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WO2008113881B1 - Compuesto inhibidor dual de las enzimas pde7 y/o pde4, composiciones farmaceúticas y sus aplicaciones - Google Patents

Compuesto inhibidor dual de las enzimas pde7 y/o pde4, composiciones farmaceúticas y sus aplicaciones

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Publication number
WO2008113881B1
WO2008113881B1 PCT/ES2008/070051 ES2008070051W WO2008113881B1 WO 2008113881 B1 WO2008113881 B1 WO 2008113881B1 ES 2008070051 W ES2008070051 W ES 2008070051W WO 2008113881 B1 WO2008113881 B1 WO 2008113881B1
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WIPO (PCT)
Prior art keywords
methylthio
oxo
dihydroquinazoline
thioxo
compound
Prior art date
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Ceased
Application number
PCT/ES2008/070051
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English (en)
French (fr)
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WO2008113881A1 (es
Inventor
Ayuso-Gontan Carmen Gil
Calduch Tania Castano
Martin Nuria Campillo
Jareno Sara Ballester
Garcia Coral Gonzalez
Torres Francisco Javier Hernandez
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Consejo Superior de Investigaciones Cientificas CSIC
Instituto de Salud Carlos III
Original Assignee
Consejo Superior de Investigaciones Cientificas CSIC
Instituto de Salud Carlos III
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Priority to CA002682259A priority Critical patent/CA2682259A1/en
Priority to JP2010500305A priority patent/JP2010522226A/ja
Priority to US12/532,104 priority patent/US20100152213A1/en
Priority to EP08736738A priority patent/EP2130823A4/en
Priority to AU2008228203A priority patent/AU2008228203A1/en
Priority to CN200880013379A priority patent/CN101679314A/zh
Publication of WO2008113881A1 publication Critical patent/WO2008113881A1/es
Publication of WO2008113881B1 publication Critical patent/WO2008113881B1/es
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • 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
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C07D239/96Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic 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
    • C07D495/04Ortho-condensed systems

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La invención describe una serie de inhibidores duales de las enzimas PDE7 y PDE4 de fórmula (I) y su utilidad para la elaboración de composiciones farmacéuticas para el tratamiento de procesos 5inflamatorios y/o autoinmunes.

Claims

44REIVINDICACIONES MODIFICADAS recibidas por Ia oficina Internacional el 04 de septiembre de 2008 (04.09.2008)REIVINDICACIONES
1.- Uso de al menos un compuesto de fórmula (I), con actividad inhibidora dual de las enzimas PDE7 y/o PDE4, junto con un portador, adyuvante o vehículo farmacéuticamente aceptable, para Ia elaboración de una composición farmacéutica o medicamento útil para el tratamiento de enfermedades inflamatorias o autoinmunes, siendo Ia fórmula (I):
Figure imgf000002_0001
donde:
A, es un carbociclo o heterociclo fusionado opcionalmente sustituido de 5, 6 ó 7 miembros saturado o insaturado, puede ser un doble enlace; X e Y, son elegidos independientemente entre el grupo consistente en hidrógeno, alquil, =0, =S, aril, O-alquil, O-aril, S-alquil o -S-aril; y
R, R1, R2 y R3 son elegidos independientemente entre el grupo consistente en hidrógeno, halógeno, alquil, haloalquil, aril, cicloalquil, (CHb)n- aril, heteroaril, -OR3; -C(O)OR3, (CH2)n-C(O)OR3 o -S(O)4-, dónde n es mayor o igual a 0 y dónde t es 1 o 2,
o bien una sal, derivado, profármaco, solvato o estereoisómero farmacéuticamente aceptables del mismo, donde el término "derivado" incluye tanto a compuestos farmacéuticamente aceptables, es decir, derivados del compuesto de fórmula (I) que pueden ser utilizados en Ia elaboración de un medicamento, como derivados farmacéuticamente no aceptables ya que éstos pueden ser útiles en Ia preparación de derivados farmacéuticamente aceptables, y dónde el término "profármaco" incluye a cualquier compuesto derivado de un compuesto de fórmula (I), que, ventajosamente, aumenta Ia biodisponibilidad del compuesto de fórmula (I) cuando se administra a un 45
individuo o que potencia Ia liberación del compuesto de fórmula (I) en un compartimento biológico.
Excepción: cuando A sea benceno sin sustituir, X=O1Y=S cuando A sea benceno sin sustituir, X=O1Y=O, cuando A sea benceno sin sustituir, X=O1Y=S-Me cuando A sea tiofeno sin sustituir, X=O1Y=S, y cuando A sea benzotiofeno sin sustituir, X=O,Y=S
2.- Compuesto según Ia reivindicación 1 caracterizado porque presenta Ia fórmula 2-metilt¡o-4-tioxo-3,4-dihidroqu¡nazolina (Compuesto Id).
3.- Compuesto según Ia reivindicación 2 caracterizado porque pertenece al siguiente grupo: - 3-Fenil-2-metiltio-4-tioxo-3,4-dihidroquinazolina,
- 3-(2,6-difluorofenil)-2-metiltio-4-tioxo-3,4-dih¡droquinazolina,
- 3-(2,3,4-trifluorofenil)-2 metiltio-4-tioxo-3,4-dihidroquinazolina, y - 3-(2-bromofenil)-2-metilt¡o-4-t¡oxo-3,4-dihidroquinazol¡na.
4.- Composición farmacéutica caracterizada porque comprende un compuesto, en cantidad terapéuticamente efectiva, de fórmula (I), o mezclas de los mismos, una sal, derivado, profármaco, solvato o estereoisómero farmacéuticamente aceptable del mismo junto con un portador, adyuvante o vehículo farmacéuticamente aceptable, para Ia administración a un paciente.
5.- Composición farmacéutica según Ia reivindicación 4 caracterizado porque el compuesto de formula (I) pertenece a una, o a varias, de las siguientes familias de compuestos:
- 4-oxo-2-tioxo-1 ,2,3,4-tetrahidroquinazolina (Compuesto Ia), - 2-metiltio-4-oxo-3,4-dihidroquinazolina (Compuesto Ib),
- 2,4-ditioxo-1 ,2,3,4-tetrahidroquinazolina (Compuesto Ic), y
- 2-metiltio-4-tioxo-3,4-dihidroquinazolina (Compuesto Id), 46
O a cualquiera de sus formas enantioméricas R, S y/o mezclas racémicas.
6.- Composición farmacéutica según Ia reivindicación 5 caracterizado porque el compuesto o mezcla de compuestos de formula (I) pertenece al siguiente grupo:
- 6-Bromo-3-fenil-4-oxo-2-tioxo-1 ,2,3,4-tetrahidroquinazolina, - 6-Bromo-3-(2,6-difluorofenil)-4-oxo-2-tioxo-1 ,2,3,4-tetrahidroquinazolina,
6-Bromo-3-(2,3,4-trifluorofen¡l)-4-oxo-2-tioxo-1 ,2,3,4- tetrahidroquinazolina,
- 6-Bromo-3-(2-bromofenil)-4-oxo-2-tioxo-1 ,2,3,4-tetrahidroquinazolina, - 3-(2,6-Difluorofenil)-8-metil-4-oxo-2-tioxo-1,2,3,4-tetrahidroquinazolina, - 3-(2,3,4-Trifluorofenil)-8-metil-4-oxo-2-tioxo-1 ,2,3,4-tetrahidroqu¡nazolina, - 3-(2-Bromofenil)-8-metil-4-oxo-2-tioxo-1 ,2,3,4-tetrahidroquinazolina, - 6-Bromo-3-fenil-2-metiltio-4-oxo-3,4-dih¡droquinazolina,
- 6-Bromo-3-(2,6-difluorofenil)-2-metiltio-4-oxo-3,4-dihidroquinazolina, - 6-Bromo-3-(2,3,4-trifluorofenil)-2-metiltio-4-oxo-3,4-dihidroquinazolina, - 6-Bromo-3-(2-bromofenil)-2-metiltio-4-oxo-3,4-dihidroquinazolina, - 3-Fenil-8-metil-2-metiltio-4-oxo-3,4-dihidroquinazolina, - 3-(2,6-Difluorofenil)-8-metil-2-metiltio-4-oxo-3,4-dihidroquinazolina,
- 3-(2I3,4-trifluorofenil)-8-metil-2-metiltio-4-oxo-3,4-dih¡droquinazolina, - 3-(2-bromofenil)-8-metil-2-metiltio-4-oxo-3,4-dihidroquinazolina,
- 3-Fenil-2,4-ditioxo-1 ,2,3,4-tetrahidroquinazolina, - 3-(2,6-D¡fluorofenil)-2,4-ditioxo-1 ,2,3,4-tetrahidroquinazolina, - 3-(2,3,4-Tr¡fluorofenil)-2,4-ditioxo-1 ,2,3,4-tetrahidroquinazolina.
- 3-Fen¡l-2-metiltio-4-tioxo-3,4-dihidroqu¡nazolina, - 3-(2,6-difluorofenil)-2-metiltio-4-tioxo-3,4-dihidroquinazolina,
- 3-(2,3,4-trifluorofenil)-2 metiltio-4-tioxo-3,4-dihidroquinazolina, y - 3-(2-bromofenil)-2-metiltio-4-tioxo-3,4-dihidroquinazolina.
7.- Uso de un compuesto según Ia reivindicación 1 caracterizado porque Ia enfermedad inflamatoria o autoinmune pertenece al siguiente grupo: enfermedad inflamatoria intestinal, patologías articulares inflamatorias, dermatitis atópicas y otras patologías dermatológicas inflamatorias, neuritis, encefalitis, encefalomielitis y patologías inflamatorias que afectan al sistema nervioso central (esclerosis múltiple) o periférico, miositis, vasculitis, lupus eritematoso sistémico, asma, enfermedad pulmonar obstructiva crónica, enfermedades infecciosas que cursan con inflamación, reacciones de rechazo de huésped contra injerto, conjuntivitis y oculopatías inflamatorias, otitis y mucositis.
PCT/ES2008/070051 2007-03-22 2008-03-14 Compuesto inhibidor dual de las enzimas pde7 y/o pde4, composiciones farmaceúticas y sus aplicaciones Ceased WO2008113881A1 (es)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CA002682259A CA2682259A1 (en) 2007-03-22 2008-03-14 Compound that is a dual inhibitor of enzymes pde7 and/or pde4, pharmaceutical compositions and uses thereof
JP2010500305A JP2010522226A (ja) 2007-03-22 2008-03-14 酵素pde7及び/又はpde4の二重阻害化合物、薬剤組成物および利用法
US12/532,104 US20100152213A1 (en) 2007-03-22 2008-03-14 Compound that is a dual inhibitor of enzymes pde7 and/or pde4, pharmaceutical compositions and uses thereof
EP08736738A EP2130823A4 (en) 2007-03-22 2008-03-14 CONNECTION AS TWO-WAY FIXTURES OF ENZYME PDE7 AND / OR PDE4, PHARMACEUTICAL COMPOSITIONS AND THEIR USE
AU2008228203A AU2008228203A1 (en) 2007-03-22 2008-03-14 Compound that is a dual inhibitor of enzymes PDE7 and/or PDE4, pharmaceutical compositions and uses thereof
CN200880013379A CN101679314A (zh) 2007-03-22 2008-03-14 酶pde7和/或pde4的双重抑制化合物、药物组合物及其用途

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200700762A ES2308916B1 (es) 2007-03-22 2007-03-22 Compuesto inhibidor dual de las enzimas pde7 y/o pde4, composiciones farmaceuticas y sus aplicaciones.
ESP200700762 2007-03-22

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WO2008113881B1 true WO2008113881B1 (es) 2008-11-06

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US (1) US20100152213A1 (es)
EP (1) EP2130823A4 (es)
JP (1) JP2010522226A (es)
CN (1) CN101679314A (es)
AU (1) AU2008228203A1 (es)
CA (1) CA2682259A1 (es)
ES (1) ES2308916B1 (es)
WO (1) WO2008113881A1 (es)

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US8637528B2 (en) 2007-03-27 2014-01-28 Omeros Corporation Use of PDE7 inhibitors for the treatment of movement disorders
KR101709492B1 (ko) 2009-03-18 2017-02-23 리스버로직스 코퍼레이션 신규한 소염제
ES2353093B1 (es) * 2009-05-20 2012-01-03 Consejo Superior De Investigaciones Científicas (Csic) Uso de derivados de quinazolinas y sus composiciones farmacéuticas en enfermedades neurodegenerativas.
US20120115849A1 (en) 2010-11-08 2012-05-10 Demopulos Gregory A Treatment of Addiction and Impulse-Control Disorders Using PDE7 Inhibitors
US9220715B2 (en) 2010-11-08 2015-12-29 Omeros Corporation Treatment of addiction and impulse-control disorders using PDE7 inhibitors
KR102662814B1 (ko) 2015-03-13 2024-05-03 리스버로직스 코퍼레이션 보체 관련 질환을 치료하기 위한 조성물 및 치료 방법
ES2544519B1 (es) 2015-05-22 2016-03-04 Consejo Superior De Investigaciones Científicas (Csic) Quinazolinas S-sustituidas y sus aplicaciones terapéuticas para el tratamiento de enfermedades mediadas por PDE7
EP4572765A1 (en) 2022-08-18 2025-06-25 Mitodicure GmbH Use of a therapeutic agent with phosphodiesterase-7 inhibitory activity for the treatment and prevention of diseases associated with chronic fatigue, exhaustion and/or exertional intolerance

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US20100152213A1 (en) 2010-06-17
CA2682259A1 (en) 2008-09-25
WO2008113881A1 (es) 2008-09-25
ES2308916B1 (es) 2009-10-29
EP2130823A4 (en) 2011-06-15
JP2010522226A (ja) 2010-07-01
AU2008228203A1 (en) 2008-09-25
ES2308916A1 (es) 2008-12-01
CN101679314A (zh) 2010-03-24
EP2130823A1 (en) 2009-12-09

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