IL289885B2 - History of N-((7,6,5,3,2,1-hexahydro-S-inden-4-yl)carbamoyl)-7,6,5,4-tetrahydrobenzofuran-2-sulfonamide and related compounds as NLPR3 modulators for the treatment of multiple sclerosis - Google Patents

History of N-((7,6,5,3,2,1-hexahydro-S-inden-4-yl)carbamoyl)-7,6,5,4-tetrahydrobenzofuran-2-sulfonamide and related compounds as NLPR3 modulators for the treatment of multiple sclerosis

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Publication number
IL289885B2
IL289885B2 IL289885A IL28988522A IL289885B2 IL 289885 B2 IL289885 B2 IL 289885B2 IL 289885 A IL289885 A IL 289885A IL 28988522 A IL28988522 A IL 28988522A IL 289885 B2 IL289885 B2 IL 289885B2
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Israel
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compound
solvate
pharmaceutically acceptable
acceptable salt
formula
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IL289885A
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English (en)
Hebrew (he)
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IL289885B1 (en
IL289885A (en
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Zomagen Biosciences Ltd
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Publication of IL289885A publication Critical patent/IL289885A/en
Publication of IL289885B1 publication Critical patent/IL289885B1/en
Publication of IL289885B2 publication Critical patent/IL289885B2/en

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    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
    • AHUMAN NECESSITIES
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    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61K31/4365Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
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    • C07D333/62Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
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IL289885A 2019-07-17 2020-07-16 History of N-((7,6,5,3,2,1-hexahydro-S-inden-4-yl)carbamoyl)-7,6,5,4-tetrahydrobenzofuran-2-sulfonamide and related compounds as NLPR3 modulators for the treatment of multiple sclerosis IL289885B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201962875402P 2019-07-17 2019-07-17
PCT/IB2020/000634 WO2021009566A1 (en) 2019-07-17 2020-07-16 N-((1,2,3,5,6,7-hexahydro-s-indacen-4-yl)carbamoyl)-4,5,6,7-tetrahydrobenzofuran -2-sulfonamide derivatives and related compounds as nlpr3 modulators for the treatment of multiple sclerosis (ms)

Publications (3)

Publication Number Publication Date
IL289885A IL289885A (en) 2022-03-01
IL289885B1 IL289885B1 (en) 2024-12-01
IL289885B2 true IL289885B2 (en) 2025-04-01

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IL289885A IL289885B2 (en) 2019-07-17 2020-07-16 History of N-((7,6,5,3,2,1-hexahydro-S-inden-4-yl)carbamoyl)-7,6,5,4-tetrahydrobenzofuran-2-sulfonamide and related compounds as NLPR3 modulators for the treatment of multiple sclerosis

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US (1) US12466800B2 (enExample)
EP (1) EP3999496B1 (enExample)
JP (1) JP7723652B2 (enExample)
KR (1) KR20220064364A (enExample)
CN (1) CN114555571B (enExample)
AU (1) AU2020312800B2 (enExample)
BR (1) BR112022000878A2 (enExample)
CA (1) CA3151865A1 (enExample)
IL (1) IL289885B2 (enExample)
MX (1) MX2022000646A (enExample)
WO (1) WO2021009566A1 (enExample)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2020312800B2 (en) 2019-07-17 2026-04-23 Zomagen Biosciences Ltd N-((1,2,3,5,6,7-hexahydro-s-indacen-4-yl)carbamoyl)-4,5,6,7-tetrahydrobenzofuran -2-sulfonamide derivatives and related compounds as NLPR3 modulators for the treatment of multiple sclerosis (ms)
JP7595642B2 (ja) 2019-07-17 2024-12-06 ズーマゲン バイオサイエンシーズ エルティーディー Nlrp3モジュレーター
KR20220154165A (ko) 2020-03-16 2022-11-21 조마젠 바이오사이언시즈 엘티디 Nlrp3 조절제
WO2023077046A1 (en) 2021-10-29 2023-05-04 Arcus Biosciences, Inc. Inhibitors of hif-2alpha and methods of use thereof
TW202333678A (zh) * 2021-12-22 2023-09-01 大陸商瑞石生物醫藥有限公司 一種磺醯脲類化合物
WO2024010772A1 (en) * 2022-07-06 2024-01-11 Kodiak Sciences Inc. Nlrp3 inhibitors
CN116283533B (zh) * 2023-02-17 2024-02-23 华南理工大学 具有nlrp3抑制活性的鸡脚参酮a及其衍生物与应用

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KR102727059B1 (ko) 2015-02-16 2024-11-05 더 유니버서티 어브 퀸슬랜드 설포닐우레아와 관련 화합물 및 그 용도
CN109071454B (zh) 2016-02-16 2023-02-17 昆士兰大学 磺酰脲和相关化合物及其用途
ES2940611T3 (es) 2016-04-18 2023-05-09 Novartis Ag Compuestos y composiciones para el tratamiento de afecciones asociadas a la actividad de NLRP
US11597706B2 (en) * 2016-04-18 2023-03-07 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
EP3272739A1 (en) * 2016-07-20 2018-01-24 NodThera Limited Sulfonyl urea derivatives and their use in the control of interleukin-1 activity
CA3047336A1 (en) 2017-01-23 2018-07-26 Jecure Therapeutics, Inc. Chemical compounds as inhibitors of interleukin-1 activity
AU2017416068A1 (en) 2017-05-24 2019-10-31 The Provost, Fellows, Foundation Scholars, And Other Members Of Board, Of The College Of The Holy And Undivided Trinity Of Queen Elizabeth Near Dublin Novel compounds and uses
US11465992B2 (en) 2017-07-07 2022-10-11 Inflazome Limited Sulfonamide carboxamide compounds
US11542255B2 (en) 2017-08-15 2023-01-03 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
MX2020001776A (es) 2017-08-15 2020-03-24 Inflazome Ltd Sulfonilureas y sulfoniltioureas como inhibidores de nlrp3.
JP2020531448A (ja) 2017-08-15 2020-11-05 インフレイゾーム リミテッド 新規なスルホンアミドカルボキサミド化合物
EP3697758B1 (en) 2017-10-17 2022-07-06 Novartis AG Sulphonamides and compositions thereof for treating conditions associated with nlrp activity
GB201721185D0 (en) 2017-12-18 2018-01-31 Nodthera Ltd Sulphonyl urea derivatives
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CN113056451A (zh) * 2018-10-24 2021-06-29 诺华股份有限公司 用于治疗与nlrp活性相关的病症的化合物和组合物
JP7595642B2 (ja) 2019-07-17 2024-12-06 ズーマゲン バイオサイエンシーズ エルティーディー Nlrp3モジュレーター
AU2020312800B2 (en) 2019-07-17 2026-04-23 Zomagen Biosciences Ltd N-((1,2,3,5,6,7-hexahydro-s-indacen-4-yl)carbamoyl)-4,5,6,7-tetrahydrobenzofuran -2-sulfonamide derivatives and related compounds as NLPR3 modulators for the treatment of multiple sclerosis (ms)
CL2022002490A1 (es) 2020-03-16 2023-05-05 Novartis Ag Derivados de biarilo como inhibidores de la interacción proteína-proteína de yap/taz-tead
KR20220154165A (ko) 2020-03-16 2022-11-21 조마젠 바이오사이언시즈 엘티디 Nlrp3 조절제
UY39129A (es) 2020-03-16 2021-10-29 Novartis Ag Derivados de biarilo como inhibidores de la interacción proteína-proteína de yap/taz-tead

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CN114555571B (zh) 2024-08-27
JP2022541254A (ja) 2022-09-22
JP7723652B2 (ja) 2025-08-14
IL289885B1 (en) 2024-12-01
AU2020312800B2 (en) 2026-04-23
US20220396559A1 (en) 2022-12-15
IL289885A (en) 2022-03-01
EP3999496B1 (en) 2024-12-18
CN114555571A (zh) 2022-05-27
WO2021009566A1 (en) 2021-01-21
US12466800B2 (en) 2025-11-11
AU2020312800A1 (en) 2022-02-24
BR112022000878A2 (pt) 2022-04-19
KR20220064364A (ko) 2022-05-18
CA3151865A1 (en) 2021-01-21
EP3999496A1 (en) 2022-05-25
MX2022000646A (es) 2022-05-20

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