| abstract |
Phosphatidyl compounds of the formula are described wherein R 'is C 3 - 14 alkanoyl, benzoyl, the acyl radical of an α-amino carboxylic acid which is different from glycine, L-alanine and their derivatives with substituted amino group, and their a-amino group by lower alkanoyl, lower alkoxycarbonyl or benzyloxycarbonyl may be substituted, or the acyl radical of a ß-amino-carboxylic acid or an α- or ß-hydroxy-carboxylic acid, T the unsubstituted or substituted by lower alkyl group NH or oxygen, Y unsubstituted or substituted by free, etherified or amidated carboxy, dimethylene, W hydrogen and Z is a 1,2-dihydroxy-ethyl, 2-hydroxy ethyl or hydroxy-methyl group, at least one of the hydroxy groups with an aliphatic C 8 - 30 carboxylic acid esterified or with a aliphauschen C a - 30 alcohol is etherified, or W and Z are each a hydroxymethyl group, with an aliphatic C 8 - 30 carboxylic acid esterified, or by an aliphatic C 8 - 30 alcohol is etherified mean, and their salts and Process for their production. The new compounds mentioned as well as structurally related compounds also described and which belong to the prior art are used for the prophylaxis and therapy of viral infections. |