EA032872B1 - Макроциклические ингибиторы rip2-киназы - Google Patents

Макроциклические ингибиторы rip2-киназы Download PDF

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Publication number
EA032872B1
EA032872B1 EA201790609A EA201790609A EA032872B1 EA 032872 B1 EA032872 B1 EA 032872B1 EA 201790609 A EA201790609 A EA 201790609A EA 201790609 A EA201790609 A EA 201790609A EA 032872 B1 EA032872 B1 EA 032872B1
Authority
EA
Eurasian Patent Office
Prior art keywords
alkyl
halogen
optionally
independently substituted
cycloalkyl
Prior art date
Application number
EA201790609A
Other languages
English (en)
Russian (ru)
Other versions
EA201790609A1 (ru
Inventor
Ян Хофлак
Петра Блом
Паскаль Бендериттер
Original Assignee
Онкодизайн С.А.
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 Онкодизайн С.А. filed Critical Онкодизайн С.А.
Publication of EA201790609A1 publication Critical patent/EA201790609A1/ru
Publication of EA032872B1 publication Critical patent/EA032872B1/ru

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Classifications

    • 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
    • A61K31/529Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim forming part of bridged ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/22Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Rheumatology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pain & Pain Management (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
EA201790609A 2014-09-17 2015-09-17 Макроциклические ингибиторы rip2-киназы EA032872B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14185130 2014-09-17
PCT/EP2015/071347 WO2016042087A1 (en) 2014-09-17 2015-09-17 Macrocyclic rip2 kinase inhibitors

Publications (2)

Publication Number Publication Date
EA201790609A1 EA201790609A1 (ru) 2017-07-31
EA032872B1 true EA032872B1 (ru) 2019-07-31

Family

ID=51687776

Family Applications (1)

Application Number Title Priority Date Filing Date
EA201790609A EA032872B1 (ru) 2014-09-17 2015-09-17 Макроциклические ингибиторы rip2-киназы

Country Status (26)

Country Link
US (1) US10676486B2 (enExample)
EP (1) EP3194407B1 (enExample)
JP (1) JP6736545B2 (enExample)
KR (1) KR102563829B1 (enExample)
CN (1) CN106687464B (enExample)
AU (1) AU2015316799B2 (enExample)
BR (1) BR112017004035B1 (enExample)
CA (1) CA2958782C (enExample)
DK (1) DK3194407T3 (enExample)
EA (1) EA032872B1 (enExample)
ES (1) ES2763344T3 (enExample)
HR (1) HRP20192334T1 (enExample)
HU (1) HUE048518T2 (enExample)
IL (1) IL250544B (enExample)
LT (1) LT3194407T (enExample)
MX (1) MX376087B (enExample)
MY (1) MY186523A (enExample)
PL (1) PL3194407T3 (enExample)
PT (1) PT3194407T (enExample)
SA (1) SA517381087B1 (enExample)
SG (1) SG11201701116XA (enExample)
SI (1) SI3194407T1 (enExample)
TW (1) TWI709563B (enExample)
UA (1) UA121315C2 (enExample)
WO (1) WO2016042087A1 (enExample)
ZA (1) ZA201701331B (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102719387B1 (ko) * 2017-01-26 2024-10-21 한미약품 주식회사 이미다조피리다진 화합물
AR124556A1 (es) 2020-01-31 2023-04-12 Oncodesign Sa Inhibidores macrocíclicos de rip2-cinasa
WO2024051631A1 (zh) * 2022-09-07 2024-03-14 苏州朗睿生物医药有限公司 一种大环咪唑并[1,2-b]哒嗪衍生物及其制备方法和用途
CN120500490A (zh) * 2023-01-03 2025-08-15 广东新契生物医药科技有限公司 作为usp1抑制剂的大环化合物
WO2025212514A2 (en) * 2024-04-02 2025-10-09 Interline Therapeutics, Inc. Methods of treating inflammatory diseases

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008058126A2 (en) * 2006-11-06 2008-05-15 Supergen, Inc. Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors
WO2011146336A1 (en) * 2010-05-20 2011-11-24 Array Biopharma Inc. Macrocyclic compounds as trk kinase inhibitors
WO2013001310A1 (en) * 2011-06-30 2013-01-03 Centro Nacional De Investigaciones Oncológicas (Cnio) Macrocyclic compounds and their use as cdk8 inhibitors
WO2013025958A1 (en) * 2011-08-18 2013-02-21 Glaxo Group Limited Amino quinazolines as kinase inhibitors
WO2013045653A1 (en) * 2011-09-30 2013-04-04 Oncodesign S.A. Macrocyclic flt3 kinase inhibitors

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IS2334B (is) 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
SK283569B6 (sk) 1993-10-01 2003-09-11 Astra Aktiebolag Spôsob spracovania jemne deleného práškového liečiva, zariadenie na vykonávanie tohto spôsobu a aglomeráty vyrobené týmto spôsobom
US6043358A (en) 1995-11-01 2000-03-28 Merck & Co., Inc. Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
US6369087B1 (en) 1999-08-26 2002-04-09 Robert R. Whittle Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
AR077468A1 (es) * 2009-07-09 2011-08-31 Array Biopharma Inc Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
ES2583477T3 (es) 2011-09-30 2016-09-21 Ipsen Pharma S.A.S. Inhibidores macrocíclicos de cinasa de LRRK2

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008058126A2 (en) * 2006-11-06 2008-05-15 Supergen, Inc. Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors
WO2011146336A1 (en) * 2010-05-20 2011-11-24 Array Biopharma Inc. Macrocyclic compounds as trk kinase inhibitors
WO2013001310A1 (en) * 2011-06-30 2013-01-03 Centro Nacional De Investigaciones Oncológicas (Cnio) Macrocyclic compounds and their use as cdk8 inhibitors
WO2013025958A1 (en) * 2011-08-18 2013-02-21 Glaxo Group Limited Amino quinazolines as kinase inhibitors
WO2013045653A1 (en) * 2011-09-30 2013-04-04 Oncodesign S.A. Macrocyclic flt3 kinase inhibitors

Also Published As

Publication number Publication date
LT3194407T (lt) 2020-01-27
DK3194407T3 (da) 2020-01-27
EP3194407A1 (en) 2017-07-26
AU2015316799B2 (en) 2019-07-11
TW201619168A (zh) 2016-06-01
TWI709563B (zh) 2020-11-11
BR112017004035A2 (pt) 2017-12-05
HUE048518T2 (hu) 2020-07-28
PT3194407T (pt) 2020-01-20
BR112017004035A8 (pt) 2023-05-09
CN106687464B (zh) 2020-03-03
CN106687464A (zh) 2017-05-17
JP6736545B2 (ja) 2020-08-05
PL3194407T3 (pl) 2020-04-30
CA2958782C (en) 2024-01-09
EA201790609A1 (ru) 2017-07-31
IL250544B (en) 2020-06-30
NZ730758A (en) 2023-09-29
WO2016042087A1 (en) 2016-03-24
JP2017528481A (ja) 2017-09-28
CA2958782A1 (en) 2016-03-24
IL250544A0 (en) 2017-03-30
HRP20192334T1 (hr) 2020-03-20
US10676486B2 (en) 2020-06-09
KR102563829B1 (ko) 2023-08-03
KR20170048596A (ko) 2017-05-08
AU2015316799A1 (en) 2017-04-27
MX376087B (es) 2025-03-07
EP3194407B1 (en) 2019-10-23
UA121315C2 (uk) 2020-05-12
SI3194407T1 (sl) 2020-03-31
ZA201701331B (en) 2020-07-29
ES2763344T3 (es) 2020-05-28
SA517381087B1 (ar) 2021-02-09
MY186523A (en) 2021-07-24
MX2017003469A (es) 2017-05-08
BR112017004035B1 (pt) 2023-11-14
US20190127390A1 (en) 2019-05-02
SG11201701116XA (en) 2017-03-30

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