Dimeric compounds and their use as anti-viral agents

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 407/12 (2006.01) A61K 31/13 (2006.01) A61K 31/351 (2006.01) A61K 31/7056 (2006.01) A61K 45/06 (2006.01) A61K 47/48 (2006.01) A61P 31/12 (2006.01) A61P 31/16 (2006.01) C07D 309/28 (2006.01)

Patent

CA 2463835

The invention relates to compounds of general formula (I), in which: R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; n and q are either the same or different and selected from 0, 1 or 2; and X is an optionally substituted phenyl, optionally substituted naphthyl or optionally substituted phenyl-Y-optionally substituted phenyl in which Y is selected from a covalent bond, CH2, CH2CH2, O or SO2, or a pharmaceutically acceptable derivative thereof, with the proviso that when X is phenyl or naphthyl, n and q are both 2 and when X is phenyl-Y-phenyl in which Y is a covalent bond, then n and q are not both 0, methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.

L'invention concerne des composés représentés par la formule générale (I), y compris leurs dérivés pharmaceutiquement acceptables. Dans ladite formule, R est un groupe amino ou guanidino; R?2¿ est acétyle ou trifluoroacétyle; n et q sont identiques ou différents, valant 0, 1 ou 2; et X est phényle éventuellement substitué, naphtyle éventuellement substitué ou phényle éventuellement substitué -Y- phényle éventuellement substitué, Y appartenant au groupe constitué par: liaison covalente, CH¿2?, CH¿2?CH¿2?, O ou SO¿2?, à condition que, lorsque X est phényle ou naphtyle, n et q valent 2 et que, lorsque X est phényle-Y-phényle, Y étant une liaison covalente, n et q ne valent pas tous les deux 0. L'invention concerne également des procédés relatifs à l'élaboration de ces composés, des formulations pharmaceutiques renfermant lesdits composés, et l'utilisation des composés en question pour la prévention ou le traitement des infections virales

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