MA55565A - Agents de dégradation de stat et leurs utilisations - Google Patents
Agents de dégradation de stat et leurs utilisationsInfo
- Publication number
- MA55565A MA55565A MA055565A MA55565A MA55565A MA 55565 A MA55565 A MA 55565A MA 055565 A MA055565 A MA 055565A MA 55565 A MA55565 A MA 55565A MA 55565 A MA55565 A MA 55565A
- Authority
- MA
- Morocco
- Prior art keywords
- stat
- degrading agents
- degrading
- agents
- stat degrading
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
- C07F9/65068—Five-membered rings having the nitrogen atoms in positions 1 and 3 condensed with carbocyclic rings or carbocyclic ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
- Steroid Compounds (AREA)
- Medicinal Preparation (AREA)
- Detergent Compositions (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962830095P | 2019-04-05 | 2019-04-05 | |
| US201962833331P | 2019-04-12 | 2019-04-12 | |
| US201962855259P | 2019-05-31 | 2019-05-31 | |
| US201962860512P | 2019-06-12 | 2019-06-12 | |
| US201962875362P | 2019-07-17 | 2019-07-17 | |
| US201962877051P | 2019-07-22 | 2019-07-22 | |
| US201962887872P | 2019-08-16 | 2019-08-16 | |
| US201962926127P | 2019-10-25 | 2019-10-25 | |
| US201962932957P | 2019-11-08 | 2019-11-08 | |
| US201962944810P | 2019-12-06 | 2019-12-06 | |
| US201962947310P | 2019-12-12 | 2019-12-12 | |
| US201962949053P | 2019-12-17 | 2019-12-17 | |
| US202062967921P | 2020-01-30 | 2020-01-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA55565A true MA55565A (fr) | 2022-02-09 |
Family
ID=72667015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA055565A MA55565A (fr) | 2019-04-05 | 2020-04-06 | Agents de dégradation de stat et leurs utilisations |
Country Status (15)
| Country | Link |
|---|---|
| US (4) | US11485750B1 (fr) |
| EP (1) | EP3946360A4 (fr) |
| JP (3) | JP2022527114A (fr) |
| KR (1) | KR102980990B1 (fr) |
| CN (2) | CN113939300A (fr) |
| AU (1) | AU2020253633A1 (fr) |
| BR (1) | BR112021019748A2 (fr) |
| CA (1) | CA3135802A1 (fr) |
| CO (1) | CO2021013339A2 (fr) |
| IL (2) | IL286969B2 (fr) |
| MA (1) | MA55565A (fr) |
| MX (1) | MX2021012216A (fr) |
| SG (1) | SG11202110829YA (fr) |
| TW (1) | TWI875749B (fr) |
| WO (1) | WO2020206424A1 (fr) |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019241766A1 (fr) * | 2018-06-15 | 2019-12-19 | City Of Hope | Chimère de ciblage de protéolyse à base d'oligonucléotides |
| AU2019389174A1 (en) | 2018-11-30 | 2021-07-01 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| WO2020205467A1 (fr) * | 2019-03-29 | 2020-10-08 | The Regents Of The University Of Michigan | Agents de dégradation de protéines stat3 |
| KR102980990B1 (ko) | 2019-04-05 | 2026-06-25 | 카이메라 쎄라퓨틱스 인코포레이티드 | Stat 분해제 및 이의 용도 |
| JP7424115B2 (ja) * | 2019-06-26 | 2024-01-30 | 住友化学株式会社 | エステル化合物の製造方法 |
| PH12022500002A1 (en) | 2019-06-28 | 2023-04-03 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
| US12558427B2 (en) | 2019-07-17 | 2026-02-24 | Kymera Therapeutics, Inc. | IRAK degraders and uses thereof |
| WO2021119159A1 (fr) | 2019-12-10 | 2021-06-17 | Kymera Therapeutics, Inc. | Agents de dégradation d'irak et leurs utilisations |
| CA3161878A1 (fr) | 2019-12-17 | 2021-06-24 | Matthew M. Weiss | Agents de degradation d'irak et leurs utilisations |
| AU2021238333A1 (en) * | 2020-03-17 | 2022-09-29 | Kymera Therapeutics, Inc. | STAT degraders and uses thereof |
| US12522623B2 (en) | 2020-03-26 | 2026-01-13 | Regents Of The University Of Michigan | Small molecule STAT protein degraders |
| US11988649B2 (en) * | 2020-10-06 | 2024-05-21 | Board Of Regents, The University Of Texas System | On-line suppressor |
| UY39671A (es) | 2021-03-15 | 2022-10-31 | Novartis Ag | Derivados de pirazolopiridina y sus usos. |
| CA3217792A1 (fr) | 2021-05-07 | 2022-11-10 | Kymera Therapeutics, Inc | Agents de degradation de cdk2 et leurs utilisations |
| CN115677831B (zh) * | 2021-07-22 | 2026-03-17 | 杭州和正医药有限公司 | 拟肽类stat降解药物、组合物及应用 |
| WO2023059792A1 (fr) * | 2021-10-06 | 2023-04-13 | C4 Thrapeutics, Inc. | Composés de dégradation de la protéine 3 non structurale de coronavirus |
| KR20240111312A (ko) * | 2021-10-25 | 2024-07-16 | 카이메라 쎄라퓨틱스 인코포레이티드 | Tyk2 분해제 및 이의 용도 |
| CA3239730A1 (fr) * | 2021-12-11 | 2023-06-15 | Christopher De Savi | Agents de degradation de stat3 et leurs utilisations |
| IL316050A (en) * | 2022-03-31 | 2024-11-01 | Recludix Pharma Inc | STAT modulators and their uses |
| CN114839372B (zh) * | 2022-04-29 | 2025-12-23 | 徐州医科大学附属医院 | 检测pSTAT3表达水平的试剂在鉴别PTCL-NOS与ALK-ALCL中的应用 |
| WO2023250058A1 (fr) * | 2022-06-22 | 2023-12-28 | Kymera Therapeutics, Inc. | Agents de dégradation de stat et leurs utilisations |
| WO2024064080A1 (fr) * | 2022-09-19 | 2024-03-28 | Kymera Therapeutics, Inc. | Agents de dégradation de stat6 et leurs utilisations |
| WO2024148041A1 (fr) * | 2023-01-04 | 2024-07-11 | Kymera Therapeutics, Inc. | Agents de dégradation de stat3 et leurs utilisations |
| KR20260019479A (ko) | 2023-05-04 | 2026-02-10 | 레볼루션 메디슨즈, 인크. | Ras 관련 질환 또는 장애를 위한 병용 요법 |
| EP4712960A2 (fr) * | 2023-05-15 | 2026-03-25 | Recludix Pharma, Inc. | Agents de dégradation de stat et leurs utilisations |
| WO2024251040A1 (fr) | 2023-06-09 | 2024-12-12 | 广州市联瑞制药有限公司 | Agent de dégradation de l'irak4 et son utilisation |
| TW202504587A (zh) * | 2023-06-12 | 2025-02-01 | 美商凱麥拉醫療公司 | Stat3降解劑及其用途 |
| WO2024263673A1 (fr) * | 2023-06-20 | 2024-12-26 | Regents Of The University Of Michigan | Composés et compositions en tant que ligands vhl et agents de dégradation de stat3 leurs utilisations |
| CN121889155A (zh) | 2023-08-07 | 2026-04-17 | 锐新医药公司 | 用于治疗ras蛋白相关疾病或病症的rmc-6291 |
| EP4759807A1 (fr) | 2023-08-11 | 2026-06-17 | Shenzhen Zhongge Biological Technology Co., Ltd. | Composé chimère ciblant la protéolyse pour dégrader irak4 et son utilisation |
| IL326621A (en) * | 2023-08-30 | 2026-04-01 | Kymera Therapeutics Inc | Stat6 degraders and uses thereof |
| AU2024360465A1 (en) | 2023-10-12 | 2026-04-09 | Revolution Medicines, Inc. | Macrocyclic ras inhibitors |
| WO2025106485A1 (fr) * | 2023-11-14 | 2025-05-22 | Kymera Therapeutics, Inc. | Agents de dégradation de stat3 destinés à être utilisés dans le traitement de la leucémie |
| WO2025103477A1 (fr) * | 2023-11-17 | 2025-05-22 | InventisBio Co., Ltd. | Composés, leurs procédés de préparation et leurs utilisations |
| WO2025128653A1 (fr) * | 2023-12-12 | 2025-06-19 | Kymera Therapeutics, Inc. | Agents de dégradation de stat3 et leurs procédés d'utilisation |
| AU2024406222A1 (en) | 2023-12-20 | 2026-06-04 | Bristol-Myers Squibb Company | Antibodies targeting il-18 receptor beta (il-18rβ) and related methods |
| WO2025147320A1 (fr) * | 2024-01-03 | 2025-07-10 | Kymera Therapeutics, Inc. | Inhibiteurs de stat6 et leurs utilisations |
| WO2025171296A1 (fr) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| TWI921181B (zh) * | 2024-04-30 | 2026-04-01 | 大陸商杭州百新生物醫藥科技有限公司 | 草醯胺類化合物及其在醫藥上的應用 |
| WO2025240847A1 (fr) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| US20250375445A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (fr) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Compositions thérapeutiques et procédés de gestion d'effets liés au traitement |
| WO2026006747A1 (fr) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026007994A1 (fr) * | 2024-07-03 | 2026-01-08 | 正大天晴药业集团股份有限公司 | Composé d'acide phosphonique et son utilisation |
| WO2026015801A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble liés à ras |
| WO2026015796A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble lié à ras |
| WO2026015790A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Méthodes de traitement d'une maladie ou d'un trouble lié à ras |
| WO2026015825A1 (fr) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Utilisation d'un inhibiteur de ras pour traiter le cancer du pancréas |
| WO2026021560A1 (fr) * | 2024-07-25 | 2026-01-29 | 杭州阿诺生物医药科技有限公司 | Agent de dégradation de protéine stat, son procédé de préparation et son utilisation |
| WO2026027675A1 (fr) | 2024-07-31 | 2026-02-05 | Guerra Gonzalez Carmen | Triple combinaison destinée à être utilisée dans le traitement du cancer |
| WO2026050446A1 (fr) | 2024-08-29 | 2026-03-05 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026072904A2 (fr) | 2024-09-26 | 2026-04-02 | Revolution Medicines, Inc. | Compositions et méthodes de traitement du cancer du poumon |
| WO2026080825A1 (fr) * | 2024-10-10 | 2026-04-16 | Revolution Medicines, Inc. | Synthèse d'inhibiteurs de ras |
| WO2026090116A2 (fr) | 2024-10-21 | 2026-04-30 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| US20260108528A1 (en) | 2024-10-22 | 2026-04-23 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2026090245A1 (fr) | 2024-10-22 | 2026-04-30 | Revolution Medicines, Inc. | Utilisation d'inhibiteurs ras pour traiter un cancer |
| WO2026106912A1 (fr) | 2024-11-12 | 2026-05-21 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026112260A1 (fr) | 2024-11-21 | 2026-05-28 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026122764A2 (fr) | 2024-12-06 | 2026-06-11 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026128688A2 (fr) | 2024-12-13 | 2026-06-18 | Revolution Medicines, Inc. | Inhibiteurs de ras |
| WO2026161839A1 (fr) | 2025-01-27 | 2026-07-30 | Revolution Medicines, Inc. | Inhibiteurs de ras |
Family Cites Families (193)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5516931A (en) | 1982-02-01 | 1996-05-14 | Northeastern University | Release tag compounds producing ketone signal groups |
| US5650270A (en) | 1982-02-01 | 1997-07-22 | Northeastern University | Molecular analytical release tags and their use in chemical analysis |
| US4709016A (en) | 1982-02-01 | 1987-11-24 | Northeastern University | Molecular analytical release tags and their use in chemical analysis |
| US4650750A (en) | 1982-02-01 | 1987-03-17 | Giese Roger W | Method of chemical analysis employing molecular release tag compounds |
| US5217866A (en) | 1985-03-15 | 1993-06-08 | Anti-Gene Development Group | Polynucleotide assay reagent and method |
| US5360811A (en) | 1990-03-13 | 1994-11-01 | Hoechst-Roussel Pharmaceuticals Incorporated | 1-alkyl-, 1-alkenyl-, and 1-alkynylaryl-2-amino-1,3-propanediols and related compounds as anti-inflammatory agents |
| JP3545461B2 (ja) | 1993-09-10 | 2004-07-21 | エーザイ株式会社 | 二環式ヘテロ環含有スルホンアミド誘導体 |
| WO1996007655A1 (fr) | 1994-09-06 | 1996-03-14 | Banyu Pharmaceutical Co., Ltd. | Nouveau derive de carbapenem |
| US6281230B1 (en) | 1996-07-24 | 2001-08-28 | Celgene Corporation | Isoindolines, method of use, and pharmaceutical compositions |
| US6306663B1 (en) | 1999-02-12 | 2001-10-23 | Proteinex, Inc. | Controlling protein levels in eucaryotic organisms |
| OA12118A (en) | 1999-12-10 | 2006-05-04 | Pfizer Prod Inc | PyrroloÄ2,3-dÜpyrimidine compounds. |
| DE10002509A1 (de) | 2000-01-21 | 2001-07-26 | Gruenenthal Gmbh | Substituierte Glutarimide |
| WO2001064681A2 (fr) | 2000-02-28 | 2001-09-07 | Sugen, Inc. | Composes de 3-(pyrolyllactone)-2-indolinone comme inhibiteurs des kinases |
| PE20020354A1 (es) | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
| AU2001295041A1 (en) | 2000-09-08 | 2002-03-22 | California Institute Of Technology | Proteolysis targeting chimeric pharmaceutical |
| US7208157B2 (en) | 2000-09-08 | 2007-04-24 | California Institute Of Technology | Proteolysis targeting chimeric pharmaceutical |
| US7998947B2 (en) | 2001-03-28 | 2011-08-16 | University Of South Florida | Materials and methods for treatment of cancer and identification of anti-cancer compounds |
| KR100833371B1 (ko) | 2001-04-27 | 2008-05-28 | 젠야쿠코교가부시키가이샤 | 헤테로시클릭 화합물 및 이를 유효 성분으로 하는 항종양제 |
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| MXPA05001766A (es) | 2002-08-14 | 2005-08-19 | Atugen Ag | Uso de proteina quinasa n beta. |
| WO2004089925A1 (fr) | 2003-04-03 | 2004-10-21 | Semafore Pharmaceuticals, Inc. | Promedicaments d'inhibiteurs de pi-3 kinase |
| ES2382377T3 (es) | 2003-05-30 | 2012-06-07 | Gemin X Pharmaceuticals Canada Inc. | Compuestos triheterocíclicos, composiciones, y métodos para tratar cáncer |
| WO2005007623A2 (fr) | 2003-07-03 | 2005-01-27 | The Trustees Of The University Of Pennsylvania | Inhibition de l'expression d'une syk kinase |
| EP2487156B1 (fr) | 2003-12-11 | 2014-07-16 | Board Of Regents The University Of Texas System | Composéspour traiter des maladies associées à une prolifération cellulaire |
| JP4398263B2 (ja) | 2004-01-13 | 2010-01-13 | 富士通株式会社 | 経路設計方法 |
| US7436318B2 (en) | 2004-04-19 | 2008-10-14 | Atg Designworks, Llc | Self contained device for displaying electronic information |
| LT2612862T (lt) | 2004-05-13 | 2017-01-25 | Icos Corporation | Chinazolinonai kaip žmogaus fosfatidilinozitol-3-kinazės delta inhibitoriai |
| US20060005147A1 (en) | 2004-06-30 | 2006-01-05 | Hammack Jason L | Methods and systems for controlling the display of maps aboard an aircraft |
| US20070010428A1 (en) | 2004-09-03 | 2007-01-11 | Mcmurray John S | Inhibitors of signal transduction and activator of transcription 3 |
| TWI309240B (en) | 2004-09-17 | 2009-05-01 | Hoffmann La Roche | Anti-ox40l antibodies |
| US7449458B2 (en) | 2005-01-19 | 2008-11-11 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
| JP2008535785A (ja) | 2005-02-25 | 2008-09-04 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | Stat3の小分子阻害剤およびその使用 |
| JP5238936B2 (ja) | 2005-03-25 | 2013-07-17 | ジーアイティーアール,インク. | Gitr結合分子およびその使用 |
| ES2493466T3 (es) | 2005-05-12 | 2014-09-11 | Abbvie Bahamas Ltd. | Promotores de la apoptosis |
| GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
| KR101704734B1 (ko) | 2005-07-01 | 2017-02-09 | 이. 알. 스퀴부 앤드 선즈, 엘.엘.씨. | 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날 항체 |
| US7402325B2 (en) | 2005-07-28 | 2008-07-22 | Phoenix Biotechnology, Inc. | Supercritical carbon dioxide extract of pharmacologically active components from Nerium oleander |
| US20080139456A1 (en) | 2005-09-30 | 2008-06-12 | Burke Terrence R | Macrocyclic Sh2 Domain Binding Inhibitors |
| HRP20140975T1 (hr) | 2005-10-07 | 2014-11-21 | Exelixis, Inc. | Derivati n-(3-amino-hinoksalin-2-il)-sulfonamida i njihova uporaba kao inhibitora fosfatidilinozitol 3-kinaze |
| BRPI0617364A2 (pt) | 2005-10-13 | 2011-07-26 | Orchid Res Lab Ltd | compostos heterocÍclicos como inibidores de pstat3/il-6 |
| WO2007053452A1 (fr) | 2005-11-01 | 2007-05-10 | Targegen, Inc. | Inhibiteurs de kinase de type biaryl-méta-pyrimidine |
| HUE028588T2 (hu) | 2005-12-13 | 2016-12-28 | Incyte Holdings Corp | Heteroaril-szubsztituált pirrolo[2,3-b]piridinek és pirrolo[2,3-b]pirimidinek mint Janus-kináz inhibitorok |
| US7622496B2 (en) | 2005-12-23 | 2009-11-24 | Zealand Pharma A/S | Modified lysine-mimetic compounds |
| JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
| KR101533461B1 (ko) | 2006-04-26 | 2015-07-02 | 에프. 호프만-라 로슈 아게 | Pi3k저해제로 유용한 티에노[3,2-d]피리미딘 유도체 |
| WO2007136858A2 (fr) | 2006-05-19 | 2007-11-29 | H. Lee Moffitt Cancer Center & Research Institute | Petites molécules inhibitrices de stat3 ayant une activité antitumorale |
| EP2529621B1 (fr) | 2006-09-22 | 2016-10-05 | Pharmacyclics LLC | Inhibiteurs de la tyrosine kinase de bruton |
| UA95978C2 (ru) | 2006-10-02 | 2011-09-26 | Оцука Фармас'Ютікел Ко., Лтд. | Ингибитор активации stat3/5 |
| WO2008067270A1 (fr) | 2006-11-27 | 2008-06-05 | Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Inhibiteurs de liaison au domaine grb2 sh2 macrocyclique |
| HUE029188T2 (en) | 2007-03-12 | 2017-03-28 | Ym Biosciences Australia Pty | Phenylamino-pyrimidine compounds and their use |
| US8394794B2 (en) | 2007-03-23 | 2013-03-12 | Regents Of The University Of Minnesota | Therapeutic compounds |
| EP1987839A1 (fr) | 2007-04-30 | 2008-11-05 | I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale | Anticorps monoclonal cytotoxique anti-LAG-3 et son utilisation pour le traitement ou la prévention d'un rejet de greffe d'organe et de maladies auto-immunes |
| PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
| WO2008156644A2 (fr) | 2007-06-14 | 2008-12-24 | Frank David A | Modulateurs de stat |
| PT2175884T (pt) | 2007-07-12 | 2016-09-21 | Gitr Inc | Terapias de combinação empregando moléculas de ligação a gitr |
| WO2009032338A1 (fr) | 2007-09-09 | 2009-03-12 | University Of Florida Research Foundation | Agents thérapeutiques à base d'apratoxine : mécanisme et procédés de traitement |
| EP2044949A1 (fr) | 2007-10-05 | 2009-04-08 | Immutep | Utilisation de lag-3 recombinant ou ses dérivatifs pour déclencher la réponse immune des monocytes |
| WO2009073620A2 (fr) | 2007-11-30 | 2009-06-11 | Newlink Genetics | Inhibiteurs de l'ido |
| FR2927330B1 (fr) | 2008-02-07 | 2010-02-19 | Sanofi Aventis | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii |
| MY165582A (en) | 2008-03-11 | 2018-04-05 | Incyte Holdings Corp | Azetidine and cyclobutane derivatives as jak inhibitors |
| JP2011518841A (ja) | 2008-04-24 | 2011-06-30 | ニューリンク ジェネティクス, インコーポレイテッド | Ido阻害剤 |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| ES2521676T3 (es) | 2008-07-08 | 2014-11-13 | Board Of Regents, The University Of Texas System | Nuevos agentes inhibidores de la proliferación y de la activación de transductores de señales y activadores de la transcripción (STATS) |
| AR072999A1 (es) | 2008-08-11 | 2010-10-06 | Medarex Inc | Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos |
| WO2010077589A2 (fr) | 2008-12-08 | 2010-07-08 | The Regents Of The University Of Michigan Office Of Technology Transfer | Inhibiteurs de stat3 et méthodes thérapeutiques les utilisant |
| MX356367B (es) | 2008-12-09 | 2018-05-25 | Genentech Inc | Anticuerpos anti-pd-l1 y su uso para mejorar la funcion de celulas t. |
| US8921037B2 (en) | 2008-12-16 | 2014-12-30 | Bo Han | PF4-depleted platelet rich plasma preparations and methods for hard and soft tissue repair |
| US8841257B2 (en) | 2009-04-10 | 2014-09-23 | Board Of Regents, The University Of Texas System | Inhibitors of STAT3 and uses thereof |
| WO2010121007A1 (fr) | 2009-04-15 | 2010-10-21 | The Ohio State University Research Foundation | Analogues de la curcumine en tant qu'inhibiteurs doubles de jak2/stat3 et leurs procédés de préparation et d'utilisation |
| IN2015DN02826A (fr) | 2009-09-03 | 2015-09-11 | Merck Sharp & Dohme | |
| EP2493862B1 (fr) | 2009-10-28 | 2016-10-05 | Newlink Genetics Corporation | Dérivés imidazole comme inhibiteurs de l'ido |
| CA2781706A1 (fr) | 2009-11-24 | 2011-06-03 | The Ohio State University | Inhibiteurs de facteur de transcription et compositions, formulations et procedes apparentes |
| DK2510010T3 (en) | 2009-12-10 | 2015-12-14 | Hoffmann La Roche | Antibodies that bind to human CSF1R extracellular domain 4 and their use |
| US8445517B2 (en) | 2009-12-11 | 2013-05-21 | Dana-Farber Cancer Institute | Stat modulators |
| JP5794922B2 (ja) | 2009-12-28 | 2015-10-14 | 一般社団法人ファルマバレープロジェクト支援機構 | 1,3,4−オキサジアゾール−2−カルボキサミド化合物 |
| DK2542256T3 (da) | 2010-03-04 | 2019-08-26 | Macrogenics Inc | Antistoffer reagerende med b7-h3, immunologisk aktive fragmenter deraf og anvendelser deraf |
| RU2617971C2 (ru) | 2010-03-05 | 2017-04-28 | Ф.Хоффманн-Ля Рош Аг | Антитела против csf-1r человека и их применение |
| CN102918061B (zh) | 2010-03-05 | 2016-06-08 | 霍夫曼-拉罗奇有限公司 | 针对人csf-1r的抗体及其用途 |
| EP3943154A1 (fr) | 2010-05-04 | 2022-01-26 | Five Prime Therapeutics, Inc. | Anticorps se liant au csf1r |
| US20130172340A1 (en) | 2010-06-22 | 2013-07-04 | University of Central Flordia Research Foundation, | Substituted 2-(9h-purin-9-yl) acetic acid analogues as inhibitors of stat3 |
| EP2588129A4 (fr) | 2010-06-30 | 2014-07-09 | Univ Brandeis | Dégradation des protéines ciblées par de petites molécules |
| US8846707B2 (en) | 2010-08-02 | 2014-09-30 | Univeristy Of Central Florida Research Foundation, Inc. | Substituted 2-hydroxy-4-(2-(phenylsulfonamido)acetamido)benzoic acid analogs as inhibitors of stat protein |
| NZ729044A (en) | 2010-09-09 | 2020-07-31 | Pfizer | 4-1bb binding molecules |
| EP2649099A4 (fr) | 2010-12-07 | 2016-10-19 | Univ Yale | Marquage hydrophobe de petites molécules de protéines de fusion et dégradation induite de celles-ci |
| PH12013501201A1 (en) | 2010-12-09 | 2013-07-29 | Univ Pennsylvania | Use of chimeric antigen receptor-modified t cells to treat cancer |
| WO2012078982A2 (fr) | 2010-12-09 | 2012-06-14 | The Ohio State University | Xzh-5 inhibe la phosphorylation de stat3 constitutive et induite par l'interleukine 6 dans des cellules de carcinome hépatocellulaire humain |
| WO2012097351A1 (fr) | 2011-01-14 | 2012-07-19 | The Ohio State University Research Foundation | Matériels et procédés d'inhibition de cellules cancéreuses de myélome multiple |
| WO2012142615A2 (fr) | 2011-04-14 | 2012-10-18 | Board Of Regents, The University Of Texas System | Auranofine et analogues d'auranofine utiles pour traiter une maladie proliférative et des troubles prolifératifs |
| NO2694640T3 (fr) | 2011-04-15 | 2018-03-17 | ||
| CA2833636A1 (fr) | 2011-04-20 | 2012-10-26 | Amplimmune, Inc. | Anticorps et autres molecules qui se lient a b7-h1 et a pd-1 |
| BR112014012819B1 (pt) | 2011-11-28 | 2022-08-16 | Merck Patent Gmbh | Anticorpo anti-pd-l1 ou fragmento de ligação ao antígeno do mesmo e composição |
| MX356337B (es) | 2011-12-15 | 2018-05-23 | Hoffmann La Roche | Anticuerpos contra csf-1r humano y sus usos. |
| KR102438072B1 (ko) | 2012-01-12 | 2022-08-31 | 예일 유니버시티 | E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법 |
| WO2013106646A2 (fr) | 2012-01-12 | 2013-07-18 | Yale University | Composés et procédés pour l'inhibition de l'ubiquitine ligase vcb e3 |
| MX2014008961A (es) | 2012-02-06 | 2014-10-14 | Genentech Inc | Composiciones y metodos para utilizar inhibidores de csf1r. |
| AR090263A1 (es) | 2012-03-08 | 2014-10-29 | Hoffmann La Roche | Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma |
| KR20150018533A (ko) | 2012-05-11 | 2015-02-23 | 파이브 프라임 테라퓨틱스, 인크. | 콜로니 자극 인자 1 수용체(csf1r)에 결속하는 항체들에 의한 질병 상태의 치료 방법 |
| HK1218709A1 (zh) | 2012-05-25 | 2017-03-10 | 多伦多大学管理委员会 | 新水楊酸衍生物、其藥學上可接受的鹽、其組合物以及其使用方法 |
| EP2861562B1 (fr) | 2012-06-14 | 2018-05-09 | Mayo Foundation For Medical Education And Research | Dérivés de pyrazole en tant qu'inhibiteurs de stat3 |
| AR091649A1 (es) | 2012-07-02 | 2015-02-18 | Bristol Myers Squibb Co | Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos |
| UA116544C2 (uk) | 2012-08-09 | 2018-04-10 | Селджин Корпорейшн | Спосіб лікування раку з використанням 3-(4-((4-(морфолінометил)бензил)оксі)-1-оксоізоіндолін-2-іл)піперидин-2,6-діону |
| EP2884971A4 (fr) | 2012-08-16 | 2016-01-06 | Ohio State Innovation Foundation | Inhibiteurs de stat3 et leur utilisation anticancéreuse |
| CN107759690A (zh) | 2012-08-31 | 2018-03-06 | 戊瑞治疗有限公司 | 用结合群落刺激因子1受体(csf1r)的抗体治疗病状的方法 |
| BR112015004547A8 (pt) | 2012-09-19 | 2018-01-23 | Hoffmann La Roche | compostos, composição farmacêutica, uso de um composto e método para o tratamento ou melhoria do cãncer |
| USRE48175E1 (en) | 2012-10-19 | 2020-08-25 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
| US9822135B2 (en) | 2012-10-30 | 2017-11-21 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | STAT3 dimerization inhibitors |
| GB201311910D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel Compounds |
| JP6197865B2 (ja) | 2013-03-15 | 2017-09-20 | 日本ゼオン株式会社 | 中空重合体粒子の水性分散液およびその製造方法 |
| JP6570512B2 (ja) | 2013-03-22 | 2019-09-04 | ユニバーシティ・オブ・ハワイUniversity Of Hawaii | 新規なStat3阻害剤 |
| WO2014182928A2 (fr) | 2013-05-08 | 2014-11-13 | Board Of Regents, The University Of Texas System | Inhibiteurs de stat6 |
| WO2014205416A1 (fr) | 2013-06-20 | 2014-12-24 | University Of Hawaii | Nouveaux inhibiteurs de stat3 sesquiterpénoïdes |
| CA2925084A1 (fr) | 2013-11-18 | 2015-05-21 | F. Hoffmann-La Roche Ag | Tetrahydro-benzodiazepinones |
| US20160058872A1 (en) | 2014-04-14 | 2016-03-03 | Arvinas, Inc. | Imide-based modulators of proteolysis and associated methods of use |
| EP4649963A3 (fr) | 2014-04-14 | 2026-05-13 | Arvinas Operations, Inc. | Modulateurs de protéolyse à base d'imide et procédés d'utilisation associés |
| US20180228907A1 (en) | 2014-04-14 | 2018-08-16 | Arvinas, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
| ES2843973T3 (es) | 2014-06-27 | 2021-07-21 | Celgene Corp | Composiciones y métodos para inducir cambios conformacionales en cereblon y otras ubiquitina ligasas E3 |
| US20160022642A1 (en) | 2014-07-25 | 2016-01-28 | Yale University | Compounds Useful for Promoting Protein Degradation and Methods Using Same |
| US10071164B2 (en) | 2014-08-11 | 2018-09-11 | Yale University | Estrogen-related receptor alpha based protac compounds and associated methods of use |
| KR101697062B1 (ko) | 2014-08-26 | 2017-01-18 | 한국생명공학연구원 | 물에 대한 용해도가 개선된 신규 제라닐 프라보노이드 유도체, 이의 제조 방법 및 이를 유효성분으로 포함하는 암 예방 및 치료용 약학적 조성물 |
| KR20160066490A (ko) | 2014-12-02 | 2016-06-10 | 주식회사 씨앤드씨신약연구소 | 헤테로사이클 유도체 및 그의 용도 |
| US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
| JP6815318B2 (ja) | 2014-12-23 | 2021-01-20 | ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド | 二官能性分子によって標的化タンパク質分解を誘導する方法 |
| WO2016115455A2 (fr) | 2015-01-15 | 2016-07-21 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | 3-(1h-pyrazol-5-yl)-7h-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines 6-aryl-7-substituées en tant qu'inhibiteurs de la voie stat3 ayant une activité anti-proliférative |
| US12312316B2 (en) | 2015-01-20 | 2025-05-27 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of androgen receptor |
| JP6817962B2 (ja) | 2015-01-20 | 2021-01-20 | アルビナス・オペレーションズ・インコーポレイテッドArvinas Operations, Inc. | ターゲティングされたアンドロゲン受容体分解のための化合物および方法 |
| CN107250108B (zh) | 2015-02-05 | 2020-11-27 | 特尔诺沃有限公司 | 用于治疗癌症的irs/stat3双重调节剂与抗癌剂的组合 |
| AU2016232705C1 (en) | 2015-03-18 | 2021-06-17 | Arvinas, Inc. | Compounds and methods for the enhanced degradation of targeted proteins |
| GB201506871D0 (en) | 2015-04-22 | 2015-06-03 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| CA2988414C (fr) | 2015-06-04 | 2023-09-26 | Arvinas, Inc. | Modulateurs a base d'imide de proteolyse et procedes d'utilisation associes |
| WO2016197114A1 (fr) | 2015-06-05 | 2016-12-08 | Arvinas, Inc. | Tank-binding kinase-1 protacs et procédés d'utilisation associés |
| SE539204C2 (en) | 2015-06-05 | 2017-05-09 | Glactone Pharma Dev Ab | Ether analogues of galiellalactone |
| CN105085620B (zh) | 2015-06-25 | 2018-05-08 | 中山大学附属第一医院 | 一种靶向泛素化降解Smad3的化合物 |
| WO2017007612A1 (fr) | 2015-07-07 | 2017-01-12 | Dana-Farber Cancer Institute, Inc. | Procédés pour induire la dégradation ciblée de protéines par des molécules bifonctionnelles |
| EP3319944A4 (fr) | 2015-07-10 | 2019-04-24 | Arvinas, Inc. | Modulateurs de protéolyse à base de mdm2 et méthodes d'utilisation associées |
| CA2988436A1 (fr) | 2015-07-13 | 2017-01-19 | Arvinas, Inc. | Modulateurs de proteolyse a base d'alanine et procedes d'utilisation associes |
| EP3322702B1 (fr) | 2015-07-14 | 2019-11-20 | Mission Therapeutics Limited | Cyanopyrrolidines en tant qu'inhibiteurs des dub pour le traitement du cancer |
| EP3337476A4 (fr) | 2015-08-19 | 2019-09-04 | Arvinas, Inc. | Composés et procédés pour la dégradation ciblée de protéines contenant un bromodomaine |
| ES2911888T3 (es) | 2015-09-18 | 2022-05-23 | Merck Patent Gmbh | Compuestos de heteroarilo como inhibidores de IRAK y usos de los mismos |
| BR112018008918A8 (pt) | 2015-11-02 | 2019-02-26 | Univ Yale | compostos de quimera proteólise dirigida e métodos para preparação e uso dos mesmos |
| WO2017117473A1 (fr) | 2015-12-30 | 2017-07-06 | Dana-Farber Cancer Institute, Inc. | Molécules bifonctionnelles de dégradation d'her3 et procédés d'utilisation |
| WO2017117474A1 (fr) | 2015-12-30 | 2017-07-06 | Dana-Farber Cancer Institute, Inc. | Composés bifonctionnels destinés à la dégradation d'her3 et procédés d'utilisation |
| CN109153644B (zh) | 2016-03-16 | 2022-10-21 | H·李·莫菲特癌症中心研究有限公司 | 用以增强效应t细胞功能的针对cereblon的小分子 |
| US20170281784A1 (en) | 2016-04-05 | 2017-10-05 | Arvinas, Inc. | Protein-protein interaction inducing technology |
| EP3440082A1 (fr) | 2016-04-06 | 2019-02-13 | The Regents of The University of Michigan | Intermédiaires monofonctionnels pour la dégradation d'une protéine cible dépendante du ligand |
| AU2017246452C1 (en) | 2016-04-06 | 2021-06-03 | The Regents Of The University Of Michigan | MDM2 protein degraders |
| CN109562107A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的杂环降解决定子体 |
| CN121974842A (zh) | 2016-05-10 | 2026-05-05 | C4医药公司 | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 |
| WO2017197056A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères ciblant un bromodomaine pour la dégradation de protéines cibles |
| WO2017197046A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères de type glutarimide liés au carbone c3 pour la dégradation de protéines cibles |
| CN109562113A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的螺环降解决定子体 |
| WO2017201069A1 (fr) | 2016-05-18 | 2017-11-23 | Biotheryx, Inc. | Dérivés d'oxoindoline utilisés comme modulateurs de la fonction protéique |
| CN109152843A (zh) | 2016-05-20 | 2019-01-04 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| GB201610147D0 (en) | 2016-06-10 | 2016-07-27 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| MX2019005007A (es) | 2016-11-01 | 2019-07-18 | Arvinas Inc | Protac dirigidos a la proteína tau y métodos asociados de uso. |
| AU2017363313B2 (en) | 2016-11-22 | 2021-06-24 | Dana-Farber Cancer Institute, Inc. | Inhibitors of interleukin-1 receptor-associated kinases and uses thereof |
| SE540295C2 (en) | 2016-12-05 | 2018-05-29 | Glactone Pharma Dev Ab | Sulfonamide analogues of galiellalactone |
| EP3570836A4 (fr) | 2017-01-23 | 2020-08-19 | The University of Hawaii | Inhibiteurs de stat3 dérivés de 2-arylsulfonamido-n-arylacétamide |
| IL319363A (en) | 2017-01-31 | 2025-05-01 | Arvinas Operations Inc | Cervalon ligands and bifunctional compounds containing them |
| EP4717317A3 (fr) * | 2017-06-20 | 2026-06-03 | C4 Therapeutics, Inc. | Dégrons et dégrons liés à n/o pour dégradation protéique |
| CN118108706A (zh) | 2017-09-04 | 2024-05-31 | C4医药公司 | 戊二酰亚胺 |
| WO2019060693A1 (fr) | 2017-09-22 | 2019-03-28 | Kymera Therapeutics, Inc. | Ligands crbn et utilisations de ces derniers |
| MX2020003190A (es) * | 2017-09-22 | 2020-11-11 | Kymera Therapeutics Inc | Degradadores de proteinas y usos de los mismos. |
| WO2019084026A1 (fr) | 2017-10-24 | 2019-05-02 | Genentech, Inc. | Composés (4-hydroxypyrrolidin-2-yl)-hétérocycliques et leurs procédés d'utilisation |
| WO2019084030A1 (fr) | 2017-10-24 | 2019-05-02 | Genentech, Inc. | Composés de (4-hydroxypyrrolidin-2-yl)-hydroxamate et leurs procédés d'utilisation |
| EP3710002A4 (fr) | 2017-11-16 | 2021-07-07 | C4 Therapeutics, Inc. | Agents de dégradation et dégrons pour dégradation protéique ciblée |
| US11065231B2 (en) | 2017-11-17 | 2021-07-20 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of interleukin-1 receptor- associated kinase 4 polypeptides |
| IL315310A (en) | 2017-12-26 | 2024-10-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
| US11512080B2 (en) | 2018-01-12 | 2022-11-29 | Kymera Therapeutics, Inc. | CRBN ligands and uses thereof |
| EP3737666A4 (fr) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Agents de dégradation de protéines et utilisations associées |
| JP7472026B2 (ja) | 2018-02-23 | 2024-04-22 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | 選択的なタンパク質分解を誘導するための低分子およびその使用法 |
| EP3578561A1 (fr) | 2018-06-04 | 2019-12-11 | F. Hoffmann-La Roche AG | Spirocomposés |
| US12454520B2 (en) | 2018-07-06 | 2025-10-28 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
| WO2020010210A1 (fr) | 2018-07-06 | 2020-01-09 | Kymera Therapeutics, Inc. | Agents de dégradation de mertk et leurs utilisations |
| US11292792B2 (en) | 2018-07-06 | 2022-04-05 | Kymera Therapeutics, Inc. | Tricyclic CRBN ligands and uses thereof |
| AU2019389174A1 (en) | 2018-11-30 | 2021-07-01 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| KR20220009941A (ko) | 2019-03-26 | 2022-01-25 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Stat3의 저분자 분해제 |
| WO2020205467A1 (fr) * | 2019-03-29 | 2020-10-08 | The Regents Of The University Of Michigan | Agents de dégradation de protéines stat3 |
| KR102980990B1 (ko) * | 2019-04-05 | 2026-06-25 | 카이메라 쎄라퓨틱스 인코포레이티드 | Stat 분해제 및 이의 용도 |
| PH12022500002A1 (en) | 2019-06-28 | 2023-04-03 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
| WO2020264490A1 (fr) | 2019-06-28 | 2020-12-30 | Kymera Therapeutics, Inc. | Agents de dégradation d'irak et leurs utilisations |
| US20220281831A1 (en) | 2019-07-15 | 2022-09-08 | Kymera Therapeutics, Inc. | Fused-glutarimide crbn ligands and uses thereof |
| US20230093080A1 (en) | 2019-07-15 | 2023-03-23 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
| US12558427B2 (en) | 2019-07-17 | 2026-02-24 | Kymera Therapeutics, Inc. | IRAK degraders and uses thereof |
| WO2021011871A1 (fr) | 2019-07-17 | 2021-01-21 | Kymera Therapeutics, Inc. | Agents de dégradation de mertk et leurs utilisations |
| WO2021119159A1 (fr) | 2019-12-10 | 2021-06-17 | Kymera Therapeutics, Inc. | Agents de dégradation d'irak et leurs utilisations |
| WO2021127278A1 (fr) | 2019-12-17 | 2021-06-24 | Kymera Therapeutics, Inc. | Agents de dégradation d'irak et leurs utilisations |
| EP4076524A4 (fr) | 2019-12-17 | 2023-11-29 | Kymera Therapeutics, Inc. | Agents de dégradation d'irak et leurs utilisations |
| CA3161878A1 (fr) | 2019-12-17 | 2021-06-24 | Matthew M. Weiss | Agents de degradation d'irak et leurs utilisations |
| US20230122219A1 (en) | 2020-02-03 | 2023-04-20 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
| AU2021238333A1 (en) | 2020-03-17 | 2022-09-29 | Kymera Therapeutics, Inc. | STAT degraders and uses thereof |
| US12522623B2 (en) | 2020-03-26 | 2026-01-13 | Regents Of The University Of Michigan | Small molecule STAT protein degraders |
| AU2021358130A1 (en) | 2020-10-07 | 2023-05-18 | Kymera Therapeutics, Inc. | Stat degraders and uses thereof |
| CA3239730A1 (fr) | 2021-12-11 | 2023-06-15 | Christopher De Savi | Agents de degradation de stat3 et leurs utilisations |
-
2020
- 2020-04-06 KR KR1020217036188A patent/KR102980990B1/ko active Active
- 2020-04-06 EP EP20785175.9A patent/EP3946360A4/fr active Pending
- 2020-04-06 WO PCT/US2020/026869 patent/WO2020206424A1/fr not_active Ceased
- 2020-04-06 TW TW109111554A patent/TWI875749B/zh active
- 2020-04-06 AU AU2020253633A patent/AU2020253633A1/en active Pending
- 2020-04-06 BR BR112021019748A patent/BR112021019748A2/pt unknown
- 2020-04-06 MA MA055565A patent/MA55565A/fr unknown
- 2020-04-06 SG SG11202110829YA patent/SG11202110829YA/en unknown
- 2020-04-06 CN CN202080040176.3A patent/CN113939300A/zh active Pending
- 2020-04-06 MX MX2021012216A patent/MX2021012216A/es unknown
- 2020-04-06 JP JP2021559270A patent/JP2022527114A/ja active Pending
- 2020-04-06 CA CA3135802A patent/CA3135802A1/fr active Pending
- 2020-04-06 IL IL286969A patent/IL286969B2/en unknown
- 2020-04-06 CN CN202510704986.9A patent/CN120574283A/zh active Pending
- 2020-04-06 US US16/841,095 patent/US11485750B1/en active Active
-
2021
- 2021-10-05 CO CONC2021/0013339A patent/CO2021013339A2/es unknown
-
2022
- 2022-05-04 US US17/736,669 patent/US12077555B2/en active Active
- 2022-10-10 US US18/045,390 patent/US11746120B2/en active Active
-
2024
- 2024-07-03 US US18/763,437 patent/US20250059221A1/en active Pending
- 2024-09-13 JP JP2024159253A patent/JP7716554B2/ja active Active
-
2025
- 2025-07-18 JP JP2025121262A patent/JP2025157450A/ja active Pending
- 2025-07-20 IL IL322230A patent/IL322230A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US11485750B1 (en) | 2022-11-01 |
| IL286969A (en) | 2021-12-01 |
| TWI875749B (zh) | 2025-03-11 |
| KR102980990B1 (ko) | 2026-06-25 |
| JP2025157450A (ja) | 2025-10-15 |
| IL322230A (en) | 2025-09-01 |
| EP3946360A4 (fr) | 2023-05-10 |
| WO2020206424A1 (fr) | 2020-10-08 |
| JP2025011088A (ja) | 2025-01-23 |
| KR20220006139A (ko) | 2022-01-14 |
| US12077555B2 (en) | 2024-09-03 |
| JP2022527114A (ja) | 2022-05-30 |
| SG11202110829YA (en) | 2021-10-28 |
| US11746120B2 (en) | 2023-09-05 |
| IL286969B2 (en) | 2025-12-01 |
| IL286969B1 (en) | 2025-08-01 |
| MX2021012216A (es) | 2022-01-24 |
| US20230120381A1 (en) | 2023-04-20 |
| CN113939300A (zh) | 2022-01-14 |
| EP3946360A1 (fr) | 2022-02-09 |
| TW202106676A (zh) | 2021-02-16 |
| US20250059221A1 (en) | 2025-02-20 |
| US20230084113A1 (en) | 2023-03-16 |
| AU2020253633A1 (en) | 2021-11-04 |
| CN120574283A (zh) | 2025-09-02 |
| BR112021019748A2 (pt) | 2021-12-07 |
| CO2021013339A2 (es) | 2022-01-17 |
| CA3135802A1 (fr) | 2020-10-08 |
| JP7716554B2 (ja) | 2025-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP3946360A4 (fr) | Agents de dégradation de stat et leurs utilisations | |
| EP3817822A4 (fr) | Agents de dégradation de protéines et leurs utilisations | |
| EP4121055A4 (fr) | Agents de dégradation de stat et leurs utilisations | |
| MA56462A (fr) | Inhibiteurs de hpk1 et leurs utilisations | |
| EP3870579A4 (fr) | Inhibiteurs de tyk2 et leurs utilisations | |
| EP3801065A4 (fr) | Compositions bactériennes spécifiques et leurs utilisations | |
| EP3746075A4 (fr) | Inhibiteurs de gcn2 et leurs utilisations | |
| EP4225303A4 (fr) | Agents dégradeurs de stat et leurs utilisations | |
| MA52483A (fr) | Dérivés de gip et leurs utilisations | |
| EP3866789A4 (fr) | Inhibiteurs de tyk2 et leurs utilisations | |
| EP3908262A4 (fr) | Vésicules dérivées de bactéries et leurs utilisations | |
| MA50618A (fr) | Polyrhérapies et leurs utilisations | |
| EP4093768A4 (fr) | Constructions cal-t et leurs utilisations | |
| EP3787607C0 (fr) | Compositions de caroténoïdes et leurs utilisations | |
| EP3886843A4 (fr) | Inhibiteurs de tyk2 et leurs utilisations | |
| EP3810182A4 (fr) | Néoantigènes et leurs utilisations | |
| EP3902530A4 (fr) | Nanovaccins polymères et leurs utilisations | |
| EP3938369A4 (fr) | Inhibiteurs de tyk2 et leurs utilisations | |
| EP3790861A4 (fr) | Compositions sénolytiques et utilisations associées | |
| EP3914357A4 (fr) | Inhibiteurs de tyk2 et leurs utilisations | |
| EP3841096A4 (fr) | Dérivés de pyridinylméthylènepipéridine et leurs utilisations | |
| EP3986397A4 (fr) | Agents de dégradation de hck et leurs utilisations | |
| EP3870162A4 (fr) | Inhibiteurs de ssao et leurs utilisations | |
| EP4363425A4 (fr) | Agents de dégradation de smarca et leurs utilisations | |
| EP4259612A4 (fr) | Agents de dégradation de smarca et leurs utilisations |