1.
    发明专利
    未知

    公开(公告)号:NO20063623L

    公开(公告)日:2006-10-12

    申请号:NO20063623

    申请日:2006-08-10

    Abstract: The invention relates to a novel use of known benzazepine, benzoxazepine, benzothiazepine-N-acetic acid and phosphono-substituted benzazepinone derivatives having neutral endopeptidase (NEP) and/or human soluble endopeptidase (hSEP) inhibitory activity. The compounds of the invention are useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders. The compounds of the invention are known from the European patents EP 0 733 642 and EP 0 916 679, and can be described by the general formula (1) wherein the symbols have the meanings as given above in the description.

    4.
    发明专利
    未知

    公开(公告)号:DK1706121T3

    公开(公告)日:2009-01-05

    申请号:DK05701469

    申请日:2005-01-10

    Abstract: The invention relates to a novel use of known benzazepine, benzoxazepine, benzothiazepine-N-acetic acid and phosphono-substituted benzazepinone derivatives having neutral endopeptidase (NEP) and/or human soluble endopeptidase (hSEP) inhibitory activity. The compounds of the invention are useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders. The compounds of the invention are known from the European patents EP 0 733 642 and EP 0 916 679, and can be described by the general formula (1) wherein the symbols have the meanings as given above in the description.

    INHIBIDORES DE ENDOPEPTIDASA NEUTRA (NEP) Y ENDOPEPTIDA SOLUBLE HUMANA (HSEP) PARA PROFILAXIS Y TRATAMIENTO DE TRASTORNOS NEUROGENERATIVOS.

    公开(公告)号:ES2313279T3

    公开(公告)日:2009-03-01

    申请号:ES05701469

    申请日:2005-01-10

    Abstract: Uso de un compuesto de fórmula general (1) (Ver fórmula) donde R1 representa un grupo de fórmula (2) o (3): (Ver fórmulas) A representa CH2, O ó S, R2 y R3 representan independientemente hidrógeno o halógeno, R4 y R6 representan independientemente hidrógeno o un grupo que forma un éster carboxílico biolábil; R5 se selecciona del grupo que consiste en alcoxi(C1-C6)alquilo(C1-C6) que puede estar substituído por alcoxi(C1-C6), fenil-alquilo(C1-C6) y feniloxi-alquilo(C1-C6) donde el grupo fenilo puede estar substituído con alquilo(C1-C6), alcoxi(C1-C6) o halógeno, y naftil-alquilo(C1-C6), R7 y R8 representan independientemente hidrógeno o un grupo que forma un éster de ácido fosfónico biolábil, todos los estereoisómeros, así como sales farmacológicamente aceptables de los mismos, para la preparación de composiciones farmacéuticas para la profilaxis y el tratamiento de afecciones seleccionadas del grupo que consiste en lesión cerebral traumática, encefalomielitis aguda diseminada, lesión cerebral relacionada con epilepsia, lesión de la médula espinal, meningitis y meningoencefalitis bacteriana o viral, enfermedades priónicas, envenenamientos con compuestos neurotóxicos, lesión cerebral inducida por radiación y para la profilaxis de íctus isquémico, con la condición de que tales composiciones farmacéuticas no contengan un antagonista del receptor de aldosterona.

    10.
    发明专利
    未知

    公开(公告)号:DE602005009487D1

    公开(公告)日:2008-10-16

    申请号:DE602005009487

    申请日:2005-01-10

    Abstract: The invention relates to a novel use of known benzazepine, benzoxazepine, benzothiazepine-N-acetic acid and phosphono-substituted benzazepinone derivatives having neutral endopeptidase (NEP) and/or human soluble endopeptidase (hSEP) inhibitory activity. The compounds of the invention are useful for the preparation of pharmaceutical compositions for prophylaxis and treatment of neurodegenerative disorders. The compounds of the invention are known from the European patents EP 0 733 642 and EP 0 916 679, and can be described by the general formula (1) wherein the symbols have the meanings as given above in the description.

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