CN117500792A - 用于抑制nlrp3的哒嗪化合物 - Google Patents
用于抑制nlrp3的哒嗪化合物 Download PDFInfo
- Publication number
- CN117500792A CN117500792A CN202280026912.9A CN202280026912A CN117500792A CN 117500792 A CN117500792 A CN 117500792A CN 202280026912 A CN202280026912 A CN 202280026912A CN 117500792 A CN117500792 A CN 117500792A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- aryl
- cycloalkyl
- compound
- membered heteroaryl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
Classifications
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- 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)
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202311481151.9A CN117510495A (zh) | 2021-04-07 | 2022-04-07 | 用于抑制nlrp3的哒嗪化合物 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202163171932P | 2021-04-07 | 2021-04-07 | |
| US63/171,932 | 2021-04-07 | ||
| US17/528,928 US11319319B1 (en) | 2021-04-07 | 2021-11-17 | Compounds for inhibiting NLRP3 and uses thereof |
| US17/528,928 | 2021-11-17 | ||
| PCT/US2022/023893 WO2022216971A1 (en) | 2021-04-07 | 2022-04-07 | Pyridazine compounds for inhibiting nlrp3 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202311481151.9A Division CN117510495A (zh) | 2021-04-07 | 2022-04-07 | 用于抑制nlrp3的哒嗪化合物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN117500792A true CN117500792A (zh) | 2024-02-02 |
Family
ID=81385286
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202280026912.9A Pending CN117500792A (zh) | 2021-04-07 | 2022-04-07 | 用于抑制nlrp3的哒嗪化合物 |
| CN202311481151.9A Pending CN117510495A (zh) | 2021-04-07 | 2022-04-07 | 用于抑制nlrp3的哒嗪化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202311481151.9A Pending CN117510495A (zh) | 2021-04-07 | 2022-04-07 | 用于抑制nlrp3的哒嗪化合物 |
Country Status (15)
| Country | Link |
|---|---|
| US (10) | US11319319B1 (enExample) |
| EP (3) | EP4331668A3 (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 |
| AU2022287224A1 (en) | 2021-06-04 | 2023-09-21 | F. Hoffmann-La Roche Ag | Triazine derivatives and their use in the treatment of cancer. |
| CN115433163A (zh) * | 2021-06-05 | 2022-12-06 | 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 |
| AR126351A1 (es) * | 2021-07-02 | 2023-10-11 | Astrazeneca Ab | Compuestos y sus sales inhibidores del inflamasoma nlrp3 |
| TW202319055A (zh) | 2021-07-21 | 2023-05-16 | 日商安斯泰來製藥股份有限公司 | 縮環噠嗪(pyridazine)化合物 |
| MX2024002342A (es) * | 2021-08-25 | 2024-05-20 | Ptc Therapeutics Inc | Inhibidores del nlrp3. |
| AU2022355409B2 (en) * | 2021-09-30 | 2025-10-16 | Origiant Pharmaceutical Co., Ltd. | Pharmaceutical use and preparation method for substituted heteroaryl phthalazine derivative |
| CN116102535A (zh) * | 2021-10-22 | 2023-05-12 | 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 |
| KR20250005125A (ko) * | 2022-03-25 | 2025-01-09 | 벤투스 테라퓨틱스 유에스 인코포레이티드 | NLRP3 유도체로서 유용한 피리도-[3,4-d]피리다진 아민 유도체 |
| CA3244129A1 (en) * | 2022-03-31 | 2023-10-05 | 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 |
| AU2023347443A1 (en) | 2022-09-23 | 2025-04-03 | Merck Sharp & Dohme Llc | Phthalazine derivatives useful as inhibitors of nod-like receptor protein 3 |
| 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 |
| TW202432551A (zh) | 2022-10-26 | 2024-08-16 | 日商安斯泰來製藥股份有限公司 | 稠環嗒嗪衍生物 |
| 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 |
| TW202419090A (zh) * | 2022-11-04 | 2024-05-16 | 大陸商藥捷安康(南京)科技股份有限公司 | Nlrp3炎症小體抑制劑及其應用 |
| 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 |
| TW202432558A (zh) * | 2022-12-27 | 2024-08-16 | 大陸商正大天晴藥業集團股份有限公司 | 一種噠嗪稠芳環化合物及其用途 |
| 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 |
| KR20250106322A (ko) * | 2022-12-28 | 2025-07-09 | 장춘 진사이언스 파마슈티컬 씨오., 엘티디. | 피리다진계 nlrp3 억제제 화합물, 약학 조성물 및 이의 제조 방법과 용도 |
| WO2024141534A1 (en) | 2022-12-28 | 2024-07-04 | Astrazeneca Ab | Crystalline forms of nlrp3 inflammasome inhibitors, chemical processes and chemical compounds |
| AU2024211840A1 (en) * | 2023-01-24 | 2025-07-03 | Daiichi Sankyo Company, Limited | Substituted benzene compound |
| EP4658654A1 (en) | 2023-01-31 | 2025-12-10 | 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 |
| EP4658649A1 (en) | 2023-01-31 | 2025-12-10 | Janssen Pharmaceutica NV | [1,2,4]triazolo[4,3-a]pyridines and [1,2,4]triazolo[4,3-a]pyrazines as nlrp3 inhibitors |
| EP4658640A1 (en) | 2023-01-31 | 2025-12-10 | Janssen Pharmaceutica NV | Pyridin-2(1h)-ones and pyrimidin-4(3h)-ones as nlrp3 inhibitors |
| WO2024160692A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | Imidazo[1,2-d][1,2,4]triazines as nlrp3 inhibitors |
| CN120435466A (zh) * | 2023-02-17 | 2025-08-05 | 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 |
| WO2024249539A1 (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 |
| US20250163060A1 (en) * | 2023-11-20 | 2025-05-22 | Ventus Therapeutics U.S., Inc. | Solid freebase forms of 5-chloro-2-(4-((2-hydroxy-2-methylpropyl)amino)pyrido[3,4-d]pyridazin-1-yl)phenol for inhibiting nlrp3 and uses thereof |
| WO2025128781A1 (en) | 2023-12-14 | 2025-06-19 | Merck Sharp & Dohme Llc | Azaindazole derivatives useful as inhibitors of nod-like receptor protein 3 |
| TW202535370A (zh) | 2023-12-14 | 2025-09-16 | 美商默沙東有限責任公司 | 作為nod樣受體蛋白3抑制劑之吲唑衍生物 |
| 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 |
|---|---|---|---|---|
| GB1293565A (en) | 1969-05-03 | 1972-10-18 | Aspro Nicholas Ltd | Aminophthalazines and pharmaceutical compositions thereof |
| GB1303061A (enExample) * | 1969-05-03 | 1973-01-17 | ||
| 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 |
| DE69105572T2 (de) | 1990-03-30 | 1995-05-11 | Mitsubishi Chem Ind | 4-Phenylphthalazin-Derivate. |
| 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 |
| WO1996005176A1 (en) * | 1994-08-09 | 1996-02-22 | Eisai Co., Ltd. | Fused pyridazine compound |
| US5763263A (en) | 1995-11-27 | 1998-06-09 | Dehlinger; Peter J. | Method and apparatus for producing position addressable combinatorial libraries |
| WO1998007430A1 (en) * | 1996-08-20 | 1998-02-26 | 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 |
| AU5614198A (en) | 1996-12-18 | 1998-07-15 | 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 |
| AU765128B2 (en) | 1999-03-22 | 2003-09-11 | Bristol-Myers Squibb Company | Fused pyridopyridazine inhibitors of cGMP phosphodiesterase |
| DE60228478D1 (de) | 2001-11-30 | 2008-10-02 | Pfizer Prod Inc | Aryl-annellierte azapolyzyklische verbindungen |
| 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 |
| WO2006004589A2 (en) * | 2004-05-08 | 2006-01-12 | Neurogen Corporation | 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 |
| BRPI0617534A2 (pt) | 2005-09-23 | 2011-07-26 | Memory Pharm Corp | Composto, composição farmacêutica, método para a ativação/estimulação seletiva de receptores nicotínicos de a-7 em um paciente, método para o tratamento de um paciente que sofre de uma doença psicótica, uma doença neurodegenerativa que envolve uma disfunção do sistema colinérgico, e/ou uma condição de degeneração da memória e/ou da cognição, método para o tratamento de um paciente que sofre de demência e/ou uma outra condição com perda da memória, método para o tratamento de um paciente que sofre de degeneração da memória devida à degeneração cognitiva suave devida ao envelhecimento, mal de alzheimer, esquizofrenia, mal de parkinson, mal de huntington, mal de pick, mal de creutzfeldt-jakob, depressão, envelhecimento, trauma na cabeça, acidente vascular cerebral, hipoxia do cns, senilidade cerebral, demência de multiinfarto, hiv e/ou doença cardiovascular, método para o tratamento e/ou a prevenção da demência em um paciente com mal de alzheimer, método para o tratamento de um paciente para a retirada do álcool ou para o tratamento de um paciente com terapia anti-intoxicação, método para o tratamento de um paciente para conferir neuroproteção contra os danos associados com acidentes vasculares cerebrais e isquemia e excitotoxicidade induzida por glutamato, método para o tratamento de um paciente que sofre de vício de nicotina, dor, tontura de fuso horário, obesidade e/ou diabetes, método de indução de um paciente a parar de fumar, método para o tratamento de um paciente que sofre de degeneração cognitiva suave (mci), demência vascular (vad), declínio cognitivo associado com a idade (aacd), amnésia associada com a cirurgia de coração aberto, apreensão cardíaca, anestesia geral, déficits da memória devido à exposição a agentes anestésicos(...) |
| US8106066B2 (en) | 2005-09-23 | 2012-01-31 | 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 |
| US7666898B2 (en) | 2005-11-03 | 2010-02-23 | Ilypsa, Inc. | Multivalent indole compounds and use thereof as phospholipase-A2 inhibitors |
| CA2627349A1 (en) | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Azaindole 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 |
| US7560551B2 (en) | 2006-01-23 | 2009-07-14 | Amgen Inc. | Aurora kinase modulators and method of use |
| CA2637658C (en) | 2006-01-23 | 2012-07-17 | Amgen Inc. | Aurora kinase modulators and method of use |
| JP2009526798A (ja) | 2006-02-16 | 2009-07-23 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 二環式ビスアミド構造を含む殺虫剤 |
| AU2007283401A1 (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 |
| AU2008248165B2 (en) | 2007-05-04 | 2011-12-08 | Amgen Inc. | Diazaquinolones that inhibit prolyl hydroxylase activity |
| US9023490B2 (en) | 2007-06-15 | 2015-05-05 | Versitech Limited | Extended pi-conjugated platinum (II) complexes |
| AU2008300019A1 (en) | 2007-09-07 | 2009-03-19 | Amgen Inc. | Annelated pyridazines for the treatment of tumors driven by inappropriate hedgehog signalling |
| US20090082358A1 (en) | 2007-09-20 | 2009-03-26 | Nobuko Nishimura | Vanilloid receptor ligands and their use in treatments |
| WO2009079008A1 (en) | 2007-12-19 | 2009-06-25 | Yangbo Feng | Benzopyrans and analogs as rho kinase inhibitors |
| AU2008345225A1 (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 |
| CN102066361B (zh) | 2008-04-11 | 2014-08-06 | 密歇根大学董事会 | 杂芳基取代的双环的smac模拟物及其用途 |
| AU2009246626A1 (en) | 2008-05-15 | 2009-11-19 | Merck Sharp & Dohme Corp. | Oxazolobenzimidazole derivatives |
| BRPI0915064B8 (pt) | 2008-06-16 | 2021-05-25 | Merck Patent Gmbh | derivados de quinoxalinadiona, seus usos, e medicamentos |
| 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 |
| AU2009296931A1 (en) | 2008-09-26 | 2010-04-01 | Merck Sharp & Dohme Corp. | Oxazolobenzimidazole derivatives |
| CA2754058A1 (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 |
| BRPI1006543A2 (pt) | 2009-04-01 | 2015-08-25 | Basf Se | "compostos de isoxazolina, composição agrícola, composição veterinária, uso de composto, método para o controle de pragas invertebradas, material de propagação de plantas e método para o tratamento, controle, prevenção ou proteção de animais contra infestação ou infecção por parasitas" |
| WO2010117936A1 (en) | 2009-04-06 | 2010-10-14 | Schering Corporation | Combinations of a hcv inhibitor such as bicyclic pyrrole derivatives and a therapeutic agent |
| US9593108B2 (en) | 2009-04-06 | 2017-03-14 | Ptc Therapeutics, Inc. | Compounds and methods for antiviral treatment |
| EA201270051A1 (ru) | 2009-06-25 | 2012-05-30 | Амген Инк. | Гетероциклические соединения и их применения |
| US8981087B2 (en) | 2009-07-29 | 2015-03-17 | Karus Therapeutics Limited | Benzo [E] [1,3] oxazin-4-one derivatives as phosphoinositide 3-kinase inhibitors |
| EP2789615B1 (en) | 2009-08-11 | 2017-05-03 | 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 |
| EP2571876B1 (en) | 2010-05-21 | 2016-09-07 | Merck Sharp & Dohme Corp. | Substituted seven-membered heterocyclic compounds as dipeptidyl peptidase-iv inhibitors for the treatment of diabetes |
| AU2011273931B2 (en) | 2010-06-28 | 2015-04-23 | Merck Patent Gmbh | 2,4- diaryl - substituted [1,8] naphthyridines as kinase inhibitors for use against cancer |
| AU2011271462A1 (en) | 2010-06-30 | 2013-01-10 | Amgen Inc. | Nitrogen containing heterocyclic compounds as PIK3 -delta inhibitors |
| AU2011302216A1 (en) | 2010-09-14 | 2013-04-04 | Exelixis, Inc. | Phtalazine derivatives as JAK1 inhibitors |
| WO2012041814A1 (en) | 2010-09-27 | 2012-04-05 | 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 |
| MX2013013211A (es) | 2011-05-18 | 2014-02-20 | Syngenta Participations Ag | Compuestos insecticidas a base de derivados de ariltioacetamida. |
| CA2844469C (en) | 2011-08-08 | 2019-08-20 | Merck Patent Gmbh | N-(benzimimdazol-2-yl)-cyclopropane carboxamides as lysophosphatidic acid antagonists |
| 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 |
| CN107011342A (zh) | 2012-05-22 | 2017-08-04 | 伊莱利利公司 | 用于检测神经功能障碍的基于咔啉和咔唑的成像剂 |
| 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 |
| WO2014079935A1 (en) | 2012-11-21 | 2014-05-30 | Syngenta Participations Ag | Insecticidal compounds based on arylthioacetamide derivatives |
| US9765039B2 (en) | 2012-11-21 | 2017-09-19 | Zenith Epigenetics Ltd. | Biaryl derivatives as bromodomain inhibitors |
| 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 |
| DK3126330T3 (en) | 2014-04-04 | 2019-04-23 | Pfizer | BICYCLE-FUSED HETEROARYL OR ARYL COMPOUNDS AND USE THEREOF AS IRAC4 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 |
| RU2021100040A (ru) | 2014-12-22 | 2021-02-02 | Акарна Терапьютикс, Лтд. | Конденсированные бициклические соединения для лечения заболевания |
| WO2016123796A1 (en) | 2015-02-06 | 2016-08-11 | Abbvie Inc. | Substituted phthalazines |
| AU2016222278B2 (en) | 2015-02-16 | 2020-07-09 | The Provost, Fellows, Foundation Scholars, And The Other Members Of Board, Of The College Of The Holy And Undivided Trinity Of Queen Elizabeth Near Dublin | Sulfonylureas and related compounds and use of same |
| EA201800367A1 (ru) | 2015-12-10 | 2019-02-28 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Способы лечения болезни хантингтона |
| FR3046933B1 (fr) | 2016-01-25 | 2018-03-02 | Galderma Research & Development | Inhibiteurs nlrp3 pour le traitement des pathologies cutanees inflammatoires |
| EP3414244A4 (en) | 2016-02-12 | 2019-11-27 | Pharmaxis Ltd. | HALOALLYLAMININDOL AND AZAINDOLDERIVATINHIBITORS OF LYSYL OXIDASES AND USES THEREOF |
| JP2019512009A (ja) | 2016-02-16 | 2019-05-09 | ザ・ユニバーシティ・オブ・クイーンズランド | スルホニルウレアおよび関連化合物ならびにこれらの利用 |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP3236267B1 (en) | 2016-04-18 | 2021-09-08 | Roche Diagnostics GmbH | Decapper and apparatus |
| ES2940611T3 (es) | 2016-04-18 | 2023-05-09 | Novartis Ag | Compuestos y composiciones para el tratamiento de afecciones asociadas a la actividad de NLRP |
| ES2855732T3 (es) | 2016-04-18 | 2021-09-24 | Novartis Ag | Compuestos y composiciones para tratar afecciones asociadas con la actividad de NLRP |
| 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 |
| KR102507847B1 (ko) * | 2016-10-28 | 2023-03-08 | 서울대학교병원 | 페닐 프탈라진 유도체, 이의 제조 방법 및 이를 포함하는 약학적 조성물 |
| WO2018138050A1 (de) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| CA3050309A1 (en) | 2017-01-31 | 2018-08-09 | Arvinas Operations, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
| WO2018172925A1 (en) | 2017-03-23 | 2018-09-27 | Vitas Pharma Research Pvt Ltd | Inhibitors of dna gyrase for treatment of bacterial infections |
| WO2018174678A1 (ko) | 2017-03-24 | 2018-09-27 | 희성소재(주) | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
| KR101943428B1 (ko) | 2017-03-24 | 2019-01-30 | 엘티소재주식회사 | 유기 발광 소자 및 유기 발광 소자의 유기물층용 조성물 |
| JOP20190272A1 (ar) | 2017-05-22 | 2019-11-21 | Amgen Inc | مثبطات kras g12c وطرق لاستخدامها |
| CN110869357A (zh) | 2017-05-25 | 2020-03-06 | 亚瑞克西斯制药公司 | 化合物及其用于治疗癌症的使用方法 |
| 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 |
| US11530225B2 (en) | 2017-07-20 | 2022-12-20 | Lg Chem, Ltd. | Compound and organic light-emitting diode comprising same |
| CA3071150A1 (en) | 2017-08-15 | 2019-02-21 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as nlrp3 inhibitors |
| JP7287952B2 (ja) | 2017-08-21 | 2023-06-06 | 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 | アデノシン受容体アンタゴニストとしてのベンズイミダゾール誘導体 |
| 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 |
| JP7682096B2 (ja) | 2019-02-04 | 2025-05-23 | スカイホーク・セラピューティクス・インコーポレーテッド | スプライシングを調節するための方法および組成物 |
| KR102721075B1 (ko) | 2019-02-15 | 2024-10-24 | 삼성전자주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| AR119731A1 (es) * | 2019-05-17 | 2022-01-05 | Novartis Ag | Inhibidores del inflamasoma nlrp3 |
| US11618751B1 (en) | 2022-03-25 | 2023-04-04 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives |
| AR121669A1 (es) * | 2020-03-27 | 2022-06-29 | Astellas Pharma Inc | Compuesto de piridazina sustituida |
| CN115667225A (zh) | 2020-05-28 | 2023-01-31 | 詹森药业有限公司 | 化合物 |
| BR112021023814A2 (pt) | 2020-06-09 | 2022-12-20 | Pardes Biosciences Inc | Inibidores de proteases de cisteína e métodos de uso das mesmas |
| US20240391895A1 (en) | 2020-12-25 | 2024-11-28 | Tuojie Biotech (Shanghai) Co., Ltd. | Pyridazine-containing compound and medicinal use thereof |
| US20240166610A1 (en) | 2021-02-08 | 2024-05-23 | Medshine Discovery Inc. | Substituted pyridazine phenol derivatives |
| KR20230167071A (ko) | 2021-04-07 | 2023-12-07 | 포르마 세라퓨틱스 인크. | 유비퀴틴-특이적 프로테아제 1 (usp1)의 억제 |
| US11319319B1 (en) | 2021-04-07 | 2022-05-03 | Ventus Therapeutics U.S., Inc. | Compounds for inhibiting NLRP3 and uses thereof |
| BR112023022451A2 (pt) | 2021-04-28 | 2024-01-02 | Astellas Pharma Inc | Composto triazina substituído |
| JP2024515817A (ja) | 2021-04-29 | 2024-04-10 | ヤンセン ファーマシューティカ エヌ.ベー. | Nlrp3インフラマソーム阻害剤としてのフタラジノン誘導体 |
| ES3031704T3 (en) | 2021-05-12 | 2025-07-10 | Hoffmann La Roche | Nlrp3 inhibitors |
| AU2022287224A1 (en) | 2021-06-04 | 2023-09-21 | F. Hoffmann-La Roche Ag | Triazine derivatives and their use in the treatment of cancer. |
| CN115433163A (zh) | 2021-06-05 | 2022-12-06 | 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 |
| WO2023278438A1 (en) | 2021-06-29 | 2023-01-05 | Zomagen Biosciences Ltd | Nlrp3 modulators |
| AR126351A1 (es) | 2021-07-02 | 2023-10-11 | Astrazeneca Ab | Compuestos y sus sales inhibidores del inflamasoma nlrp3 |
| CA3224494A1 (en) | 2021-07-09 | 2023-01-12 | Koen Vandyck | Anti-viral compounds |
| TW202319055A (zh) | 2021-07-21 | 2023-05-16 | 日商安斯泰來製藥股份有限公司 | 縮環噠嗪(pyridazine)化合物 |
| WO2023028536A1 (en) | 2021-08-25 | 2023-03-02 | Ptc Therapeutics, Inc. | 1,2,4-triazine derivatives useful as inhibitors of nlrp3 |
| CA3226855A1 (en) | 2021-08-25 | 2023-03-02 | Zydus Lifesciences Limited | Treatment for neuroinflammatory disorders |
| MX2024002342A (es) | 2021-08-25 | 2024-05-20 | Ptc Therapeutics Inc | Inhibidores del nlrp3. |
| AU2022355409B2 (en) | 2021-09-30 | 2025-10-16 | Origiant Pharmaceutical Co., Ltd. | Pharmaceutical use and preparation method for substituted heteroaryl phthalazine derivative |
| MX2024004503A (es) | 2021-10-19 | 2024-05-06 | Hoffmann La Roche | Compuestos heteroarilo biciclicos fusionados utiles como inhibidores de proteina 3 que contiene dominios de pirina (nlrp3). |
| CN116102535A (zh) | 2021-10-22 | 2023-05-12 | 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 |
| WO2023088856A1 (en) | 2021-11-17 | 2023-05-25 | F. Hoffmann-La Roche Ag | Heterocyclic nlrp3 inhibitors |
| JP2024540525A (ja) | 2021-11-19 | 2024-10-31 | エフ. ホフマン-ラ ロシュ アーゲー | Nlrp3の阻害剤としてのピリダジン誘導体 |
| WO2023129987A1 (en) | 2021-12-29 | 2023-07-06 | Neumora Therapeutics, Inc. | Pyridazine derivatives as modulators of nlrp3 inflammasome and related methods |
| MX2024008548A (es) | 2022-01-07 | 2024-07-19 | Transthera Sciences Nanjing Inc | Inhibidor del inflamosoma nlrp3 y uso del mismo. |
| 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 |
| AU2023234527A1 (en) | 2022-03-15 | 2024-10-31 | Zomagen Biosciences Ltd | Nlrp3 modulators |
| KR20250005125A (ko) | 2022-03-25 | 2025-01-09 | 벤투스 테라퓨틱스 유에스 인코포레이티드 | NLRP3 유도체로서 유용한 피리도-[3,4-d]피리다진 아민 유도체 |
| CA3244129A1 (en) | 2022-03-31 | 2023-10-05 | 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 |
| CN119546586A (zh) | 2022-05-13 | 2025-02-28 | 纽摩拉治疗公司 | Nlrp3炎症小体的调节剂和相关产品以及方法 |
| US20250353830A1 (en) | 2022-06-03 | 2025-11-20 | Hoffmann-La Roche Inc. | 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 |
| JP2025526423A (ja) | 2022-07-28 | 2025-08-13 | エーシー・イミューン・エス・アー | 新規化合物 |
| UY40374A (es) | 2022-08-03 | 2024-02-15 | Novartis Ag | Inhibidores de inflamasoma nlrp3 |
| WO2024033845A1 (en) | 2022-08-10 | 2024-02-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| 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 |
| AU2023347443A1 (en) | 2022-09-23 | 2025-04-03 | Merck Sharp & Dohme Llc | Phthalazine derivatives useful as inhibitors of nod-like receptor protein 3 |
| TW202432551A (zh) | 2022-10-26 | 2024-08-16 | 日商安斯泰來製藥股份有限公司 | 稠環嗒嗪衍生物 |
| 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 |
| WO2024097598A1 (en) | 2022-11-02 | 2024-05-10 | Merck Sharp & Dohme Llc | Triazines useful as inhibitors of nod-like receptor protein 3 |
| WO2024094150A1 (en) | 2022-11-04 | 2024-05-10 | Insilico Medicine Ip Limited | Nlrp3 inflammasome inhibitors and uses thereof |
| TW202419090A (zh) | 2022-11-04 | 2024-05-16 | 大陸商藥捷安康(南京)科技股份有限公司 | Nlrp3炎症小體抑制劑及其應用 |
| PE20251696A1 (es) | 2022-11-09 | 2025-07-02 | Hoffmann La Roche | Derivados de triazinona como inhibidores de nlrp3 |
| WO2024099993A1 (en) | 2022-11-09 | 2024-05-16 | F. Hoffmann-La Roche Ag | Triazinone derivatives as nlrp3 inhibitors |
| WO2024099996A1 (en) | 2022-11-09 | 2024-05-16 | F. Hoffmann-La Roche Ag | Triazinone derivatives as nlrp3 inhibitors |
| 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 |
| WO2024121086A1 (en) | 2022-12-07 | 2024-06-13 | F. Hoffmann-La Roche Ag | Novel compounds as modulators of nlrp3 inhibition |
| CN120303272A (zh) | 2022-12-08 | 2025-07-11 | 豪夫迈·罗氏有限公司 | Nlrp3的抑制剂 |
| 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 |
| TW202432558A (zh) | 2022-12-27 | 2024-08-16 | 大陸商正大天晴藥業集團股份有限公司 | 一種噠嗪稠芳環化合物及其用途 |
| KR20250106322A (ko) | 2022-12-28 | 2025-07-09 | 장춘 진사이언스 파마슈티컬 씨오., 엘티디. | 피리다진계 nlrp3 억제제 화합물, 약학 조성물 및 이의 제조 방법과 용도 |
| 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 |
| AU2023414924A1 (en) | 2022-12-30 | 2025-07-03 | Ptc Therapeutics, Inc. | Heterocyclic and heteroaryl compounds as inhibitors of nlrp3 |
| AU2024206808A1 (en) | 2023-01-03 | 2025-07-17 | Kodiak Sciences Inc. | Organic compounds as nlrp3 inhibitors |
| EP4658640A1 (en) | 2023-01-31 | 2025-12-10 | Janssen Pharmaceutica NV | Pyridin-2(1h)-ones and pyrimidin-4(3h)-ones as nlrp3 inhibitors |
| EP4658649A1 (en) | 2023-01-31 | 2025-12-10 | Janssen Pharmaceutica NV | [1,2,4]triazolo[4,3-a]pyridines and [1,2,4]triazolo[4,3-a]pyrazines as nlrp3 inhibitors |
| EP4658654A1 (en) | 2023-01-31 | 2025-12-10 | Janssen Pharmaceutica NV | Pyrrolo[1,2-d][1,2,4]triazines and pyrazolo[1,5-d] [1,2,4]triazines as nlrp3 inhibitors |
| WO2024160692A1 (en) | 2023-01-31 | 2024-08-08 | Janssen Pharmaceutica Nv | Imidazo[1,2-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 |
-
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 EP EP23208386.5A patent/EP4331668A3/en active Pending
- 2022-04-07 EP EP22719717.5A patent/EP4320102A1/en active Pending
- 2022-04-07 BR BR112023020483A patent/BR112023020483A2/pt unknown
- 2022-04-07 TW TW111113264A patent/TW202304905A/zh unknown
- 2022-04-07 IL IL308378A patent/IL308378A/en unknown
- 2022-04-07 KR KR1020237037922A patent/KR20230167394A/ko active Pending
- 2022-04-07 IL IL307303A patent/IL307303A/en unknown
- 2022-04-07 EP EP25153415.2A patent/EP4537900A3/en active Pending
- 2022-04-07 PE PE2023002788A patent/PE20240765A1/es unknown
- 2022-04-07 MX MX2023011576A patent/MX2023011576A/es unknown
- 2022-04-07 CN CN202280026912.9A patent/CN117500792A/zh active Pending
- 2022-04-07 AU AU2022256052A patent/AU2022256052B2/en active Active
- 2022-04-07 CA CA3214676A patent/CA3214676A1/en active Pending
- 2022-04-07 JP JP2023561765A patent/JP7620120B2/ja active Active
- 2022-04-07 CN CN202311481151.9A patent/CN117510495A/zh active Pending
- 2022-04-07 WO PCT/US2022/023893 patent/WO2022216971A1/en not_active Ceased
- 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 AU AU2023263450A patent/AU2023263450C1/en active Active
- 2023-11-07 JP JP2023190081A patent/JP2024050527A/ja active Pending
- 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 US18/763,258 patent/US12312350B2/en active Active
- 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
- 2024-09-20 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 |
|---|---|---|
| CN117500792A (zh) | 用于抑制nlrp3的哒嗪化合物 | |
| IL275058B2 (en) | Sulfonylurea derivatives as modulators of the NLRP3 inflammasome | |
| CN119137121A (zh) | 可用作NLRP3衍生物的吡啶并-[3,4-d]哒嗪胺衍生物 | |
| US12312351B2 (en) | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors | |
| HK40100030A (en) | Compounds for inhibiting nlrp3 and uses thereof | |
| KR20230157535A (ko) | Nlrp3을 저해하기 위한 피리다진 화합물 | |
| BR122024000756A2 (pt) | Compostos inibidores de nlrp3, derivado isotópico dos mesmos, composição farmacêutica que compreende os mesmos, bem como uso dos ditos compostos para tratar ou prevenir uma doença ou distúrbio relacionado a nlrp3 | |
| US20250346600A1 (en) | Tricyclic derivatives and related uses |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination |