MX390082B - Derivados de adenina como inhibidores de proteína quinasa - Google Patents

Derivados de adenina como inhibidores de proteína quinasa

Info

Publication number
MX390082B
MX390082B MX2018013325A MX2018013325A MX390082B MX 390082 B MX390082 B MX 390082B MX 2018013325 A MX2018013325 A MX 2018013325A MX 2018013325 A MX2018013325 A MX 2018013325A MX 390082 B MX390082 B MX 390082B
Authority
MX
Mexico
Prior art keywords
sub
protein kinase
pharmaceutically acceptable
formula
diseases
Prior art date
Application number
MX2018013325A
Other languages
English (en)
Other versions
MX2018013325A (es
Inventor
Claire Amiable
Dominique Surleraux
Rémi Guillon
Original Assignee
B C I Pharma
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 B C I Pharma filed Critical B C I Pharma
Publication of MX2018013325A publication Critical patent/MX2018013325A/es
Publication of MX390082B publication Critical patent/MX390082B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
    • 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
    • A61K31/52Purines, e.g. adenine
    • 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente invención se refiere a un compuesto adecuado para usarse como un inhibidor de cinasa de conformidad con la fórmula general (I) [compuesto (C), en lo sucesivo], o el N-óxido, sal farmacéuticamente aceptable, solvato farmacéuticamente aceptable, o estereoisómero del mismo, fórmula (I) en donde A, R1, R2, R3, R3', R4, R4', X, Y, Z, T son como se define en las reivindicaciones; la invención además se refiere a un método in vitro para inhibir actividad de proteína cinasa que comprende poner en contacto una proteína cinasa con un compuesto de la fórmula (I), o el N-óxido, sal farmacéuticamente aceptable, solvato farmacéuticamente aceptable, o estereoisómero del mismo; la invención además se refiere a los compuestos de la fórmula (I) por sí mismos, así como a su uso como un medicamente, y para usarse o en un método de tratamiento de una enfermedad mediada por una proteína cinasa seleccionada de cáncer, trastornos inflamatorios, enfermedades cardiovasculares, enfermedades inducidas virales, enfermedades circulatorias, enfermedades fibro-proliferativas y trastornos de sensibilización al dolor. (ver fórmula I)
MX2018013325A 2016-05-04 2017-05-04 Derivados de adenina como inhibidores de proteína quinasa MX390082B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP16305530 2016-05-04
PCT/EP2017/060730 WO2017191297A1 (en) 2016-05-04 2017-05-04 Adenine derivatives as protein kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2018013325A MX2018013325A (es) 2019-08-16
MX390082B true MX390082B (es) 2025-03-20

Family

ID=55953089

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2018013325A MX390082B (es) 2016-05-04 2017-05-04 Derivados de adenina como inhibidores de proteína quinasa

Country Status (12)

Country Link
US (1) US11236093B2 (es)
EP (1) EP3452477B1 (es)
JP (1) JP7485502B2 (es)
KR (1) KR102479746B1 (es)
CN (1) CN109311882B (es)
AU (1) AU2017260298B9 (es)
EA (1) EA201892460A1 (es)
IL (1) IL262700B (es)
MX (1) MX390082B (es)
SG (1) SG11201809674QA (es)
WO (1) WO2017191297A1 (es)
ZA (1) ZA201808014B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6920411B2 (ja) * 2016-07-25 2021-08-18 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ コリンキナーゼ阻害剤としてのプリン及び3−デアザプリンアナログ
WO2018229197A1 (en) * 2017-06-14 2018-12-20 European Molecular Biology Laboratory Bicyclic heteroaromatic urea or carbamate compounds for use in therapy
US12303515B2 (en) * 2019-04-30 2025-05-20 City University Of Hong Kong PIM1 inhibitors for use in treatment of viral infection and pharmaceutical compositions thereof
JP7371221B2 (ja) * 2019-07-26 2023-10-30 珠海宇繁生物科技有限責任公司 Irak4キナーゼ阻害剤及びその調製方法
CN111560389B (zh) * 2020-06-11 2022-07-01 云南中烟工业有限责任公司 烟草丝裂原活化蛋白激酶基因NtMAPK8及其应用
JP7728367B2 (ja) 2021-06-14 2025-08-22 スコーピオン・セラピューティクス・インコーポレイテッド がんを処置するために使用され得る尿素誘導体

Family Cites Families (15)

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Publication number Priority date Publication date Assignee Title
GB9010404D0 (en) * 1990-05-09 1990-06-27 Pfizer Ltd Therapeutic agents
FR2686084B1 (fr) * 1992-01-10 1995-12-22 Bioprojet Soc Civ Nouveaux derives de l'imidazole, leur preparation et leurs applications therapeutiques.
US6110923A (en) * 1994-06-22 2000-08-29 Biochem Pharma Inc. Method for treating cancer using novel substituted purinyl derivatives with immunomodulating activity
US6713474B2 (en) * 1998-09-18 2004-03-30 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as therapeutic agents
US6258793B1 (en) * 1999-12-03 2001-07-10 Cv Therapeutics, Inc. N6 heterocyclic 5′ modified adenosine derivatives
AU2002951247A0 (en) * 2002-09-06 2002-09-19 Alchemia Limited Compounds that interact with kinases
WO2005009348A2 (en) * 2003-06-25 2005-02-03 Ariad Pharmaceuticals, Inc. Substituted purine derivatives
WO2005117882A2 (en) * 2004-04-20 2005-12-15 Incyte Corporation Hydroxamic acid derivatives as metalloprotease inhibitors
EP2532667A1 (en) 2005-09-30 2012-12-12 Vertex Pharmaceuticals Incorporated Deazapurines useful as inhibitors of janus kinases
US20070238746A1 (en) * 2006-04-06 2007-10-11 Trixi Brandl Thiazolyl-dihydro-chinazoline
TWI444384B (zh) * 2008-02-20 2014-07-11 Gilead Sciences Inc 核苷酸類似物及其在治療惡性腫瘤上的用途
US20120034250A1 (en) 2009-04-14 2012-02-09 Astellas Pharma Inc. Condensed pyrrolopyridine derivative
EP2508607A1 (en) 2011-04-07 2012-10-10 Helmholtz-Zentrum für Infektionsforschung GmbH Medicament for liver regeneration and for treatment of liver failure
SG11201503893RA (en) * 2012-11-19 2015-06-29 Agency Science Tech & Res Method of treating cancer
WO2014141129A2 (en) * 2013-03-14 2014-09-18 Grueneberg Dorre A Novel methods, compounds, and compositions for inhibition of ros

Also Published As

Publication number Publication date
AU2017260298B2 (en) 2021-09-02
EP3452477B1 (en) 2023-09-13
NZ748751A (en) 2024-12-20
CN109311882B (zh) 2022-02-11
WO2017191297A1 (en) 2017-11-09
JP2019516688A (ja) 2019-06-20
US11236093B2 (en) 2022-02-01
US20190127379A1 (en) 2019-05-02
KR20190003968A (ko) 2019-01-10
AU2017260298B9 (en) 2021-09-30
CN109311882A (zh) 2019-02-05
IL262700A (en) 2018-12-31
JP7485502B2 (ja) 2024-05-16
BR112018072468A2 (pt) 2019-02-19
SG11201809674QA (en) 2018-11-29
KR102479746B1 (ko) 2022-12-21
AU2017260298A1 (en) 2018-12-13
CA3022896A1 (en) 2017-11-09
EP3452477A1 (en) 2019-03-13
ZA201808014B (en) 2020-02-26
MX2018013325A (es) 2019-08-16
EP3452477C0 (en) 2023-09-13
EA201892460A1 (ru) 2019-09-30
IL262700B (en) 2022-02-01

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