MA42456B1 - Inhibiteurs de hpk1 et leurs procédés d'utilisation - Google Patents

Inhibiteurs de hpk1 et leurs procédés d'utilisation

Info

Publication number
MA42456B1
MA42456B1 MA42456A MA42456A MA42456B1 MA 42456 B1 MA42456 B1 MA 42456B1 MA 42456 A MA42456 A MA 42456A MA 42456 A MA42456 A MA 42456A MA 42456 B1 MA42456 B1 MA 42456B1
Authority
MA
Morocco
Prior art keywords
compounds
methods
formula
pharmaceutically acceptable
inhibitors
Prior art date
Application number
MA42456A
Other languages
English (en)
Other versions
MA42456A (fr
Inventor
Peter Brent Sampson
Narendra Kumar B Patel
Heinz W Pauls
Sze-Wan Li
Grace Ng
Radoslaw Laufer
Yong Liu
Yunhui Lang
Original Assignee
Univ Health Network
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Health Network filed Critical Univ Health Network
Publication of MA42456A publication Critical patent/MA42456A/fr
Publication of MA42456B1 publication Critical patent/MA42456B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic 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
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/4355Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/4365Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/5355Non-condensed oxazines and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], 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
    • C07K16/2818Immunoglobulins [IGs], 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

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).
MA42456A 2015-06-25 2016-06-23 Inhibiteurs de hpk1 et leurs procédés d'utilisation MA42456B1 (fr)

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 MA42456A (fr) 2018-05-23
MA42456B1 true 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 (27)

Country Link
US (3) US10501474B2 (fr)
EP (1) EP3322711B1 (fr)
JP (3) JP6898868B2 (fr)
KR (2) KR20240000617A (fr)
CN (2) CN107922431B (fr)
AU (1) AU2016282289B2 (fr)
BR (2) BR122023006150B1 (fr)
CA (1) CA2989684A1 (fr)
CY (1) CY1124489T1 (fr)
DK (1) DK3322711T3 (fr)
EA (1) EA035421B1 (fr)
ES (1) ES2872555T3 (fr)
HK (1) HK1255833A1 (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) MX2018000048A (fr)
PL (1) PL3322711T3 (fr)
PT (1) PT3322711T (fr)
RS (1) RS61919B1 (fr)
SG (1) SG10202105964RA (fr)
SI (1) SI3322711T1 (fr)
TW (1) TWI733679B (fr)
WO (1) WO2016205942A1 (fr)

Families Citing this family (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2989684A1 (fr) * 2015-06-25 2016-12-29 University Health Network Inhibiteurs de hpk1 et leurs procedes d'utilisation
WO2018049191A1 (fr) 2016-09-09 2018-03-15 Incyte Corporation Dérivés de pyrazolopyridone en tant que modulateurs de hpk1 et leurs utilisations pour le traitement du cancer
US20180072718A1 (en) 2016-09-09 2018-03-15 Incyte Corporation Pyrazolopyridine compounds and uses thereof
MX2019002750A (es) 2016-09-09 2019-07-04 Incyte Corp Derivados de pirazolopiridina como moduladores de cinasa 1 progenitora hematopoyetica (hpk1) y usos de los mismos para tratamiento de cancer.
TW201811799A (zh) 2016-09-09 2018-04-01 美商英塞特公司 吡唑并嘧啶化合物及其用途
US20180228786A1 (en) 2017-02-15 2018-08-16 Incyte Corporation Pyrazolopyridine compounds and uses thereof
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
AU2018243770A1 (en) * 2017-03-30 2019-09-19 F. Hoffmann-La Roche Ag Isoquinolines as inhibitors of HPK1
WO2018183956A1 (fr) * 2017-03-30 2018-10-04 Genentech, Inc. Naphtyridines utilisés en tant qu'inhibiteurs de hpk1
CA3066859A1 (fr) 2017-06-13 2018-12-20 Bayer Pharma Aktiengesellschaft Derives de pyrrolopyridine substitues
CA3079060A1 (fr) 2017-06-13 2018-12-20 Bayer Pharma Aktiengesellschaft Derives de pyrrolopyridine substitues utilises en tant que modulateurs de map4k1 pour le traitement de maladies cancereuses
US20200246347A1 (en) 2017-06-13 2020-08-06 Bayer Pharma Aktiengesellschaft Substituted Pyrrolopyridine-Derivatives
WO2019016071A1 (fr) 2017-07-18 2019-01-24 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
CN111527084B (zh) * 2017-11-06 2023-07-18 百时美施贵宝公司 可用作hpk1抑制剂的异呋喃酮化合物
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
MD3755703T2 (ro) 2018-02-20 2022-10-31 Incyte Corp Derivați N-(fenil)-2-(fenil)pirimidin-4-carboxamidă și compuși înrudiți ca inhibitori HPK1 pentru tratarea cancerului
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
JP7399968B2 (ja) 2018-09-25 2023-12-18 インサイト・コーポレイション Alk2及び/またはfgfr調節剤としてのピラゾロ[4,3-d]ピリミジン化合物
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
JP2022504080A (ja) * 2018-10-03 2022-01-13 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト 8-アミノイソキノリン化合物およびその使用
US11612606B2 (en) 2018-10-03 2023-03-28 Genentech, Inc. 8-aminoisoquinoline compounds and uses thereof
EP3873903B1 (fr) 2018-10-31 2024-01-24 Gilead Sciences, Inc. Composés de 6-azabenzimidazole substitués en tant qu'inhibiteurs de hpk1
US11071730B2 (en) 2018-10-31 2021-07-27 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds
US20220047603A1 (en) 2018-12-11 2022-02-17 Bayer Aktiengesellschaft Substituted pyrrolopyridine-derivatives
TW202039481A (zh) 2018-12-21 2020-11-01 美商西建公司 Ripk2之噻吩并吡啶抑制劑
KR20210108433A (ko) * 2018-12-26 2021-09-02 얀센 파마슈티카 엔.브이. 티에노피리디논 화합물
EP3947373A1 (fr) 2019-03-26 2022-02-09 Janssen Pharmaceutica NV Inhibiteurs bicycliques de hpk1
CA3129768A1 (fr) 2019-03-26 2020-10-01 Laurence Anne Mevellec Inhibiteurs de hpk1
EP3971190A4 (fr) * 2019-05-17 2023-06-14 Voronoi Inc. 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
PE20220231A1 (es) 2019-06-25 2022-02-07 Gilead Sciences Inc Proteinas de fusion flt3l-fc y metodos de uso
BR112022002059A2 (pt) 2019-08-06 2022-06-07 Incyte Corp Formas sólidas de um inibidor de hpk1
KR20220105631A (ko) 2019-09-13 2022-07-27 님버스 새턴 인코포레이티드 Hpk1 길항제 및 이의 용도
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
KR20220085796A (ko) 2019-10-18 2022-06-22 포티 세븐, 인코포레이티드 골수이형성 증후군 및 급성 골수성 백혈병을 치료하기 위한 조합 치료
CA3153636A1 (fr) 2019-10-31 2021-05-06 Forty Seven, Inc. Traitement d'un cancer du sang base sur une therapie anti-cd47 et anti-cd20
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
PE20230376A1 (es) 2019-12-24 2023-03-06 Carna Biosciences Inc Compuestos moduladores de la diacilglicerol quinasa
US20230115523A1 (en) * 2020-01-09 2023-04-13 Sumitomo Chemical Company, Limited Heterocyclic compound and harmful arthropod-controlling composition including same
IL295023A (en) 2020-02-14 2022-09-01 Jounce Therapeutics Inc Antibodies and fusion proteins that bind to ccr8 and their uses
BR112022020814A2 (pt) * 2020-04-13 2022-11-29 Univ Health Network Métodos para tratamento de síndrome de liberação de citocina
CN115698009A (zh) 2020-05-01 2023-02-03 吉利德科学公司 抑制cd73的2,4-二氧代嘧啶化合物
EP4149946A1 (fr) * 2020-05-11 2023-03-22 University Health Network Formes salines et cristallines de 4-amino-5-(6-(4-méthylpipérazin-1-yl)-1h-benzo[d]imidazol-2-yl)thiéno[2,3-b]pyridin-6(7h)-one
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
EP4222150A1 (fr) * 2020-09-30 2023-08-09 BeiGene, Ltd. Composés de 3-[(1h-pyrazol-4-yl)oxy]pyrazin-2-amine utilisés en tant qu'inhibiteur de hpk1 et leur utilisation
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
WO2022167627A1 (fr) 2021-02-05 2022-08-11 Bayer Aktiengesellschaft Inhibiteurs de map4k1
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
CN116981666A (zh) * 2021-03-26 2023-10-31 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
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
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
US11932634B2 (en) 2021-06-23 2024-03-19 Gilead Sciences, Inc. Diacylglycerol kinase modulating compounds
CA3222595A1 (fr) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Composes de modulation de la diacylglycerol kinase
US20230046340A1 (en) 2021-06-23 2023-02-16 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
AU2022299051A1 (en) 2021-06-23 2023-12-07 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
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
WO2023057882A1 (fr) * 2021-10-05 2023-04-13 Pfizer Inc. Combinaisons de composés d'azalactam avec un antagoniste de liaison à l'axe pd-1 pour le traitement du cancer
AU2022364646A1 (en) * 2021-10-15 2024-03-28 Lomond Therapeutics, Inc. SUBSTITUTED 1H-PYRAZOLO [4,3-c] QUINOLINES, METHODS OF PREPARATION, AND USE THEREOF
US20230183216A1 (en) 2021-10-28 2023-06-15 Gilead Sciences, Inc. Pyridizin-3(2h)-one derivatives
WO2023077030A1 (fr) 2021-10-29 2023-05-04 Gilead Sciences, Inc. Composés cd73
WO2023107956A1 (fr) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Protéines se liant à nkg2d, cd16 et 5t4
WO2023107954A1 (fr) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Anticorps ciblant 5t4 et leurs utilisations
TW202333754A (zh) * 2021-12-17 2023-09-01 大陸商海思科醫藥集團股份有限公司 並環雜環衍生物及其在醫藥上的應用
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
WO2023122581A2 (fr) 2021-12-22 2023-06-29 Gilead Sciences, Inc. Agents de dégradation de doigt de zinc de la famille ikaros et utilisations associées
US20230242508A1 (en) 2021-12-22 2023-08-03 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
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
CN116462685A (zh) * 2022-02-08 2023-07-21 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
US20230373950A1 (en) 2022-03-17 2023-11-23 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
US20230355796A1 (en) 2022-03-24 2023-11-09 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
TW202345901A (zh) 2022-04-05 2023-12-01 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
WO2023205719A1 (fr) 2022-04-21 2023-10-26 Gilead Sciences, Inc. Composés modulateurs de kras g12d
WO2024006929A1 (fr) 2022-07-01 2024-01-04 Gilead Sciences, Inc. Composés cd73
WO2024064668A1 (fr) 2022-09-21 2024-03-28 Gilead Sciences, Inc. POLYTHÉRAPIE ANTICANCÉREUSE PAR RAYONNEMENT IONISANT FOCAL ET PERTURBATION CD47/SIRPα

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001021615A1 (fr) * 1999-09-17 2001-03-29 Yamanouchi Pharmaceutical Co., Ltd. Dérivés de benzimidazole
CA2387840A1 (fr) 1999-10-19 2001-04-26 Scott R. Hambaugh Inhibiteurs tyrosine kinase
DE60140456D1 (de) * 2000-09-01 2009-12-24 Novartis Vaccines & Diagnostic Aza heterocyclische derivate und ihre therapeutische verwendung
AU2003249540A1 (en) 2002-08-13 2004-02-25 Warner-Lambert Company Llc Fused bicyclic metalloproteinase inhibitors
US7119205B2 (en) 2003-05-16 2006-10-10 Abbott Laboratories Thienopyridones as AMPK activators for the treatment of diabetes and obesity
WO2008143262A1 (fr) 2007-05-21 2008-11-27 Takeda Pharmaceutical Company Limited Composé hétérocyclique et son utilisation
PL2262500T3 (pl) * 2008-04-11 2016-09-30 Pochodne tienopirydonowe jako aktywatory kinazy białkowej aktywowanej przez amp (ampk)
CA2723429C (fr) 2008-05-05 2016-10-11 Daniel Cravo Derives de thienopyridone comme activateurs de la proteine kinase activee par l'amp (ampk)
JP5766820B2 (ja) 2011-02-09 2015-08-19 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Pi3キナーゼ阻害剤としての複素環化合物
GB201114212D0 (en) * 2011-08-18 2011-10-05 Ucb Pharma Sa Therapeutic agents
CA2989684A1 (fr) * 2015-06-25 2016-12-29 University Health Network Inhibiteurs de hpk1 et leurs procedes d'utilisation

Also Published As

Publication number Publication date
PL3322711T3 (pl) 2021-10-25
EP3322711A1 (fr) 2018-05-23
IL283353B (en) 2022-09-01
SI3322711T1 (sl) 2021-08-31
HRP20210895T1 (hr) 2021-08-20
CN107922431A (zh) 2018-04-17
KR102614872B1 (ko) 2023-12-15
PT3322711T (pt) 2021-05-13
JP6898868B2 (ja) 2021-07-07
BR112017027241A2 (fr) 2018-08-21
HK1255833A1 (zh) 2019-08-30
US11059832B2 (en) 2021-07-13
EA035421B1 (ru) 2020-06-11
CA2989684A1 (fr) 2016-12-29
US20180179221A1 (en) 2018-06-28
SG10202105964RA (en) 2021-07-29
MX2018000048A (es) 2018-06-06
US20220002313A1 (en) 2022-01-06
EA201890059A1 (ru) 2018-07-31
RS61919B1 (sr) 2021-06-30
DK3322711T3 (en) 2021-04-26
IL283353A (en) 2021-07-29
CN113214287B (zh) 2023-10-20
CY1124489T1 (el) 2022-07-22
US20200190104A1 (en) 2020-06-18
JP2018522858A (ja) 2018-08-16
MX2021011435A (es) 2021-10-13
AU2016282289A1 (en) 2018-01-04
TWI733679B (zh) 2021-07-21
JP7241810B2 (ja) 2023-03-17
BR112017027241B1 (pt) 2023-09-26
WO2016205942A1 (fr) 2016-12-29
HUE054159T2 (hu) 2021-08-30
AU2016282289B2 (en) 2020-12-24
EP3322711A4 (fr) 2018-12-19
IL256250A (en) 2018-02-28
BR122023006150B1 (pt) 2023-12-12
CN107922431B (zh) 2021-06-04
KR20180015255A (ko) 2018-02-12
TW201718597A (zh) 2017-06-01
US10501474B2 (en) 2019-12-10
CN113214287A (zh) 2021-08-06
MD3322711T2 (ro) 2021-07-31
ES2872555T3 (es) 2021-11-02
JP2023071911A (ja) 2023-05-23
LT3322711T (lt) 2021-05-10
JP2021138754A (ja) 2021-09-16
KR20240000617A (ko) 2024-01-02
MA42456A (fr) 2018-05-23
EP3322711B1 (fr) 2021-03-10
IL256250B (en) 2021-06-30

Similar Documents

Publication Publication Date Title
MA42456B1 (fr) Inhibiteurs de hpk1 et leurs procédés d'utilisation
MA46452B1 (fr) Composés de benzo[b]thiophéne en tant qu'agonistes de sting
MA39554A3 (fr) Spirocycloheptanes utilisés en tant qu'inhibiteurs de rock
MA47079B1 (fr) Composés amino-triazolopyidines et leur utilisation pour traiter le cancer
ZA202101960B (en) Protein tyrosine phosphatase inhibitors
CR20210501A (es) Inhibidores de la proteína tirosina fosfatasa
MA44674B1 (fr) Inhibiteurs de bromodomaine
MA42678B1 (fr) Nouveaux analogues nucléosidiques substitués à cycle aromatique bicyclique 6-6 pour une utilisation en tant qu'inhibiteurs de prmt5
MA38393B1 (fr) Composés hétéroaryle et utilisations associées
MA37762B1 (fr) Composés n-aryltriazole utilisés comme antagonistes de lpar
MA40225B1 (fr) Composés dihydroisoquinolinone substitués
MA29909B1 (fr) Derives de pyridazine
MA32134B1 (fr) Composés hétérocycliques
MA29856B1 (fr) Derives de diacylindazole en tant qu'inhibiteurs de lipases et de phospholipases
PH12013502369A1 (en) Diazacarbazoles and methods of use
MA34234B1 (fr) Composes pyrazol-4-yl-heterocyclyle-carboxamide et leurs procedes d'utilisation
MA37142B1 (fr) Dérivés de dihydro-benzo-oxazine et de dihydro-pyrido-oxazine
MX2018013164A (es) Compuestos novedosos de imidazopiridina sustituida como inhibidores de indolamina-2,3-dioxigenasa y/o triptofano-2,3-dioxigenasa.
SG156681A1 (en) Use of ranolazine in combination with at least one remodeling agent for reversing left ventricular remodeling in the treatment of heart failure
MA39335B1 (fr) Inhibiteurs mgat2 de dihydropyridinone à substitution tétrazolone
MA37765A1 (fr) Composés de pyrazole substitués utilisés comme antagonistes de lpar
MA43052B1 (fr) Inhibiteurs de la kallicréine plasmatique humaine
AU2020258568A8 (en) CD73 inhibitors
MX2021002878A (es) Inhibidores de cd73 y usos farmaceuticos de los mismos.
MA39926B1 (fr) Dérivés de dihétérocycle liés à cycloalkyle