[go: up one dir, main page]

AR126351A1 - Compuestos y sus sales inhibidores del inflamasoma nlrp3 - Google Patents

Compuestos y sus sales inhibidores del inflamasoma nlrp3

Info

Publication number
AR126351A1
AR126351A1 ARP220101723A ARP220101723A AR126351A1 AR 126351 A1 AR126351 A1 AR 126351A1 AR P220101723 A ARP220101723 A AR P220101723A AR P220101723 A ARP220101723 A AR P220101723A AR 126351 A1 AR126351 A1 AR 126351A1
Authority
AR
Argentina
Prior art keywords
compounds
independently selected
nlrp3
salts
inflamasoma
Prior art date
Application number
ARP220101723A
Other languages
English (en)
Inventor
Lars Anders Mikael Johansson
Henrik Gradn
Giulia Bergonzini
Hiroshi Sugama
Takehiko Matsumura
Original Assignee
Astrazeneca Ab
Mitsubishi Tanabe Pharma Corp
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 Astrazeneca Ab, Mitsubishi Tanabe Pharma Corp filed Critical Astrazeneca Ab
Publication of AR126351A1 publication Critical patent/AR126351A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/28Cinnolines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • 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
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • 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
    • 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
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/30Phthalazines
    • C07D237/34Phthalazines with nitrogen atoms directly attached to carbon atoms of the nitrogen-containing ring, e.g. hydrazine radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La memoria descriptiva se refiere en general a compuestos de fórmula (1) y sales farmacéuticamente aceptables de los mismos. Dichos compuestos son útiles para inhibir la actividad del inflamasoma NLRP3 y pueden ser útiles como agentes terapéuticos. La memoria descriptiva también se refiere al uso de dichos compuestos para tratar o prevenir enfermedades y afecciones en las que está implicado el inflamasoma NLRP3. La memoria descriptiva se refiere además a composiciones que comprenden dichos compuestos. Reivindicación 1: Un compuesto caracterizado porque es de fórmula (1) o una sal farmacéuticamente aceptable del mismo, en donde R¹ se selecciona entre los compuestos del grupo de fórmulas (2); cada R³ se selecciona independientemente entre -H y -alquilo C₁₋₃; R⁴ se selecciona entre -H y -alquilo C₁₋₃; R²A, R²B, R²C y R²D se seleccionan cada uno independientemente entre -H, -F, -Cl, -alquilo C₁₋₃ sustituido con 0 - 3 sustituyentes -F, ciclopropilo, -OCF₃ y -SO₂Me; W, X, Y y Z se seleccionan cada uno independientemente entre CR⁵ y N; cero o uno de W, X, Y y Z son N y el resto de W, X, Y y Z son CR⁵; cada R⁵ se selecciona independientemente entre -H, -Me y -F.
ARP220101723A 2021-07-02 2022-07-01 Compuestos y sus sales inhibidores del inflamasoma nlrp3 AR126351A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US202163217970P 2021-07-02 2021-07-02

Publications (1)

Publication Number Publication Date
AR126351A1 true AR126351A1 (es) 2023-10-11

Family

ID=82611090

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP220101723A AR126351A1 (es) 2021-07-02 2022-07-01 Compuestos y sus sales inhibidores del inflamasoma nlrp3

Country Status (29)

Country Link
US (2) US11970463B2 (es)
EP (2) EP4363406B1 (es)
JP (1) JP2024523623A (es)
KR (1) KR20240031343A (es)
CN (1) CN117580826A (es)
AR (1) AR126351A1 (es)
AU (2) AU2022304254B2 (es)
BR (1) BR112023026976A2 (es)
CA (1) CA3224513A1 (es)
CL (1) CL2023003939A1 (es)
CO (1) CO2024000565A2 (es)
CR (1) CR20240038A (es)
DK (1) DK4363406T3 (es)
DO (1) DOP2024000002A (es)
EC (1) ECSP24008862A (es)
FI (1) FI4363406T3 (es)
HR (1) HRP20251513T1 (es)
IL (1) IL309680A (es)
LT (1) LT4363406T (es)
MA (1) MA65277B1 (es)
MX (1) MX2024000234A (es)
PE (1) PE20250122A1 (es)
PL (1) PL4363406T3 (es)
PT (1) PT4363406T (es)
RS (1) RS67463B1 (es)
SM (1) SMT202500441T1 (es)
TW (1) TW202321201A (es)
UY (1) UY39839A (es)
WO (1) WO2023275366A1 (es)

Families Citing this family (14)

* 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
KR20240019083A (ko) 2021-06-04 2024-02-14 에프. 호프만-라 로슈 아게 트리아진 유도체 및 암 치료에서 이의 용도
IL310264A (en) 2021-07-21 2024-03-01 Nico Therapeutics Inc Annulated pyridazine compound
US20240262806A1 (en) 2021-08-25 2024-08-08 Pct Therapeutics, Inc. Inhibitors of nlrp3
US20240391881A1 (en) * 2021-09-30 2024-11-28 Origiant Pharmaceutical Co., Ltd. Pharmaceutical use and preparation method for substituted heteroaryl phthalazine derivative
WO2023066377A1 (zh) 2021-10-22 2023-04-27 索智生物科技(浙江)有限公司 一种含氮化合物、其制备方法及应用
US12331048B2 (en) 2022-10-31 2025-06-17 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors
CN120418236A (zh) 2022-12-28 2025-08-01 长春金赛药业有限责任公司 哒嗪类nlrp3抑制剂化合物、药物组合物及其制备方法和应用
AU2023417850A1 (en) * 2022-12-28 2025-08-14 Astrazeneca Ab Crystalline forms of nlrp3 inflammasome inhibitors, chemical processes and chemical compounds
AU2024280075A1 (en) 2023-06-02 2025-12-11 Merck Sharp & Dohme Llc 5,6-Unsaturated Bicyclic Heterocycles Useful as Inhibitors of Nod-Like Receptor Protein 3
TW202521535A (zh) * 2023-11-20 2025-06-01 美商凡特斯治療美國公司 用於抑制NLRP3之固態游離鹼形式的5-氯-2-(4-((2-羥基-2-甲基丙基)胺基)吡啶并[3,4-d]嗒嗪-1-基)酚及其用途
WO2025153532A1 (en) 2024-01-16 2025-07-24 NodThera Limited Nlrp3 inhibitors and glp-1 agonists combination therapies
WO2026002229A1 (zh) * 2024-06-28 2026-01-02 长春金赛药业有限责任公司 一种nlrp3抑制剂化合物及其制备方法和应用

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5221952B2 (ja) 2004-05-08 2013-06-26 ノバルティス・インターナショナル・ファーマシューティカル・リミテッド 3−アリール−5,6−ジ置換ピリダジン類
JP2021502364A (ja) 2017-11-09 2021-01-28 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
AR119731A1 (es) * 2019-05-17 2022-01-05 Novartis Ag Inhibidores del inflamasoma nlrp3
US20230107277A1 (en) 2020-03-27 2023-04-06 Astellas Pharma Inc. Substituted pyridazine compound
CN116390914A (zh) * 2020-12-25 2023-07-04 上海拓界生物医药科技有限公司 一类含哒嗪的化合物及其医药用途
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
US11319319B1 (en) 2021-04-07 2022-05-03 Ventus Therapeutics U.S., Inc. Compounds for inhibiting NLRP3 and uses thereof
US20240239758A1 (en) 2021-04-28 2024-07-18 Astellas Pharma Inc. Substituted triazine compound
US20240327413A1 (en) 2021-06-29 2024-10-03 Zomagen Biosciences Ltd Nlrp3 modulators

Also Published As

Publication number Publication date
IL309680A (en) 2024-02-01
TW202321201A (zh) 2023-06-01
CA3224513A1 (en) 2023-01-05
US12503445B2 (en) 2025-12-23
PE20250122A1 (es) 2025-01-16
LT4363406T (lt) 2025-12-29
HRP20251513T1 (hr) 2026-01-02
MX2024000234A (es) 2024-04-16
PL4363406T3 (pl) 2026-01-05
AU2022304254A1 (en) 2024-02-08
EP4363406A1 (en) 2024-05-08
CN117580826A (zh) 2024-02-20
CL2023003939A1 (es) 2024-08-30
ECSP24008862A (es) 2024-03-01
PT4363406T (pt) 2025-12-15
DK4363406T3 (da) 2025-12-01
EP4628490A3 (en) 2025-12-03
EP4363406B1 (en) 2025-09-10
US20230110122A1 (en) 2023-04-13
US20240383862A1 (en) 2024-11-21
CO2024000565A2 (es) 2024-04-18
FI4363406T3 (fi) 2025-12-02
JP2024523623A (ja) 2024-06-28
CR20240038A (es) 2024-05-24
BR112023026976A2 (pt) 2024-03-12
UY39839A (es) 2023-01-31
EP4628490A2 (en) 2025-10-08
MA65277B1 (fr) 2025-12-31
WO2023275366A1 (en) 2023-01-05
US11970463B2 (en) 2024-04-30
DOP2024000002A (es) 2024-05-15
AU2025223957A1 (en) 2025-09-18
AU2022304254B2 (en) 2025-06-12
KR20240031343A (ko) 2024-03-07
SMT202500441T1 (it) 2026-01-12
RS67463B1 (sr) 2025-12-31

Similar Documents

Publication Publication Date Title
AR126351A1 (es) Compuestos y sus sales inhibidores del inflamasoma nlrp3
AR119731A1 (es) Inhibidores del inflamasoma nlrp3
PE20230825A1 (es) Inhibidores de kras triciclicos fusionados
AR127235A1 (es) Pirazoloquinolinas inhibidoras de kras
PE20221905A1 (es) Aminas biciclicas como inhibidoras de la cdk2
CL2020002146A1 (es) Derivados de n-(fenil)-2-(fenil)pirimidina-4-carboxamida y compuestos relacionados como inhibidores hpki para tratar el cáncer.
AR110139A1 (es) COMPUESTOS MONO Y ESPIROCÍCLICOS QUE CONTIENEN CICLOBUTANO Y AZETIDINA COMO INHIBIDORES DE LA INTEGRINA aV
AR090590A1 (es) COMPUESTOS 1,3,4-OXADIAZOL Y 1,3,4-TIADIAZOL COMO INHIBIDORES DE b-LACTAMASA
AR078157A1 (es) Derivados de pirazol-[4,5-d]pirrolo[2,3-b]piridina inhibidores de tirosinquinasas jak 2, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del cancer
AR090589A1 (es) INHIBIDORES DE b-LACTAMASA ISOXAZOL
AR089143A1 (es) Triazolopiridinas sustituidas con actividad inhibidora de ttk
AR087915A1 (es) N-(3-(2-amino-6,6-difluor-4,4a,5,6,7,7a-hexahidro-ciclopenta-[e][1,3]oxazin-4-il)-fenil)-amidas como inhibidores de la bace1
UY33961A (es) Compuestos de bis(fuoroalquil)-1,4-benziodiazepinona
AR050952A1 (es) Derivados de indazolona; procesos para su obtencion; composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades mediadas por la inhibicion de la enzima 11beta - hsd1.
AR100714A1 (es) Derivados de alquilo y arilo de compuestos de 1-oxa-4,9-diazaespiro undecano que tienen actividad multimodal contra el dolor
AR123435A1 (es) Derivados de sulfamoil urea que contienen resto alquilo-oxacicloalquilo, y usos de los mismos
CL2022002975A1 (es) Compuestos y composiciones para inhibir la actividad de hif2-alfa y sus métodos de uso
AR103629A1 (es) Compuestos con actividad antitumoral
AR126892A1 (es) Compuestos de aminopiridina sustituidos como inhibidores de egfr
PE20181328A1 (es) Compuestos de dihidroquinolinsulfonamida de alquilo
AR091731A1 (es) Antagonistas del receptor de mineralocorticoides
AR088639A1 (es) Composicion farmaceutica oftalmica, compuestos antimicrobianos a base de carbolina
AR125479A1 (es) Inhibidores de il4i1 y métodos de uso
BR112023014549A2 (pt) Compostos derivados substituídos com ip4-4,6
AR108535A1 (es) Derivados de tetrahidropirano y tiopirano que tienen actividad multimodal contra el dolor