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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
- A61K31/33—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
-
- 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
-
- 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
- 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
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- 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)
- Veterinary Medicine (AREA)
- Public Health (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)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (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) | KR102614872B1 (fr) |
| CN (2) | CN113214287B (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 (119)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MA42456B1 (fr) * | 2015-06-25 | 2021-06-30 | Univ Health Network | Inhibiteurs de hpk1 et leurs procédés d'utilisation |
| US10280164B2 (en) | 2016-09-09 | 2019-05-07 | Incyte Corporation | Pyrazolopyridone compounds and uses thereof |
| WO2018049214A1 (fr) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Dérivés de pyrazolopyridine comme modulateurs de hpk1 et leurs utilisations pour le traitement du cancer |
| CN115819417A (zh) | 2016-09-09 | 2023-03-21 | 因赛特公司 | 作为hpk1调节剂的吡唑并吡啶衍生物及其用于治疗癌症的用途 |
| US20180072741A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
| WO2018152220A1 (fr) * | 2017-02-15 | 2018-08-23 | Incyte Corporation | Composés de pyrazolopyridine et leurs utilisations |
| CN110402248B (zh) * | 2017-03-15 | 2023-01-06 | 豪夫迈·罗氏有限公司 | 作为hpk1抑制剂的氮杂吲哚类 |
| EP3601259B1 (fr) | 2017-03-30 | 2022-02-23 | F. Hoffmann-La Roche AG | Isoquinoléines utilisées en tant qu'inhibiteurs de hpk1 |
| AU2018244935A1 (en) * | 2017-03-30 | 2019-08-15 | F. Hoffmann-La Roche Ag | Naphthyridines as inhibitors of HPK1 |
| WO2018228925A1 (fr) | 2017-06-13 | 2018-12-20 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| EP3638670B1 (fr) | 2017-06-13 | 2021-07-21 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués utilisés en tant que modulateurs de map4k1 pour le traitement de maladies cancéreuses |
| EP3638669A1 (fr) | 2017-06-13 | 2020-04-22 | Bayer Pharma Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| CA3070013A1 (fr) | 2017-07-18 | 2019-01-24 | Bayer Pharma Aktiengesellschaft | Derives de pyrrolopyridine substitues |
| 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 |
| EP3707138B1 (fr) * | 2017-11-06 | 2022-07-13 | Bristol-Myers Squibb Company | Composés d'isofuranone utiles en tant qu'inhibiteurs de hpk1 |
| EP3755703B1 (fr) * | 2018-02-20 | 2022-05-04 | Incyte Corporation | Dérivés n-(phényl)-2-(phényl)pyrimidine-4-carboxamide et composés similaires en tant qu'inhibiteurs de hpk1 pour le traitemant du cancer |
| US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
| US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
| US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
| TW202012405A (zh) * | 2018-07-24 | 2020-04-01 | 瑞士商赫孚孟拉羅股份公司 | 萘啶化合物及其用途 |
| TW202019905A (zh) | 2018-07-24 | 2020-06-01 | 瑞士商赫孚孟拉羅股份公司 | 異喹啉化合物及其用途 |
| 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 |
| US11612606B2 (en) | 2018-10-03 | 2023-03-28 | Genentech, Inc. | 8-aminoisoquinoline compounds and uses thereof |
| WO2020072695A1 (fr) * | 2018-10-03 | 2020-04-09 | Genentech, Inc. | Composés de 8-aminoisoquinoline et leurs utilisations |
| US12331320B2 (en) | 2018-10-10 | 2025-06-17 | The Research Foundation For The State University Of New York | Genome edited cancer cell vaccines |
| WO2020092528A1 (fr) | 2018-10-31 | 2020-05-07 | Gilead Sciences, Inc. | Composés 6-azabenzimidazole substitués ayant une activité inhibitrice de hpk1 |
| US11203591B2 (en) | 2018-10-31 | 2021-12-21 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds |
| WO2020120257A1 (fr) | 2018-12-11 | 2020-06-18 | Bayer Aktiengesellschaft | Dérivés de pyrrolopyridine substitués |
| WO2020132384A1 (fr) | 2018-12-21 | 2020-06-25 | Celgene Corporation | Inhibiteurs thiénopyridine de ripk2 |
| WO2020135483A1 (fr) * | 2018-12-26 | 2020-07-02 | Janssen Pharmaceutica Nv | Composés de thiénopyridinone |
| US12492194B2 (en) | 2019-03-26 | 2025-12-09 | Janssen Pharmaceutica Nv | HPK1 inhibitors |
| US12486264B2 (en) | 2019-03-26 | 2025-12-02 | Janssen Pharmaceutica Nv | Bicyclic HPK1 inhibitors |
| WO2020235902A1 (fr) * | 2019-05-17 | 2020-11-26 | 주식회사 보로노이 | Dérivé de pyrimidine condensé avec un hétérocycle et son utilisation |
| EP3972695A1 (fr) | 2019-05-23 | 2022-03-30 | Gilead Sciences, Inc. | Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1 |
| WO2020263830A1 (fr) | 2019-06-25 | 2020-12-30 | Gilead Sciences, Inc. | Protéines de fusion flt3l-fc et procédés d'utilisation |
| 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 |
| BR112022002059A2 (pt) | 2019-08-06 | 2022-06-07 | Incyte Corp | Formas sólidas de um inibidor de hpk1 |
| MX2022002877A (es) * | 2019-09-13 | 2022-08-08 | Nimbus Saturn Inc | Antagonistas de cinasa progenitora hematopoyetica 1 (hpk1) y sus usos. |
| 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 |
| ES2973832T3 (es) | 2019-10-18 | 2024-06-24 | Forty Seven Inc | Terapias combinadas para el tratamiento de síndromes mielodisplásicos y leucemia mieloide aguda |
| JP2022552748A (ja) | 2019-10-31 | 2022-12-19 | フォーティ セブン, インコーポレイテッド | 抗cd47及び抗cd20による血液癌の治療 |
| TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
| IL294032A (en) | 2019-12-24 | 2022-08-01 | Carna Biosciences Inc | Compounds that regulate diacylglycerol kinase |
| JP7667745B2 (ja) * | 2020-01-09 | 2025-04-23 | 住友化学株式会社 | 複素環化合物及びそれを含有する有害節足動物防除組成物 |
| 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 |
| IL297327B2 (en) | 2020-05-01 | 2026-01-01 | Gilead Sciences Inc | 4,2-dioxopyrimidine compounds CD73 inhibitors |
| KR20230019110A (ko) * | 2020-05-11 | 2023-02-07 | 유니버시티 헬스 네트워크 | 4-아미노-5-(6-(4-메틸피페라진-1-일)-1H-벤조[D]이미다졸-2-일)티에노[2,3-b]피리딘-6(7H)-온(one)의 염 및 결정형 |
| 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 |
| WO2022064459A1 (fr) * | 2020-09-28 | 2022-03-31 | 1ST Biotherapeutics, Inc. | Indazoles utilisés en tant qu'inhibiteurs de kinase 1 progénitrice hématopoïétique (hpk1) et leurs procédés d'utilisation |
| HRP20260277T1 (hr) * | 2020-09-30 | 2026-04-10 | Beone Medicines I Gmbh | Spojevi 3-[(1h-pirazol-4-il)oksi]pirazin-2-amina kao inhibitori hpk1 i njihova upotreba |
| US20230406864A1 (en) * | 2020-11-09 | 2023-12-21 | Merck Sharp & Dohme Llc | 7-azole substituted 2-aminoquinazoline inhibitors of 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 |
| US20240174683A1 (en) | 2021-02-05 | 2024-05-30 | Bayer Aktiengesellschaft | Map4k1 inhibitors |
| CN114907377A (zh) * | 2021-02-10 | 2022-08-16 | 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 |
| EP4291235A4 (fr) | 2021-02-12 | 2025-01-08 | Nimbus Saturn, Inc. | Antagonistes de hpk1 et leurs utilisations |
| US11926625B2 (en) | 2021-03-05 | 2024-03-12 | Nimbus Saturn, Inc. | HPK1 antagonists and uses thereof |
| TW202246284A (zh) * | 2021-03-10 | 2022-12-01 | 大陸商山東軒竹醫藥科技有限公司 | 三并環類hpk1抑制劑及其用途 |
| 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 |
| US20240425479A1 (en) * | 2021-04-30 | 2024-12-26 | Ontario Institute For Cancer Research (Oicr) | Halo-substituted amino aza-heteroaryl compounds as inhibitors of the haematopoietic progenitor kinase 1 (hpk1) |
| JP2024517771A (ja) * | 2021-04-30 | 2024-04-23 | オンタリオ・インスティテュート・フォー・キャンサー・リサーチ(オーアイシーアール) | 造血前駆キナーゼ1(hpk1)の阻害剤としての置換アミノアザヘテロアリール化合物 |
| 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) |
| 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 |
| WO2022258044A1 (fr) * | 2021-06-11 | 2022-12-15 | 杭州中美华东制药有限公司 | Composé de pyrrolopyridinone, son procédé de préparation et son utilisation |
| MX2023014762A (es) | 2021-06-23 | 2024-01-15 | Gilead Sciences Inc | Compuestos moduladores de diacilglicerol quinasa. |
| JP7686091B2 (ja) | 2021-06-23 | 2025-05-30 | 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 |
| AU2022299051B2 (en) | 2021-06-23 | 2025-03-13 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| 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 |
| WO2023288254A1 (fr) * | 2021-07-14 | 2023-01-19 | Blueprint Medicines Corporation | Composés hétérocycliques utilisés en tant qu'inhibiteurs de map4k1 |
| TW202321239A (zh) | 2021-07-20 | 2023-06-01 | 瑞典商阿斯特捷利康公司 | 作為hpk1抑制劑用於治療癌症之經取代的吡𠯤—2—甲醯胺 |
| WO2023015199A1 (fr) * | 2021-08-03 | 2023-02-09 | 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 |
| EP4416146A4 (fr) * | 2021-10-15 | 2025-11-05 | Lomond Therapeutics Inc | 1h-pyrazolo[4,3-c]quinoléines substituées, leurs procédés de préparation et leur utilisation |
| AU2022375782B2 (en) | 2021-10-28 | 2026-02-26 | Gilead Sciences, Inc. | Pyridizin-3(2h)-one derivatives |
| JP7787991B2 (ja) | 2021-10-29 | 2025-12-17 | ギリアード サイエンシーズ, インコーポレイテッド | Cd73化合物 |
| WO2023107956A1 (fr) | 2021-12-08 | 2023-06-15 | Dragonfly Therapeutics, Inc. | Protéines se liant à nkg2d, cd16 et 5t4 |
| US20230220106A1 (en) | 2021-12-08 | 2023-07-13 | Dragonfly Therapeutics, Inc. | Antibodies targeting 5t4 and uses thereof |
| 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 |
| US12122764B2 (en) | 2021-12-22 | 2024-10-22 | Gilead Sciences, Inc. | IKAROS zinc finger family degraders and uses thereof |
| KR20240123836A (ko) | 2021-12-22 | 2024-08-14 | 길리애드 사이언시즈, 인코포레이티드 | 이카로스 아연 핑거 패밀리 분해제 및 이의 용도 |
| US20250049787A1 (en) * | 2021-12-22 | 2025-02-13 | University Health Network | Treatment for acute myeloid leukemia or lymphoma |
| 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 |
| TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
| WO2023151559A1 (fr) * | 2022-02-08 | 2023-08-17 | 和径医药科技(上海)有限公司 | Composé hétérocyclique, composition pharmaceutique le contenant et utilisation anti-tumorale associée |
| WO2023178181A1 (fr) | 2022-03-17 | 2023-09-21 | Gilead Sciences, Inc. | Agents de dégradation des doigts de zinc de la famille ikaros et leurs utilisations |
| KR20240165995A (ko) | 2022-03-24 | 2024-11-25 | 길리애드 사이언시즈, 인코포레이티드 | Trop-2 발현 암의 치료를 위한 병용요법 |
| 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 |
| CR20240451A (es) | 2022-04-21 | 2024-12-04 | Gilead Sciences Inc | Compuestos de modulación de kras g12d |
| KR20250028371A (ko) | 2022-07-01 | 2025-02-28 | 길리애드 사이언시즈, 인코포레이티드 | Cd73 화합물 |
| WO2024064668A1 (fr) | 2022-09-21 | 2024-03-28 | Gilead Sciences, Inc. | POLYTHÉRAPIE ANTICANCÉREUSE PAR RAYONNEMENT IONISANT FOCAL ET PERTURBATION CD47/SIRPα |
| 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 |
| AU2023409398A1 (en) | 2022-12-22 | 2025-06-05 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| 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 |
| AU2024252725A1 (en) | 2023-04-11 | 2025-11-06 | Gilead Sciences, Inc. | Kras modulating compounds |
| CR20250446A (es) | 2023-04-21 | 2025-12-02 | Gilead Sciences Inc | Inhibidores de prmt5 y usos de los mismos |
| AU2024306338A1 (en) | 2023-06-30 | 2026-01-08 | Gilead Sciences, Inc. | Kras modulating compounds |
| CN121620513A (zh) | 2023-07-26 | 2026-03-06 | 吉利德科学公司 | Parp7抑制剂 |
| KR20260046403A (ko) | 2023-07-26 | 2026-04-07 | 길리애드 사이언시즈, 인코포레이티드 | Parp7 저해제 |
| US20250109147A1 (en) | 2023-09-08 | 2025-04-03 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| US20250101042A1 (en) | 2023-09-08 | 2025-03-27 | Gilead Sciences, Inc. | Kras g12d modulating compounds |
| 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 |
| US20250154172A1 (en) | 2023-11-03 | 2025-05-15 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
| WO2025137640A1 (fr) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Inhibiteurs azaspiro de wrn |
| 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 |
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 |
| ATE448226T1 (de) * | 2000-09-01 | 2009-11-15 | Novartis Vaccines & Diagnostic | Aza heterocyclische derivate und ihre therapeutische verwendung |
| 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 |
| JPWO2008143262A1 (ja) | 2007-05-21 | 2010-08-12 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| UA103321C2 (ru) * | 2008-04-11 | 2013-10-10 | Мерк Патент Гмбх | Производные тиенопиридона как активаторы amp-активированной протеинкиназы (амрк) |
| HRP20120549T1 (hr) | 2008-05-05 | 2012-07-31 | Merck@Patent@GmbH | Derivati tienopiridona kao amp aktivirani aktivatori protein kinaze ampk |
| RU2013138835A (ru) | 2011-02-09 | 2015-03-20 | Ф. Хоффманн-Ля Рош Аг | Гетероциклические соединения в качестве ингибиторов pi3 киназы |
| GB201114212D0 (en) * | 2011-08-18 | 2011-10-05 | Ucb Pharma Sa | Therapeutic agents |
| MA42456B1 (fr) | 2015-06-25 | 2021-06-30 | Univ Health Network | Inhibiteurs de hpk1 et leurs procédés d'utilisation |
-
2016
- 2016-06-23 MA MA42456A patent/MA42456B1/fr unknown
- 2016-06-23 US US15/738,286 patent/US10501474B2/en active Active
- 2016-06-23 BR BR122023006150-0A patent/BR122023006150B1/pt active IP Right Grant
- 2016-06-23 AU AU2016282289A patent/AU2016282289B2/en active Active
- 2016-06-23 HU HUE16813437A patent/HUE054159T2/hu unknown
- 2016-06-23 HR HRP20210895TT patent/HRP20210895T1/hr unknown
- 2016-06-23 IL IL283353A patent/IL283353B/en unknown
- 2016-06-23 EP EP16813437.7A patent/EP3322711B1/fr active Active
- 2016-06-23 SI SI201631189T patent/SI3322711T1/sl unknown
- 2016-06-23 LT LTEP16813437.7T patent/LT3322711T/lt unknown
- 2016-06-23 KR KR1020187001327A patent/KR102614872B1/ko active Active
- 2016-06-23 MX MX2018000048A patent/MX386480B/es unknown
- 2016-06-23 CN CN202110534553.5A patent/CN113214287B/zh active Active
- 2016-06-23 JP JP2017566338A patent/JP6898868B2/ja active Active
- 2016-06-23 BR BR112017027241-5A patent/BR112017027241B1/pt active IP Right Grant
- 2016-06-23 WO PCT/CA2016/050734 patent/WO2016205942A1/fr not_active Ceased
- 2016-06-23 ES ES16813437T patent/ES2872555T3/es active Active
- 2016-06-23 RS RS20210675A patent/RS61919B1/sr unknown
- 2016-06-23 PT PT168134377T patent/PT3322711T/pt unknown
- 2016-06-23 SM SM20210324T patent/SMT202100324T1/it unknown
- 2016-06-23 PL PL16813437T patent/PL3322711T3/pl unknown
- 2016-06-23 SG SG10202105964RA patent/SG10202105964RA/en unknown
- 2016-06-23 KR KR1020237042987A patent/KR102740623B1/ko active Active
- 2016-06-23 DK DK16813437.7T patent/DK3322711T3/da active
- 2016-06-23 CN CN201680048058.0A patent/CN107922431B/zh active Active
- 2016-06-23 MD MDE20180529T patent/MD3322711T2/ro unknown
- 2016-06-23 EA EA201890059A patent/EA035421B1/ru not_active IP Right Cessation
- 2016-06-24 TW TW105120043A patent/TWI733679B/zh active
-
2017
- 2017-12-11 IL IL256250A patent/IL256250B/en active IP Right Grant
-
2018
- 2018-01-08 MX MX2021011435A patent/MX2021011435A/es unknown
-
2019
- 2019-12-06 US US16/705,458 patent/US11059832B2/en active Active
-
2021
- 2021-06-08 CY CY20211100498T patent/CY1124489T1/el unknown
- 2021-06-11 JP JP2021097834A patent/JP7241810B2/ja active Active
- 2021-07-12 US US17/372,717 patent/US20220002313A1/en not_active Abandoned
-
2023
- 2023-03-07 JP JP2023034474A patent/JP2023071911A/ja active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA42456A (fr) | Inhibiteurs de hpk1 et leurs procédés d'utilisation | |
| MA54229B1 (fr) | Composés et compositions destinés au traitement d'états pathologiques associés à une activité de nlrp | |
| MA39554A3 (fr) | Spirocycloheptanes utilisés en tant qu'inhibiteurs de rock | |
| MA40111A1 (fr) | Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1 | |
| MX2021012122A (es) | Inhibidores de la proteina tirosina fosfatasa. | |
| CR20210189A (es) | Inhibidores de la proteina tirosina fosfatasa | |
| MA35753B1 (fr) | Aryl-dihydropyridinones et pipéridinones en tant qu'inhibiteurs de mgat2 | |
| WO2018112365A3 (fr) | Procédés de traitement du cancer colorectal et d'un mélanome en utilisant parabacteroides goldsteinii | |
| MA43131B1 (fr) | Compositions et procédés d'inhibition de l'activité de l'arginase | |
| MA37762A1 (fr) | Composés n-aryltriazole utilisés comme antagonistes de lpar | |
| MA38175A1 (fr) | Lactames fusionnés à un aryle et hétéroaryle | |
| MA45920A (fr) | Inhibiteurs de pyridopyrimidinone cdk2/4/6 | |
| MA37764A1 (fr) | Composés n-alkyltriazole utilisés comme antagonistes de lpar | |
| MA38393A3 (fr) | Composés hétéroaryle et utilisations associées | |
| MA52492B1 (fr) | Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés | |
| MA32134B1 (fr) | Composés hétérocycliques | |
| MA29909B1 (fr) | Derives de pyridazine | |
| MA29856B1 (fr) | Derives de diacylindazole en tant qu'inhibiteurs de lipases et de phospholipases | |
| UA116774C2 (uk) | Інгібітори серин/треонінкінази | |
| MA43364B1 (fr) | Composés d'alcènes tétrasubstitués et leur utilisation | |
| MA42145A (fr) | Triazoles agonistes du récepteur apj | |
| EP2595482A4 (fr) | Inhibiteurs de l'aldostérone synthase | |
| Liu et al. | Synthesis and characterization of 1H-phenanthro [9, 10-d] imidazole derivatives as multifunctional agents for treatment of Alzheimer's disease | |
| MA39152A1 (fr) | Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine | |
| PH12021552588A1 (en) | Cd73 inhibitors |