SG11202012321PA - Nlrp3 inflammasome inhibitors - Google Patents

Nlrp3 inflammasome inhibitors

Info

Publication number
SG11202012321PA
SG11202012321PA SG11202012321PA SG11202012321PA SG11202012321PA SG 11202012321P A SG11202012321P A SG 11202012321PA SG 11202012321P A SG11202012321P A SG 11202012321PA SG 11202012321P A SG11202012321P A SG 11202012321PA SG 11202012321P A SG11202012321P A SG 11202012321PA
Authority
SG
Singapore
Prior art keywords
nlrp3 inflammasome
inflammasome inhibitors
inhibitors
nlrp3
inflammasome
Prior art date
Application number
SG11202012321PA
Other languages
English (en)
Inventor
Christopher Farady
Nina Gommermann
Philipp Janser
Angela Mackay
Henri Mattes
Nikolaus Johannes Stiefl
Juraj Velcicky
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 SG11202012321PA publication Critical patent/SG11202012321PA/en

Links

Classifications

    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/60Salicylic acid; Derivatives thereof
    • A61K31/612Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid
    • A61K31/616Salicylic acid; Derivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
    • 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
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D515/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D515/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D515/14Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
SG11202012321PA 2018-07-25 2019-07-23 Nlrp3 inflammasome inhibitors SG11202012321PA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP18185580 2018-07-25
EP19175246 2019-05-17
PCT/IB2019/056278 WO2020021447A1 (en) 2018-07-25 2019-07-23 Nlrp3 inflammasome inhibitors

Publications (1)

Publication Number Publication Date
SG11202012321PA true SG11202012321PA (en) 2021-02-25

Family

ID=67989037

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202012321PA SG11202012321PA (en) 2018-07-25 2019-07-23 Nlrp3 inflammasome inhibitors

Country Status (22)

Country Link
US (1) US20210308140A1 (es)
EP (1) EP3827008A1 (es)
JP (1) JP2021532124A (es)
KR (1) KR20210038877A (es)
CN (1) CN112424207B (es)
AU (1) AU2019309727B2 (es)
BR (1) BR112021000964A2 (es)
CA (1) CA3103943A1 (es)
CL (1) CL2021000191A1 (es)
CO (1) CO2021000537A2 (es)
CR (1) CR20210045A (es)
CU (1) CU20210009A7 (es)
DO (1) DOP2021000019A (es)
EC (1) ECSP21004787A (es)
IL (1) IL280336A (es)
JO (1) JOP20210017A1 (es)
MA (1) MA53388A (es)
MX (1) MX2021000925A (es)
PE (1) PE20210406A1 (es)
PH (1) PH12021550166A1 (es)
SG (1) SG11202012321PA (es)
WO (1) WO2020021447A1 (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4126015A4 (en) * 2020-03-31 2024-04-24 Olatec Therapeutics, Inc. METHOD FOR PREVENTING OR TREATING PULMONARY INFECTION AND PULMONARY INFLAMMATION
WO2021209552A1 (en) 2020-04-15 2021-10-21 Janssen Pharmaceutica Nv Pyrazolo[1,5-d][1,2,4]triazine-5(4h)-acetamides as inhibitors of the nlrp3 inflammasome pathway
WO2021209539A1 (en) 2020-04-15 2021-10-21 Janssen Pharmaceutica Nv Pyrrolo[1,2-d][1,2,4]triazine-2-yl-acetamides as inhibitors of the nlrp3 inflammasome pathway
WO2021214284A1 (en) 2020-04-23 2021-10-28 Janssen Pharmaceutica Nv Tricyclic compounds as inhibitors of nlrp3
WO2021219784A1 (en) 2020-04-30 2021-11-04 Janssen Pharmaceutica Nv New triazinoindole compounds
AU2021279305A1 (en) 2020-05-28 2023-02-09 Janssen Pharmaceutica Nv Compounds
BR112022025612A2 (pt) 2020-06-19 2023-01-17 Ac Immune Sa Derivados de di-hidro-oxazol e tioureia modulando a via do inflamassoma nlrp3
CN116194445A (zh) 2020-09-24 2023-05-30 詹森药业有限公司 新化合物
EP3974415A1 (en) 2020-09-24 2022-03-30 Janssen Pharmaceutica NV Nlrp3 modulators
CN114478537B (zh) * 2020-11-13 2024-02-02 上海拓界生物医药科技有限公司 环酰胺并环化合物及其医药用途
EP4301754A1 (en) 2021-03-04 2024-01-10 Janssen Pharmaceutica NV 4-amino-6-oxo-pyridazine derivatives modulating nlrp3
EP4301753A1 (en) 2021-03-04 2024-01-10 Janssen Pharmaceutica NV 4-alkoxy-6-oxo-pyridazine derivatives modulating nlrp3
CN113230240B (zh) * 2021-03-22 2022-12-27 广州医科大学 1,3-二苯基丙-2-烯-1-酮衍生物及其应用
US11951115B2 (en) 2021-04-13 2024-04-09 Unity Biotechnology, Inc. Methods of treating retinal vasculopathies
US11932630B2 (en) 2021-04-16 2024-03-19 Novartis Ag Heteroaryl aminopropanol derivatives
BR112023022471A2 (pt) * 2021-04-29 2024-01-16 Janssen Pharmaceutica Nv Derivados de ftalazinona como inibidores de inflamassoma nlrp3
IL294231A (en) 2021-06-23 2023-01-01 Yoda Pharmaceuticals Inc History of benzimidazole for the treatment and/or prevention of nlrp3-mediated diseases and disorders
KR20240029027A (ko) 2021-07-01 2024-03-05 얀센 파마슈티카 엔브이 5-옥소-피리도[2,3-d]피리다진-6(5H)-일 아세트아미드
WO2023028536A1 (en) * 2021-08-25 2023-03-02 Ptc Therapeutics, Inc. 1,2,4-triazine derivatives useful as inhibitors of nlrp3
WO2023044043A1 (en) * 2021-09-17 2023-03-23 Denali Therapeutics Inc. Compounds, compositions and methods
KR20230066899A (ko) 2021-11-08 2023-05-16 제일약품주식회사 Nlrp3 저해제로서의 신규한 화합물 및 이를 포함하는 약학적 조성물
WO2023118521A1 (en) 2021-12-22 2023-06-29 Ac Immune Sa Dihydro-oxazol derivative compounds
WO2023156643A1 (en) * 2022-02-21 2023-08-24 Sanofi Thienopyrrolotriazine compounds, their preparation and their therapeutic use
US20240034735A1 (en) 2022-07-14 2024-02-01 Ac Immune Sa Novel compounds
US20240101563A1 (en) 2022-07-28 2024-03-28 Ac Immune Sa Novel compounds
WO2024033845A1 (en) * 2022-08-10 2024-02-15 Takeda Pharmaceutical Company Limited Heterocyclic compound
KR20240022938A (ko) 2022-08-12 2024-02-20 제일약품주식회사 Nlrp3 저해제로서의 신규한 화합물 및 이를 포함하는 약학적 조성물
WO2024064245A1 (en) 2022-09-23 2024-03-28 Merck Sharp & Dohme Llc Phthalazine derivatives useful as inhibitors of nod-like receptor protein 3

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009008906A2 (en) * 2007-02-06 2009-01-15 The Trustees Of The University Of Pennsylvania Therapeutic compounds for blocking dna synthesis of pox viruses
WO2010128152A1 (en) 2009-05-07 2010-11-11 Novartis Ag Fused heterocyclic c-glycosides for the treatment of diabetes
US8163704B2 (en) 2009-10-20 2012-04-24 Novartis Ag Glycoside derivatives and uses thereof
BR112012008924A2 (pt) 2009-10-20 2019-09-24 Novartis Ag derivado de glicosídeo e usos do mesmo
TR201821217T4 (tr) 2010-06-23 2019-01-21 Hanmi Science Co Ltd Tirozin kinaz aktivitesinin inhibisyonu için yeni kaynaşmış pirimidin türevleri.
CN105566229A (zh) 2010-08-10 2016-05-11 西建阿维拉米斯研究公司 Btk抑制剂的苯磺酸盐及其用途和制备方法
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
EA031153B1 (ru) 2011-06-10 2018-11-30 Мерк Патент Гмбх Применение пиримидиновых соединений с btk ингибирующей активностью
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
DK3181567T3 (da) 2012-09-10 2019-06-11 Principia Biopharma Inc Pyrazolopyrimidinforbindelser som kinasehæmmere
EP2925328A1 (en) 2012-11-28 2015-10-07 Intercept Pharmaceuticals, Inc. Treatment of pulmonary disease
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
MX367918B (es) 2013-04-25 2019-09-11 Beigene Ltd Compuestos heterociclicos fusionados como inhibidores de proteina quinasa.
SG11201603026PA (en) 2013-11-05 2016-05-30 Novartis Ag Compositions and methods for modulating farnesoid x receptors
US9512084B2 (en) 2013-11-29 2016-12-06 Novartis Ag Amino pyrimidine derivatives
JP2016540053A (ja) 2013-12-05 2016-12-22 アセルタ ファーマ ビー.ブイ. Pi3k阻害剤とbtk阻害剤の治療的組み合わせ
LT3083564T (lt) 2013-12-20 2018-09-25 Novartis Ag Heteroarilo butano rūgšties dariniai, kaip lta4h inhibitoriai
WO2015110923A2 (en) 2014-01-21 2015-07-30 Acerta Pharma B.V. Methods of treating chronic lymphocytic leukemia and small lymphocytic leukemia usng a btk inhibitor
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
EP3116909B1 (en) 2014-03-14 2019-11-13 Novartis Ag Antibody molecules to lag-3 and uses thereof
BR112016025659B1 (pt) 2014-05-13 2023-03-07 Novartis Ag Indutores de condrogênese, seu uso, e composição farmacêutica
EP4245376A3 (en) 2014-10-14 2023-12-13 Novartis AG Antibody molecules to pd-l1 and uses thereof
SI3461821T1 (sl) 2014-10-24 2020-09-30 Bristol-Myers Squibb Company Spojine indol karboksamida, uporabne kot kinazni inhibitorji
MX2017008386A (es) 2014-12-24 2018-03-23 Principia Biopharma Inc Administración específica del sitio de un inhibidor de btk.
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
US20180282310A1 (en) 2015-06-10 2018-10-04 Biogen Ma Inc. Forms and compositions of biaryl inhibitors of bruton's tyrosine kinase
CA3001744A1 (en) 2015-10-09 2017-04-13 ACEA Therapeutics, Inc. Pharmaceutical salts, physical forms, and compositions of pyrrolopyrimidine kinase inhibitors, and methods of making same
WO2017079542A1 (en) 2015-11-04 2017-05-11 Merck Patent Gmbh Methods for treating cancer using pyrimidine and pyridine compounds with btk inhibitory activity
US9630968B1 (en) 2015-12-23 2017-04-25 Arqule, Inc. Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof
MX2018008131A (es) 2016-01-05 2018-09-03 Jiangsu Hengrui Medicine Co Forma cristalina del inhibidor de la btk quinasa y metodo de preparacion de la misma.
EP3445761A1 (en) * 2016-04-19 2019-02-27 Innate Tumor Immunity, Inc. Nlrp3 modulators
KR101865120B1 (ko) 2016-06-29 2018-06-08 숭실대학교 산학협력단 테스트 노드 기반의 무선 측위 방법 및 그 장치
CA3028169A1 (en) 2016-06-29 2018-01-04 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
GB201712282D0 (en) * 2017-07-31 2017-09-13 Nodthera Ltd Selective inhibitors of NLRP3 inflammasome
US11926600B2 (en) * 2017-08-15 2024-03-12 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors

Also Published As

Publication number Publication date
IL280336A (en) 2021-03-01
CN112424207B (zh) 2024-03-19
PH12021550166A1 (en) 2021-09-13
AU2019309727B2 (en) 2021-12-23
ECSP21004787A (es) 2021-03-31
BR112021000964A2 (pt) 2021-04-20
WO2020021447A1 (en) 2020-01-30
PE20210406A1 (es) 2021-03-02
US20210308140A1 (en) 2021-10-07
JOP20210017A1 (ar) 2021-01-21
CR20210045A (es) 2021-06-18
AU2019309727A1 (en) 2021-01-07
EP3827008A1 (en) 2021-06-02
CN112424207A (zh) 2021-02-26
JP2021532124A (ja) 2021-11-25
CL2021000191A1 (es) 2021-08-20
CU20210009A7 (es) 2021-08-06
KR20210038877A (ko) 2021-04-08
MX2021000925A (es) 2021-03-31
DOP2021000019A (es) 2021-02-15
CA3103943A1 (en) 2020-01-30
MA53388A (fr) 2021-06-02
CO2021000537A2 (es) 2021-01-29

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