
pmid: 8215846
AbstractPhenytoin‐1‐triglycerides and phenytoin‐2‐triglycerides were synthesized as potential prodrugs of phenytoin by covalent binding of 3‐hydroxymethylphenytoin by succinic acid to the positions 1 and 2 of diglycerides, respectively. The corresponding 1‐ and 2‐monoglycerides were prepared. In addition, replacement of glycerol by 3‐hydroxy‐2‐hydroxymethylpropionic acid furnished lipids that allowed direct coupling of 3‐hydroxyme‐thylphenytoin. The lipid conjugates proved to be substrates for pancreatic lipase in vitro.
Swine, Phenytoin, Animals, Prodrugs, Lipase, Lipids, Pancreas, Triglycerides
Swine, Phenytoin, Animals, Prodrugs, Lipase, Lipids, Pancreas, Triglycerides
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