SG11202005912PA - Irak degraders and uses thereof - Google Patents
Irak degraders and uses thereofInfo
- Publication number
- SG11202005912PA SG11202005912PA SG11202005912PA SG11202005912PA SG11202005912PA SG 11202005912P A SG11202005912P A SG 11202005912PA SG 11202005912P A SG11202005912P A SG 11202005912PA SG 11202005912P A SG11202005912P A SG 11202005912PA SG 11202005912P A SG11202005912P A SG 11202005912PA
- Authority
- SG
- Singapore
- Prior art keywords
- degraders
- irak
- irak degraders
- Prior art date
Links
- 239000001064 degrader Substances 0.000 title 1
Classifications
-
- 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
- A61K47/545—Heterocyclic compounds
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles 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
- A61K31/41—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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
-
- 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
- C07D401/14—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 three or more hetero 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
- C07D417/14—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 three or more hetero rings
-
- 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
- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Liquid Crystal Substances (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Saccharide Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762610397P | 2017-12-26 | 2017-12-26 | |
US201862653178P | 2018-04-05 | 2018-04-05 | |
US201862694955P | 2018-07-06 | 2018-07-06 | |
US201862712377P | 2018-07-31 | 2018-07-31 | |
PCT/US2018/067304 WO2019133531A1 (en) | 2017-12-26 | 2018-12-21 | Irak degraders and uses thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11202005912PA true SG11202005912PA (en) | 2020-07-29 |
Family
ID=66949188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11202005912PA SG11202005912PA (en) | 2017-12-26 | 2018-12-21 | Irak degraders and uses thereof |
Country Status (11)
Country | Link |
---|---|
US (4) | US10874743B2 (en) |
EP (1) | EP3731869A4 (en) |
JP (2) | JP2021508703A (en) |
CN (1) | CN112105385A (en) |
AU (1) | AU2018396142A1 (en) |
BR (1) | BR112020012997A2 (en) |
CA (1) | CA3086763A1 (en) |
IL (2) | IL275649B2 (en) |
MX (1) | MX2020006812A (en) |
SG (1) | SG11202005912PA (en) |
WO (1) | WO2019133531A1 (en) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2018338314A1 (en) * | 2017-09-22 | 2020-04-09 | Kymera Therapeutics, Inc | Protein degraders and uses thereof |
EP3684366A4 (en) | 2017-09-22 | 2021-09-08 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
JP2021508703A (en) | 2017-12-26 | 2021-03-11 | カイメラ セラピューティクス, インコーポレイテッド | IRAK Degradants and Their Use |
EP3737675A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
EP3737666A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
KR102548191B1 (en) * | 2018-04-09 | 2023-06-28 | 상하이테크 유니버시티 | Targeted proteolytic compounds, their antitumor applications, their intermediates and applications of intermediates |
EP3817748A4 (en) | 2018-07-06 | 2022-08-24 | Kymera Therapeutics, Inc. | Tricyclic crbn ligands and uses thereof |
US20220348556A1 (en) * | 2018-07-06 | 2022-11-03 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
WO2020010451A1 (en) * | 2018-07-10 | 2020-01-16 | Trillium Therapeutics Inc. | Heteroaromatic-fused imidazolyl amides, compositions and uses thereof as sting agonists |
JPWO2020027225A1 (en) | 2018-07-31 | 2021-11-11 | ファイメクス株式会社 | Heterocyclic compound |
EP3862348A4 (en) * | 2018-09-30 | 2022-06-22 | Shanghai Institute of Materia Medica, Chinese Academy of Sciences | Isoindoline compound, preparation method, pharmaceutical composition and use thereof |
EP3873898A4 (en) * | 2018-11-02 | 2022-11-30 | Dana-Farber Cancer Institute, Inc. | Acetylation writer inhibitor development and uses thereof |
SG11202105424PA (en) * | 2018-11-30 | 2021-06-29 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
CN113677668A (en) | 2019-01-30 | 2021-11-19 | 蒙特利诺治疗公司 | Bifunctional compounds and methods for androgen receptor targeted ubiquitination |
SG11202110829YA (en) | 2019-04-05 | 2021-10-28 | Kymera Therapeutics Inc | Stat degraders and uses thereof |
WO2021011868A1 (en) * | 2019-07-17 | 2021-01-21 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
JP2021024787A (en) | 2019-07-31 | 2021-02-22 | ファイメクス株式会社 | Heterocyclic compound |
JPWO2021020585A1 (en) | 2019-07-31 | 2021-02-04 | ||
MX2022003504A (en) * | 2019-09-24 | 2022-07-19 | Shanghai Meiyue Biotech Dev Co Ltd | Irak inhibitor and preparation method therefor and use thereof. |
CN114929223A (en) * | 2019-11-05 | 2022-08-19 | 德米拉公司 | Topical composition comprising an IRAK4 inhibitor for the treatment of skin conditions characterized by inflammation |
WO2021119159A1 (en) * | 2019-12-10 | 2021-06-17 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
EP4076524A4 (en) * | 2019-12-17 | 2023-11-29 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
IL293917A (en) * | 2019-12-17 | 2022-08-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
CA3164832A1 (en) | 2019-12-18 | 2021-06-24 | Novartis Ag | 3-(5-methoxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
WO2021133920A1 (en) | 2019-12-23 | 2021-07-01 | Kymera Therapeutics, Inc. | Smarca degraders and uses thereof |
US20230122219A1 (en) * | 2020-02-03 | 2023-04-20 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
WO2021162493A1 (en) * | 2020-02-14 | 2021-08-19 | 보로노이 주식회사 | Protein kinase degradation inducing compound, and use thereof |
CA3165009A1 (en) | 2020-02-19 | 2021-08-26 | Wylie Solang Palmer | Bifunctional degraders of interleukin-1 receptor-associated kinases and therapeutic use thereof |
EP4122925A4 (en) * | 2020-03-17 | 2024-04-17 | Medshine Discovery Inc | Proteolysis regulator and method for using same |
CN115776887A (en) | 2020-03-19 | 2023-03-10 | 凯麦拉医疗公司 | MDM2 degrading agents and uses thereof |
WO2021198966A1 (en) * | 2020-03-31 | 2021-10-07 | Orum Therapeutics, Inc. | Conjugates |
US11116737B1 (en) | 2020-04-10 | 2021-09-14 | University Of Georgia Research Foundation, Inc. | Methods of using probenecid for treatment of coronavirus infections |
US20230167081A1 (en) * | 2020-04-30 | 2023-06-01 | President And Fellows Of Harvard College | 5-amino-2-piperidinon-3-yl-1-oxoisoindoline derivatives for degradation of ikzf2 degraders |
TW202208381A (en) | 2020-05-06 | 2022-03-01 | 美商紐力克斯醫療股份有限公司 | Bifunctional degraders of hematopoietic progenitor kinase and therapeutic uses thereof |
EP4153587A1 (en) * | 2020-05-18 | 2023-03-29 | Montelino Therapeutics, Inc. | Bi-functional compounds and methods for targeted ubiquitination of androgen receptor |
TW202210483A (en) | 2020-06-03 | 2022-03-16 | 美商凱麥拉醫療公司 | Crystalline forms of irak degraders |
EP4161521A1 (en) * | 2020-06-03 | 2023-04-12 | Kymera Therapeutics, Inc. | Deuterated irak degraders and uses thereof |
EP4168410A1 (en) | 2020-06-22 | 2023-04-26 | The United States of America, as represented by the Secretary, Department of Health and Human Services | Methotrexate analogs and methods of use |
US11857551B1 (en) | 2020-07-10 | 2024-01-02 | Ting Therapeutics Llc | Methods for the prevention and treatment of hearing loss |
WO2022027058A1 (en) * | 2020-07-30 | 2022-02-03 | Kymera Therapeutics, Inc. | Methods of treating mutant lymphomas |
US20230416242A1 (en) * | 2020-10-21 | 2023-12-28 | Kymera Therapeutics, Inc. | Double degraders and uses thereof |
IL303458A (en) * | 2020-12-09 | 2023-08-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
MX2023008296A (en) | 2021-01-13 | 2023-09-29 | Monte Rosa Therapeutics Inc | Isoindolinone compounds. |
WO2022161414A1 (en) * | 2021-01-26 | 2022-08-04 | 成都茵创园医药科技有限公司 | Aromatic compound, pharmaceutical composition containing same, and application thereof |
CN116847848A (en) * | 2021-02-10 | 2023-10-03 | 百济神州有限公司 | EGFR degrading agents and methods of use |
IL304905A (en) * | 2021-02-15 | 2023-10-01 | Kymera Therapeutics Inc | Irak4 degraders and uses thereof |
WO2022229466A2 (en) | 2021-04-30 | 2022-11-03 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e. V. | Non-covalent halotag ligands |
WO2022236339A1 (en) * | 2021-05-07 | 2022-11-10 | Kymera Therapeutics, Inc. | Deuterated irak degraders and uses thereof |
CN113549060A (en) * | 2021-07-28 | 2021-10-26 | 派普医药(江苏)有限公司 | Synthetic method of 3-amino-1- (tetrahydrofuran-2-yloxy) -1H-pyrazole-4-carbonitrile |
TW202315632A (en) | 2021-08-18 | 2023-04-16 | 美商新銳思生物製藥股份有限公司 | Bifunctional degraders of interleukin-1 receptor-associated kinases and therapeutic use thereof |
CN115772180A (en) * | 2021-09-08 | 2023-03-10 | 南京明德新药研发有限公司 | Glutarimide compound and application thereof |
US11981672B2 (en) | 2021-09-13 | 2024-05-14 | Montelino Therapeutics Inc. | Bi-functional compounds and methods for targeted ubiquitination of androgen receptor |
WO2023045978A1 (en) * | 2021-09-26 | 2023-03-30 | 南京明德新药研发有限公司 | 2,6-piperidinedione compound and application thereof |
AU2022378463A1 (en) * | 2021-10-25 | 2024-05-09 | Kymera Therapeutics, Inc. | Tyk2 degraders and uses thereof |
WO2023104155A1 (en) * | 2021-12-08 | 2023-06-15 | 标新生物医药科技(上海)有限公司 | Ligand compounds for e3 ubiquitin ligase, protein degraders developed on basis of ligand compounds, and uses thereof |
TW202333670A (en) * | 2022-01-04 | 2023-09-01 | 大陸商海思科醫藥集團股份有限公司 | Compound for inhibiting and degrading irak4, and pharmaceutical composition and pharmaceutical application thereof |
CN114213283B (en) * | 2022-01-04 | 2023-06-02 | 攀枝花学院 | Method for preparing [2- [1- (Fmoc-amino) ethoxy ] acetic acid by one-pot method |
TW202345827A (en) * | 2022-01-14 | 2023-12-01 | 美商凱麥拉醫療公司 | Irak4 degraders and uses thereof |
WO2023180388A1 (en) | 2022-03-24 | 2023-09-28 | Glaxosmithkline Intellectual Property Development Limited | 2,4-dioxotetrahydropyrimidinyl derivatives as degrons in protacs |
WO2023186069A1 (en) * | 2022-03-31 | 2023-10-05 | 石药集团中奇制药技术(石家庄)有限公司 | Bifunctional chimeric heterocyclic compound of interleukin-1 receptor-associated kinase 4, preparation method therefor, pharmaceutical composition thereof and use thereof |
WO2023192586A1 (en) * | 2022-03-31 | 2023-10-05 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
US20230405014A1 (en) | 2022-04-12 | 2023-12-21 | Genzyme Corporation | Use of an irak4 modulator for gene therapy |
US20230405151A1 (en) | 2022-04-12 | 2023-12-21 | Genzyme Corporation | Use of irak4 modulators for gene therapy |
WO2023237049A1 (en) * | 2022-06-09 | 2023-12-14 | Beigene, Ltd. | Degradation of irak4 by conjugation of irak4 inhibitors with e3 ligase ligand and methods of use |
CN114843114B (en) * | 2022-06-30 | 2022-10-25 | 深圳市今朝时代股份有限公司 | Nitrogen-doping-based electrode material and application thereof to supercapacitor |
WO2024073507A1 (en) | 2022-09-28 | 2024-04-04 | Theseus Pharmaceuticals, Inc. | Macrocyclic compounds and uses thereof |
CN115626916B (en) * | 2022-10-24 | 2024-01-30 | 河南科技大学第一附属医院 | Pomalidomide derivative as well as preparation method and application thereof |
WO2024099908A1 (en) | 2022-11-09 | 2024-05-16 | Boehringer Ingelheim International Gmbh | Cyclic pyridine derivatives as cgas inhibitors |
CN115872877A (en) * | 2022-12-21 | 2023-03-31 | 南京安伦化工科技有限公司 | Synthesis method of aminotetraethyleneglycol |
Family Cites Families (219)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5650270A (en) | 1982-02-01 | 1997-07-22 | 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 |
US4709016A (en) | 1982-02-01 | 1987-11-24 | Northeastern University | Molecular analytical release tags and their use in chemical analysis |
US4650750A (en) | 1982-02-01 | 1987-03-17 | Giese Roger W | Method of chemical analysis employing molecular release tag compounds |
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 (en) | 1993-09-10 | 2004-07-21 | エーザイ株式会社 | Bicyclic heterocycle-containing sulfonamide derivatives |
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 (en) | 1999-12-10 | 2008-04-23 | ファイザー・プロダクツ・インク | Pyrrolo [2,3-d] pyrimidine compound |
DE10002509A1 (en) | 2000-01-21 | 2001-07-26 | Gruenenthal Gmbh | New substituted glutarimide derivatives are IL-12 antagonists, are useful as immunomodulators and for the treatment of angiopathy, hematological or oncological disorders |
AU2001241798A1 (en) | 2000-02-28 | 2001-09-12 | Sugen, Inc. | 3-(pyrolyllactone)-2-indolinone compounds as kinase inhibitors |
PE20020354A1 (en) | 2000-09-01 | 2002-06-12 | Novartis Ag | HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS |
US7208157B2 (en) | 2000-09-08 | 2007-04-24 | California Institute Of Technology | Proteolysis targeting chimeric pharmaceutical |
EP1322750A4 (en) | 2000-09-08 | 2004-09-29 | California Inst Of Techn | Proteolysis targeting chimeric pharmaceutical |
DE60217322T2 (en) | 2001-04-27 | 2007-10-04 | Zenyaku Kogyo K.K. | Heterocyclic compound and antitumor agent containing it as an active ingredient |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
WO2004019973A1 (en) | 2002-08-14 | 2004-03-11 | Atugen Ag | Use of protein kinase n beta |
SG160211A1 (en) | 2003-04-03 | 2010-04-29 | Semafore Pharmaceuticals Inc | Pi-3 kinase inhibitor prodrugs |
CA2527583C (en) | 2003-05-30 | 2013-12-17 | Giorgio Attardo | Triheterocyclic compounds, compositions, and methods for treating cancer or viral diseases |
AU2004257167B2 (en) | 2003-07-03 | 2012-03-29 | The Trustees Of The University Of Pennsylvania | Inhibition of Syk kinase expression |
JP4398263B2 (en) | 2004-01-13 | 2010-01-13 | 富士通株式会社 | Route design method |
CN101031569B (en) | 2004-05-13 | 2011-06-22 | 艾科斯有限公司 | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
TWI380996B (en) | 2004-09-17 | 2013-01-01 | Hoffmann La Roche | Anti-ox40l antibodies |
EP2161275A1 (en) | 2005-01-19 | 2010-03-10 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
EP2343320B1 (en) | 2005-03-25 | 2017-10-25 | GITR, Inc. | Anti-gitr antibodies and uses thereof |
KR101509440B1 (en) | 2005-05-12 | 2015-04-07 | 애브비 바하마스 리미티드 | Apoptosis promoters |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
MX2007015942A (en) | 2005-07-01 | 2008-03-07 | Medarex Inc | Human monoclonal antibodies to programmed death ligand 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 |
CN103819416A (en) | 2005-10-07 | 2014-05-28 | 埃克塞里艾克西斯公司 | N-(3-amino-quinoxalin-2-yl)-sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors |
WO2007053452A1 (en) | 2005-11-01 | 2007-05-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
HUE030235T2 (en) | 2005-12-13 | 2017-04-28 | Incyte Holdings Corp | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
WO2007078990A2 (en) | 2005-12-23 | 2007-07-12 | Zealand Pharma A/S | Modified lysine-mimetic compounds |
JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | PI-3 Kinase inhibitors and methods of their use |
CN101472930B (en) | 2006-04-26 | 2011-12-14 | 霍夫曼-拉罗奇有限公司 | Thieno [3, 2-d] pyrimidine derivative useful as pi3K inhibitor |
EP2526933B1 (en) | 2006-09-22 | 2015-02-25 | Pharmacyclics, Inc. | Inhibitors of Bruton's tyrosine kinase |
US20100279316A1 (en) * | 2007-01-19 | 2010-11-04 | Leonid Gorelik | Antibodies to Phosphorylated IRAK4 |
ES2557930T3 (en) | 2007-03-12 | 2016-01-29 | Ym Biosciences Australia Pty Ltd | Phenylaminopyrimidine compounds and uses thereof |
WO2008118802A1 (en) | 2007-03-23 | 2008-10-02 | Regents Of The University Of Minnesota | Therapeutic compounds |
EP1987839A1 (en) | 2007-04-30 | 2008-11-05 | I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale | Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease |
PE20090717A1 (en) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS |
ES2591281T3 (en) | 2007-07-12 | 2016-11-25 | Gitr, Inc. | Combination therapies that employ GITR binding molecules |
EP2044949A1 (en) | 2007-10-05 | 2009-04-08 | Immutep | Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response |
CA2960659C (en) | 2007-11-09 | 2021-07-13 | The Salk Institute For Biological Studies | Use of tam receptor inhibitors as immunoenhancers and tam activators as immunosuppressors |
CN101932325B (en) | 2007-11-30 | 2014-05-28 | 新联基因公司 | Ido inhibitors |
ES2602577T3 (en) | 2008-03-11 | 2017-02-21 | Incyte Holdings Corporation | Azetidine and cyclobutane derivatives as JAK inhibitors |
EP2291187B1 (en) | 2008-04-24 | 2018-08-15 | Newlink Genetics Corporation | Ido inhibitors |
US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
AR072999A1 (en) | 2008-08-11 | 2010-10-06 | Medarex Inc | HUMAN ANTIBODIES THAT JOIN GEN 3 OF LYMPHOCYTARY ACTIVATION (LAG-3) AND THE USES OF THESE |
TWI686405B (en) | 2008-12-09 | 2020-03-01 | 建南德克公司 | Anti-pd-l1 antibodies and their use to enhance t-cell function |
US8921037B2 (en) | 2008-12-16 | 2014-12-30 | Bo Han | PF4-depleted platelet rich plasma preparations and methods for hard and soft tissue repair |
KR101790802B1 (en) | 2009-09-03 | 2017-10-27 | 머크 샤프 앤드 돔 코포레이션 | Anti-gitr antibodies |
JP2012254939A (en) | 2009-10-07 | 2012-12-27 | Astellas Pharma Inc | Oxazole compound |
US8722720B2 (en) | 2009-10-28 | 2014-05-13 | Newlink Genetics Corporation | Imidazole derivatives as IDO inhibitors |
ES2722300T3 (en) | 2009-12-10 | 2019-08-09 | Hoffmann La Roche | Antibodies that preferentially bind to extracellular domain 4 of CSF1R and its use |
PH12018501083A1 (en) | 2010-03-04 | 2019-02-18 | Macrogenics Inc | Antibodies reactive with b7-h3, immunologically active fragments thereof and uses thereof |
CN102918060B (en) | 2010-03-05 | 2016-04-06 | 霍夫曼-拉罗奇有限公司 | Anti-human CSF-1R antibody and uses thereof |
US9221910B2 (en) | 2010-03-05 | 2015-12-29 | Hoffmann-La Roche Inc. | Antibodies against human CSF-1R |
US8114621B2 (en) | 2010-03-12 | 2012-02-14 | Saladax Biomedical Inc. | Lenalidomide and thalidomide immunoassays |
SI2566517T1 (en) | 2010-05-04 | 2019-01-31 | Five Prime Therapeutics, Inc. | Antibodies that bind csf1r |
CN103153335A (en) | 2010-06-30 | 2013-06-12 | 布兰代斯大学 | Small-molecule-targeted protein degradation |
RU2604062C2 (en) | 2010-07-13 | 2016-12-10 | Ф.Хоффманн-Ля Рош Аг | PYRAZOLO[1,5-a]PYRIMIDINE AND THIENO[3,2-b]PYRIMIDINE DERIVATIVES AS MODULATORS OF IRAK-4 |
EP2614082B1 (en) | 2010-09-09 | 2018-10-03 | Pfizer Inc | 4-1bb binding molecules |
EP2730564B1 (en) | 2010-11-19 | 2018-04-18 | Ligand Pharmaceuticals Inc. | Heterocycle amines and uses thereof |
WO2012078559A2 (en) | 2010-12-07 | 2012-06-14 | Yale University | Small-molecule hydrophobic tagging of fusion proteins and induced degradation of same |
BR122021026169B1 (en) | 2010-12-09 | 2023-12-12 | The Trustees Of The University Of Pennsylvania | USE OF A CELL |
US9073892B2 (en) | 2010-12-20 | 2015-07-07 | Merck Serono S.A. | Indazolyl triazol derivatives |
WO2012097013A1 (en) | 2011-01-10 | 2012-07-19 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
EP2688872A4 (en) | 2011-03-22 | 2014-08-27 | Merck Sharp & Dohme | Amidopyrazole inhibitors of interleukin receptor-associated kinases |
NO2694640T3 (en) | 2011-04-15 | 2018-03-17 | ||
RU2625034C2 (en) | 2011-04-20 | 2017-07-11 | МЕДИММЬЮН, ЭлЭлСи | Antibodies and other molecules binding b7-h1 and pd-1 |
WO2013042137A1 (en) | 2011-09-19 | 2013-03-28 | Aurigene Discovery Technologies Limited | Bicyclic heterocycles as irak4 inhibitors |
WO2013066729A1 (en) | 2011-10-31 | 2013-05-10 | Merck Sharp & Dohme Corp. | Aminopyrimidinones as interleukin receptor-associated kinase inhibitors |
BR112014012819B1 (en) | 2011-11-28 | 2022-08-16 | Merck Patent Gmbh | ANTI-PD-L1 ANTIBODY OR ANTIGEN BINDING FRAGMENT AND COMPOSITION |
WO2013087699A1 (en) | 2011-12-15 | 2013-06-20 | F. Hoffmann-La Roche Ag | Antibodies against human csf-1r and uses thereof |
TW201728592A (en) | 2012-01-10 | 2017-08-16 | 林伯士艾瑞斯公司 | IRAK inhibitors and uses thereof |
WO2013106646A2 (en) | 2012-01-12 | 2013-07-18 | Yale University | Compounds and methods for the inhibition of vcb e3 ubiquitin ligase |
CA2861066C (en) | 2012-01-12 | 2024-01-02 | Yale University | Compounds and methods for the enhanced degradation of targeted proteins and other polypeptides by an e3 ubiquitin ligase |
ES2630705T3 (en) | 2012-01-13 | 2017-08-23 | Bristol-Myers Squibb Company | Triazolyl substituted pyridyl compounds useful as kinase inhibitors |
WO2013106612A1 (en) | 2012-01-13 | 2013-07-18 | Bristol-Myers Squibb Company | Heterocyclic-substituted pyridyl compounds useful as kinase inhibitors |
CN104254533B (en) | 2012-01-13 | 2017-09-08 | 百时美施贵宝公司 | The pyridinyl compounds of thiazole or thiadiazoles substitution as kinase inhibitor |
CA2861122A1 (en) | 2012-02-06 | 2013-08-15 | Genentech, Inc. | Compositions and methods for using csf1r inhibitors |
AR090263A1 (en) | 2012-03-08 | 2014-10-29 | Hoffmann La Roche | COMBINED ANTIBODY THERAPY AGAINST HUMAN CSF-1R AND USES OF THE SAME |
BR112014028013A2 (en) | 2012-05-11 | 2018-02-27 | Five Prime Therapeutics Inc | methods for treating a condition associated with rheumatoid arthritis, rheumatoid arthritis, skin lesions, lupus nephritis, lupus, an inflammatory condition, cd16 + disorder, method for reducing the number of cd16 + monocytes, methods for slowing the progression of a renal condition, rag and bone loss |
UY34887A (en) | 2012-07-02 | 2013-12-31 | Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware | OPTIMIZATION OF ANTIBODIES THAT FIX THE LYMPHOCYTE ACTIVATION GEN 3 (LAG-3) AND ITS USES |
ES2589558T3 (en) | 2012-07-10 | 2016-11-15 | Ares Trading S.A. | Pyrimidin Pyrazolyl Derivatives |
WO2014011911A2 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2014011906A2 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2014011902A1 (en) | 2012-07-11 | 2014-01-16 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
US20140079699A1 (en) | 2012-08-31 | 2014-03-20 | Five Prime Therapeutics, Inc. | Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r) |
JP6302912B2 (en) | 2012-09-19 | 2018-03-28 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | 2-oxo-2,3,4,5-tetrahydro-1H-benzo [B] diazepine and its use in the treatment of cancer |
US9586948B2 (en) | 2012-10-08 | 2017-03-07 | Merck Sharp & Dohme Corp. | Inhibitors of IRAK4 activity |
US9598440B2 (en) | 2012-10-08 | 2017-03-21 | Merck Sharp & Dohme Corp. | Inhibitors of IRAK4 activity |
USRE48175E1 (en) | 2012-10-19 | 2020-08-25 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
KR102233252B1 (en) * | 2012-11-08 | 2021-03-26 | 브리스톨-마이어스 스큅 컴퍼니 | ALKYL-AMIDE-SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFNα RESPONSES |
JP6215338B2 (en) * | 2012-11-08 | 2017-10-18 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Bicyclic heterocycle-substituted pyridyl compounds useful as kinase modulators |
PE20150953A1 (en) * | 2012-11-08 | 2015-06-20 | Bristol Myers Squibb Co | HETEROARYL SUBSTITUTE PYRIDYL COMPOUNDS USEFUL AS KINASE MODULATORS |
GB201311910D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel Compounds |
AU2014214254B2 (en) | 2013-02-07 | 2018-03-29 | Merck Patent Gmbh | Macrocyclic Pyridazinone derivatives |
SG11201506100XA (en) | 2013-02-07 | 2015-09-29 | Merck Patent Gmbh | Pyridazinone-amides derivatives |
WO2014143672A1 (en) | 2013-03-15 | 2014-09-18 | Biogen Idec Ma Inc. | Macrocyclic compounds as irak4 inhibitors for the treatment of inflammatory diseases |
EP3049086A4 (en) | 2013-09-27 | 2017-02-22 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
EA201690713A1 (en) | 2013-10-04 | 2016-08-31 | Инфинити Фармасьютикалз, Инк. | HETEROCYCLIC COMPOUNDS AND THEIR APPLICATIONS |
EA201690952A1 (en) | 2013-11-08 | 2016-08-31 | Такеда Фармасьютикал Компани Лимитед | PYRAZOL FOR THE TREATMENT OF AUTOIMMUNE DISORDERS |
RU2016122563A (en) | 2013-11-18 | 2017-12-25 | Ф. Хоффманн-Ля Рош Аг | TETRAHYDROBENZODIAZEPINONES |
CN110156770B (en) | 2013-11-27 | 2022-10-04 | 圣诺康生命科学公司 | Aminopyridine derivatives as inhibitors of TAM family kinases |
TWI667233B (en) | 2013-12-19 | 2019-08-01 | 德商拜耳製藥公司 | Novel indazolecarboxamides, processes for their preparation, pharmaceutical preparations comprising them and their use for producing medicaments |
UY35935A (en) | 2014-01-03 | 2015-06-30 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | NICOTINAMIDE COMPOUNDS REPLACED WITH HETEROARILO AS QUINASE INHIBITORS AND MODULATORS OF IRAK-4 |
SG11201605408RA (en) | 2014-01-10 | 2016-07-28 | Aurigene Discovery Tech Ltd | Indazole compounds as irak4 inhibitors |
DK3094329T3 (en) | 2014-01-13 | 2018-11-19 | Aurigene Discovery Tech Ltd | BICYCLIC HETEROCYCLYL DERIVATIVES AS IRAC4 INHIBITORS |
EP3119760A1 (en) | 2014-03-17 | 2017-01-25 | F. Hoffmann-La Roche AG | Piperidine-dione derivatives |
WO2015140051A1 (en) | 2014-03-19 | 2015-09-24 | Boehringer Ingelheim International Gmbh | Heteroaryl sik inhibitors |
EA032559B1 (en) | 2014-04-04 | 2019-06-28 | Пфайзер Инк. | Bicyclic-fused heteroaryl or aryl compounds and their use as irak4 inhibitors |
US20180228907A1 (en) | 2014-04-14 | 2018-08-16 | Arvinas, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
JP6778114B2 (en) | 2014-04-14 | 2020-10-28 | 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. | Imid-based proteolysis modulators and related uses |
US20160058872A1 (en) | 2014-04-14 | 2016-03-03 | Arvinas, Inc. | Imide-based modulators of proteolysis and associated methods of use |
CA2945819A1 (en) | 2014-04-22 | 2015-10-29 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
BR112016029853A2 (en) | 2014-06-20 | 2017-08-22 | Aurigene Discovery Tech Ltd | substituted indazole compounds as irak4 inhibitors |
WO2015200795A1 (en) | 2014-06-27 | 2015-12-30 | Celgene Corporation | Compositions and methods for inducing conformational changes in cereblon other e3 ubiquitin ligases |
TW201613872A (en) | 2014-07-18 | 2016-04-16 | Biogen Ma Inc | IRAK4 inhibiting agents |
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 |
WO2016053769A1 (en) | 2014-09-30 | 2016-04-07 | Merck Sharp & Dohme Corp. | Inhibitors of irak4 activity |
US9943516B2 (en) | 2014-09-30 | 2018-04-17 | Merck Sharp & Dohme Corp. | Inhibitors of IRAK4 activity |
EP3200787B1 (en) | 2014-09-30 | 2019-09-04 | Merck Sharp & Dohme Corp. | Inhibitors of irak4 activity |
US9932350B2 (en) | 2014-09-30 | 2018-04-03 | Merck Sharp & Dohme Corp. | Inhibitors of IRAK4 activity |
AU2015349899B9 (en) | 2014-11-20 | 2020-06-25 | Merck Patent Gmbh | Heteroaryl compounds as IRAK inhibitors and uses thereof |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
JP6815318B2 (en) | 2014-12-23 | 2021-01-20 | ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド | How to Induce Targeted Proteolysis by Bifunctional Molecules |
WO2016105581A1 (en) * | 2014-12-23 | 2016-06-30 | South Dakota Board Of Regents | Electrospun three-dimensional nanofibrous scaffolds with interconnected and hierarchically structured pores |
US20170327469A1 (en) | 2015-01-20 | 2017-11-16 | Arvinas, Inc. | Compounds and methods for the targeted degradation of androgen receptor |
KR20220029783A (en) | 2015-01-20 | 2022-03-08 | 아비나스 오퍼레이션스, 인코포레이티드 | Compounds and Methods for the Targeted Degradation of the Androgen Receptor |
US10155765B2 (en) | 2015-03-12 | 2018-12-18 | Merck Sharp & Dohme Corp. | Carboxamide inhibitors of IRAK4 activity |
WO2016144847A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Pyrrolopyridazine inhibitors of irak4 activity |
EP3268003B1 (en) | 2015-03-12 | 2020-07-29 | Merck Sharp & Dohme Corp. | Thienopyrazine inhibitors of irak4 activity |
WO2016144846A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Pyrazolopyrimidine inhibitors of irak4 activity |
EP3268006B1 (en) | 2015-03-12 | 2020-01-08 | Merck Sharp & Dohme Corp. | Pyrrolotriazine inhibitors of irak4 activity |
MX2017011919A (en) | 2015-03-18 | 2018-05-22 | Arvinas Inc | Compounds and methods for the enhanced degradation of targeted proteins. |
GB201506871D0 (en) | 2015-04-22 | 2015-06-03 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
EP3286181B1 (en) | 2015-04-22 | 2021-01-27 | Rigel Pharmaceuticals, Inc. | Pyrazole compounds and method for making and using the compounds |
WO2016174183A1 (en) | 2015-04-30 | 2016-11-03 | Bayer Pharma Aktiengesellschaft | Combinations of inhibitors of irak4 with inhibitors of btk |
EP3302572B8 (en) | 2015-06-04 | 2021-03-24 | Arvinas Operations, Inc. | Imide-based modulators of proteolysis and associated methods of use |
EP3302482A4 (en) | 2015-06-05 | 2018-12-19 | Arvinas, Inc. | Tank-binding kinase-1 protacs and associated methods of use |
JP6720355B2 (en) * | 2015-06-24 | 2020-07-08 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Heteroaryl-substituted aminopyridine compounds |
CN107849039B (en) | 2015-06-24 | 2020-07-03 | 百时美施贵宝公司 | Heteroaryl substituted aminopyridine compounds |
CN105085620B (en) | 2015-06-25 | 2018-05-08 | 中山大学附属第一医院 | A kind of compound for targeting ubiquitination degraded Smad3 |
WO2017004134A1 (en) | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2017004133A1 (en) | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2017007612A1 (en) * | 2015-07-07 | 2017-01-12 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
AU2016291578C1 (en) | 2015-07-10 | 2021-07-15 | Arvinas Operations, Inc. | MDM2-based modulators of proteolysis and associated methods of use |
RU2018105094A (en) | 2015-07-13 | 2019-08-14 | Арвинас, Инк. | ALANINE-BASED PROTEOLYSIS MODULATORS AND RELATED APPLICATION METHODS |
BR112018000624A2 (en) | 2015-07-15 | 2018-09-18 | Aurigene Discovery Technologies Limited | indazole and azaindazole compounds as irak-4 inhibitors |
AU2016293446A1 (en) | 2015-07-15 | 2018-02-15 | Aurigene Discovery Technologies Limited | Substituted aza compounds as IRAK-4 inhibitors |
WO2017030814A1 (en) | 2015-08-19 | 2017-02-23 | Arvinas, Inc. | Compounds and methods for the targeted degradation of bromodomain-containing proteins |
WO2017033093A1 (en) | 2015-08-27 | 2017-03-02 | Pfizer Inc. | Bicyclic-fused heteroaryl or aryl compounds as irak4 modulators |
CA2996318C (en) | 2015-09-18 | 2023-10-10 | Merck Patent Gmbh | Heteroaryl compounds as irak inhibitors and uses thereof |
EP3350177B1 (en) | 2015-09-18 | 2021-07-07 | Merck Patent GmbH | Heteroaryl compounds as irak inhibitors and uses thereof |
WO2017059280A1 (en) | 2015-10-02 | 2017-04-06 | The University Of North Carolina At Chapel Hill | Novel pan-tam inhibitors and mer/axl dual inhibitors |
CN108366992A (en) | 2015-11-02 | 2018-08-03 | 耶鲁大学 | Proteolysis targets chimera compound and its methods for making and using same |
WO2017108723A2 (en) | 2015-12-22 | 2017-06-29 | F. Hoffmann-La Roche Ag | PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS |
US20200216454A1 (en) | 2015-12-30 | 2020-07-09 | Dana-Farber Cancer Institute, Inc. | Bifunctional molecules for her3 degradation and methods of use |
US20190016703A1 (en) | 2015-12-30 | 2019-01-17 | Dana-Farber Cancer Institute, Inc. | Bifunctional compounds for her3 degradation and methods of use |
ES2904557T3 (en) | 2016-01-20 | 2022-04-05 | Biogen Ma Inc | Iraq4 inhibitory agents |
US11395820B2 (en) | 2016-03-16 | 2022-07-26 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Small molecules against cereblon to enhance effector t cell function |
US20170281784A1 (en) | 2016-04-05 | 2017-10-05 | Arvinas, Inc. | Protein-protein interaction inducing technology |
CN113788818A (en) | 2016-04-06 | 2021-12-14 | 密执安大学评议会 | MDM2 protein degrading agent |
US10759808B2 (en) | 2016-04-06 | 2020-09-01 | The Regents Of The University Of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
WO2017197055A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Heterocyclic degronimers for target protein degradation |
EP3455218A4 (en) | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | C3-carbon linked glutarimide degronimers for target protein degradation |
WO2017197051A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Amine-linked c3-glutarimide degronimers for target protein degradation |
WO2017197056A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Bromodomain targeting degronimers for target protein degradation |
CN109562113A (en) | 2016-05-10 | 2019-04-02 | C4医药公司 | Loop coil degron body for target protein degradation |
WO2017201069A1 (en) | 2016-05-18 | 2017-11-23 | Biotheryx, Inc. | Oxoindoline derivatives as protein function modulators |
EP3458101B1 (en) * | 2016-05-20 | 2020-12-30 | H. Hoffnabb-La Roche Ag | Protac antibody conjugates and methods of use |
WO2017205762A1 (en) | 2016-05-27 | 2017-11-30 | Pharmacyclics Llc | Inhibitors of interleukin-1 receptor-associated kinase |
WO2017205766A1 (en) | 2016-05-27 | 2017-11-30 | Pharmacyclics Llc | Inhibitors of interleukin-1 receptor-associated kinase |
WO2017207385A1 (en) | 2016-05-31 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Substituted 3-methylindazoles, methods for the production thereof, pharmaceutical preparations containing same, and use thereof for the production of medicaments |
GB201610147D0 (en) | 2016-06-10 | 2016-07-27 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
JP7065840B2 (en) | 2016-06-27 | 2022-05-12 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 2,4-Diamino-pyrimidine compound and method for producing and using the compound |
US10646488B2 (en) | 2016-07-13 | 2020-05-12 | Araxes Pharma Llc | Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof |
JP2019196309A (en) | 2016-09-15 | 2019-11-14 | 武田薬品工業株式会社 | Heterocyclic compound |
WO2018089736A1 (en) | 2016-11-10 | 2018-05-17 | Dana-Farber Cancer Institute, Inc. | Degradation of protein kinases by conjugation of protein kinase inhibitors with e3 ligase ligand and methods of use |
JP7308146B2 (en) | 2016-11-22 | 2023-07-13 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | INHIBITORS OF INTERLEUKIN-1 RECEPTOR-ASSOCIATED KINASE AND USES THEREOF |
CN108322937B (en) | 2017-01-18 | 2020-08-11 | 上海诺基亚贝尔股份有限公司 | Resource allocation method and orchestrator for network slices in a radio access network |
MX2019009046A (en) | 2017-01-31 | 2019-10-30 | Arvinas Operations Inc | Cereblon ligands and bifunctional compounds comprising the same. |
JOP20180011A1 (en) | 2017-02-16 | 2019-01-30 | Gilead Sciences Inc | PYRROLO[1,2-b] PYRIDAZINE DERIVATIVES |
PT3621960T (en) | 2017-05-11 | 2021-09-16 | Bristol Myers Squibb Co | Thienopyridines and benzothiophenes useful as irak4 inhibitors |
CN110769822A (en) | 2017-06-20 | 2020-02-07 | C4医药公司 | N/O-linked degron and degron bodies for protein degradation |
EP3679026A1 (en) | 2017-09-04 | 2020-07-15 | C4 Therapeutics, Inc. | Glutarimide |
AU2018338314A1 (en) | 2017-09-22 | 2020-04-09 | Kymera Therapeutics, Inc | Protein degraders and uses thereof |
EP3684366A4 (en) | 2017-09-22 | 2021-09-08 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
EP3700901A1 (en) | 2017-10-24 | 2020-09-02 | Genentech, Inc. | (4-hydroxypyrrolidin-2-yl)-heterocyclic compounds and methods of use thereof |
WO2019084030A1 (en) | 2017-10-24 | 2019-05-02 | Genentech, Inc. | (4-hydroxypyrrolidin-2-yl)-hydroxamate compounds and methods of use thereof |
WO2019099868A2 (en) | 2017-11-16 | 2019-05-23 | C4 Therapeutics, Inc. | Degraders and degrons for targeted protein degradation |
WO2019099926A1 (en) | 2017-11-17 | 2019-05-23 | Arvinas, Inc. | Compounds and methods for the targeted degradation of interleukin-1 receptor-associated kinase 4 polypeptides |
JP2021508703A (en) | 2017-12-26 | 2021-03-11 | カイメラ セラピューティクス, インコーポレイテッド | IRAK Degradants and Their Use |
EP3737675A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
EP3737666A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
WO2019160915A1 (en) | 2018-02-14 | 2019-08-22 | Dana-Farber Cancer Institute, Inc. | Irak degraders and uses thereof |
AU2019225166A1 (en) | 2018-02-23 | 2020-08-06 | Dana-Farber Cancer Institute, Inc. | Small molecules for inducing selective protein degradation and uses thereof |
EP3578561A1 (en) | 2018-06-04 | 2019-12-11 | F. Hoffmann-La Roche AG | Spiro compounds |
US20220348556A1 (en) | 2018-07-06 | 2022-11-03 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
WO2020010210A1 (en) | 2018-07-06 | 2020-01-09 | Kymera Therapeutics, Inc. | Mertk degraders and uses thereof |
EP3817748A4 (en) | 2018-07-06 | 2022-08-24 | Kymera Therapeutics, Inc. | Tricyclic crbn ligands and uses thereof |
AU2019307631A1 (en) | 2018-07-20 | 2020-12-17 | Dana-Farber Cancer Institute, Inc. | Degraders that target proteins via KEAP1 |
SG11202105424PA (en) | 2018-11-30 | 2021-06-29 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
US20230149549A1 (en) | 2019-06-10 | 2023-05-18 | Kymera Therapeutics, Inc | Smarca degraders and uses thereof |
US20220324880A1 (en) | 2019-06-10 | 2022-10-13 | Kymara Therapeutics, Inc. | Smarca inhibitors and uses thereof |
US20230072658A1 (en) | 2019-06-10 | 2023-03-09 | Kymera Therapeutics, Inc. | Smarca degraders and uses thereof |
WO2020251969A1 (en) | 2019-06-10 | 2020-12-17 | Kymera Therapeutics, Inc. | Smarca degraders and uses thereof |
EP3989966A4 (en) | 2019-06-28 | 2023-09-27 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
WO2020264490A1 (en) | 2019-06-28 | 2020-12-30 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
WO2021011631A1 (en) | 2019-07-15 | 2021-01-21 | Kymera Therapeutics, Inc. | Fused-glutarimide crbn ligands and uses thereof |
US20230093080A1 (en) | 2019-07-15 | 2023-03-23 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
WO2021011868A1 (en) | 2019-07-17 | 2021-01-21 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
WO2021011871A1 (en) | 2019-07-17 | 2021-01-21 | Kymera Therapeutics, Inc. | Mertk degraders and uses thereof |
WO2021127278A1 (en) | 2019-12-17 | 2021-06-24 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
IL293917A (en) | 2019-12-17 | 2022-08-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
EP4076524A4 (en) | 2019-12-17 | 2023-11-29 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
-
2018
- 2018-12-21 JP JP2020535655A patent/JP2021508703A/en active Pending
- 2018-12-21 SG SG11202005912PA patent/SG11202005912PA/en unknown
- 2018-12-21 IL IL275649A patent/IL275649B2/en unknown
- 2018-12-21 MX MX2020006812A patent/MX2020006812A/en unknown
- 2018-12-21 BR BR112020012997-6A patent/BR112020012997A2/en unknown
- 2018-12-21 US US16/230,792 patent/US10874743B2/en active Active
- 2018-12-21 EP EP18894876.4A patent/EP3731869A4/en active Pending
- 2018-12-21 CA CA3086763A patent/CA3086763A1/en active Pending
- 2018-12-21 IL IL304055A patent/IL304055A/en unknown
- 2018-12-21 CN CN201880089841.0A patent/CN112105385A/en active Pending
- 2018-12-21 WO PCT/US2018/067304 patent/WO2019133531A1/en unknown
- 2018-12-21 AU AU2018396142A patent/AU2018396142A1/en active Pending
-
2020
- 2020-10-16 US US17/073,019 patent/US11318205B1/en active Active
-
2022
- 2022-02-10 US US17/650,545 patent/US11723980B2/en active Active
-
2023
- 2023-04-24 US US18/305,911 patent/US20230398223A1/en active Pending
-
2024
- 2024-01-11 JP JP2024002339A patent/JP2024038329A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
IL275649B2 (en) | 2023-12-01 |
US11318205B1 (en) | 2022-05-03 |
AU2018396142A1 (en) | 2020-07-16 |
EP3731869A1 (en) | 2020-11-04 |
WO2019133531A1 (en) | 2019-07-04 |
IL304055A (en) | 2023-08-01 |
IL275649B1 (en) | 2023-08-01 |
US11723980B2 (en) | 2023-08-15 |
US20230106066A1 (en) | 2023-04-06 |
CA3086763A1 (en) | 2019-07-04 |
US10874743B2 (en) | 2020-12-29 |
JP2024038329A (en) | 2024-03-19 |
EP3731869A4 (en) | 2021-09-22 |
US20190192668A1 (en) | 2019-06-27 |
MX2020006812A (en) | 2020-11-06 |
CN112105385A (en) | 2020-12-18 |
IL275649A (en) | 2020-08-31 |
BR112020012997A2 (en) | 2020-12-01 |
JP2021508703A (en) | 2021-03-11 |
US20230398223A1 (en) | 2023-12-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL275649A (en) | Irak degraders and uses thereof | |
IL283471A (en) | Irak degraders and uses thereof | |
IL289267A (en) | Irak degraders and uses thereof | |
IL273432A (en) | Protein degraders and uses thereof | |
IL273236A (en) | Pyrazolopyrimidinone compounds and uses thereof | |
EP4076520A4 (en) | Irak degraders and uses thereof | |
EP4076536A4 (en) | Irak degraders and uses thereof | |
EP3752504A4 (en) | Irak degraders and uses thereof | |
IL293377A (en) | Hsd17b13 variants and uses thereof | |
GB201714745D0 (en) | New compounds and uses | |
GB201714740D0 (en) | New compounds and uses | |
EP4081308A4 (en) | Smarca degraders and uses thereof | |
GB201714734D0 (en) | New compounds and uses | |
HUE060805T2 (en) | Pyridinamine-pyridone and pyrimidinamine-pyridone compounds | |
EP4072591A4 (en) | Irak degraders and uses thereof | |
GB201714736D0 (en) | New compounds and uses | |
IL265531A (en) | N 3 -cyclically substituted thienouraciles and use thereof | |
IL264473A (en) | Gpr156 variants and uses thereof | |
SG11201912432VA (en) | Emm-23 materials and processes and uses thereof | |
IL273671A (en) | Cornulin (crnn) variants and uses thereof | |
IL275211A (en) | Fast and partition-resilient blockchains | |
IL269836B (en) | Substituted n-arylethyl-2-aminoquinoline-4-carboxamides and use thereof | |
ZA201905513B (en) | Rorgamma modulators and uses thereof | |
ZA201905511B (en) | Rorgamma modulators and uses thereof | |
GB201712110D0 (en) | New compounds and uses |