608A5 - - Google Patents

Info

Publication number
JP2023538608A5
JP2023538608A5 JP2023512162A JP2023512162A JP2023538608A5 JP 2023538608 A5 JP2023538608 A5 JP 2023538608A5 JP 2023512162 A JP2023512162 A JP 2023512162A JP 2023512162 A JP2023512162 A JP 2023512162A JP 2023538608 A5 JP2023538608 A5 JP 2023538608A5
Authority
JP
Japan
Prior art keywords
phenyl
pyrrolo
pyridine
dimethyl
methylsulfonyl
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
JP2023512162A
Other languages
English (en)
Japanese (ja)
Other versions
JP2023538608A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2021/046434 external-priority patent/WO2022040267A1/en
Publication of JP2023538608A publication Critical patent/JP2023538608A/ja
Publication of JP2023538608A5 publication Critical patent/JP2023538608A5/ja
Pending legal-status Critical Current

Links

JP2023512162A 2020-08-19 2021-08-18 線維症の処置のためのtlr9阻害剤阻害剤としての1h-ピロロ[3,2-c]ピリジンおよび1h-ピロロ[2,3-c]ピリジン誘導体 Pending JP2023538608A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202063067465P 2020-08-19 2020-08-19
US63/067,465 2020-08-19
PCT/US2021/046434 WO2022040267A1 (en) 2020-08-19 2021-08-18 1h-pyrrolo[3,2-c]pyridine and 1h-pyrrolo[2,3-c]pyridine derivatives as tlr9 inhibitors for the treatment of fibrosis

Publications (2)

Publication Number Publication Date
JP2023538608A JP2023538608A (ja) 2023-09-08
JP2023538608A5 true JP2023538608A5 (enExample) 2024-08-26

Family

ID=77711459

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2023512162A Pending JP2023538608A (ja) 2020-08-19 2021-08-18 線維症の処置のためのtlr9阻害剤阻害剤としての1h-ピロロ[3,2-c]ピリジンおよび1h-ピロロ[2,3-c]ピリジン誘導体

Country Status (14)

Country Link
US (1) US12590091B2 (enExample)
EP (1) EP4200298B1 (enExample)
JP (1) JP2023538608A (enExample)
KR (1) KR20230053646A (enExample)
CN (1) CN115867549A (enExample)
AR (1) AR123285A1 (enExample)
AU (1) AU2021328577A1 (enExample)
BR (1) BR112023002646A2 (enExample)
CA (1) CA3189826A1 (enExample)
ES (1) ES3034264T3 (enExample)
IL (1) IL300643A (enExample)
MX (1) MX2023001929A (enExample)
TW (1) TW202214233A (enExample)
WO (1) WO2022040267A1 (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11807622B2 (en) 2019-01-30 2023-11-07 Insilico Medicine Ip Limited TLR 9 inhibitors
EP4479135A1 (en) * 2022-02-18 2024-12-25 Bristol-Myers Squibb Company Substituted imidazopyridinyl compounds useful as inhibitors of tlr9
KR20250109202A (ko) * 2022-11-10 2025-07-16 브리스톨-마이어스 스큅 컴퍼니 Tlr9의 억제제로서 유용한 치환된 벤즈이미다졸 화합물
CN120152957A (zh) * 2022-11-10 2025-06-13 百时美施贵宝公司 用作tlr9抑制剂的经取代的喹诺酮
WO2024163380A1 (en) * 2023-01-31 2024-08-08 Bristol-Myers Squibb Company Substituted benzimidazole compounds useful as inhibitors of tlr9
TW202504599A (zh) 2023-06-30 2025-02-01 美商必治妥美雅史谷比公司 Kras抑制劑
WO2026039512A1 (en) 2024-08-14 2026-02-19 Bristol-Myers Squibb Company Kras inhibitors

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US20060235037A1 (en) 2005-04-15 2006-10-19 Purandare Ashok V Heterocyclic inhibitors of protein arginine methyl transferases
GB0602178D0 (en) 2006-02-03 2006-03-15 Merck Sharp & Dohme Therapeutic treatment
JP2009532501A (ja) 2006-04-04 2009-09-10 ミリアド ジェネティクス, インコーポレイテッド 疾患および障害のための化合物
US8785489B2 (en) 2008-10-17 2014-07-22 Boehringer Ingelheim International Gmbh Heteroaryl substituted indole compounds useful as MMP-13 inhibitors
US20130158066A1 (en) 2011-12-20 2013-06-20 Hoffmann-La Roche Inc. 4-azaindole inhibitors of crac
US20130158049A1 (en) 2011-12-20 2013-06-20 Hoffmann-La Roche Inc. 7-azaindole inhibitors of crac
WO2013156431A1 (en) 2012-04-17 2013-10-24 Syngenta Participations Ag Pesticidally active pyridyl- and pyrimidyl- substituted thiazole and thiadiazole derivatives
EP2738172A1 (en) 2012-11-28 2014-06-04 Almirall, S.A. New bicyclic compounds as crac channel modulators
CA2933466A1 (en) * 2013-12-13 2015-06-18 Takeda Pharmaceutical Company Limited Pyrrolo[3,2-c]pyridine derivatives as tlr inhibitors
AR107032A1 (es) 2015-12-09 2018-03-14 Padlock Therapeutics Inc Inhibidores bicíclicos de pad4
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
MX391344B (es) 2016-07-30 2025-03-21 Bristol Myers Squibb Co Compuestos indol sustituidos con dimetoxifenilo como inhibidores de receptores tipo toll 7, 8 o 9 (tlr7, tlr8 o tlr9).
JP7028861B2 (ja) 2016-09-09 2022-03-02 ブリストル-マイヤーズ スクイブ カンパニー ピリジル置換のインドール化合物
EP3538513A1 (en) 2016-11-11 2019-09-18 Dynavax Technologies Corporation Toll-like receptor antagonist compounds and methods of use
US11399542B2 (en) 2017-07-05 2022-08-02 Syngenta Participations Ag Pesticidally active heterocyclic derivatives with sulfur containing substituents
ES2921020T3 (es) 2017-08-04 2022-08-16 Bristol Myers Squibb Co Compuestos de indol sustituidos con [1,2,4]triazolo[4,3-a]piridinilo
CN110997656B (zh) 2017-08-04 2023-04-14 百时美施贵宝公司 用作tlr7/8/9抑制剂的取代的吲哚化合物
WO2019099336A1 (en) 2017-11-14 2019-05-23 Bristol-Myers Squibb Company Substituted indole compounds
AU2018386201A1 (en) 2017-12-15 2020-07-30 Bristol-Myers Squibb Company Substituted indole ether compounds
JP7289301B2 (ja) 2017-12-18 2023-06-09 ブリストル-マイヤーズ スクイブ カンパニー 4-アザインドール化合物
SG11202005704RA (en) * 2017-12-19 2020-07-29 Bristol Myers Squibb Co 6-azaindole compounds
US11878975B2 (en) 2017-12-19 2024-01-23 Bristol-Myers Squibb Company Substituted indole compounds useful as TLR inhibitors
CN111511730B (zh) 2017-12-19 2023-07-25 百时美施贵宝公司 可用作tlr抑制剂的被酰胺取代的吲哚化合物
CA3085937A1 (en) 2017-12-20 2019-06-27 Bristol-Myers Squibb Company Diazaindole compounds
KR102730859B1 (ko) 2017-12-20 2024-11-15 브리스톨-마이어스 스큅 컴퍼니 아릴 및 헤테로아릴 치환된 인돌 화합물
SG11202005694RA (en) 2017-12-20 2020-07-29 Bristol Myers Squibb Co Amino indole compounds useful as tlr inhibitors
AU2019319835A1 (en) 2018-08-08 2021-03-25 Bristol-Myers Squibb Company Indole and azaindole inhibitors of PAD enzymes

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