CL2023002973A1 - Compuestos para la inhibición de nlrp3 y usos de estos. - Google Patents
Compuestos para la inhibición de nlrp3 y usos de estos.Info
- Publication number
- CL2023002973A1 CL2023002973A1 CL2023002973A CL2023002973A CL2023002973A1 CL 2023002973 A1 CL2023002973 A1 CL 2023002973A1 CL 2023002973 A CL2023002973 A CL 2023002973A CL 2023002973 A CL2023002973 A CL 2023002973A CL 2023002973 A1 CL2023002973 A1 CL 2023002973A1
- Authority
- CL
- Chile
- Prior art keywords
- nlrp3
- inhibition
- compounds
- inhibited
- disorders
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
- 102000000874 Pyrin Domain-Containing 3 Protein NLR Family Human genes 0.000 abstract 1
- 108010001946 Pyrin Domain-Containing 3 Protein NLR Family Proteins 0.000 abstract 1
- 208000037765 diseases and disorders Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic 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
- C07D237/10—Heterocyclic 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
- C07D237/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
- C07D237/34—Phthalazines with nitrogen atoms directly attached to carbon atoms of the nitrogen-containing ring, e.g. hydrazine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic 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 two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202163171932P | 2021-04-07 | 2021-04-07 | |
| US17/528,928 US11319319B1 (en) | 2021-04-07 | 2021-11-17 | Compounds for inhibiting NLRP3 and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2023002973A1 true CL2023002973A1 (es) | 2024-03-08 |
Family
ID=81385286
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2023002973A CL2023002973A1 (es) | 2021-04-07 | 2023-10-04 | Compuestos para la inhibición de nlrp3 y usos de estos. |
| CL2024001964A CL2024001964A1 (es) | 2021-04-07 | 2024-06-26 | Compuestos para la inhibición de nlrp3 y usos de estos |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2024001964A CL2024001964A1 (es) | 2021-04-07 | 2024-06-26 | Compuestos para la inhibición de nlrp3 y usos de estos |
Country Status (15)
| Country | Link |
|---|---|
| US (10) | US11319319B1 (enExample) |
| EP (3) | EP4320102A1 (enExample) |
| JP (2) | JP7620120B2 (enExample) |
| KR (1) | KR20230167394A (enExample) |
| CN (2) | CN117500792A (enExample) |
| AU (3) | AU2022256052B2 (enExample) |
| BR (1) | BR112023020483A2 (enExample) |
| CA (1) | CA3214676A1 (enExample) |
| CL (2) | CL2023002973A1 (enExample) |
| CO (1) | CO2023013356A2 (enExample) |
| IL (2) | IL308378A (enExample) |
| MX (2) | MX2023011576A (enExample) |
| PE (1) | PE20240765A1 (enExample) |
| TW (1) | TW202304905A (enExample) |
| WO (1) | WO2022216971A1 (enExample) |
Families Citing this family (42)
| 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 |
| TW202313577A (zh) | 2021-06-04 | 2023-04-01 | 瑞士商赫孚孟拉羅股份公司 | 新穎化合物 |
| WO2022253326A1 (zh) * | 2021-06-05 | 2022-12-08 | 药捷安康(南京)科技股份有限公司 | Nlrp3炎症小体抑制剂及其应用 |
| EP4363406B1 (en) * | 2021-07-02 | 2025-09-10 | Astrazeneca AB | Nlrp3 inflammasome inhibitors |
| CA3226995A1 (en) | 2021-07-21 | 2023-01-26 | Nico Therapeutics, Inc. | Annulated pyridazine compound |
| JP2024534162A (ja) * | 2021-08-25 | 2024-09-18 | ピーティーシー セラピューティクス, インコーポレイテッド | Nlrp3の阻害剤 |
| EP4410787A4 (en) * | 2021-09-30 | 2025-10-15 | Origiant Pharmaceutical Co Ltd | PHARMACEUTICAL USE AND PROCESS FOR PREPARING A SUBSTITUTED HETEROARYL-PHTHALAZINE DERIVATIVE |
| EP4421068A1 (en) * | 2021-10-22 | 2024-08-28 | Zhejiang Aixplorer Biotech Co., Ltd. | Nitrogen-containing compound, preparation method therefor and application thereof |
| CN119137121A (zh) * | 2022-03-25 | 2024-12-13 | 万特斯治疗美国公司 | 可用作NLRP3衍生物的吡啶并-[3,4-d]哒嗪胺衍生物 |
| AU2023245348A1 (en) * | 2022-03-31 | 2024-09-12 | Hangzhou Highlightll Pharmaceutical Co., Ltd | Nlrp3 inflammasome inhibitors |
| KR20250036233A (ko) * | 2022-07-14 | 2025-03-13 | 에이씨 이뮨 에스에이 | Nlrp3 인플라마좀 경로의 조절제로서의 피롤로트리아진 및 이미다조트리아진 유도체 |
| JP2025023868A (ja) * | 2022-09-23 | 2025-02-17 | メルク・シャープ・アンド・ドーム・エルエルシー | Nod様受容体タンパク質3の阻害剤として有用なフタラジン誘導体 |
| WO2024064245A1 (en) | 2022-09-23 | 2024-03-28 | Merck Sharp & Dohme Llc | Phthalazine derivatives useful as inhibitors of nod-like receptor protein 3 |
| CN120152974A (zh) | 2022-10-26 | 2025-06-13 | 天维生物制药有限公司 | 缩环哒嗪衍生物 |
| TW202419449A (zh) * | 2022-10-31 | 2024-05-16 | 美商凡特斯治療美國公司 | 可用作nlrp3抑制劑之橋接雙環雜環烷基吡啶并-〔3,4-d〕噠嗪胺衍生物 |
| US12331048B2 (en) | 2022-10-31 | 2025-06-17 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors |
| CN121045190A (zh) * | 2022-11-04 | 2025-12-02 | 药捷安康(南京)科技股份有限公司 | Nlrp3炎症小体抑制剂及其应用 |
| WO2024109922A1 (zh) * | 2022-11-25 | 2024-05-30 | 成都赜灵生物医药科技有限公司 | 桥环并哒嗪类化合物及其用途 |
| EP4637746A1 (en) * | 2022-12-19 | 2025-10-29 | Merck Sharp & Dohme LLC | 6,6 bicyclic heterocyles useful as inhibitors of nod-like receptor protein 3 |
| CN120379995A (zh) * | 2022-12-27 | 2025-07-25 | 正大天晴药业集团股份有限公司 | 一种哒嗪稠芳环化合物及其用途 |
| EP4642763A1 (en) | 2022-12-28 | 2025-11-05 | Astrazeneca AB | Crystalline forms of nlrp3 inflammasome inhibitors, chemical processes and chemical compounds |
| TW202440107A (zh) | 2022-12-28 | 2024-10-16 | 瑞典商阿斯特捷利康公司 | Nlrp3炎症小體抑制劑 |
| EP4644380A1 (en) * | 2022-12-28 | 2025-11-05 | Changchun Genescience Pharmaceutical Co., Ltd. | Pyridazine nlrp3 inhibitor compound, pharmaceutical composition, and preparation method therefor and use thereof |
| EP4656635A1 (en) | 2023-01-24 | 2025-12-03 | Daiichi Sankyo Company, Limited | Substituted benzene compound |
| KR20250152599A (ko) | 2023-01-31 | 2025-10-23 | 얀센 파마슈티카 엔브이 | NLRP3 억제제로서의 [1,2,4]트라이아졸로[4,3-a]피리딘 및 [1,2,4]트라이아졸로[4,3-a]피라진 |
| AU2024213537A1 (en) | 2023-01-31 | 2025-09-11 | Janssen Pharmaceutica Nv | Imidazo[1,2-d][1,2,4]triazines as nlrp3 inhibitors |
| CN121001996A (zh) | 2023-01-31 | 2025-11-21 | 詹森药业有限公司 | 作为nlrp3抑制剂的吡啶-2(1h)-酮和嘧啶-4(3h)-酮 |
| WO2024160690A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | 2-(pyridazin-3-yl)-5-(trifluoromethyl)phenols as nlrp3 inhibitors |
| WO2024160691A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | PYRROLO[1,2-d][1,2,4]TRIAZINES AND PYRAZOLO[1,5-d] [1,2,4]TRIAZINES AS NLRP3 INHIBITORS |
| WO2024169858A1 (zh) * | 2023-02-17 | 2024-08-22 | 成都赜灵生物医药科技有限公司 | 六元氮杂环类化合物及其用途 |
| WO2024217462A1 (zh) * | 2023-04-18 | 2024-10-24 | 南京明德新药研发有限公司 | 五氟化硫取代的芳环化合物及其应用 |
| US20240400571A1 (en) | 2023-06-02 | 2024-12-05 | Merck Sharp & Dohme Llc | 5,6 unsaturated bicyclic heterocyles useful as inhibitors of nod-like receptor protein 3 |
| WO2025006681A2 (en) * | 2023-06-27 | 2025-01-02 | Viva Star Biosciences (Us) Inc. | Substituted pyridazine compounds as inhibitors of nlrp3 activity and therapeutic uses thereof |
| WO2025036275A1 (zh) * | 2023-08-11 | 2025-02-20 | 药捷安康(南京)科技股份有限公司 | Nlrp3炎症小体抑制剂及其应用 |
| CN117143027B (zh) * | 2023-08-31 | 2024-12-20 | 四川大学 | 3-苄氧基-6-羟苯基哒嗪类化合物及其制备方法和用途 |
| WO2025059069A1 (en) * | 2023-09-12 | 2025-03-20 | Zomagen Biosciences Ltd | Nlrp3 modulators |
| WO2025059481A1 (en) * | 2023-09-13 | 2025-03-20 | Ventus Therapeutics U.S., Inc. | Solid forms of an nlrp3 inhibitor and uses thereof |
| KR20250074627A (ko) * | 2023-11-20 | 2025-05-27 | 벤투스 테라퓨틱스 유에스 인코포레이티드 | NLRP3을 억제하기 위한 5-클로로-2-(4-((2-하이드록시-2-메틸프로필)아미노)피리도[3,4-d]피리다진-1-일)페놀의 고형 유리염기 형태 및 이의 용도 |
| US20250195511A1 (en) | 2023-12-14 | 2025-06-19 | Merck Sharp & Dohme Llc | Indazole derivatives useful as inhibitors of nod-like receptor protein 3 |
| WO2025128781A1 (en) | 2023-12-14 | 2025-06-19 | Merck Sharp & Dohme Llc | Azaindazole derivatives useful as inhibitors of nod-like receptor protein 3 |
| WO2025153532A1 (en) | 2024-01-16 | 2025-07-24 | NodThera Limited | Nlrp3 inhibitors and glp-1 agonists combination therapies |
Family Cites Families (190)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1303061A (enExample) * | 1969-05-03 | 1973-01-17 | ||
| GB1293565A (en) | 1969-05-03 | 1972-10-18 | Aspro Nicholas Ltd | Aminophthalazines and pharmaceutical compositions thereof |
| GB2063249A (en) * | 1979-10-09 | 1981-06-03 | Mitsubishi Yuka Pharma | 4-Phenylphthalazine derivatives |
| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| WO1989011279A1 (en) | 1988-05-16 | 1989-11-30 | Georgia State University Foundation, Inc. | Nucleic acid interacting unfused heteropolycyclic compounds |
| ES2068413T3 (es) | 1990-03-30 | 1995-04-16 | Mitsubishi Chem Ind | Derivados de 4-fenilftalazina. |
| JPH03284669A (ja) * | 1990-03-30 | 1991-12-16 | Mitsubishi Kasei Corp | 4―フェニルフタラジン誘導体 |
| TW279162B (enExample) * | 1991-09-26 | 1996-06-21 | Mitsubishi Chem Corp | |
| WO1993015058A1 (en) | 1992-01-23 | 1993-08-05 | Pfizer Inc. | 4-aryl-3-(heteroarylureido)-1,2-dihydro-2-oxo-quinoline derivatives as antihypercholesterolemic and antiatherosclerotic agents |
| US5565472A (en) | 1992-12-21 | 1996-10-15 | Pfizer Inc. | 4-aryl-3-(heteroarylureido)-1,2-dihydro-2-oxo-quinoline derivatives as antihypercholesterolemic and antiatherosclerotic agents |
| DE4417746A1 (de) | 1994-05-20 | 1995-11-23 | Bayer Ag | Neue Farbstoffe zum Massefärben von Kunststoffen |
| NZ290952A (en) | 1994-08-09 | 1998-05-27 | Eisai Co Ltd | Phthalazine derivatives optionally substituted in position-1 by (generally benzyl) amino groups |
| US5763263A (en) | 1995-11-27 | 1998-06-09 | Dehlinger; Peter J. | Method and apparatus for producing position addressable combinatorial libraries |
| US6288064B1 (en) | 1996-08-20 | 2001-09-11 | Eisai Co., Ltd. | Remedy for erection failure comprising fused pyridazine compound |
| US20030124053A1 (en) | 1996-10-07 | 2003-07-03 | Barrett John Andrew | Radiopharmaceuticals for imaging infection and inflammation |
| CA2275686C (en) | 1996-12-18 | 2006-10-17 | Neurogen Corporation | Isoquinolinamine and phthalazinamine derivatives which interact with crf receptors |
| US6486158B1 (en) | 1998-08-14 | 2002-11-26 | Cell Pathways, Inc. | [4,5]-fused-3,6-disubstituted-pyridazines with sulfur-containing substituents in position three for the treatment of neoplasia |
| JP2002540102A (ja) | 1999-03-22 | 2002-11-26 | ブリストル−マイヤーズ スクイブ カンパニー | cGMPホスホジエステラーゼの縮合ピリドピリダジン阻害剤 |
| PL369886A1 (en) | 2001-11-30 | 2005-05-02 | Pfizer Products Inc. | Aryl fused azapolycyclic compounds |
| WO2004099158A1 (en) | 2003-04-30 | 2004-11-18 | Ricerca Biosciences, Llc. | Monocyclic diazodioxide based bcl-2 protein antagonists |
| WO2005016000A1 (en) | 2003-08-05 | 2005-02-24 | Avalon Pharmaceuticals | Derivatives of cyclic quinone and uses thereof |
| US7087621B2 (en) | 2003-09-05 | 2006-08-08 | Bristol-Myers Squibb Company | Benzo- and azabenzodithiazole compounds |
| WO2005033288A2 (en) | 2003-09-29 | 2005-04-14 | The Johns Hopkins University | Hedgehog pathway antagonists |
| CA2564996A1 (en) | 2004-05-08 | 2006-01-12 | Taeyoung Yoon | 3-aryl-5,6-disubstituted pyridazines |
| CA2569849C (en) | 2004-06-09 | 2012-11-27 | Erick M. Carreira | Monophosphine compounds, transition metal complexes thereof and production of optically active compounds using the complexes as asymmetric catalysts |
| US20060156485A1 (en) | 2005-01-14 | 2006-07-20 | The Procter & Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| WO2006090273A2 (en) | 2005-02-22 | 2006-08-31 | Warner-Lambert Company Llc | [1,8]naphthyridin-2-ones and related compounds with keto or hydroxyl linkers for the treatment of schizophrenia |
| WO2006110516A1 (en) | 2005-04-11 | 2006-10-19 | Abbott Laboratories | Acylhydrazide p2x7 antagonists and uses thereof |
| US8106066B2 (en) | 2005-09-23 | 2012-01-31 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof |
| WO2007038367A1 (en) | 2005-09-23 | 2007-04-05 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof |
| FR2891828B1 (fr) | 2005-10-12 | 2007-12-21 | Sanofi Aventis Sa | Derives de la 1-amino-phtalazine substituee, leur preparation et leur application en therapeutique |
| MX2008005662A (es) | 2005-11-03 | 2008-12-15 | Ilypsa Inc | Compuestos de azaindol y uso de los mismos como inhibidores de la fosfolipasa a2. |
| US7666898B2 (en) | 2005-11-03 | 2010-02-23 | Ilypsa, Inc. | Multivalent indole compounds and use thereof as phospholipase-A2 inhibitors |
| US20070179123A1 (en) | 2005-11-08 | 2007-08-02 | Chiang Peter K | Methods and compositions for treating diseases associated with pathogenic proteins |
| JP2009120486A (ja) | 2005-12-05 | 2009-06-04 | Mitsubishi Pharma Corp | 核内オーファン受容体の新規活性化剤及びその用途 |
| MY161884A (en) | 2006-01-23 | 2017-05-15 | Amgen Inc | Aurora kinase modulators and method of use |
| US7560551B2 (en) | 2006-01-23 | 2009-07-14 | Amgen Inc. | Aurora kinase modulators and method of use |
| BRPI0709555B1 (pt) | 2006-02-16 | 2015-11-03 | Syngenta Ltd | compostos pesticidas contendo uma estrutura de bisamida bicíclica, composição pesticida, e método para controlar pestes. |
| CA2660114A1 (en) | 2006-08-09 | 2008-02-14 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| CN101679299A (zh) | 2007-04-19 | 2010-03-24 | 诺瓦提斯公司 | 作为代谢型谷氨酸受体-5调节剂的烟酸衍生物 |
| CA2685219C (en) | 2007-05-04 | 2012-06-19 | Amgen Inc. | Diazaquinolones that inhibit prolyl hydroxylase activity |
| US9023490B2 (en) | 2007-06-15 | 2015-05-05 | Versitech Limited | Extended pi-conjugated platinum (II) complexes |
| WO2009035568A1 (en) | 2007-09-07 | 2009-03-19 | Amgen Inc. | Annelated pyridazines for the treatment of tumors driven by inappropriate hedgehog signalling |
| WO2009038812A1 (en) | 2007-09-20 | 2009-03-26 | Amgen Inc. | Condensed piperidine derivatives useful as vanilloid receptor ligands |
| US20110150833A1 (en) | 2007-12-21 | 2011-06-23 | The Scripps Research Institute | Benzopyrans and analogs as rho kinase inhibitors |
| CA2709784A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| US8932557B2 (en) | 2008-02-14 | 2015-01-13 | Eli Lilly And Company | Imaging agents for detecting neurological dysfunction |
| CA2725398A1 (en) | 2008-04-11 | 2009-10-15 | The Regents Of The University Of Michigan | Heteroaryl-substituted bicyclic smac mimetics and the uses thereof |
| AU2009246626A1 (en) | 2008-05-15 | 2009-11-19 | Merck Sharp & Dohme Corp. | Oxazolobenzimidazole derivatives |
| MX2010013577A (es) | 2008-06-16 | 2010-12-21 | Merck Patent Gmbh | Derivados de quinoxalindiona. |
| WO2009157386A1 (ja) | 2008-06-25 | 2009-12-30 | 住友化学株式会社 | 光学活性アミン化合物の製造方法 |
| NZ590500A (en) | 2008-08-16 | 2012-06-29 | Genentech Inc | Azaindole inhibitors of iap |
| US20110178117A1 (en) | 2008-09-26 | 2011-07-21 | Merck Sharp & Dohme Corp. | Oxazolobenzimidazole derivatives |
| WO2010101949A1 (en) | 2009-03-02 | 2010-09-10 | Sirtris Pharmaceuticals, Inc. | 8-substituted quinolines and related analogs as sirtuin modulators |
| TW201040191A (en) | 2009-03-27 | 2010-11-16 | Abbott Gmbh & Co Kg | Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors |
| JP2012522750A (ja) | 2009-04-01 | 2012-09-27 | ビーエーエスエフ ソシエタス・ヨーロピア | 無脊椎動物害虫を駆除するためのイソキサゾリン化合物 |
| WO2010117935A1 (en) | 2009-04-06 | 2010-10-14 | Schering Corporation | Compounds and methods for antiviral treatment |
| WO2010117936A1 (en) | 2009-04-06 | 2010-10-14 | Schering Corporation | Combinations of a hcv inhibitor such as bicyclic pyrrole derivatives and a therapeutic agent |
| WO2010151791A1 (en) | 2009-06-25 | 2010-12-29 | Amgen Inc. | Heterocyclic compounds and their uses |
| US8981087B2 (en) | 2009-07-29 | 2015-03-17 | Karus Therapeutics Limited | Benzo [E] [1,3] oxazin-4-one derivatives as phosphoinositide 3-kinase inhibitors |
| EP2464647B1 (en) | 2009-08-11 | 2016-09-21 | Bristol-Myers Squibb Company | Azaindazoles as btk kinase modulators and use thereof |
| WO2011075607A1 (en) | 2009-12-18 | 2011-06-23 | Intermune, Inc. | Novel inhibitors of hepatitis c virus replication |
| US8759535B2 (en) | 2010-02-18 | 2014-06-24 | High Point Pharmaceuticals, Llc | Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof |
| UY33304A (es) | 2010-04-02 | 2011-10-31 | Amgen Inc | Compuestos heterocíclicos y sus usos |
| US8980929B2 (en) | 2010-05-21 | 2015-03-17 | Merck Sharp & Dohme Corp. | Substituted seven-membered heterocyclic compounds as dipeptidyl peptidase-iv inhibitors for the treatment of diabetes |
| PE20130376A1 (es) | 2010-06-28 | 2013-03-30 | Merck Patent Gmbh | [1,8]naftiridinas sustituidas por 2,4-diarilo como inhibidores de quinasas para uso contra el cancer |
| MX2012015143A (es) | 2010-06-30 | 2013-07-03 | Amgen Inc | Compuestos heterociclicos que contienen nitrogeno como inhibidores de pi3k delta. |
| EP2616443A1 (en) | 2010-09-14 | 2013-07-24 | Exelixis, Inc. | Phtalazine derivatives as jak1 inhibitors |
| EP2621914B1 (en) | 2010-09-27 | 2016-12-28 | Abbott GmbH & Co. KG | Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors |
| US20140107151A1 (en) | 2011-05-17 | 2014-04-17 | Principia Biophama Inc. | Tyrosine kinase inhibitors |
| US8895587B2 (en) | 2011-05-18 | 2014-11-25 | Syngenta Participations Ag | Insecticidal compounds based on arylthioacetamide derivatives |
| ES2609003T3 (es) | 2011-08-08 | 2017-04-18 | Merck Patent Gmbh | Carboxamidas de n-(bencimimazol-2-il) -ciclopropano como antagonistas de ácido lisofosfatídico |
| WO2013026939A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Methods for the control of termites and ants |
| WO2013078254A1 (en) | 2011-11-22 | 2013-05-30 | Array Biopharma Inc. | Bicyclic heteroaryl derivatives as kinase inhibitors |
| UA112897C2 (uk) | 2012-05-09 | 2016-11-10 | Байєр Фарма Акцієнгезелльшафт | Біциклічно заміщені урацили та їх застосування для лікування і/або профілактики захворювань |
| ES2792830T3 (es) | 2012-05-22 | 2020-11-12 | Lilly Co Eli | Agentes para formación de imagen en base a carbolina y carbazol, para la detección de disfunción neurológica |
| TWI610916B (zh) | 2012-08-03 | 2018-01-11 | 廣東東陽光藥業有限公司 | 作爲丙型肝炎抑制劑的橋環化合物及其在藥物中的應用 |
| WO2014079941A1 (en) | 2012-11-21 | 2014-05-30 | Syngenta Participations Ag | Insecticidal compounds based on n-(arylsulfanylmethyl) carboxamide derivatives |
| WO2014080291A2 (en) | 2012-11-21 | 2014-05-30 | Rvx Therapeutics Inc. | Biaryl derivatives as bromodomain inhibitors |
| WO2014079935A1 (en) | 2012-11-21 | 2014-05-30 | Syngenta Participations Ag | Insecticidal compounds based on arylthioacetamide derivatives |
| WO2014086737A1 (de) | 2012-12-06 | 2014-06-12 | Bayer Cropscience Ag | Kondensierte 2-pyridon-3-carboxamide und ihre verwendung als herbizide |
| TW201439060A (zh) | 2013-02-27 | 2014-10-16 | Sunshine Lake Pharma Co Ltd | 作爲丙型肝炎抑制劑的橋環化合物及其藥物組合物和用途 |
| GB201311953D0 (en) | 2013-07-03 | 2013-08-14 | Redx Pharma Ltd | Compounds |
| AR097631A1 (es) | 2013-09-16 | 2016-04-06 | Bayer Pharma AG | Trifluorometilpirimidinonas sustituidas con heterociclos y sus usos |
| UY35809A (es) | 2013-11-05 | 2015-05-29 | Bayer Pharma AG | (aza)piridopirazolopirimidinonas e indazolopirimidinonas y sus usos |
| WO2015150995A1 (en) | 2014-04-04 | 2015-10-08 | Pfizer Inc. | Bicyclic-fused heteroaryl or aryl compounds and their use as irak4 inhibitors |
| CN103992311B (zh) | 2014-06-20 | 2017-01-25 | 东南大学 | Hedgehog信号通路抑制剂 |
| US9617279B1 (en) | 2014-06-24 | 2017-04-11 | Bristol-Myers Squibb Company | Imidazooxadiazole compounds |
| WO2016086200A1 (en) | 2014-11-27 | 2016-06-02 | Genentech, Inc. | 4,5,6,7-tetrahydro-1 h-pyrazolo[4,3-c]pyridin-3-amine compounds as cbp and/or ep300 inhibitors |
| MX369623B (es) | 2014-12-22 | 2019-11-14 | Akarna Therapeutics Ltd | Compuestos biciclicos fusionados para el tratamiento de enfermedades. |
| US20180093956A1 (en) | 2015-02-06 | 2018-04-05 | Abbvie Inc. | Substituted phthalazines |
| PE20221627A1 (es) | 2015-02-16 | 2022-10-19 | Univ Queensland | Sulfonilureas y compuestos relacionados y uso de estos |
| CN108697709A (zh) | 2015-12-10 | 2018-10-23 | Ptc医疗公司 | 用于治疗亨廷顿病的方法 |
| FR3046933B1 (fr) | 2016-01-25 | 2018-03-02 | Galderma Research & Development | Inhibiteurs nlrp3 pour le traitement des pathologies cutanees inflammatoires |
| CA3013850C (en) | 2016-02-12 | 2024-01-30 | Pharmaxis Ltd. | Haloallylamine indole and azaindole derivative inhibitors of lysyl oxidases and uses thereof |
| HK1257569A1 (zh) | 2016-02-16 | 2019-10-25 | The University Of Queensland | 磺醯脲和相关化合物及其用途 |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP3445749B1 (en) | 2016-04-18 | 2022-12-21 | Novartis AG | Compounds and compositions for treating conditions associated with nlrp activity |
| WO2017184623A1 (en) | 2016-04-18 | 2017-10-26 | Ifm Therapeutics, Inc | Compounds and compositions for treating conditions associated with nlrp activity |
| EP3236267B1 (en) | 2016-04-18 | 2021-09-08 | Roche Diagnostics GmbH | Decapper and apparatus |
| EP3272739A1 (en) | 2016-07-20 | 2018-01-24 | NodThera Limited | Sulfonyl urea derivatives and their use in the control of interleukin-1 activity |
| WO2018031680A1 (en) | 2016-08-10 | 2018-02-15 | Fronthera U.S. Pharmaceuticals Llc | Novel compounds, uses and methods for their preparation |
| US10947241B2 (en) * | 2016-10-28 | 2021-03-16 | Seoul National University Hospital | Phenyl phthalazine derivative, method for the preparation thereof, and pharmaceutical composition comprising the same |
| WO2018138050A1 (de) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP3577109A4 (en) | 2017-01-31 | 2020-11-18 | Arvinas Operations, Inc. | CEREMONY LIGANDS AND BIFUNCTIONAL COMPOUNDS CONTAINING THEM |
| WO2018172925A1 (en) | 2017-03-23 | 2018-09-27 | Vitas Pharma Research Pvt Ltd | Inhibitors of dna gyrase for treatment of bacterial infections |
| KR101943428B1 (ko) | 2017-03-24 | 2019-01-30 | 엘티소재주식회사 | 유기 발광 소자 및 유기 발광 소자의 유기물층용 조성물 |
| WO2018174678A1 (ko) | 2017-03-24 | 2018-09-27 | 희성소재(주) | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
| JOP20190272A1 (ar) | 2017-05-22 | 2019-11-21 | Amgen Inc | مثبطات kras g12c وطرق لاستخدامها |
| WO2018218071A1 (en) | 2017-05-25 | 2018-11-29 | Araxes Pharma Llc | Compounds and methods of use thereof for treatment of cancer |
| WO2018221433A1 (ja) | 2017-05-29 | 2018-12-06 | 第一三共株式会社 | ヘテロアリールアミン誘導体 |
| JP6849248B2 (ja) | 2017-07-20 | 2021-03-24 | エルジー・ケム・リミテッド | 化合物およびこれを含む有機発光素子 |
| JP2020531453A (ja) | 2017-08-15 | 2020-11-05 | インフレイゾーム リミテッド | Nlrp3阻害剤としてのスルホニルウレアおよびスルホニルチオウレア |
| CN110997662B (zh) | 2017-08-21 | 2023-10-31 | 默克专利股份公司 | 作为腺苷受体拮抗剂的苯并咪唑衍生物 |
| CN110526898A (zh) | 2018-05-25 | 2019-12-03 | 北京诺诚健华医药科技有限公司 | 3-吲唑啉酮类化合物、其制备方法及其在医药学上的应用 |
| CN110563722A (zh) | 2018-06-06 | 2019-12-13 | 上海青煜医药科技有限公司 | 吡啶或哒嗪并环化合物及其应用 |
| WO2020021015A1 (en) | 2018-07-26 | 2020-01-30 | Esteve Pharmaceuticals, S.A. | New imidazopyridine derivatives for treating pain and pain related conditions |
| US12453279B2 (en) | 2018-08-22 | 2025-10-21 | Universal Display Corporation | Organic electroluminescent materials and devices |
| WO2020163248A1 (en) | 2019-02-04 | 2020-08-13 | Skyhawk Therapeutics, Inc. | Methods and compositions for modulating splicing |
| KR102721075B1 (ko) | 2019-02-15 | 2024-10-24 | 삼성전자주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| UY38687A (es) * | 2019-05-17 | 2023-05-15 | Novartis Ag | Inhibidores del inflamasoma nlrp3, composiciones, combinaciones de los mismos y métodos para su uso |
| US11618751B1 (en) | 2022-03-25 | 2023-04-04 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives |
| WO2021193897A1 (ja) * | 2020-03-27 | 2021-09-30 | アステラス製薬株式会社 | 置換ピリダジン化合物 |
| KR20230016658A (ko) | 2020-05-28 | 2023-02-02 | 얀센 파마슈티카 엔.브이. | 화합물 |
| JP2023530627A (ja) | 2020-06-09 | 2023-07-19 | パルデス バイオサイエンシーズ, インコーポレイテッド | システインプロテアーゼの阻害剤及びその使用方法 |
| 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 |
| TN2023000250A1 (en) | 2021-04-07 | 2025-07-02 | Forma Therapeutics Inc | Inhibiting ubiquitin-specific protease 1 (usp1) |
| US11319319B1 (en) * | 2021-04-07 | 2022-05-03 | Ventus Therapeutics U.S., Inc. | Compounds for inhibiting NLRP3 and uses thereof |
| CA3218212A1 (en) | 2021-04-28 | 2022-11-03 | Astellas Pharma Inc. | Substituted triazine compound |
| AU2022263621A1 (en) | 2021-04-29 | 2023-12-14 | Janssen Pharmaceutica Nv | Phthalazinone derivatives as nlrp3 inflammasome inhibitors |
| CR20230529A (es) | 2021-05-12 | 2023-12-04 | Hoffmann La Roche | Inhibidores de nlrp3 |
| TW202313577A (zh) | 2021-06-04 | 2023-04-01 | 瑞士商赫孚孟拉羅股份公司 | 新穎化合物 |
| WO2022253326A1 (zh) | 2021-06-05 | 2022-12-08 | 药捷安康(南京)科技股份有限公司 | Nlrp3炎症小体抑制剂及其应用 |
| JP2024529839A (ja) | 2021-06-29 | 2024-08-14 | 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 |
| EP4363406B1 (en) | 2021-07-02 | 2025-09-10 | Astrazeneca AB | Nlrp3 inflammasome inhibitors |
| WO2023283256A1 (en) | 2021-07-09 | 2023-01-12 | Aligos Therapeutics, Inc. | Anti-viral compounds |
| CA3226995A1 (en) | 2021-07-21 | 2023-01-26 | Nico Therapeutics, Inc. | Annulated pyridazine compound |
| JP2024534162A (ja) | 2021-08-25 | 2024-09-18 | ピーティーシー セラピューティクス, インコーポレイテッド | Nlrp3の阻害剤 |
| KR20240052009A (ko) | 2021-08-25 | 2024-04-22 | 자이두스 라이프사이언시즈 리미티드 | 신경염증성 장애의 치료 |
| WO2023028536A1 (en) | 2021-08-25 | 2023-03-02 | Ptc Therapeutics, Inc. | 1,2,4-triazine derivatives useful as inhibitors of nlrp3 |
| EP4410787A4 (en) | 2021-09-30 | 2025-10-15 | Origiant Pharmaceutical Co Ltd | PHARMACEUTICAL USE AND PROCESS FOR PREPARING A SUBSTITUTED HETEROARYL-PHTHALAZINE DERIVATIVE |
| AU2022369332A1 (en) | 2021-10-19 | 2024-02-08 | F. Hoffmann-La Roche Ag | Fused bicyclic heteroaryl compounds useful as nlrp3 inhibitors |
| EP4421068A1 (en) | 2021-10-22 | 2024-08-28 | Zhejiang Aixplorer Biotech Co., Ltd. | Nitrogen-containing compound, preparation method therefor and application thereof |
| EP4433480A1 (en) | 2021-11-17 | 2024-09-25 | F. Hoffmann-La Roche AG | Heterocyclic nlrp3 inhibitors |
| AR127704A1 (es) | 2021-11-19 | 2024-02-21 | Hoffmann La Roche | Derivados de piridazina inhibidores de nlrp3 |
| WO2023129987A1 (en) | 2021-12-29 | 2023-07-06 | Neumora Therapeutics, Inc. | Pyridazine derivatives as modulators of nlrp3 inflammasome and related methods |
| CA3246797A1 (en) | 2022-01-07 | 2025-07-08 | Transthera Sciences Nanjing Inc | NUCLEOTIDE-BINDING OLIGOMERIZATION DOMAIN 3 INFLAMMASOME INHIBITOR, A LEUCINE-RICH REPEATING DOMAIN AND A PYRINE-CONTAINING DOMAIN, AND RELATED USES |
| CN116726020A (zh) | 2022-03-08 | 2023-09-12 | 上海拓界生物医药科技有限公司 | 一类含哒嗪的化合物的药物组合物及其医药用途 |
| WO2023178099A1 (en) | 2022-03-15 | 2023-09-21 | Zomagen Biosciences Ltd | Nlrp3 modulators |
| CN119137121A (zh) | 2022-03-25 | 2024-12-13 | 万特斯治疗美国公司 | 可用作NLRP3衍生物的吡啶并-[3,4-d]哒嗪胺衍生物 |
| AU2023245348A1 (en) | 2022-03-31 | 2024-09-12 | Hangzhou Highlightll Pharmaceutical Co., Ltd | Nlrp3 inflammasome inhibitors |
| AR129012A1 (es) | 2022-04-07 | 2024-07-03 | Takeda Pharmaceuticals Co | Derivados de piridazina fusionados |
| CN116969920A (zh) | 2022-04-29 | 2023-10-31 | 上海辉启生物医药科技有限公司 | 稠合哒嗪衍生物及其制备方法与医药用途 |
| JP2025517702A (ja) | 2022-05-13 | 2025-06-10 | ニューモラ セラピューティクス インコーポレイテッド | Nlrp3インフラマソームのモジュレーターならびに関連製品および方法 |
| WO2023232917A1 (en) | 2022-06-03 | 2023-12-07 | F. Hoffmann-La Roche Ag | Novel compounds |
| WO2024006559A1 (en) | 2022-07-01 | 2024-01-04 | Neumora Therapeutics, Inc. | Modulators of nlrp3 inflammasome and related products and methods |
| KR20250036233A (ko) | 2022-07-14 | 2025-03-13 | 에이씨 이뮨 에스에이 | Nlrp3 인플라마좀 경로의 조절제로서의 피롤로트리아진 및 이미다조트리아진 유도체 |
| CN119546599A (zh) | 2022-07-14 | 2025-02-28 | 南京明德新药研发有限公司 | 氘取代的哒嗪苯并噻吩化合物及其应用 |
| WO2024017924A1 (en) | 2022-07-21 | 2024-01-25 | F. Hoffmann-La Roche Ag | Nlrp3 inhibitors |
| US20240101563A1 (en) | 2022-07-28 | 2024-03-28 | Ac Immune Sa | Novel compounds |
| UY40374A (es) | 2022-08-03 | 2024-02-15 | Novartis Ag | Inhibidores de inflamasoma nlrp3 |
| JP2025526692A (ja) | 2022-08-10 | 2025-08-15 | 武田薬品工業株式会社 | 複素環式化合物 |
| CN116789674B (zh) | 2022-08-24 | 2024-05-24 | 杭州高光制药有限公司 | Nlrp3炎性小体抑制剂 |
| WO2024064245A1 (en) | 2022-09-23 | 2024-03-28 | Merck Sharp & Dohme Llc | Phthalazine derivatives useful as inhibitors of nod-like receptor protein 3 |
| CN120152974A (zh) | 2022-10-26 | 2025-06-13 | 天维生物制药有限公司 | 缩环哒嗪衍生物 |
| US12331048B2 (en) | 2022-10-31 | 2025-06-17 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors |
| TW202419449A (zh) | 2022-10-31 | 2024-05-16 | 美商凡特斯治療美國公司 | 可用作nlrp3抑制劑之橋接雙環雜環烷基吡啶并-〔3,4-d〕噠嗪胺衍生物 |
| EP4611743A1 (en) | 2022-11-02 | 2025-09-10 | Merck Sharp & Dohme LLC | Triazines useful as inhibitors of nod-like receptor protein 3 |
| CN121045190A (zh) | 2022-11-04 | 2025-12-02 | 药捷安康(南京)科技股份有限公司 | Nlrp3炎症小体抑制剂及其应用 |
| WO2024094150A1 (en) | 2022-11-04 | 2024-05-10 | Insilico Medicine Ip Limited | Nlrp3 inflammasome inhibitors and uses thereof |
| EP4615830A1 (en) | 2022-11-09 | 2025-09-17 | F. Hoffmann-La Roche AG | Triazinone derivatives as nlrp3 inhibitors |
| JP2025537237A (ja) | 2022-11-09 | 2025-11-14 | エフ. ホフマン-ラ ロシュ アーゲー | Nlrp3阻害剤としてのトリアジノン誘導体 |
| AR130984A1 (es) | 2022-11-09 | 2025-02-05 | Hoffmann La Roche | Compuestos novedosos |
| CN118056822A (zh) | 2022-11-18 | 2024-05-21 | 正大天晴药业集团股份有限公司 | 一种哒嗪并环化合物及其用途 |
| WO2024109922A1 (zh) | 2022-11-25 | 2024-05-30 | 成都赜灵生物医药科技有限公司 | 桥环并哒嗪类化合物及其用途 |
| CN120322432A (zh) | 2022-12-07 | 2025-07-15 | 豪夫迈·罗氏有限公司 | 作为nlrp3抑制的调节剂的新颖化合物 |
| AR131282A1 (es) | 2022-12-08 | 2025-03-05 | Hoffmann La Roche | Compuestos novedosos |
| EP4637746A1 (en) | 2022-12-19 | 2025-10-29 | Merck Sharp & Dohme LLC | 6,6 bicyclic heterocyles useful as inhibitors of nod-like receptor protein 3 |
| EP4638434A1 (en) | 2022-12-23 | 2025-10-29 | Neumora Therapeutics, Inc. | Modulators of nlrp3 inflammasome and related products and methods |
| CN120379995A (zh) | 2022-12-27 | 2025-07-25 | 正大天晴药业集团股份有限公司 | 一种哒嗪稠芳环化合物及其用途 |
| TW202440107A (zh) | 2022-12-28 | 2024-10-16 | 瑞典商阿斯特捷利康公司 | Nlrp3炎症小體抑制劑 |
| EP4644380A1 (en) | 2022-12-28 | 2025-11-05 | Changchun Genescience Pharmaceutical Co., Ltd. | Pyridazine nlrp3 inhibitor compound, pharmaceutical composition, and preparation method therefor and use thereof |
| WO2024145623A1 (en) | 2022-12-30 | 2024-07-04 | Ptc Therapeutics, Inc. | Heterocyclic and heteroaryl compounds as inhibitors of nlrp3 |
| CN120813345A (zh) | 2023-01-03 | 2025-10-17 | 科达制药 | 作为nlrp3抑制剂的有机化合物 |
| KR20250152599A (ko) | 2023-01-31 | 2025-10-23 | 얀센 파마슈티카 엔브이 | NLRP3 억제제로서의 [1,2,4]트라이아졸로[4,3-a]피리딘 및 [1,2,4]트라이아졸로[4,3-a]피라진 |
| AU2024213537A1 (en) | 2023-01-31 | 2025-09-11 | Janssen Pharmaceutica Nv | Imidazo[1,2-d][1,2,4]triazines as nlrp3 inhibitors |
| WO2024160691A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | PYRROLO[1,2-d][1,2,4]TRIAZINES AND PYRAZOLO[1,5-d] [1,2,4]TRIAZINES AS NLRP3 INHIBITORS |
| WO2024160690A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | 2-(pyridazin-3-yl)-5-(trifluoromethyl)phenols as nlrp3 inhibitors |
| CN121001996A (zh) | 2023-01-31 | 2025-11-21 | 詹森药业有限公司 | 作为nlrp3抑制剂的吡啶-2(1h)-酮和嘧啶-4(3h)-酮 |
-
2021
- 2021-11-17 US US17/528,928 patent/US11319319B1/en active Active
-
2022
- 2022-02-24 US US17/679,898 patent/US20220340567A1/en not_active Abandoned
- 2022-04-07 CN CN202280026912.9A patent/CN117500792A/zh active Pending
- 2022-04-07 CA CA3214676A patent/CA3214676A1/en active Pending
- 2022-04-07 BR BR112023020483A patent/BR112023020483A2/pt unknown
- 2022-04-07 JP JP2023561765A patent/JP7620120B2/ja active Active
- 2022-04-07 AU AU2022256052A patent/AU2022256052B2/en active Active
- 2022-04-07 IL IL308378A patent/IL308378A/en unknown
- 2022-04-07 EP EP22719717.5A patent/EP4320102A1/en active Pending
- 2022-04-07 KR KR1020237037922A patent/KR20230167394A/ko active Pending
- 2022-04-07 TW TW111113264A patent/TW202304905A/zh unknown
- 2022-04-07 IL IL307303A patent/IL307303A/en unknown
- 2022-04-07 MX MX2023011576A patent/MX2023011576A/es unknown
- 2022-04-07 WO PCT/US2022/023893 patent/WO2022216971A1/en not_active Ceased
- 2022-04-07 EP EP23208386.5A patent/EP4331668A3/en active Pending
- 2022-04-07 EP EP25153415.2A patent/EP4537900A3/en active Pending
- 2022-04-07 PE PE2023002788A patent/PE20240765A1/es unknown
- 2022-04-07 CN CN202311481151.9A patent/CN117510495A/zh active Pending
- 2022-10-26 US US17/974,342 patent/US12351578B2/en active Active
-
2023
- 2023-09-29 MX MX2024000820A patent/MX2024000820A/es unknown
- 2023-10-03 US US18/480,164 patent/US12410167B2/en active Active
- 2023-10-04 CL CL2023002973A patent/CL2023002973A1/es unknown
- 2023-10-04 US US18/480,925 patent/US12441728B2/en active Active
- 2023-10-06 CO CONC2023/0013356A patent/CO2023013356A2/es unknown
- 2023-11-07 JP JP2023190081A patent/JP2024050527A/ja active Pending
- 2023-11-07 AU AU2023263450A patent/AU2023263450C1/en active Active
- 2023-12-11 US US18/534,906 patent/US20240158396A1/en not_active Abandoned
-
2024
- 2024-06-26 CL CL2024001964A patent/CL2024001964A1/es unknown
- 2024-07-03 US US18/763,302 patent/US20240368160A1/en not_active Abandoned
- 2024-07-03 US US18/763,243 patent/US12281112B2/en active Active
- 2024-07-03 US US18/763,258 patent/US12312350B2/en active Active
- 2024-09-20 US US18/891,602 patent/US20250250270A1/en active Pending
-
2025
- 2025-08-08 AU AU2025213656A patent/AU2025213656A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CL2023002973A1 (es) | Compuestos para la inhibición de nlrp3 y usos de estos. | |
| CO2022018811A2 (es) | Inhibidores de la proteína kras g12c y usos de estos | |
| ECSP23054131A (es) | Cocristal de un inhibidor de cdk | |
| UY40021A (es) | Inhibidores lisina acetiltransferasa 6a (kat6a) y usos de los mismos | |
| CO2023010023A2 (es) | Inhibidores de cdk2 y métodos de uso de los mismos | |
| CO2024005925A2 (es) | Moléculas pequeñas para el tratamiento del cáncer | |
| CO2022011258A2 (es) | Pirazolo-pirimidinas sustituidas y usos de las mismas | |
| UY40587A (es) | Inhibidores del inflamasoma nlrp3 | |
| MX2025010799A (es) | Inhibidores de acilsulfonamida para lisina acetiltransferasa 6a (kat6a) | |
| CO2025003090A2 (es) | Compuestos de piridinona sustituida como inhibidores de cbl-b | |
| CL2023001637A1 (es) | Inhibidores de la vía jak1 para el tratamiento del vitíligo. | |
| UY40772A (es) | Inhibidores de wrn | |
| BR112023017371A2 (pt) | Compostos que têm ((3-nitrofenil)sulfonil)acetamida como inibidores de bcl-2 | |
| ECSP23091984A (es) | Compuestos y usos de estos | |
| MX2025008741A (es) | Inhibidores de la proteina 3 que contiene los dominios nod, lrr y pirina (nlrp3) | |
| MX2025005720A (es) | Inhibidores de la tirosina-cinasa 2 (tyk2) | |
| BR112020026507A8 (pt) | Composto de isotiazolo[5,4-d]pirimidinas como inibidor de irak4 | |
| BR112023017344A2 (pt) | Compostos que têm tetra-hidroindolizina-1-carboxamida como inibidores de bcl-2 | |
| CO2024017422A2 (es) | Composiciones y métodos para inhibir la expresión de serina proteasa transmembrana 6 (tmprss6) | |
| CL2021000282A1 (es) | Inhibidores de ckd8/19 | |
| MX2023000198A (es) | Inhibidores de atr y usos de estos. | |
| CO2024012770A2 (es) | Inhibidores de proteínas de unión a emopamilo y usos de estos | |
| ECSP24007193A (es) | Compuestos pirimidínicos para usar como inhibidores de map4k1 | |
| UY38133A (es) | Nuevos inhibidores de cdk8/19 | |
| UY40353A (es) | Inhibidores de proteína de unión a emopamil y usos de estos |