MA42456A - Inhibiteurs de hpk1 et leurs procédés d'utilisation - Google Patents
Inhibiteurs de hpk1 et leurs procédés d'utilisationInfo
- Publication number
- MA42456A MA42456A MA42456A MA42456A MA42456A MA 42456 A MA42456 A MA 42456A MA 42456 A MA42456 A MA 42456A MA 42456 A MA42456 A MA 42456A MA 42456 A MA42456 A MA 42456A
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- methods
- formula
- pharmaceutically acceptable
- inhibitors
- Prior art date
Links
Classifications
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- 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
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- 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
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- 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
- A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
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- 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
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- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2818—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
L'invention concerne des composés de thiénopyridinone de formule (i) et des sels de ceux-ci pharmaceutiquement acceptables. Dans ces composés, l'un de x1, x2, et x3 est s et les deux autres sont chacun indépendamment cr, r et toutes les autres variables sont telles que définies dans la description. Ces composés sont connus pour inhiber l'activité de la kinase hpk1 et pour avoir une activité antitumorale in vivo. Ces composés peuvent être efficacement combinés avec des vecteurs pharmaceutiquement acceptables, ainsi qu'avec d'autres techniques immunomodulatrices, telles qu'une inhibition de points de contrôle ou des inhibiteurs de l'oxydation du tryptophane. Formule (i).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562184348P | 2015-06-25 | 2015-06-25 | |
| PCT/CA2016/050734 WO2016205942A1 (fr) | 2015-06-25 | 2016-06-23 | Inhibiteurs de hpk1 et leurs procédés d'utilisation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA42456A true MA42456A (fr) | 2018-05-23 |
| MA42456B1 MA42456B1 (fr) | 2021-06-30 |
Family
ID=57584335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA42456A MA42456B1 (fr) | 2015-06-25 | 2016-06-23 | Inhibiteurs de hpk1 et leurs procédés d'utilisation |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US10501474B2 (fr) |
| EP (1) | EP3322711B1 (fr) |
| JP (3) | JP6898868B2 (fr) |
| KR (2) | KR102740623B1 (fr) |
| CN (2) | CN107922431B (fr) |
| AU (1) | AU2016282289B2 (fr) |
| BR (2) | BR122023006150B1 (fr) |
| CY (1) | CY1124489T1 (fr) |
| DK (1) | DK3322711T3 (fr) |
| EA (1) | EA035421B1 (fr) |
| ES (1) | ES2872555T3 (fr) |
| HR (1) | HRP20210895T1 (fr) |
| HU (1) | HUE054159T2 (fr) |
| IL (2) | IL283353B (fr) |
| LT (1) | LT3322711T (fr) |
| MA (1) | MA42456B1 (fr) |
| MD (1) | MD3322711T2 (fr) |
| MX (2) | MX386480B (fr) |
| PL (1) | PL3322711T3 (fr) |
| PT (1) | PT3322711T (fr) |
| RS (1) | RS61919B1 (fr) |
| SG (1) | SG10202105964RA (fr) |
| SI (1) | SI3322711T1 (fr) |
| SM (1) | SMT202100324T1 (fr) |
| TW (1) | TWI733679B (fr) |
| WO (1) | WO2016205942A1 (fr) |
Families Citing this family (121)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS61919B1 (sr) * | 2015-06-25 | 2021-06-30 | Univ Health Network | Inhibitori hpk1 i postupci za njihovo korišćenje |
| US20180072741A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
| US20180072718A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| US10280164B2 (en) | 2016-09-09 | 2019-05-07 | Incyte Corporation | Pyrazolopyridone compounds and uses thereof |
| AR109596A1 (es) | 2016-09-09 | 2018-12-26 | Incyte Corp | Compuestos pirazolopiridina y sus usos |
| WO2018152220A1 (fr) | 2017-02-15 | 2018-08-23 | Incyte Corporation | Composés de pyrazolopyridine et leurs utilisations |
| EP3596075B1 (fr) | 2017-03-15 | 2023-10-11 | F. Hoffmann-La Roche AG | Azaindoles utilisés en tant qu'inhibiteurs de hpk1 |
| CN110678466B (zh) | 2017-03-30 | 2023-01-31 | 豪夫迈·罗氏有限公司 | 作为hpk1抑制剂的二氮杂萘类 |
| MX2019010302A (es) * | 2017-03-30 | 2019-11-21 | Hoffmann La Roche | Isoquinolinas como inhibidores de hpk1. |
| EP3638669A1 (fr) | 2017-06-13 | 2020-04-22 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| WO2018228923A1 (fr) | 2017-06-13 | 2018-12-20 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués utilisés en tant que modulateurs de map4k1 pour le traitement de maladies cancéreuses |
| WO2018228925A1 (fr) | 2017-06-13 | 2018-12-20 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| EP3655406A1 (fr) | 2017-07-18 | 2020-05-27 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| US10722495B2 (en) | 2017-09-08 | 2020-07-28 | Incyte Corporation | Cyanoindazole compounds and uses thereof |
| CN109721620B (zh) * | 2017-10-27 | 2022-05-13 | 药捷安康(南京)科技股份有限公司 | Hpk1抑制剂及其用途 |
| WO2019090198A1 (fr) * | 2017-11-06 | 2019-05-09 | Bristol-Myers Squibb Company | Composés d'isofuranone utiles en tant qu'inhibiteurs de hpk1 |
| DK3755703T3 (da) * | 2018-02-20 | 2022-06-27 | Incyte Corp | N-(phenyl)-2-(phenyl)pyrimidin-4-carboxamidderivater og relaterede forbindelser som hpk1-inhibitorer til behandling af kræft |
| US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
| US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
| US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
| JP7386841B2 (ja) | 2018-07-24 | 2023-11-27 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | イソキノリン化合物及びその使用 |
| JP7386842B2 (ja) * | 2018-07-24 | 2023-11-27 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | ナフチリジン化合物およびその使用 |
| US10899755B2 (en) | 2018-08-08 | 2021-01-26 | Incyte Corporation | Benzothiazole compounds and uses thereof |
| WO2020068729A1 (fr) | 2018-09-25 | 2020-04-02 | Incyte Corporation | Composés pyrazolo[4,3-d]pyrimidine en tant que modulateurs des alk2 et/ou fgfr |
| TW202024053A (zh) | 2018-10-02 | 2020-07-01 | 美商建南德克公司 | 異喹啉化合物及其用途 |
| TW202023558A (zh) * | 2018-10-03 | 2020-07-01 | 美商建南德克公司 | 8-胺基異喹啉化合物及其用途 |
| US12331320B2 (en) | 2018-10-10 | 2025-06-17 | The Research Foundation For The State University Of New York | Genome edited cancer cell vaccines |
| EP4371987B9 (fr) | 2018-10-31 | 2025-11-26 | Gilead Sciences, Inc. | Composés de 6-azabenzimidazole substitués utilisés en tant qu'inhibiteurs de hpk1 |
| EP3873608A1 (fr) * | 2018-10-31 | 2021-09-08 | Gilead Sciences, Inc. | Composés 6-azabenzimidazole substitués ayant une activité inhibitrice de hpk1 |
| US20220047603A1 (en) | 2018-12-11 | 2022-02-17 | Bayer Aktiengesellschaft | Substituted pyrrolopyridine-derivatives |
| ES2974634T3 (es) | 2018-12-21 | 2024-06-28 | Celgene Corp | Inhibidores de tienopiridinas de RIPK2 |
| US12398155B2 (en) | 2018-12-26 | 2025-08-26 | Janssen Pharmaceutica Nv | Thienopyridinone compounds |
| TW202102488A (zh) | 2019-03-26 | 2021-01-16 | 比利時商健生藥品公司 | Hpk1抑制劑 |
| MA55478A (fr) | 2019-03-26 | 2022-02-09 | Janssen Pharmaceutica Nv | Inhibiteurs bicycliques de hpk1 |
| WO2020235902A1 (fr) * | 2019-05-17 | 2020-11-26 | 주식회사 보로노이 | Dérivé de pyrimidine condensé avec un hétérocycle et son utilisation |
| US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
| CN114245807B (zh) | 2019-06-25 | 2025-05-02 | 吉利德科学公司 | Flt3l-fc融合蛋白和使用方法 |
| TWI848141B (zh) | 2019-07-04 | 2024-07-11 | 英屬開曼群島商百濟神州有限公司 | 及其用途 |
| US12459958B2 (en) | 2019-07-17 | 2025-11-04 | Beone Medicines I Gmbh | Tricyclic compounds as HPK1 inhibitor and the use thereof |
| KR20220059480A (ko) * | 2019-08-06 | 2022-05-10 | 인사이트 코포레이션 | 고체 형태의 hpk1 억제제 |
| US12673933B2 (en) | 2019-08-21 | 2026-07-07 | Beone Medicines I Gmbh | Aminopyrazine compounds as HPK1 inhibitor and the use thereof |
| US12215105B2 (en) * | 2019-09-13 | 2025-02-04 | Nimbus Saturn, Inc. | HPK1 antagonists and uses thereof |
| CN112552293A (zh) * | 2019-09-25 | 2021-03-26 | 珠海宇繁生物科技有限责任公司 | 一种protac小分子化合物及其应用 |
| PH12022550835A1 (en) | 2019-10-18 | 2023-07-03 | Forty Seven Inc | Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia |
| NZ786589A (en) | 2019-10-31 | 2025-03-28 | Forty Seven Llc | Anti-cd47 and anti-cd20 based treatment of blood cancer |
| TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
| CN115362003B (zh) | 2019-12-24 | 2024-03-22 | 卡尔那生物科学株式会社 | 二酰基甘油激酶调节化合物 |
| EP4089096A4 (fr) * | 2020-01-09 | 2024-01-03 | Sumitomo Chemical Company, Limited | Composé hétérocyclique et composition de lutte contre les arthropodes nuisibles le comprenant |
| TWI890283B (zh) | 2020-02-14 | 2025-07-11 | 美商基利科學股份有限公司 | 結合ccr8之抗體及融合蛋白及其用途 |
| CN115867275A (zh) * | 2020-04-13 | 2023-03-28 | 大学健康网络 | 治疗细胞因子释放综合征的方法 |
| JP7564888B2 (ja) | 2020-05-01 | 2024-10-09 | ギリアード サイエンシーズ, インコーポレイテッド | Cd73阻害性2,4-ジオキソピリミジン化合物 |
| TWI920085B (zh) | 2020-05-11 | 2026-04-01 | 加拿大健康網路大學 | 4-胺基-5-(6-(4-甲基哌-1-基)-1h-苯并[d]咪唑-2-基)噻吩并[2,3-b]吡啶-6(7h)-酮之鹽及晶形 |
| WO2021249913A1 (fr) | 2020-06-09 | 2021-12-16 | Bayer Aktiengesellschaft | Dérivés de 2'-(quinolin-3-yl)-5',6'-dihydrospiro[azétidine-3,4'-pyrrolo[1,2-b]pyrazole]-1-carboxylate et des composés apparentés servant d'inhibiteurs de map4k1 (hpk1) pour le traitement du cancer |
| CN113845531B (zh) * | 2020-06-28 | 2025-06-27 | 四川科伦博泰生物医药股份有限公司 | 吡唑并环类化合物、包含其的药物组合物、其制备方法及其用途 |
| WO2022064458A1 (fr) * | 2020-09-28 | 2022-03-31 | 1ST Biotherapeutics, Inc. | Indazoles en tant qu'inhibiteurs de kinase 1 progénitrice hématopoïétique (hpk1) et leurs procédés d'utilisation |
| CN117624131A (zh) | 2020-09-30 | 2024-03-01 | 百济神州有限公司 | 作为hpk1抑制剂的3-[(1h-吡唑-4-基)氧基]吡嗪-2-胺化合物和其用途 |
| EP4240361A4 (fr) * | 2020-11-09 | 2024-09-25 | Merck Sharp & Dohme LLC | Inhibiteurs, du type 2-aminoquinazoline à substitution 7-azole, de hpk1 |
| US20240002394A1 (en) * | 2020-11-24 | 2024-01-04 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Deuterium-modified thienopyridone compound |
| CN121851009A (zh) * | 2021-01-22 | 2026-04-14 | 苏州信诺维医药科技股份有限公司 | Hpk1抑制剂、其制备方法、药物组合物及其应用 |
| WO2022167627A1 (fr) | 2021-02-05 | 2022-08-11 | Bayer Aktiengesellschaft | Inhibiteurs de map4k1 |
| CN114907377B (zh) * | 2021-02-10 | 2026-05-12 | 江苏恒瑞医药股份有限公司 | 稠合四环类化合物、其制备方法及其在医药上的应用 |
| WO2022174253A1 (fr) | 2021-02-12 | 2022-08-18 | Nimbus Saturn, Inc. | Antagonistes de hpk1 et leurs utilisations |
| CN117295737A (zh) | 2021-03-05 | 2023-12-26 | 林伯士萨顿公司 | Hpk1拮抗剂和其用途 |
| WO2022188823A1 (fr) * | 2021-03-10 | 2022-09-15 | 山东轩竹医药科技有限公司 | Inhibiteur de hpk1 tricyclique et son utilisation |
| WO2022199676A1 (fr) * | 2021-03-26 | 2022-09-29 | 江苏恒瑞医药股份有限公司 | Composé tétracyclique fusionné, son procédé de préparation et son utilisation en médecine |
| WO2022213062A1 (fr) | 2021-03-29 | 2022-10-06 | Nimbus Saturn, Inc. | Antagonistes de hpk1 et leurs utilisations |
| TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
| CN117597336A (zh) * | 2021-04-30 | 2024-02-23 | 安大略省癌症研究所(Oicr) | 作为造血祖细胞激酶1(hpk1)抑制剂的卤素取代的氨基氮杂-杂芳基化合物 |
| WO2022226667A1 (fr) * | 2021-04-30 | 2022-11-03 | Ontario Institute For Cancer Research (Oicr) | Composés aminopyridine substitués utilisés en tant qu'inhibiteurs de la kinase progénitrice hématopoïétique 1 (hpk1) |
| EP4330252A4 (fr) * | 2021-04-30 | 2025-04-02 | Ontario Institute for Cancer Research (OICR) | Composés amino aza-hétéroaryles substitués utilisés en tant qu'inhibiteurs de la kinase des progéniteurs hématopoïétiques 1 (hpk1) |
| WO2022245671A1 (fr) | 2021-05-18 | 2022-11-24 | Gilead Sciences, Inc. | Méthodes d'utilisation de protéines de fusion flt3l-fc |
| WO2022253252A1 (fr) * | 2021-06-03 | 2022-12-08 | Silexon Biotech Co., Ltd. | Composés hétérocycliques utiles en tant qu'inhibiteurs de hpk1 |
| CN115433161A (zh) * | 2021-06-04 | 2022-12-06 | 轶诺(浙江)药业有限公司 | 新型hpk1抑制剂及其制备方法和应用 |
| CN117460732A (zh) * | 2021-06-11 | 2024-01-26 | 杭州中美华东制药有限公司 | 吡咯并吡啶酮类化合物及其制备方法和用途 |
| JP7651018B2 (ja) | 2021-06-23 | 2025-03-25 | ギリアード サイエンシーズ, インコーポレイテッド | ジアシルグリセロールキナーゼ調節化合物 |
| CN117355531A (zh) | 2021-06-23 | 2024-01-05 | 吉利德科学公司 | 二酰基甘油激酶调节化合物 |
| MX2023014762A (es) | 2021-06-23 | 2024-01-15 | Gilead Sciences Inc | Compuestos moduladores de diacilglicerol quinasa. |
| EP4359413A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés de modulation de la diacylglycérol kinase |
| MX2024000751A (es) * | 2021-07-14 | 2024-03-25 | Blueprint Medicines Corp | Compuestos heterociclicos como inhibidores de map4k1. |
| WO2023001794A1 (fr) | 2021-07-20 | 2023-01-26 | Astrazeneca Ab | Pyrazine-2-carboxamides substituées utilisées en tant qu'inhibiteurs de hpk1 pour le traitement du cancer |
| EP4380565A4 (fr) * | 2021-08-03 | 2025-05-21 | Nimbus Saturn, Inc. | Antagonistes de hpk1 et leurs utilisations |
| WO2023023942A1 (fr) * | 2021-08-24 | 2023-03-02 | Biofront Ltd (Cayman) | Inhibiteurs de hpk1, compositions comprenant un inhibiteur de hpk1 et leurs procédés d'utilisation |
| TW202327595A (zh) * | 2021-10-05 | 2023-07-16 | 美商輝瑞大藥廠 | 用於治療癌症之氮雜內醯胺化合物的組合 |
| US20250011319A1 (en) * | 2021-10-15 | 2025-01-09 | Lomond Therapeutics, Inc. | SUBSTITUTED 1H-PYRAZOLO [4,3-c] QUINOLINES, METHODS OF PREPARATION, AND USE THEREOF |
| EP4423078A1 (fr) | 2021-10-28 | 2024-09-04 | Gilead Sciences, Inc. | Dérivés de pyridine-3(2h)-one |
| PE20241186A1 (es) | 2021-10-29 | 2024-06-03 | Gilead Sciences Inc | Compuestos de cd73 |
| US20230203202A1 (en) | 2021-12-08 | 2023-06-29 | Dragonfly Therapeutics, Inc. | Proteins binding nkg2d, cd16 and 5t4 |
| WO2023107954A1 (fr) | 2021-12-08 | 2023-06-15 | Dragonfly Therapeutics, Inc. | Anticorps ciblant 5t4 et leurs utilisations |
| CN118339168A (zh) * | 2021-12-17 | 2024-07-12 | 西藏海思科制药有限公司 | 一种并环杂环衍生物及其在医药上的应用 |
| US20240124412A1 (en) | 2021-12-22 | 2024-04-18 | Gilead Sciences, Inc. | Ikaros zinc finger family degraders and uses thereof |
| CN118488948A (zh) | 2021-12-22 | 2024-08-13 | 吉利德科学公司 | Ikaros锌指家族降解剂及其用途 |
| TW202333712A (zh) * | 2021-12-22 | 2023-09-01 | 加拿大健康網路大學 | 於急性骨髓性白血病或淋巴瘤之治療 |
| WO2023138612A1 (fr) * | 2022-01-19 | 2023-07-27 | Silexon Ai Technology Co., Ltd. | Composés hétérocycliques utiles en tant qu'inhibiteurs de hpk1 |
| WO2023143384A1 (fr) * | 2022-01-27 | 2023-08-03 | 四川海思科制药有限公司 | Composé pour inhiber ou dégrader la kinase hpk1 et son utilisation médicale |
| CA3248911A1 (fr) | 2022-01-28 | 2023-08-03 | Gilead Sciences, Inc. | Inhibiteurs de poly(adénosine diphosphate-ribose) polymérase 7 |
| CN116462685B (zh) * | 2022-02-08 | 2025-02-11 | 和径医药科技(上海)有限公司 | 杂环化合物、包含其的药物组合物及其抗肿瘤应用 |
| PL4245756T3 (pl) | 2022-03-17 | 2025-02-17 | Gilead Sciences, Inc. | Środki degradujące palec cynkowy z rodziny ikaros i ich zastosowania |
| AU2023240346A1 (en) | 2022-03-24 | 2024-09-19 | Gilead Sciences, Inc. | Combination therapy for treating trop-2 expressing cancers |
| TWI876305B (zh) | 2022-04-05 | 2025-03-11 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
| EP4511127A1 (fr) | 2022-04-21 | 2025-02-26 | Gilead Sciences, Inc. | Composés modulateurs de kras g12d |
| WO2024006929A1 (fr) | 2022-07-01 | 2024-01-04 | Gilead Sciences, Inc. | Composés cd73 |
| US20240091351A1 (en) | 2022-09-21 | 2024-03-21 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY |
| CN117624187B (zh) * | 2022-11-17 | 2025-11-04 | 杭州阿诺生物医药科技有限公司 | 一种高效的hpk1降解剂化合物及其制备方法和应用 |
| KR102855849B1 (ko) | 2022-11-25 | 2025-09-08 | 충남대학교산학협력단 | 이미다조피리딘 유도체, 이를 유효성분으로 포함하는 약제학적 조성물 및 이를 이용하는 암의 치료 방법 |
| EP4638436A1 (fr) | 2022-12-22 | 2025-10-29 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| WO2024206869A2 (fr) * | 2023-03-30 | 2024-10-03 | Board Of Regents, The University Of Texas System | Combinaison d'inhibiteur de hpk1 et d'inhibiteur d'axl dans une thérapie anticancéreuse |
| WO2024215754A1 (fr) | 2023-04-11 | 2024-10-17 | Gilead Sciences, Inc. | Composés modulateurs de kras |
| PE20260121A1 (es) | 2023-04-21 | 2026-01-16 | Gilead Sciences Inc | Inhibidores de prmt5 y usos de los mismos |
| JP2026522894A (ja) | 2023-06-30 | 2026-07-09 | ギリアード サイエンシーズ, インコーポレイテッド | Kras調節化合物 |
| AU2024297978A1 (en) | 2023-07-26 | 2026-02-05 | Gilead Sciences, Inc. | Parp7 inhibitors |
| CN121568935A (zh) | 2023-07-26 | 2026-02-24 | 吉利德科学公司 | Parp7抑制剂 |
| US20250109147A1 (en) | 2023-09-08 | 2025-04-03 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| EP4774280A1 (fr) | 2023-09-08 | 2026-07-15 | Gilead Sciences, Inc. | Composés de modulation de kras g12d |
| WO2025080099A1 (fr) * | 2023-10-13 | 2025-04-17 | 주식회사유한양행 | Dérivé 7,7-diméthylfuro[3,4-b] pyridin-5(7h)-one ou sel de celui-ci, et composition pharmaceutique le comprenant |
| WO2025096647A1 (fr) * | 2023-10-30 | 2025-05-08 | Nimbus Saturn, Inc. | Méthodes de traitement de tumeurs |
| WO2025096589A1 (fr) | 2023-11-03 | 2025-05-08 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| US20250230168A1 (en) | 2023-12-22 | 2025-07-17 | Gilead Sciences, Inc. | Azaspiro wrn inhibitors |
| WO2025245003A1 (fr) | 2024-05-21 | 2025-11-27 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
| US20260098049A1 (en) | 2024-08-12 | 2026-04-09 | Gilead Sciences, Inc. | Kras modulating compounds |
| US20260130893A1 (en) | 2024-10-21 | 2026-05-14 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| WO2026136515A1 (fr) | 2024-12-19 | 2026-06-25 | Gilead Sciences, Inc. | Inhibiteurs de parp7 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU7314200A (en) * | 1999-09-17 | 2001-04-24 | Yamanouchi Pharmaceutical Co., Ltd. | Benzimidazole derivatives |
| AU778042B2 (en) * | 1999-10-19 | 2004-11-11 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| JP4341949B2 (ja) | 2000-09-01 | 2009-10-14 | ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド | アザ複素環式誘導体およびその治療的使用 |
| WO2004014375A2 (fr) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Inhibiteurs de metalloprotease bicycliques condenses |
| US7119205B2 (en) | 2003-05-16 | 2006-10-10 | Abbott Laboratories | Thienopyridones as AMPK activators for the treatment of diabetes and obesity |
| EP2151440A4 (fr) | 2007-05-21 | 2010-10-20 | Takeda Pharmaceutical | Composé hétérocyclique et son utilisation |
| KR101630466B1 (ko) * | 2008-04-11 | 2016-06-14 | 메르크 파텐트 게엠베하 | Amp-활성화 단백질 키나아제(ampk) 활성화제로서의 티에노피리돈 유도체 |
| KR101648593B1 (ko) | 2008-05-05 | 2016-08-16 | 메르크 파텐트 게엠베하 | Amp-활성화된 단백질 키나아제 (ampk) 활성화제로서의 티에노피리돈 유도체 |
| US8653089B2 (en) | 2011-02-09 | 2014-02-18 | F. Hoffmann-La Roche Ag | Heterocyclic compounds and methods of use |
| GB201114212D0 (en) * | 2011-08-18 | 2011-10-05 | Ucb Pharma Sa | Therapeutic agents |
| RS61919B1 (sr) * | 2015-06-25 | 2021-06-30 | Univ Health Network | Inhibitori hpk1 i postupci za njihovo korišćenje |
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