NUEVOS DERIVADOS NAFTALENICOS, SU PROCEDIMIENTO DE PREPARACION Y COMPOSICIONES FARMACEUTICAS QUE LOS CONTIENEN

Compuesto de fórmula (I) **(Ver fórmula)** o N-[3-hidroxi-2-(7-metoxi-1-naftil)propil]propanoamida sus enantiómeros, así como sus sales de adición de una base farmacéuticamente aceptable. N-[3-Hydroxy-2-(7-methoxy-1-naphthyl)propyl] propanamide (I), its enantiomers and base addition salts, are new....

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Main Authors YOUS, SAID, DELAGRANGE, PHILIPPE, BERTHELOT, PASCAL, PERES, BASILE, SABAOUNI, AHMED, SPEDDING, MICHAEL
Format Patent
LanguageSpanish
Published 08.03.2010
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Summary:Compuesto de fórmula (I) **(Ver fórmula)** o N-[3-hidroxi-2-(7-metoxi-1-naftil)propil]propanoamida sus enantiómeros, así como sus sales de adición de una base farmacéuticamente aceptable. N-[3-Hydroxy-2-(7-methoxy-1-naphthyl)propyl] propanamide (I), its enantiomers and base addition salts, are new. N-[3-Hydroxy-2-(7-methoxy-1-naphthyl)propyl] propanamide of formula (I), its enantiomers and base addition salts, are new. An independent claim is included for the preparation of (I). [Image] ACTIVITY : Hypnotic; Tranquilizer; Antidepressant; Cardiovascular-Gen; Gastrointestinal-Gen; Neuroleptic; Anorectic; Anticonvulsant; Antidiabetic; Antiparkinsonian; Nootropic; Antimigraine; Neuroprotective; Cerebroprotective; Contraceptive; Endocrine-Gen; Immunomodulator; Cytostatic. MECHANISM OF ACTION : Melatonin receptor binder. The ability of (I) to bind with melatonin was tested. The results showed that N-[3-hydroxy-2-(7-methoxy-1-naphthyl)propyl] propanamide exhibited an inhibition constant value of 1.4 nM and 3.2 nM to bind with melatonin receptors MT 1 and MT 2, respectively.
Bibliography:Application Number: ES20070290819T