[go: up one dir, main page]

MA71689A - Inhibiteurs de l'inflammasome nlrp3 - Google Patents

Inhibiteurs de l'inflammasome nlrp3

Info

Publication number
MA71689A
MA71689A MA71689A MA71689A MA71689A MA 71689 A MA71689 A MA 71689A MA 71689 A MA71689 A MA 71689A MA 71689 A MA71689 A MA 71689A MA 71689 A MA71689 A MA 71689A
Authority
MA
Morocco
Prior art keywords
nlrp3 inflammasome
inflammasome inhibitors
inhibitors
nlrp3
inflammasome
Prior art date
Application number
MA71689A
Other languages
English (en)
Inventor
Xiaobin GE
Henri Mattes
Zhicong SHI
Mei XIA
Ning Ye
Original Assignee
Novartis Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MA71689A publication Critical patent/MA71689A/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
    • C07D237/20Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
MA71689A 2022-08-03 2023-08-02 Inhibiteurs de l'inflammasome nlrp3 MA71689A (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US202263370300P 2022-08-03 2022-08-03
CN2023097282 2023-05-30
PCT/IB2023/057819 WO2024028782A1 (fr) 2022-08-03 2023-08-02 Inhibiteurs de l'inflammasome nlrp3
EP23755486.0A EP4565326A1 (fr) 2022-08-03 2023-08-02 Inhibiteurs de l'inflammasome nlrp3

Publications (1)

Publication Number Publication Date
MA71689A true MA71689A (fr) 2025-05-30

Family

ID=87580191

Family Applications (1)

Application Number Title Priority Date Filing Date
MA71689A MA71689A (fr) 2022-08-03 2023-08-02 Inhibiteurs de l'inflammasome nlrp3

Country Status (19)

Country Link
US (2) US20240067627A1 (fr)
EP (1) EP4565326A1 (fr)
JP (1) JP2025525866A (fr)
KR (1) KR20250043519A (fr)
CN (1) CN119677725A (fr)
AR (1) AR130094A1 (fr)
AU (1) AU2023318764A1 (fr)
CA (1) CA3262660A1 (fr)
CL (1) CL2025000285A1 (fr)
CO (1) CO2025002057A2 (fr)
CR (1) CR20250063A (fr)
DO (1) DOP2025000013A (fr)
IL (1) IL318533A (fr)
MA (1) MA71689A (fr)
MX (1) MX2025001273A (fr)
PE (1) PE20251255A1 (fr)
TW (1) TW202406550A (fr)
UY (1) UY40374A (fr)
WO (1) WO2024028782A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11618751B1 (en) 2022-03-25 2023-04-04 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives
US11319319B1 (en) 2021-04-07 2022-05-03 Ventus Therapeutics U.S., Inc. Compounds for inhibiting NLRP3 and uses thereof
US12331048B2 (en) 2022-10-31 2025-06-17 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors
WO2025153532A1 (fr) 2024-01-16 2025-07-24 NodThera Limited Polythérapies faisant intervenir des inhibiteurs de nlrp3 et des agonistes de glp-1

Family Cites Families (80)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2510997A1 (fr) 1981-08-10 1983-02-11 Sanofi Sa Nouveaux derives de la methyl-4 phenyl-6 pyridazine, procede pour leur preparation et medicaments actifs sur le systeme nerveux central en contenant
PT93060B (pt) 1989-02-07 1995-12-29 Sanofi Sa Processo para a obtencao de derivados de piridazina e de composicoes farmaceuticas que os contem
FR2663326B2 (fr) 1989-11-17 1992-10-16 Sanofi Sa Derives de la pyridazine, procede de preparation et compositions pharmaceutiques en contenant.
FR2676444B1 (fr) 1991-05-16 1995-03-10 Sanofi Elf Nouveaux derives d'amino-3 pyridazines actifs sur le systeme nerveux central, procede de preparation et compositions pharmaceutiques en contenant.
US6602872B1 (en) 1999-12-13 2003-08-05 Merck & Co., Inc. Substituted pyridazines having cytokine inhibitory activity
GB0220581D0 (en) 2002-09-04 2002-10-09 Novartis Ag Organic Compound
EP1631260A2 (fr) 2003-02-28 2006-03-08 Transform Pharmaceuticals, Inc. Compositions pharmaceutiques a base d'un co-cristal
US8338591B2 (en) 2004-05-08 2012-12-25 Novartis International Pharmaceutical Ltd. 3-aryl-5,6-disubstituted pyridazines
GB0415746D0 (en) 2004-07-14 2004-08-18 Novartis Ag Organic compounds
GB0521508D0 (en) 2005-10-21 2005-11-30 Novartis Ag Organic compounds
WO2008058064A1 (fr) 2006-11-07 2008-05-15 Lexicon Pharmaceuticals, Inc. Composés multicycliques liés à une amine et leurs méthodes d'utilisation
GB0720444D0 (en) 2007-10-18 2007-11-28 Glaxo Group Ltd Novel compounds
WO2010048149A2 (fr) 2008-10-20 2010-04-29 Kalypsys, Inc. Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
WO2010128152A1 (fr) 2009-05-07 2010-11-11 Novartis Ag C-glycosides hétérocycliques condensés pour le traitement du diabète
US8163704B2 (en) 2009-10-20 2012-04-24 Novartis Ag Glycoside derivatives and uses thereof
AU2010309788A1 (en) 2009-10-20 2012-04-05 Novartis Ag Glycoside derivative and uses thereof
BR112012033253A2 (pt) 2010-06-23 2016-11-22 Hanmi Science Co Ltd novos derivados de pirimidina fundidos para inibição da atividade de tirosina quinase
WO2012016133A2 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
NZ607845A (en) 2010-08-10 2015-03-27 Celgene Avilomics Res Inc Besylate salt of a btk inhibitor
US8835472B2 (en) 2010-09-02 2014-09-16 Boehringer Ingelheim International Gmbh Compounds, pharmaceutical compositions and uses thereof
JP5937102B2 (ja) 2010-12-14 2016-06-22 エレクトロフォレティクス リミテッド カゼインキナーゼ1デルタ(ck1デルタ)阻害剤
CU24152B1 (es) 2010-12-20 2016-02-29 Irm Llc 1,2 oxazol-8-azabiciclo[3,2,1]octano 8 il como moduladores de fxr
JP2014517016A (ja) 2011-06-10 2014-07-17 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング Btk阻害活性を有するピリミジンおよびピリミジン化合物の組成物と製造方法
UA111756C2 (uk) 2011-11-03 2016-06-10 Ф. Хоффманн-Ля Рош Аг Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона
BR112014012727B1 (pt) 2011-11-29 2022-10-25 Ono Pharmaceutical Co., Ltd Cloridrato de 6-amino-9-[(3r)-1-(2-butinoil)-3-pirrolidinil]-7-(4-fenoxifenil)-7,9-di-hidro-8h-puri- 8-ona e composição farmacêutica
US9353087B2 (en) 2012-06-08 2016-05-31 Biogen Ma Inc. Inhibitors of Bruton's tyrosine kinase
US8729263B2 (en) 2012-08-13 2014-05-20 Novartis Ag 1,4-disubstituted pyridazine analogs there of and methods for treating SMN-deficiency-related conditions
RS58956B1 (sr) 2012-09-10 2019-08-30 Principia Biopharma Inc Jedinjenja pirazolopirimidina kao inhibitori kinaze
WO2014085474A1 (fr) 2012-11-28 2014-06-05 Intercept Pharmaceuticals, Inc. Traitement d'une maladie pulmonaire
UY35368A (es) 2013-03-08 2014-10-31 Irm Llc Péptidos y composiciones para el tratamiento de daño articular
JO3377B1 (ar) 2013-03-11 2019-03-13 Takeda Pharmaceuticals Co مشتقات بيريدينيل وبيريدينيل مندمج
AU2014256633B2 (en) 2013-04-25 2017-02-02 Beone Medicines I Gmbh Fused heterocyclic compounds as protein kinase inhibitors
EA030430B1 (ru) 2013-11-05 2018-08-31 Новартис Аг Композиции и способы модуляции фарнезоидных х-рецепторов
US9512084B2 (en) 2013-11-29 2016-12-06 Novartis Ag Amino pyrimidine derivatives
BR112016012794A2 (pt) 2013-12-05 2017-08-08 Acerta Pharma Bv Combinação terapêutica de um inibidor de pi3k e um inibidor de btk
AP2016009301A0 (en) 2013-12-20 2016-06-30 Novartis Ag Heteroaryl butanoic acid derivatives as lta4h inhibitors
WO2015110923A2 (fr) 2014-01-21 2015-07-30 Acerta Pharma B.V. Méthodes de traitement de la leucémie lymphoïde chronique et du lymphome à petits lymphocytes en utilisant un inhibiteur de btk
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
JOP20200096A1 (ar) 2014-01-31 2017-06-16 Children’S Medical Center Corp جزيئات جسم مضاد لـ tim-3 واستخداماتها
PH12016501545B1 (en) 2014-03-14 2023-12-06 Immutep Sas Antibody molecules to lag-3 and uses thereof
WO2015175487A1 (fr) 2014-05-13 2015-11-19 Novartis Ag Composés et compositions d'induction de la chondrogenèse
CN103965169A (zh) 2014-05-30 2014-08-06 彭正中 一种化合物及其制备方法与用途
WO2016022626A1 (fr) 2014-08-06 2016-02-11 Merck Sharp & Dohme Corp. Antagonistes hétérocycliques des récepteurs cgrp
CA2964367C (fr) 2014-10-14 2024-01-30 Novartis Ag Molecules d'anticorps de pd-l1 et leurs utilisations
LT3461821T (lt) 2014-10-24 2020-08-10 Bristol-Myers Squibb Company Indolo karboksamido junginiai, naudotini kaip kinazės inhibitoriai
MA41256B1 (fr) 2014-12-24 2021-02-26 Principia Biopharma Inc Dosage spécifique de site d'un inhibiteur de btk
CA2973873A1 (fr) 2015-01-20 2016-07-28 Merial, Inc. Composes anthelmintiques, compositions et leur procede d'utilisation
US20180008629A1 (en) 2015-01-29 2018-01-11 Yale University Compositions and Methods for Treating NLRP3 Inflammasome-Related Diseases and Disorders
WO2016128343A1 (fr) 2015-02-09 2016-08-18 F. Hoffmann-La Roche Ag Composés pour le traitement d'un cancer
SI3578547T1 (sl) 2015-02-16 2021-09-30 The University Of Queensland Sulfonilsečnine in sorodne spojine ter njihova uporaba
MA41598A (fr) 2015-02-25 2018-01-02 Constellation Pharmaceuticals Inc Composés thérapeutiques de pyridazine et leurs utilisations
TWI810582B (zh) 2015-06-03 2023-08-01 美商普林斯匹亞生物製藥公司 酪胺酸激酶抑制劑
WO2016201280A1 (fr) 2015-06-10 2016-12-15 Biogen Ma Inc. Formes et compositions d'inhibiteurs biaryles de la tyrosine kinase de bruton
WO2017059702A1 (fr) 2015-10-09 2017-04-13 Acea Biosciences, Inc Sels pharmaceutiques, formes physiques, et compositions d'inhibiteurs pyrrolopyrimidine de kinases, et leurs procédés de préparation
KR20250133463A (ko) 2015-11-04 2025-09-05 메르크 파텐트 게엠베하 Btk 억제 활성을 갖는 피리미딘 및 피리딘 화합물을 사용하여 암 치료하는 방법
ES2879995T3 (es) 2015-12-10 2021-11-23 Ptc Therapeutics Inc Métodos para el tratamiento de la enfermedad de Huntington
US9630968B1 (en) 2015-12-23 2017-04-25 Arqule, Inc. Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof
EP3372607B1 (fr) 2016-01-05 2021-04-28 Jiangsu Hengrui Medicine Co. Ltd. Forme cristalline d'un inhibiteur de la tyrosine kinase de bruton (btk) et son procédé de préparation
CA3011465A1 (fr) 2016-01-15 2017-07-20 The Brigham And Women's Hospital, Inc. Derives de pyridazine en tant qu'activateurs d'eaat2
US20190231784A1 (en) 2016-06-29 2019-08-01 Principia Biopharma Inc. Modified release formulations of 2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4-methyl-4-[4-(oxetan-3-yl)piperazin-1-yl]pent-2-enenitrile
KR101865120B1 (ko) 2016-06-29 2018-06-08 숭실대학교 산학협력단 테스트 노드 기반의 무선 측위 방법 및 그 장치
EP3272739A1 (fr) 2016-07-20 2018-01-24 NodThera Limited Derives de sulfonyluree et leur application en matiere de regulation de l'activite de l'interleukine-1
TWI674261B (zh) 2017-02-17 2019-10-11 美商英能腫瘤免疫股份有限公司 Nlrp3 調節劑
AU2018284853A1 (en) 2017-06-14 2019-12-19 Ptc Therapeutics, Inc. Methods for modifying RNA splicing
CA3067410A1 (fr) 2017-07-07 2019-01-10 Inflazome Limited Nouveaux composes de sulfonamide carboxamide
CN110914258A (zh) 2017-07-14 2020-03-24 先天肿瘤免疫公司 Nlrp3调节剂
IL273741B (en) 2017-08-04 2022-09-01 Skyhawk Therapeutics Inc Methods and compositions for fusion modulation
UY37847A (es) 2017-08-15 2019-03-29 Inflazome Ltd Sulfonilureas y sulfoniltioureas útiles como inhibidores de nlrp3
CN111373057A (zh) 2017-09-25 2020-07-03 斯基霍克疗法公司 用于筛选和鉴定剪接调节剂的方法和组合物
CA3078565A1 (fr) 2017-10-12 2019-04-18 Revolution Medicines, Inc. Pyridine, pyrazine et composes de triazine utilises en tant qu'inhibiteurs allosteriques de shp2
BR112020008981A2 (pt) 2017-11-09 2020-11-17 Inflazome Limited novos compostos de sulfonamida carboxamida
MX2020009957A (es) 2018-03-27 2021-01-15 Ptc Therapeutics Inc Compuestos para el tratamiento de enfermedad de hungtinton.
US11530207B2 (en) 2018-04-10 2022-12-20 Skyhawk Therapeutics, Inc. Compounds for the treatment of cancer
WO2019207538A1 (fr) 2018-04-26 2019-10-31 Aurigene Discovery Technologies Limited Dérivés de pyridazine en tant qu'agents de dégradation de smarca2/4
UY38687A (es) * 2019-05-17 2023-05-15 Novartis Ag Inhibidores del inflamasoma nlrp3, composiciones, combinaciones de los mismos y métodos para su uso
US20230107277A1 (en) * 2020-03-27 2023-04-06 Astellas Pharma Inc. Substituted pyridazine compound
US20230348437A1 (en) * 2020-07-02 2023-11-02 Denali Therapeutics Inc. Compounds, compositions and methods
US20240391895A1 (en) * 2020-12-25 2024-11-28 Tuojie Biotech (Shanghai) Co., Ltd. Pyridazine-containing compound and medicinal use thereof
CN116867769A (zh) * 2021-02-08 2023-10-10 南京明德新药研发有限公司 取代的哒嗪苯酚类衍生物
US11932630B2 (en) 2021-04-16 2024-03-19 Novartis Ag Heteroaryl aminopropanol derivatives

Also Published As

Publication number Publication date
US20240067627A1 (en) 2024-02-29
DOP2025000013A (es) 2025-02-28
WO2024028782A1 (fr) 2024-02-08
US20250034114A1 (en) 2025-01-30
KR20250043519A (ko) 2025-03-28
CN119677725A (zh) 2025-03-21
MX2025001273A (es) 2025-03-07
EP4565326A1 (fr) 2025-06-11
CR20250063A (es) 2025-03-27
JP2025525866A (ja) 2025-08-07
UY40374A (es) 2024-02-15
TW202406550A (zh) 2024-02-16
PE20251255A1 (es) 2025-05-06
IL318533A (en) 2025-03-01
CO2025002057A2 (es) 2025-03-06
US12378222B2 (en) 2025-08-05
CA3262660A1 (fr) 2024-02-08
CL2025000285A1 (es) 2025-06-13
AU2023318764A1 (en) 2025-01-09
AR130094A1 (es) 2024-10-30

Similar Documents

Publication Publication Date Title
MA71689A (fr) Inhibiteurs de l'inflammasome nlrp3
MA53388A (fr) Inhibiteurs d'inflammasome nlrp3
ES3054790T3 (en) Nlrp3 inflammasome inhibitors
DK4337652T3 (da) NLRP3-hæmmere
IL287042A (en) Inflammatory inhibitors of nlrp3
IL315027A (en) Inhibitors of nlrp3
IL318258A (en) NLRP3 inflammasome inhibitors
EP4362946A4 (fr) Modulateurs de nlrp3
EP4251630A4 (fr) Inhibiteurs d'inflammasome de nlrp3 sulfonylurée
IL306022A (en) NLRP3 inflammasome inhibitors
EP3999045A4 (fr) Composés en tant qu'inhibiteurs d'inflammasome de nlrp3 et compositions et utilisations de ceux-ci
EP4129996A4 (fr) Nouvel inhibiteur aminopyrimidine d'egfr
EP4121059A4 (fr) Modulateurs de nlrp3
EP4217346C0 (fr) Modulateurs du nlrp3
MX2025011086A (es) Inhibidores de inflamasoma nlrp3 y usos de los mismos
ITFI20050239A1 (it) Idrossammati come inibitori dell'istone deacetilasi e formulazioni farmaceutiche che li contegono
SMT202500216T1 (it) Composti e composizioni come inibitori di sppl2a
EP1829864A4 (fr) Derives d'isoquiline utiles en tant qu'inhibiteurs de la calpaine
PT4337652T (pt) Inibidores do nlrp3
EP4293018A4 (fr) Composé servant d'inhibiteur de nlrp3
IT202200008321A1 (it) Composti tetraidroisochinolinici come inibitori dell’inflammasoma nlrp3 e loro uso come medicamenti
IT202200008246A1 (it) Composti solfonammidici come inibitori dell’inflammasoma nlrp3 e loro uso come medicamenti
IT202200008294A1 (it) Composti pirrolidinici e piperidinici come inibitori dell’inflammasoma nlrp3 e loro uso come medicamenti
HK40099180A (en) Inhibitors of nlrp3 inflammasome
AU2024325221A1 (en) Nlrp3 inflammasome inhibitor and use thereof