MA55565A - Agents de dégradation de stat et leurs utilisations - Google Patents

Agents de dégradation de stat et leurs utilisations

Info

Publication number
MA55565A
MA55565A MA055565A MA55565A MA55565A MA 55565 A MA55565 A MA 55565A MA 055565 A MA055565 A MA 055565A MA 55565 A MA55565 A MA 55565A MA 55565 A MA55565 A MA 55565A
Authority
MA
Morocco
Prior art keywords
stat
degrading agents
degrading
agents
stat degrading
Prior art date
Application number
MA055565A
Other languages
English (en)
Inventor
Nan Ji
Nello Mainolfi
Bin Yang
Yi Zhang
Original Assignee
Kymera Therapeutics Inc
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 Kymera Therapeutics Inc filed Critical Kymera Therapeutics Inc
Publication of MA55565A publication Critical patent/MA55565A/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/06—Peri-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503—Five-membered rings
    • C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
    • C07F9/65068—Five-membered rings having the nitrogen atoms in positions 1 and 3 condensed with carbocyclic rings or carbocyclic ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Detergent Compositions (AREA)
MA055565A 2019-04-05 2020-04-06 Agents de dégradation de stat et leurs utilisations MA55565A (fr)

Applications Claiming Priority (13)

Application Number Priority Date Filing Date Title
US201962830095P 2019-04-05 2019-04-05
US201962833331P 2019-04-12 2019-04-12
US201962855259P 2019-05-31 2019-05-31
US201962860512P 2019-06-12 2019-06-12
US201962875362P 2019-07-17 2019-07-17
US201962877051P 2019-07-22 2019-07-22
US201962887872P 2019-08-16 2019-08-16
US201962926127P 2019-10-25 2019-10-25
US201962932957P 2019-11-08 2019-11-08
US201962944810P 2019-12-06 2019-12-06
US201962947310P 2019-12-12 2019-12-12
US201962949053P 2019-12-17 2019-12-17
US202062967921P 2020-01-30 2020-01-30

Publications (1)

Publication Number Publication Date
MA55565A true MA55565A (fr) 2022-02-09

Family

ID=72667015

Family Applications (1)

Application Number Title Priority Date Filing Date
MA055565A MA55565A (fr) 2019-04-05 2020-04-06 Agents de dégradation de stat et leurs utilisations

Country Status (15)

Country Link
US (3) US11485750B1 (fr)
EP (1) EP3946360A4 (fr)
JP (1) JP2022527114A (fr)
KR (1) KR20220006139A (fr)
CN (1) CN113939300A (fr)
AU (1) AU2020253633A1 (fr)
BR (1) BR112021019748A2 (fr)
CA (1) CA3135802A1 (fr)
CO (1) CO2021013339A2 (fr)
IL (1) IL286969A (fr)
MA (1) MA55565A (fr)
MX (1) MX2021012216A (fr)
SG (1) SG11202110829YA (fr)
TW (1) TW202106676A (fr)
WO (1) WO2020206424A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019241766A1 (fr) * 2018-06-15 2019-12-19 City Of Hope Chimère de ciblage de protéolyse à base d'oligonucléotides
CA3135802A1 (fr) 2019-04-05 2020-10-08 Kymera Therapeutics, Inc. Agents de degradation de stat et leurs utilisations
JP7424115B2 (ja) * 2019-06-26 2024-01-30 住友化学株式会社 エステル化合物の製造方法
EP4121055A4 (fr) * 2020-03-17 2024-04-24 Kymera Therapeutics, Inc. Agents de dégradation de stat et leurs utilisations
WO2021195481A1 (fr) * 2020-03-26 2021-09-30 The Regents Of The University Of Michigan Agents de dégradation de protéine stat à petites molécules
US11988649B2 (en) * 2020-10-06 2024-05-21 Board Of Regents, The University Of Texas System On-line suppressor
UY39671A (es) 2021-03-15 2022-10-31 Novartis Ag Derivados de pirazolopiridina y sus usos.
WO2023059792A1 (fr) * 2021-10-06 2023-04-13 C4 Thrapeutics, Inc. Composés de dégradation de la protéine 3 non structurale de coronavirus
CA3236262A1 (fr) * 2021-10-25 2023-05-04 Isaac Marx Agents de degradation de tyk2 et leurs utilisations
IL313123A (en) * 2021-12-11 2024-07-01 Kymera Therapeutics Inc STAT3 compounds and their uses
AU2023244363A1 (en) * 2022-03-31 2024-09-19 Recludix Pharma, Inc. Stat modulators and uses thereof
WO2023250058A1 (fr) * 2022-06-22 2023-12-28 Kymera Therapeutics, Inc. Agents de dégradation de stat et leurs utilisations
WO2024064080A1 (fr) * 2022-09-19 2024-03-28 Kymera Therapeutics, Inc. Agents de dégradation de stat6 et leurs utilisations
WO2024148041A1 (fr) * 2023-01-04 2024-07-11 Kymera Therapeutics, Inc. Agents de dégradation de stat3 et leurs utilisations

Family Cites Families (193)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4650750A (en) 1982-02-01 1987-03-17 Giese Roger W Method of chemical analysis employing molecular release tag compounds
US4709016A (en) 1982-02-01 1987-11-24 Northeastern University Molecular analytical release tags and their use in chemical analysis
US5516931A (en) 1982-02-01 1996-05-14 Northeastern University Release tag compounds producing ketone signal groups
US5650270A (en) 1982-02-01 1997-07-22 Northeastern University Molecular analytical release tags and their use in chemical analysis
US5217866A (en) 1985-03-15 1993-06-08 Anti-Gene Development Group Polynucleotide assay reagent and method
US5360811A (en) 1990-03-13 1994-11-01 Hoechst-Roussel Pharmaceuticals Incorporated 1-alkyl-, 1-alkenyl-, and 1-alkynylaryl-2-amino-1,3-propanediols and related compounds as anti-inflammatory agents
JP3545461B2 (ja) 1993-09-10 2004-07-21 エーザイ株式会社 二環式ヘテロ環含有スルホンアミド誘導体
AU4596096A (en) 1994-09-06 1996-03-27 Banyu Pharmaceutical Co., Ltd. Novel carbapenem derivative
US6281230B1 (en) 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
US6306663B1 (en) 1999-02-12 2001-10-23 Proteinex, Inc. Controlling protein levels in eucaryotic organisms
JP4078074B2 (ja) 1999-12-10 2008-04-23 ファイザー・プロダクツ・インク ピロロ［２，３−ｄ］ピリミジン化合物
DE10002509A1 (de) 2000-01-21 2001-07-26 Gruenenthal Gmbh Substituierte Glutarimide
JP2003525296A (ja) 2000-02-28 2003-08-26 スージェン・インコーポレーテッド キナーゼ阻害剤としての３−（ピロリルラクトン）−２−インドリノン化合物
PE20020354A1 (es) 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
US7208157B2 (en) 2000-09-08 2007-04-24 California Institute Of Technology Proteolysis targeting chimeric pharmaceutical
WO2002020740A2 (fr) 2000-09-08 2002-03-14 California Institute Of Technology Medicament chimere de ciblage de proteolyse
AU2002307217A1 (en) * 2001-03-28 2002-10-15 University Of South Florida Materials and methods for treatment of cancer and identification of anti-cancer compounds
JP3836436B2 (ja) 2001-04-27 2006-10-25 全薬工業株式会社 複素環式化合物及びそれを有効成分とする抗腫瘍剤
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
DE60325740D1 (de) 2002-08-14 2009-02-26 Silence Therapeutics Ag Verwendung von protein-kinase-n-beta
WO2004089925A1 (fr) 2003-04-03 2004-10-21 Semafore Pharmaceuticals, Inc. Promedicaments d'inhibiteurs de pi-3 kinase
DK1644363T3 (da) 2003-05-30 2012-05-29 Gemin X Pharmaceuticals Canada Inc Triheterocykliske forbindelser, sammensætninger og fremgangsmåder til behandling af cancer eller virussygdomme
EP1692153A4 (fr) 2003-07-03 2007-03-21 Univ Pennsylvania Inhibition de l'expression d'une syk kinase
WO2005058829A1 (fr) 2003-12-11 2005-06-30 Board Of Regents, The University Of Texas System Composes pour traiter des maladies associees a une proliferation cellulaire
JP4398263B2 (ja) 2004-01-13 2010-01-13 富士通株式会社 経路設計方法
US7436318B2 (en) 2004-04-19 2008-10-14 Atg Designworks, Llc Self contained device for displaying electronic information
LT2612862T (lt) 2004-05-13 2017-01-25 Icos Corporation Chinazolinonai kaip žmogaus fosfatidilinozitol-3-kinazės delta inhibitoriai
US20060005147A1 (en) 2004-06-30 2006-01-05 Hammack Jason L Methods and systems for controlling the display of maps aboard an aircraft
US20070010428A1 (en) 2004-09-03 2007-01-11 Mcmurray John S Inhibitors of signal transduction and activator of transcription 3
TWI309240B (en) 2004-09-17 2009-05-01 Hoffmann La Roche Anti-ox40l antibodies
DK1856135T3 (da) 2005-01-19 2010-04-12 Rigel Pharmaceuticals Inc Prodrugs af 2,4-pyrimidindiamin-forbindelser og deres anvendelser
US20060247318A1 (en) 2005-02-25 2006-11-02 Hui Song Small molecule inhibitors of STAT3 and the uses thereof
US7812135B2 (en) 2005-03-25 2010-10-12 Tolerrx, Inc. GITR-binding antibodies
WO2007040650A2 (fr) 2005-05-12 2007-04-12 Abbott Laboratories Promoteurs d'apoptose
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
SI1907424T1 (sl) 2005-07-01 2015-12-31 E. R. Squibb & Sons, L.L.C. Humana monoklonska protitelesa proti programiranem smrtnem ligandu 1 (PD-L1)
US7402325B2 (en) 2005-07-28 2008-07-22 Phoenix Biotechnology, Inc. Supercritical carbon dioxide extract of pharmacologically active components from Nerium oleander
US20080139456A1 (en) 2005-09-30 2008-06-12 Burke Terrence R Macrocyclic Sh2 Domain Binding Inhibitors
EA024305B1 (ru) 2005-10-07 2016-09-30 Экселиксис, Инк. Ингибиторы фосфатидилинозит-3-киназы и их применение
BRPI0617364A2 (pt) 2005-10-13 2011-07-26 Orchid Res Lab Ltd compostos heterocÍclicos como inibidores de pstat3/il-6
BR122021011788B1 (pt) 2005-11-01 2022-01-25 Impact Biomedicines, Inc Inibidores de biaril meta pirimidina de cinases, composição farmacêutica e processo para preparar uma composição farmacêutica
MY159449A (en) 2005-12-13 2017-01-13 Incyte Holdings Corp Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors
WO2007078990A2 (fr) 2005-12-23 2007-07-12 Zealand Pharma A/S Composés modifiés mimétiques de la lysine
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
NZ572812A (en) 2006-04-26 2010-09-30 Hoffmann La Roche THIENO [3, 2-D] PYRIMIDINE Indazole DERIVATIVE USEFUL AS PI3K INHIBITOR
WO2007136858A2 (fr) 2006-05-19 2007-11-29 H. Lee Moffitt Cancer Center & Research Institute Petites molécules inhibitrices de stat3 ayant une activité antitumorale
EP2532235A1 (fr) 2006-09-22 2012-12-12 Pharmacyclics, Inc. Inhibiteurs de la tyrosine kinase de bruton
UA95978C2 (ru) 2006-10-02 2011-09-26 Оцука Фармас'Ютікел Ко., Лтд. Ингибитор активации stat3/5
WO2008067270A1 (fr) 2006-11-27 2008-06-05 Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Inhibiteurs de liaison au domaine grb2 sh2 macrocyclique
KR101566840B1 (ko) 2007-03-12 2015-11-06 와이엠 바이오사이언시즈 오스트레일리아 피티와이 엘티디 페닐 아미노 피리미딘 화합물 및 이의 용도
US8394794B2 (en) 2007-03-23 2013-03-12 Regents Of The University Of Minnesota Therapeutic compounds
EP1987839A1 (fr) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Anticorps monoclonal cytotoxique anti-LAG-3 et son utilisation pour le traitement ou la prévention d'un rejet de greffe d'organe et de maladies auto-immunes
PE20090717A1 (es) 2007-05-18 2009-07-18 Smithkline Beecham Corp Derivados de quinolina como inhibidores de la pi3 quinasa
WO2008156644A2 (fr) 2007-06-14 2008-12-24 Frank David A Modulateurs de stat
EP3124046B1 (fr) 2007-07-12 2019-12-25 GITR, Inc. Thérapies combinées utilisant des molécules de liaison gitr
WO2009032338A1 (fr) 2007-09-09 2009-03-12 University Of Florida Research Foundation Agents thérapeutiques à base d'apratoxine : mécanisme et procédés de traitement
EP2044949A1 (fr) 2007-10-05 2009-04-08 Immutep Utilisation de lag-3 recombinant ou ses dérivatifs pour déclencher la réponse immune des monocytes
CA2932121A1 (fr) 2007-11-30 2009-06-11 Newlink Genetics Corporation Inhibiteurs de l'ido
FR2927330B1 (fr) 2008-02-07 2010-02-19 Sanofi Aventis Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii
UA101493C2 (ru) 2008-03-11 2013-04-10 Инсайт Корпорейшн Производные азетидина и циклобутана как ингибиторы jak
CN102083429B (zh) 2008-04-24 2014-05-28 新联基因公司 Ido抑制剂
US8338439B2 (en) 2008-06-27 2012-12-25 Celgene Avilomics Research, Inc. 2,4-disubstituted pyrimidines useful as kinase inhibitors
KR20110033922A (ko) 2008-07-08 2011-04-01 더 보드 오브 리전츠 오브 더 유니버시티 오브 텍사스 시스템 전사의 신호 변환자 및 활성제（ｓｔａｔｓ）의 증식 및 활성화의 신규한 억제제
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
EP2373658A4 (fr) 2008-12-08 2012-05-23 Univ Michigan Office Of Technology Transfer Inhibiteurs de stat3 et méthodes thérapeutiques les utilisant
CN114835812A (zh) 2008-12-09 2022-08-02 霍夫曼-拉罗奇有限公司 抗-pd-l1抗体及它们用于增强t细胞功能的用途
US8921037B2 (en) 2008-12-16 2014-12-30 Bo Han PF4-depleted platelet rich plasma preparations and methods for hard and soft tissue repair
US8841257B2 (en) 2009-04-10 2014-09-23 Board Of Regents, The University Of Texas System Inhibitors of STAT3 and uses thereof
JP2012524106A (ja) 2009-04-15 2012-10-11 ジ・オハイオ・ステイト・ユニバーシティ・リサーチ・ファウンデイション 二重ｊａｋ２／ｓｔａｔ３阻害剤としてのクルクミン類似体ならびにその同じ物を作る、および用いる方法
RU2595409C2 (ru) 2009-09-03 2016-08-27 Мерк Шарп И Доум Корп., Анти-gitr-антитела
EP2493862B1 (fr) 2009-10-28 2016-10-05 Newlink Genetics Corporation Dérivés imidazole comme inhibiteurs de l'ido
CA2781706A1 (fr) 2009-11-24 2011-06-03 The Ohio State University Inhibiteurs de facteur de transcription et compositions, formulations et procedes apparentes
ES2557454T3 (es) 2009-12-10 2016-01-26 F. Hoffmann-La Roche Ag Anticuerpos que se unen al dominio extracelular 4 de CSF1R humana y su utilización
US8445517B2 (en) 2009-12-11 2013-05-21 Dana-Farber Cancer Institute Stat modulators
CN102725287B (zh) 2009-12-28 2015-07-01 一般社团法人创药分子谷项目支援机构 1,3,4-噁二唑-2-甲酰胺化合物
CN106279416B (zh) 2010-03-04 2019-08-30 宏观基因有限公司 与b7-h3反应性的抗体、其免疫学活性片段及其用途
EP2542587A1 (fr) 2010-03-05 2013-01-09 F. Hoffmann-La Roche AG Anticorps dirigés contre le csf-1r humain et utilisations associées
MX336682B (es) 2010-03-05 2016-01-27 Hoffmann La Roche Anticuerpos contra csf-1r humanos y usos de los mismos.
CN106977603B (zh) 2010-05-04 2020-11-27 戊瑞治疗有限公司 结合csf1r的抗体
WO2011163424A2 (fr) 2010-06-22 2011-12-29 University Of Central Florida Research Foundation, Inc. Analogues d'acide 2-(9h-purin-9-yl)acétique substitués en tant qu'inhibiteurs de stat3
US9765019B2 (en) 2010-06-30 2017-09-19 Brandeis University Small-molecule-targeted protein degradation
KR20130121818A (ko) 2010-08-02 2013-11-06 유니버시티 오브 센트럴 플로리다 리서치 파운데이션, 인코포레이티드 Stat 단백질의 저해제로서의 치환된 2-히드록시-4-(2-(페닐설폰아미도)아세트아미도)벤조산 유사체
CN105481983B (zh) 2010-09-09 2021-09-03 辉瑞公司 4-1bb结合分子
CN103502275A (zh) 2010-12-07 2014-01-08 耶鲁大学 融合蛋白的小分子疏水性标记和引起的其降解
WO2012078982A2 (fr) 2010-12-09 2012-06-14 The Ohio State University Xzh-5 inhibe la phosphorylation de stat3 constitutive et induite par l'interleukine 6 dans des cellules de carcinome hépatocellulaire humain
SG190997A1 (en) 2010-12-09 2013-07-31 Univ Pennsylvania Use of chimeric antigen receptor-modified t cells to treat cancer
WO2012097351A1 (fr) 2011-01-14 2012-07-19 The Ohio State University Research Foundation Matériels et procédés d'inhibition de cellules cancéreuses de myélome multiple
WO2012142615A2 (fr) 2011-04-14 2012-10-18 Board Of Regents, The University Of Texas System Auranofine et analogues d'auranofine utiles pour traiter une maladie proliférative et des troubles prolifératifs
NO2694640T3 (fr) 2011-04-15 2018-03-17
RS57324B1 (sr) 2011-04-20 2018-08-31 Medimmune Llc Antitela i drugi molekuli koji vezuju b7-h1 i pd-1
EA036814B9 (ru) 2011-11-28 2021-12-27 Мерк Патент Гмбх Антитело против pd-l1 (варианты), композиция, содержащая это антитело, и их применение
MX356337B (es) 2011-12-15 2018-05-23 Hoffmann La Roche Anticuerpos contra csf-1r humano y sus usos.
EP3608317A1 (fr) 2012-01-12 2020-02-12 Yale University Composés et procédés pour la dégradation améliorée de protéines cibles et d'autres polypeptides par une e3 ubiquitine ligase
WO2013106646A2 (fr) 2012-01-12 2013-07-18 Yale University Composés et procédés pour l'inhibition de l'ubiquitine ligase vcb e3
KR20140127855A (ko) 2012-02-06 2014-11-04 제넨테크, 인크. Csf1r 억제제를 사용하는 조성물 및 방법
AR090263A1 (es) 2012-03-08 2014-10-29 Hoffmann La Roche Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
EP3539984A1 (fr) 2012-05-11 2019-09-18 Five Prime Therapeutics, Inc. Procédés de traitement de maladies avec des anticorps qui se lient au récepteur 1 du facteur de stimulation de colonie (csf1r)
CN110003104A (zh) 2012-05-25 2019-07-12 多伦多大学管理委员会 水杨酸衍生物、其药学上可接受的盐、其组合物以及其使用方法
EP3406598B1 (fr) 2012-06-14 2020-01-29 Mayo Foundation for Medical Education and Research Dérivés de pyrazole en tant qu'inhibiteurs de stat3
UY34887A (es) 2012-07-02 2013-12-31 Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos
KR102146848B1 (ko) 2012-08-09 2020-08-21 셀진 코포레이션 3-(4-((4-모르포리노메틸)벤질)옥시)-1-옥소이소인돌린-2-일)피페리딘-2,6-디온을 이용한 암의 치료방법
US9783513B2 (en) 2012-08-16 2017-10-10 Ohio State Innovation Foundation STAT3 inhibitors and their anticancer use
SG10201906328RA (en) 2012-08-31 2019-08-27 Five Prime Therapeutics Inc Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
US9422331B2 (en) 2012-09-19 2016-08-23 Hoffmann-La Roche Inc. 2-oxo-2,3,4,5-tetrahydro-1 H-benzo[B]diazepines and their use in the treatment of cancer
USRE48175E1 (en) 2012-10-19 2020-08-25 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
WO2014070859A1 (fr) 2012-10-30 2014-05-08 H. Lee Moffitt Cancer Center And Research Institute, Inc. Inhibiteurs de dimérisation de stat3
GB201311910D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel Compounds
US9777144B2 (en) 2013-03-15 2017-10-03 Zeon Corporation Aqueous dispersion of hollow polymer particles and method of production of same
US9802888B2 (en) 2013-03-22 2017-10-31 University Of Hawaii STAT3 inhibitors
EP2994143A4 (fr) 2013-05-08 2017-02-01 Board of Regents, The University of Texas System Inhibiteurs de stat6
WO2014205416A1 (fr) 2013-06-20 2014-12-24 University Of Hawaii Nouveaux inhibiteurs de stat3 sesquiterpénoïdes
WO2015071393A1 (fr) 2013-11-18 2015-05-21 F. Hoffmann-La Roche Ag Tétrahydro-benzodiazépinones
US20160058872A1 (en) 2014-04-14 2016-03-03 Arvinas, Inc. Imide-based modulators of proteolysis and associated methods of use
US20180228907A1 (en) 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
KR20240038809A (ko) 2014-04-14 2024-03-25 아비나스 오퍼레이션스, 인코포레이티드 단백질분해의 이미드-기초된 조절인자 및 연관된 이용 방법
EP3160486B1 (fr) 2014-06-27 2020-11-18 Celgene Corporation Compositions et procédés pour induire des modifications conformationnelles dans céréblon et d'autres ubiquitine ligases e3
US20160022642A1 (en) 2014-07-25 2016-01-28 Yale University Compounds Useful for Promoting Protein Degradation and Methods Using Same
US10071164B2 (en) 2014-08-11 2018-09-11 Yale University Estrogen-related receptor alpha based protac compounds and associated methods of use
KR101697062B1 (ko) 2014-08-26 2017-01-18 한국생명공학연구원 물에 대한 용해도가 개선된 신규 제라닐 프라보노이드 유도체, 이의 제조 방법 및 이를 유효성분으로 포함하는 암 예방 및 치료용 약학적 조성물
KR20160066490A (ko) 2014-12-02 2016-06-10 주식회사 씨앤드씨신약연구소 헤테로사이클 유도체 및 그의 용도
US9694084B2 (en) 2014-12-23 2017-07-04 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
CN107257800B (zh) 2014-12-23 2020-06-30 达纳-法伯癌症研究所股份有限公司 通过双功能分子诱导靶蛋白降解的方法
WO2016115455A2 (fr) 2015-01-15 2016-07-21 University Of Pittsburgh - Of The Commonwealth System Of Higher Education 3-(1h-pyrazol-5-yl)-7h-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines 6-aryl-7-substituées en tant qu'inhibiteurs de la voie stat3 ayant une activité anti-proliférative
US20170327469A1 (en) 2015-01-20 2017-11-16 Arvinas, Inc. Compounds and methods for the targeted degradation of androgen receptor
JP6817962B2 (ja) 2015-01-20 2021-01-20 アルビナス・オペレーションズ・インコーポレイテッドＡｒｖｉｎａｓ Ｏｐｅｒａｔｉｏｎｓ， Ｉｎｃ． ターゲティングされたアンドロゲン受容体分解のための化合物および方法
EP3750530A1 (fr) 2015-02-05 2020-12-16 TyrNovo Ltd. Combinaisons de doubles modulateurs d'irs/stat3 et d'agents anticancéreux pour le traitement du cancer
CN108601764A (zh) 2015-03-18 2018-09-28 阿尔维纳斯股份有限公司 用于靶蛋白的增强降解的化合物和方法
GB201506871D0 (en) 2015-04-22 2015-06-03 Glaxosmithkline Ip Dev Ltd Novel compounds
ES2862469T3 (es) 2015-06-04 2021-10-07 Arvinas Operations Inc Moduladores de proteólisis a base de imidas y métodos de uso asociados
EP3302482A4 (fr) 2015-06-05 2018-12-19 Arvinas, Inc. Tank-binding kinase-1 protacs et procédés d'utilisation associés
SE539204C2 (en) 2015-06-05 2017-05-09 Glactone Pharma Dev Ab Ether analogues of galiellalactone
CN105085620B (zh) 2015-06-25 2018-05-08 中山大学附属第一医院 一种靶向泛素化降解Smad3的化合物
WO2017007612A1 (fr) 2015-07-07 2017-01-12 Dana-Farber Cancer Institute, Inc. Procédés pour induire la dégradation ciblée de protéines par des molécules bifonctionnelles
KR20180035828A (ko) 2015-07-10 2018-04-06 아비나스 인코포레이티드 단백질 분해의 mdm2계 조절인자 및 관련된 이용 방법
WO2017011590A1 (fr) 2015-07-13 2017-01-19 Arvinas, Inc. Modulateurs de protéolyse à base d'alanine et procédés d'utilisation associés
JP6802251B2 (ja) 2015-07-14 2020-12-16 ミッション セラピューティクス リミティド 癌の処置のためのｄｕｂ阻害剤としてのシアノピロリジン
WO2017030814A1 (fr) 2015-08-19 2017-02-23 Arvinas, Inc. Composés et procédés pour la dégradation ciblée de protéines contenant un bromodomaine
AU2016323613B2 (en) 2015-09-18 2020-12-10 Merck Patent Gmbh Heteroaryl compounds as IRAK inhibitors and uses thereof
AU2016349781A1 (en) 2015-11-02 2018-05-10 Yale University Proteolysis targeting chimera compounds and methods of preparing and using same
US20200216454A1 (en) 2015-12-30 2020-07-09 Dana-Farber Cancer Institute, Inc. Bifunctional molecules for her3 degradation and methods of use
WO2017117474A1 (fr) 2015-12-30 2017-07-06 Dana-Farber Cancer Institute, Inc. Composés bifonctionnels destinés à la dégradation d'her3 et procédés d'utilisation
MX2018011216A (es) 2016-03-16 2019-08-29 H Lee Moffitt Cancer Ct & Res Moléculas pequeñas contra cereblon para mejorar la función efectora de los linfocitos t.
US20170281784A1 (en) 2016-04-05 2017-10-05 Arvinas, Inc. Protein-protein interaction inducing technology
JP7001614B2 (ja) 2016-04-06 2022-02-03 ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン リガンド依存性の標的タンパク質分解のための単官能性中間体
UA123786C2 (uk) 2016-04-06 2021-06-02 Дзе Ріджентс Оф Дзе Юніверсіті Оф Мічіган Деструктори білка mdm2
WO2017197056A1 (fr) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Dégronimères ciblant un bromodomaine pour la dégradation de protéines cibles
WO2017197036A1 (fr) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Dégronimères spirocycliques pour la dégradation de protéines cibles
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN109562107A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的杂环降解决定子体
WO2017201069A1 (fr) 2016-05-18 2017-11-23 Biotheryx, Inc. Dérivés d'oxoindoline utilisés comme modulateurs de la fonction protéique
CN109152843A (zh) 2016-05-20 2019-01-04 豪夫迈·罗氏有限公司 Protac抗体缀合物及其使用方法
GB201610147D0 (en) 2016-06-10 2016-07-27 Glaxosmithkline Ip Dev Ltd Novel compounds
CN110234646A (zh) 2016-11-01 2019-09-13 阿尔维纳斯股份有限公司 靶向PROTAC的Tau蛋白及相关使用方法
AU2017363313B2 (en) 2016-11-22 2021-06-24 Dana-Farber Cancer Institute, Inc. Inhibitors of interleukin-1 receptor-associated kinases and uses thereof
SE540295C2 (en) 2016-12-05 2018-05-29 Glactone Pharma Dev Ab Sulfonamide analogues of galiellalactone
WO2018136935A1 (fr) 2017-01-23 2018-07-26 University Of Hawaii Inhibiteurs de stat3 dérivés de 2-arylsulfonamido-n-arylacétamide
KR20190116315A (ko) 2017-01-31 2019-10-14 아비나스 오퍼레이션스, 인코포레이티드 세레블론 리간드 및 이를 포함하는 이작용성 화합물
WO2018237026A1 (fr) 2017-06-20 2018-12-27 C4 Therapeutics, Inc. Dégrons et dégronimères à liaison n/o pour la dégradation de protéines
CN118108706A (zh) 2017-09-04 2024-05-31 C4医药公司 戊二酰亚胺
IL295603B2 (en) 2017-09-22 2024-03-01 Kymera Therapeutics Inc Protein compounds and their uses
US11358948B2 (en) 2017-09-22 2022-06-14 Kymera Therapeutics, Inc. CRBN ligands and uses thereof
WO2019084030A1 (fr) 2017-10-24 2019-05-02 Genentech, Inc. Composés de (4-hydroxypyrrolidin-2-yl)-hydroxamate et leurs procédés d'utilisation
WO2019084026A1 (fr) 2017-10-24 2019-05-02 Genentech, Inc. Composés (4-hydroxypyrrolidin-2-yl)-hétérocycliques et leurs procédés d'utilisation
WO2019099868A2 (fr) 2017-11-16 2019-05-23 C4 Therapeutics, Inc. Agents de dégradation et dégrons pour dégradation protéique ciblée
EP3710443A1 (fr) 2017-11-17 2020-09-23 Arvinas Operations, Inc. Composés et procédés pour la dégradation ciblée de polypeptides de kinase 4 associés au récepteur de l'interleukine 1
AU2018396142A1 (en) 2017-12-26 2020-07-16 Kymera Therapeutics, Inc. IRAK degraders and uses thereof
EP3737666A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Agents de dégradation de protéines et utilisations associées
EP3737675A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Ligands crbn et leurs utilisations
US11802132B2 (en) 2018-02-23 2023-10-31 Dana-Farber Cancer Institute, Inc. Small molecules for inducing selective protein degradation and uses thereof
EP3578561A1 (fr) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spirocomposés
WO2020010210A1 (fr) 2018-07-06 2020-01-09 Kymera Therapeutics, Inc. Agents de dégradation de mertk et leurs utilisations
US20220348556A1 (en) 2018-07-06 2022-11-03 Kymera Therapeutics, Inc. Protein degraders and uses thereof
WO2020010177A1 (fr) 2018-07-06 2020-01-09 Kymera Therapeutics, Inc. Ligands crbn tricycliques et leurs utilisations
CA3119773A1 (fr) 2018-11-30 2020-06-04 Kymera Therapeutics, Inc. Agents de degradation de kinases de type irak et leurs utilisations
CA3134822A1 (fr) 2019-03-26 2020-10-01 The Regents Of The Universtiy Of Michigan Agents de degradation, a petites molecules, de stat3
WO2020205467A1 (fr) * 2019-03-29 2020-10-08 The Regents Of The University Of Michigan Agents de dégradation de protéines stat3
CA3135802A1 (fr) 2019-04-05 2020-10-08 Kymera Therapeutics, Inc. Agents de degradation de stat et leurs utilisations
WO2020264499A1 (fr) 2019-06-28 2020-12-30 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
WO2020264490A1 (fr) 2019-06-28 2020-12-30 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
US20220281831A1 (en) 2019-07-15 2022-09-08 Kymera Therapeutics, Inc. Fused-glutarimide crbn ligands and uses thereof
WO2021011634A1 (fr) 2019-07-15 2021-01-21 Kymera Therapeutics, Inc. Agents de dégradation de protéines et leurs utilisations
WO2021011871A1 (fr) 2019-07-17 2021-01-21 Kymera Therapeutics, Inc. Agents de dégradation de mertk et leurs utilisations
US20230132715A1 (en) 2019-07-17 2023-05-04 Kymera Therapeutics, Inc. Irak degraders and uses thereof
EP4072591A4 (fr) 2019-12-10 2024-06-05 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
EP4076536A4 (fr) 2019-12-17 2024-05-01 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
JP2023509366A (ja) 2019-12-17 2023-03-08 カイメラ セラピューティクス， インコーポレイテッド Ｉｒａｋ分解剤およびそれらの使用
WO2021127283A2 (fr) 2019-12-17 2021-06-24 Kymera Therapeutics, Inc. Agents de dégradation d'irak et leurs utilisations
WO2021158634A1 (fr) 2020-02-03 2021-08-12 Kymera Therapeutics, Inc. Agents de dégradation de kinases irak et leurs utilisations
EP4121055A4 (fr) 2020-03-17 2024-04-24 Kymera Therapeutics, Inc. Agents de dégradation de stat et leurs utilisations
WO2021195481A1 (fr) 2020-03-26 2021-09-30 The Regents Of The University Of Michigan Agents de dégradation de protéine stat à petites molécules
US20240293423A1 (en) 2020-10-07 2024-09-05 Kymera Therapeutics, Inc. Stat degraders and uses thereof
IL313123A (en) 2021-12-11 2024-07-01 Kymera Therapeutics Inc STAT3 compounds and their uses

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EP3946360A4 (fr) 2023-05-10
US11485750B1 (en) 2022-11-01
CO2021013339A2 (es) 2022-01-17
US12077555B2 (en) 2024-09-03
TW202106676A (zh) 2021-02-16
EP3946360A1 (fr) 2022-02-09
US11746120B2 (en) 2023-09-05
IL286969A (en) 2021-12-01
BR112021019748A2 (pt) 2021-12-07
CA3135802A1 (fr) 2020-10-08
US20230120381A1 (en) 2023-04-20
KR20220006139A (ko) 2022-01-14
MX2021012216A (es) 2022-01-24
AU2020253633A1 (en) 2021-11-04
US20230084113A1 (en) 2023-03-16
CN113939300A (zh) 2022-01-14

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