MX2022013064A - Nuevos derivados de imidazolona como inhibidores de proteinas cinasas en particular cinasa 1a regulada por fosforilacion de la tirosina de especificidad dual (dyrk1a), cinasa 1 similar a las citolisinas dependientes del colesterol (clk1) y/o cinasa 4 similar a las citolisinas dependientes del colesterol (clk4). - Google Patents

Nuevos derivados de imidazolona como inhibidores de proteinas cinasas en particular cinasa 1a regulada por fosforilacion de la tirosina de especificidad dual (dyrk1a), cinasa 1 similar a las citolisinas dependientes del colesterol (clk1) y/o cinasa 4 similar a las citolisinas dependientes del colesterol (clk4).

Info

Publication number
MX2022013064A
MX2022013064A MX2022013064A MX2022013064A MX2022013064A MX 2022013064 A MX2022013064 A MX 2022013064A MX 2022013064 A MX2022013064 A MX 2022013064A MX 2022013064 A MX2022013064 A MX 2022013064A MX 2022013064 A MX2022013064 A MX 2022013064A
Authority
MX
Mexico
Prior art keywords
sub
group
sup
compound
phenyl group
Prior art date
Application number
MX2022013064A
Other languages
English (en)
Inventor
Laurent Meijer
Frédéric Miege
Emmanuel Deau
Pascal George
Original Assignee
Perha Pharmaceuticals
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 EP20305421.8A external-priority patent/EP3904354A1/en
Application filed by Perha Pharmaceuticals filed Critical Perha Pharmaceuticals
Publication of MX2022013064A publication Critical patent/MX2022013064A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La presente invención se refiere a un compuesto de fórmula (I) S N N HN O R NH 1 (I) R2 en donde R1 representa un grupo alquilo (C1-C6), un anillo espirobicíclico (C5-C11), un grupo fenilo fusionado, un fenil sustituido, un grupo R'-L-, en donde L es ya sea un enlace sencillo o un grupo alcandiilo (C1-C3), y R' representa un grupo cicloalquilo (C3-C8), un grupo cicloalquilo (C6-C10) puenteado, un grupo heterocicloalquilo (C3-C8), o un grupo heteroarilo (C3-C8), o un grupo R'-L- en donde L es un grupo alcandiilo (C1-C3), y R' es un grupo fenilo opcionalmente sustituido, y en donde R2 representa un átomo de hidrógeno o un grupo alquilo (C1-C3) o cualquiera de sus sales farmacéuticamente aceptables. La presente invención se refiere además a una composición que comprende un compuesto de fórmula (I) y un proceso para manufacturar tal compuesto, así como también sus intermediarios de síntesis. También se refiere a tal compuesto para uso como un medicamento, en particular en el tratamiento y/o prevención de déficits cognitivos asociados con déficits cognitivos asociados al síndrome de Down; enfermedad de Alzheimer; demencia; tauopatías; Enfermedad de Parkinson; trastorno por deficiencia de CDKL5; síndrome de Phelan-McDermid; autismo; diabetes tipo 1 y tipo 2; metabolismo anormal del folato y la metionina; osteoartritis; Distrofia muscular de Duchenne; varios cánceres; neuroinflamación, anemia e infecciones virales y unicelulares y para regular la temperatura corporal.
MX2022013064A 2020-04-30 2021-04-29 Nuevos derivados de imidazolona como inhibidores de proteinas cinasas en particular cinasa 1a regulada por fosforilacion de la tirosina de especificidad dual (dyrk1a), cinasa 1 similar a las citolisinas dependientes del colesterol (clk1) y/o cinasa 4 similar a las citolisinas dependientes del colesterol (clk4). MX2022013064A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20305421.8A EP3904354A1 (en) 2020-04-30 2020-04-30 New imidazolone derivatives as inhibitors of protein kinases in particular dyrk1a, clk1 and/or clk4
EP21305361 2021-03-24
PCT/EP2021/061349 WO2021219828A1 (en) 2020-04-30 2021-04-29 New imidazolone derivatives as inhibitors of protein kinases in particular dyrk1a, clk1 and/or clk4

Publications (1)

Publication Number Publication Date
MX2022013064A true MX2022013064A (es) 2023-04-12

Family

ID=75690302

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2022013064A MX2022013064A (es) 2020-04-30 2021-04-29 Nuevos derivados de imidazolona como inhibidores de proteinas cinasas en particular cinasa 1a regulada por fosforilacion de la tirosina de especificidad dual (dyrk1a), cinasa 1 similar a las citolisinas dependientes del colesterol (clk1) y/o cinasa 4 similar a las citolisinas dependientes del colesterol (clk4).

Country Status (14)

Country Link
US (1) US20230167104A1 (es)
EP (1) EP4143185A1 (es)
JP (1) JP2023523788A (es)
KR (1) KR20230005197A (es)
CN (1) CN115515953A (es)
AU (1) AU2021266141A1 (es)
BR (1) BR112022021442A2 (es)
CA (1) CA3174844A1 (es)
CL (1) CL2022002996A1 (es)
CO (1) CO2022015361A2 (es)
IL (1) IL297767B1 (es)
MX (1) MX2022013064A (es)
WO (1) WO2021219828A1 (es)
ZA (1) ZA202210885B (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021114314A1 (en) * 2019-12-14 2021-06-17 Tongji University Novel heterocyclic derivatives with cardiomyocyte proliferation activity for treatment of heart diseases

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005082901A1 (en) * 2004-02-25 2005-09-09 Smithkline Beecham Corporation Novel chemical compounds
KR100875408B1 (ko) * 2004-10-14 2008-12-23 에프. 호프만-라 로슈 아게 Cdk1 항증식성 활성을 갖는 1,5-나프티리딘 아졸리디논
US7304074B2 (en) * 2005-04-05 2007-12-04 Hoffmann-La Roche Inc. Substituted 1,5-naphthyridine azolinones
JP2009528384A (ja) * 2006-03-02 2009-08-06 スミスクライン・ビーチャム・コーポレイション Pi3キナーゼ阻害剤として用いるためのチアゾロン
FR2919608B1 (fr) 2007-08-01 2012-10-05 Univ Rennes Derives d'imidazolones,procede de preparation et applications biologiques

Also Published As

Publication number Publication date
CO2022015361A2 (es) 2022-11-08
EP4143185A1 (en) 2023-03-08
ZA202210885B (en) 2024-02-28
IL297767A (en) 2022-12-01
AU2021266141A1 (en) 2022-12-01
US20230167104A1 (en) 2023-06-01
KR20230005197A (ko) 2023-01-09
CL2022002996A1 (es) 2023-05-26
WO2021219828A1 (en) 2021-11-04
JP2023523788A (ja) 2023-06-07
CN115515953A (zh) 2022-12-23
BR112022021442A2 (pt) 2022-12-13
IL297767B1 (en) 2024-02-01
CA3174844A1 (en) 2021-11-04

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