MA56038B1 - Inhibiteurs à petite molécule de kinase induisant nf-kb - Google Patents

Inhibiteurs à petite molécule de kinase induisant nf-kb

Info

Publication number
MA56038B1
MA56038B1 MA56038A MA56038A MA56038B1 MA 56038 B1 MA56038 B1 MA 56038B1 MA 56038 A MA56038 A MA 56038A MA 56038 A MA56038 A MA 56038A MA 56038 B1 MA56038 B1 MA 56038B1
Authority
MA
Morocco
Prior art keywords
disorders
small molecule
compounds
molecule inhibitors
inducing kinase
Prior art date
Application number
MA56038A
Other languages
English (en)
Other versions
MA56038A (fr
Inventor
Alec D. Lebsack
Kevin D. Kreutter
Wenying Chai
Paul J. KRAWCZUK
J. Kent Barbay
Wendy Eccles
Michael D. Hack
Aaron T. HERRMANN
William M. Jones
Daniel J. Pippel
Alexander R. ROVIRA
Ronald L. Wolin
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of MA56038A publication Critical patent/MA56038A/fr
Publication of MA56038B1 publication Critical patent/MA56038B1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D475/00—Heterocyclic compounds containing pteridine ring systems
    • C07D475/06—Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Transplantation (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention concerne des composés agissant en tant qu'inhibiteurs de NIK, des compositions pharmaceutiques comprenant de tels composés, et des procédés d'utilisation de ces derniers. Ces composés et compositions pharmaceutiques sont destinés pour être utilisés dans la prévention ou le traitement de maladies telles que le cancer (notamment des malignités à lymphocytes B, y compris les leucémies, les lymphomes et le myélome), des troubles inflammatoires, des troubles auto-immuns, des troubles immunodermatologiques tels que la pustulose palmoplantaire et la hidradenite suppurativa, ainsi que des troubles métaboliques tels que l'obésité et le diabète.
MA56038A 2019-05-31 2020-05-29 Inhibiteurs à petite molécule de kinase induisant nf-kb MA56038B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201962855144P 2019-05-31 2019-05-31
US201962907833P 2019-09-30 2019-09-30
EP20733688.4A EP3976597B1 (fr) 2019-05-31 2020-05-29 Inhibiteurs à petite molécule de kinase induisant nf-kb
PCT/EP2020/065024 WO2020239999A1 (fr) 2019-05-31 2020-05-29 Inhibiteurs à petite molécule de kinase induisant nf-kb

Publications (2)

Publication Number Publication Date
MA56038A MA56038A (fr) 2022-04-06
MA56038B1 true MA56038B1 (fr) 2024-11-29

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
MA56038A MA56038B1 (fr) 2019-05-31 2020-05-29 Inhibiteurs à petite molécule de kinase induisant nf-kb

Country Status (37)

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US (3) US11254673B2 (fr)
EP (2) EP3976597B1 (fr)
JP (2) JP7547387B2 (fr)
KR (1) KR20220027871A (fr)
CN (2) CN114222737B (fr)
AU (1) AU2020282005B2 (fr)
BR (1) BR112021023796A2 (fr)
CL (1) CL2021003142A1 (fr)
CO (1) CO2021017838A2 (fr)
CR (1) CR20210587A (fr)
DK (1) DK3976597T3 (fr)
DO (1) DOP2021000244A (fr)
EC (1) ECSP21093623A (fr)
ES (1) ES2989387T3 (fr)
FI (1) FI3976597T3 (fr)
HR (1) HRP20241352T1 (fr)
HU (1) HUE068694T2 (fr)
IL (1) IL288387B2 (fr)
JO (1) JOP20210318B1 (fr)
LT (1) LT3976597T (fr)
MA (1) MA56038B1 (fr)
MD (1) MD3976597T2 (fr)
MX (1) MX2021014679A (fr)
MY (1) MY205653A (fr)
PE (1) PE20220768A1 (fr)
PH (1) PH12021553011A1 (fr)
PL (1) PL3976597T3 (fr)
PT (1) PT3976597T (fr)
RS (1) RS66105B1 (fr)
SA (1) SA521430960B1 (fr)
SG (1) SG11202112994WA (fr)
SI (1) SI3976597T1 (fr)
SM (1) SMT202400418T1 (fr)
TW (2) TWI850390B (fr)
UA (1) UA130430C2 (fr)
UY (1) UY38721A (fr)
WO (1) WO2020239999A1 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114222737B (zh) * 2019-05-31 2024-07-26 詹森药业有限公司 NF-κB诱导激酶的小分子抑制剂
WO2020243423A1 (fr) 2019-05-31 2020-12-03 Ikena Oncology, Inc. Inhibiteurs de tead et leurs utilisations
KR20220030222A (ko) 2019-05-31 2022-03-10 이케나 온콜로지, 인코포레이티드 Tead 억제제 및 이의 용도
IL316886A (en) * 2022-05-11 2025-01-01 Janssen Pharmaceutica Nv History of pyrrolidinones as NF kappa B kinase inhibitors
CA3257152A1 (fr) * 2022-05-11 2023-11-16 Janssen Pharmaceutica Nv Dérivés de pyrrolidinone utiles comme inhibiteurs de la kinase d'induction de nf-kb
EP4637773A1 (fr) 2022-12-22 2025-10-29 Boehringer Ingelheim International GmbH Formes cristallines d'un inhibiteur de her2
WO2025020886A1 (fr) * 2023-07-27 2025-01-30 浙江星浩澎博医药有限公司 Dérivé cyclique d'azaquinazoline et son utilisation
IL326016A (en) 2023-07-28 2026-03-01 Boehringer Ingelheim Int Process for manufacturing a HER2 inhibitor
WO2025235874A1 (fr) * 2024-05-10 2025-11-13 Schrödinger, Inc. Hétérocycles utiliséés en tant qu'inhibiteurs d'egfr
JP2026022634A (ja) * 2024-07-30 2026-02-12 日本たばこ産業株式会社 ピラゾロピリミジン化合物及びその医薬用途

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9930616D0 (en) 1999-12-24 2000-02-16 Mathilda & Terence Kennedy Ins Activation and inhibition of the immune system
US7132428B2 (en) 2003-07-03 2006-11-07 Aventis Pharmaceuticals Inc. Pyrazoloisoquinoline derivative as kinase inhibitors for the treatment of various disorders
JP2008509138A (ja) * 2004-08-03 2008-03-27 ワイス 心臓血管疾患の治療に有用なインダゾール類
WO2006053277A2 (fr) 2004-11-12 2006-05-18 Chippac, Inc. Interconnexion par microcablage
AU2009263037B2 (en) * 2008-06-26 2011-10-06 Amgen Inc. Alkynyl alcohols as kinase inhibitors
WO2010042337A1 (fr) 2008-10-07 2010-04-15 Merck Sharp & Dohme Corp. Nouveaux dérivés de 6-azaindole aminopyrimidine ayant une activité inhibitrice de nik
MX2013010513A (es) * 2011-03-16 2013-10-07 Hoffmann La Roche Compuestos de alcohol 6,5-heterociclil-propargilico y usos de los mismos.
JP2015507001A (ja) 2012-02-17 2015-03-05 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ 三環式化合物及びその使用方法
US8859553B2 (en) * 2012-07-30 2014-10-14 Astar Biotech Llc Protein kinase inhibitors
TWI663166B (zh) 2013-04-24 2019-06-21 健生藥品公司 新化合物
US20150057260A1 (en) * 2013-08-22 2015-02-26 Genentech, Inc. Alkynyl alcohols and methods of use
US20160096850A9 (en) * 2013-08-22 2016-04-07 Genentech, Inc. Alkynyl alcohols and methods of use
TWI704146B (zh) 2013-09-26 2020-09-11 比利時商健生藥品公司 用作ＮＩＫ抑制劑之新的1-(４-嘧啶基)-１Ｈ-吡唑並[３,２-ｃ]吡啶衍生物
TWI627173B (zh) 2013-09-26 2018-06-21 比利時商健生藥品公司 作為ＮＩＫ抑制劑的新穎３－（１Ｈ－吡唑－４－基）－１Ｈ－吡咯并［２，３－ｃ］吡啶衍生物
AU2015334917B2 (en) 2014-10-23 2019-08-29 Janssen Pharmaceutica Nv New compounds as NIK inhibitors
BR112017008039B1 (pt) 2014-10-23 2023-04-11 Janssen Pharmaceutica N.V. Derivados de pirazol como inibidores de nik, seu uso no tratamento ou prevenção de câncer e composição farmacêutica que os compreende
JP6616412B2 (ja) 2014-10-23 2019-12-04 ヤンセン ファーマシューティカ エヌ．ベー． Ｎｉｋ阻害剤としての新規のピラゾロピリミジン誘導体
MX371151B (es) 2014-10-23 2020-01-20 Janssen Pharmaceutica Nv NUEVOS DERIVADOS DE TIENOPIRIMIDINA EN CALIDAD DE INHIBIDORES DE LA CINASA INDUCTORA DE NF-kB (NIK).
JP2018510140A (ja) 2015-02-25 2018-04-12 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ アルキニルアルコール及び使用方法
ES2775449T3 (es) 2016-01-22 2020-07-27 Janssen Pharmaceutica Nv Nuevos derivados de cianoindolina sustituida como inhibidores de nik
EP3405464B1 (fr) 2016-01-22 2019-12-04 Janssen Pharmaceutica NV Nouveaux dérivés de pyridinone substituée 5- (2-amino-4-pyrimidinyle)-cyanoindoline en tant qu'inhibiteurs de nik
ES2837157T3 (es) 2016-06-30 2021-06-29 Janssen Pharmaceutica Nv Derivados de cianoindolina como inhibidores de NIK
WO2018002217A1 (fr) 2016-06-30 2018-01-04 Janssen Pharmaceutica Nv Dérivés hétéroaromatiques en tant qu'inhibiteurs de nik
WO2018037058A1 (fr) * 2016-08-24 2018-03-01 F. Hoffmann-La Roche Ag Dérivés de 2-azabicyclo [3.1.0] hexan-3-one et procédés d'utilisation
WO2018037059A1 (fr) 2016-08-24 2018-03-01 F. Hoffmann-La Roche Ag Dérivés de 2-azabicyclo [3.1.0] hexan-3-one et procédés d'utilisation
CN110831940B (zh) 2017-07-06 2023-06-20 詹森药业有限公司 作为nik抑制剂的新取代的氮杂吲哚啉衍生物
CN109810110B (zh) * 2017-11-22 2023-01-24 中国科学院上海药物研究所 一种具有2-氨基嘧啶结构的化合物，其制备方法和用途
CN114222737B (zh) * 2019-05-31 2024-07-26 詹森药业有限公司 NF-κB诱导激酶的小分子抑制剂
WO2020243423A1 (fr) 2019-05-31 2020-12-03 Ikena Oncology, Inc. Inhibiteurs de tead et leurs utilisations
CR20240234A (es) 2019-05-31 2024-07-09 Sage Therapeutics Inc ESTEROIDES NEUROACTIVOS Y COMPOSICIONES DE ESTOS (Divisional 2021-629)
KR20220030222A (ko) 2019-05-31 2022-03-10 이케나 온콜로지, 인코포레이티드 Tead 억제제 및 이의 용도
BR112021022099A2 (pt) 2019-05-31 2021-12-28 Chiesi Farm Spa Derivados de amino quinazolina como inibidores de p2x3
WO2021067217A1 (fr) 2019-09-30 2021-04-08 Incyte Corporation Composés pyrido[3,2-d]pyrimidine en tant qu'immunomodulateurs

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US20230080834A1 (en) 2023-03-16
WO2020239999A1 (fr) 2020-12-03
ES2989387T3 (es) 2024-11-26
EP4467199A3 (fr) 2025-03-05
US20210300918A1 (en) 2021-09-30
SMT202400418T1 (it) 2024-11-15
IL288387B1 (en) 2025-09-01
UY38721A (es) 2020-11-30
FI3976597T3 (fi) 2024-09-25
BR112021023796A2 (pt) 2022-02-08
TW202110842A (zh) 2021-03-16
MD3976597T2 (ro) 2025-01-31
MY205653A (en) 2024-11-02
KR20220027871A (ko) 2022-03-08
LT3976597T (lt) 2024-10-10
PE20220768A1 (es) 2022-05-16
US20240199605A1 (en) 2024-06-20
RS66105B1 (sr) 2024-11-29
JP7547387B2 (ja) 2024-09-09
JP2024167319A (ja) 2024-12-03
SG11202112994WA (en) 2021-12-30
IL288387A (en) 2022-01-01
TWI906955B (zh) 2025-12-01
TW202517638A (zh) 2025-05-01
EP3976597B1 (fr) 2024-08-28
CN118908957A (zh) 2024-11-08
TWI850390B (zh) 2024-08-01
UA130430C2 (uk) 2026-02-18
SI3976597T1 (sl) 2024-11-29
JOP20210318B1 (ar) 2025-10-01
EP3976597A1 (fr) 2022-04-06
HRP20241352T1 (hr) 2024-12-20
CR20210587A (es) 2022-02-11
US11827634B2 (en) 2023-11-28
SA521430960B1 (ar) 2024-11-12
PH12021553011A1 (en) 2022-11-07
DK3976597T3 (da) 2024-09-09
ECSP21093623A (es) 2022-01-31
PT3976597T (pt) 2024-10-22
HUE068694T2 (hu) 2025-01-28
MA56038A (fr) 2022-04-06
AU2020282005A1 (en) 2021-12-23
CN114222737A (zh) 2022-03-22
PL3976597T3 (pl) 2024-12-16
JOP20210318A1 (ar) 2023-01-30
CN114222737B (zh) 2024-07-26
CO2021017838A2 (es) 2022-01-17
CL2021003142A1 (es) 2022-08-19
IL288387B2 (en) 2026-01-01
AU2020282005B2 (en) 2026-02-12
MX2021014679A (es) 2022-04-06
CA3143350A1 (fr) 2020-12-03
US11254673B2 (en) 2022-02-22
JP2022534302A (ja) 2022-07-28
EP4467199A2 (fr) 2024-11-27
DOP2021000244A (es) 2022-04-18

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