PL3601296T3 - Pochodne 2-okso-tiazolowe jako inhibitory i związki a2a do stosowania w leczeniu nowotworów złośliwych - Google Patents

Pochodne 2-okso-tiazolowe jako inhibitory i związki a2a do stosowania w leczeniu nowotworów złośliwych

Info

Publication number
PL3601296T3
PL3601296T3 PL18716193.0T PL18716193T PL3601296T3 PL 3601296 T3 PL3601296 T3 PL 3601296T3 PL 18716193 T PL18716193 T PL 18716193T PL 3601296 T3 PL3601296 T3 PL 3601296T3
Authority
PL
Poland
Prior art keywords
cancers
oxo
inhibitors
compounds
treatment
Prior art date
Application number
PL18716193.0T
Other languages
English (en)
Inventor
Stefano Crosignani
Bruno GOMES
Erica HOUTHUYS
Original Assignee
iTeos Belgium SA
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
Priority claimed from ARP180100778A external-priority patent/AR111200A1/es
Application filed by iTeos Belgium SA filed Critical iTeos Belgium SA
Priority claimed from PCT/EP2018/058301 external-priority patent/WO2018178338A1/en
Publication of PL3601296T3 publication Critical patent/PL3601296T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D497/00Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D497/12Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D497/14Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PL18716193.0T 2017-03-30 2018-03-30 Pochodne 2-okso-tiazolowe jako inhibitory i związki a2a do stosowania w leczeniu nowotworów złośliwych PL3601296T3 (pl)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP17163781 2017-03-30
US201762565281P 2017-09-29 2017-09-29
EP17194084 2017-09-29
ARP180100778A AR111200A1 (es) 2017-03-30 2018-03-28 Derivados de tiocarbamato como inhibidores de a2a y métodos para usar en el tratamiento de cánceres
PCT/EP2018/058301 WO2018178338A1 (en) 2017-03-30 2018-03-30 2-oxo-thiazole derivatives as a2a inhibitors and compounds for use in the treatment of cancers

Publications (1)

Publication Number Publication Date
PL3601296T3 true PL3601296T3 (pl) 2022-10-10

Family

ID=61911575

Family Applications (1)

Application Number Title Priority Date Filing Date
PL18716193.0T PL3601296T3 (pl) 2017-03-30 2018-03-30 Pochodne 2-okso-tiazolowe jako inhibitory i związki a2a do stosowania w leczeniu nowotworów złośliwych

Country Status (19)

Country Link
US (3) US10995101B2 (pl)
EP (2) EP3601296B1 (pl)
JP (2) JP7197558B2 (pl)
KR (2) KR20240027885A (pl)
CN (3) CN115991679A (pl)
AU (1) AU2018246355B2 (pl)
BR (1) BR112019020421A8 (pl)
CA (1) CA3058260A1 (pl)
DK (1) DK3601296T3 (pl)
ES (1) ES2926158T3 (pl)
HR (1) HRP20221039T1 (pl)
HU (1) HUE059990T2 (pl)
IL (2) IL300149A (pl)
LT (1) LT3601296T (pl)
MX (2) MX2019011743A (pl)
PL (1) PL3601296T3 (pl)
RS (1) RS63557B1 (pl)
SI (1) SI3601296T1 (pl)
TW (1) TWI836960B (pl)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11202000431PA (en) 2017-07-18 2020-02-27 Nuvation Bio Inc 1,8-naphthyridinone compounds and uses thereof
AU2018302179A1 (en) 2017-07-18 2020-02-13 Nuvation Bio Inc. Heterocyclic compounds as adenosine antagonists
US11376255B2 (en) 2018-09-11 2022-07-05 iTeos Belgium SA Thiocarbamate derivatives as A2A inhibitors, pharmaceutical composition thereof and combinations with anticancer agents
JP2022500496A (ja) * 2018-09-11 2022-01-04 アイテオ ベルギウム エスエー A2a阻害剤としてのチオカルバメート誘導体、その医薬組成物、及び抗がん剤との組み合わせ
US11427594B2 (en) 2018-09-27 2022-08-30 iTeos Belgium SA Non brain penetrant A2A inhibitors and methods for use in the treatment of cancers
AU2020208644A1 (en) 2019-01-18 2021-08-26 Nuvation Bio Inc. Heterocyclic compounds as adenosine antagonists
CN113939291A (zh) 2019-01-18 2022-01-14 诺维逊生物股份有限公司 1,8-萘啶酮化合物及其用途
CN114539265B (zh) * 2022-03-02 2023-07-21 中山大学 靶向a2a的苯并咪唑并吡嗪-3-甲酰胺及其肿瘤免疫功能

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6448253B1 (en) 1998-09-16 2002-09-10 King Pharmaceuticals Research And Development, Inc. Adenosine A3 receptor modulators
US6921825B2 (en) 1998-09-16 2005-07-26 King Pharmaceuticuals Research & Development, Inc. Adenosine A3 receptor modulators
ES2237576T3 (es) * 2000-05-26 2005-08-01 Schering Corporation Antagonistas del receptor a2a de adenosina.
WO2004092171A2 (en) * 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolo[1,5-a]pyrimidines and pyrazolo[1,5-a]pyrimidines useful as a2a adenosin e receptor antagonists
US7709492B2 (en) * 2004-04-21 2010-05-04 Schering Corporation Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists
WO2007140181A2 (en) 2006-05-26 2007-12-06 King Pharmaceuticals Research And Development, Inc. Combination therapy comprising an adenosine uptake inhibitor and a non-selective adenosine receptor antagonist
US7691869B2 (en) * 2007-03-30 2010-04-06 King Pharmaceuticals Research And Development, Inc. Pyrrolotriazolopyrimidine derivatives, pharmaceutical compositions containing them and methods of treating conditions and diseases mediated by the adenosine A2A receptor activity
CA2694987A1 (en) 2007-07-17 2009-01-22 Combinatorx, Incorporated Combinations for the treatment of b-cell proliferative disorders
WO2011112687A2 (en) 2010-03-10 2011-09-15 Kalypsys, Inc. Heterocyclic inhibitors of histamine receptors for the treatment of disease
CA2812378C (en) 2010-09-24 2016-11-29 Advinus Therapeutics Limited Fused tricyclic compounds as adenosine receptor antagonist
WO2012055015A1 (en) 2010-10-26 2012-05-03 Alberta Health Services Combination comprising an atp analog and an adenosine receptor antagonist or a nucleobase/nucleoside analog for the treatment of cancer
WO2012135084A1 (en) * 2011-03-31 2012-10-04 Merck Sharp & Dohme Corp. METABOLITES OF 2-(FURAN-2-YL)-7-(2-(4-(4-(2-METHOXYETHOXY)PHENYL)PIPERAZIN-1-YL)ETHYL)-7H-PYRAZOLO[4,3-e][1,2,4]TRIAZOLO[1,5-c]PYRIMIDIN-5-AMINE AND THEIR UTILITY AS ADENOSINE A2a RECEPTOR ANTAGONISTS
CA3047600A1 (en) 2017-01-20 2018-07-26 Arcus Biosciences, Inc. Azolopyrimidine for the treatment of cancer-related disorders
WO2018178338A1 (en) 2017-03-30 2018-10-04 Iteos Therapeutics 2-oxo-thiazole derivatives as a2a inhibitors and compounds for use in the treatment of cancers
US20200316077A1 (en) 2017-12-19 2020-10-08 Impetis Biosciences Ltd. Pharmaceutical composition for the treatment of cancer
JP2022500496A (ja) 2018-09-11 2022-01-04 アイテオ ベルギウム エスエー A2a阻害剤としてのチオカルバメート誘導体、その医薬組成物、及び抗がん剤との組み合わせ
US11427594B2 (en) 2018-09-27 2022-08-30 iTeos Belgium SA Non brain penetrant A2A inhibitors and methods for use in the treatment of cancers
WO2020065036A1 (en) 2018-09-27 2020-04-02 Iteos Therapeutics S.A. Use of an inhibitor of an ent family transporter in the treatment of cancer and combination thereof with an adenosine receptor antagonist

Also Published As

Publication number Publication date
CN110678472A (zh) 2020-01-10
LT3601296T (lt) 2022-09-26
TW202344508A (zh) 2023-11-16
AU2018246355B2 (en) 2021-12-09
HUE059990T2 (hu) 2023-01-28
US20230159564A1 (en) 2023-05-25
IL300149A (en) 2023-03-01
CA3058260A1 (en) 2018-10-04
KR20240027885A (ko) 2024-03-04
JP7197558B2 (ja) 2022-12-27
CN115991679A (zh) 2023-04-21
HRP20221039T1 (hr) 2022-11-11
EP3601296B1 (en) 2022-05-25
ES2926158T3 (es) 2022-10-24
MX2022005298A (es) 2022-05-26
JP2020512407A (ja) 2020-04-23
US10995101B2 (en) 2021-05-04
US20190276473A1 (en) 2019-09-12
CN115873022A (zh) 2023-03-31
CN110678472B (zh) 2023-01-24
RU2019134724A3 (pl) 2021-06-28
JP2023027282A (ja) 2023-03-01
IL269710B2 (en) 2023-06-01
BR112019020421A8 (pt) 2022-11-08
BR112019020421A2 (pt) 2020-04-28
KR20190141156A (ko) 2019-12-23
US20210198281A1 (en) 2021-07-01
RU2019134724A (ru) 2021-04-30
IL269710A (en) 2019-11-28
AU2018246355A1 (en) 2019-10-17
KR102640927B1 (ko) 2024-02-27
EP4112623A1 (en) 2023-01-04
SI3601296T1 (sl) 2022-10-28
DK3601296T3 (da) 2022-08-29
RS63557B1 (sr) 2022-10-31
TWI836960B (zh) 2024-03-21
MX2019011743A (es) 2020-01-20
EP3601296A1 (en) 2020-02-05

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