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Merck

Competitive inhibition of lipolytic enzymes. II. Preparation of 'monoacylamino' phospholipids.

Biochimica et biophysica acta (1990-03-12)
R Dijkman, N Dekker, G H de Haas
RESUMEN

This paper describes the synthesis of a number of phosphatidylcholines and phosphatidylglycols, in which one fatty acyl ester group is replaced by an acylamino function. The phospholipids, both of the alpha- and beta-type, are prepared in racemic and enantiomeric pure forms.

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Sigma-Aldrich
(±)-3-Amino-1,2-propanediol, 97%