| 摘要 |
<p>The present invention provides a novel lipophilic disaccharide-tripeptide derivative of the known base compound muramyl dipeptide (MDP). The compound of the invention is preferably encapsulated into multilamellar liposomes, which can be formed from phosphatidyl choline and phosphatidyl glycerol. The compound is effective in activating human monocytes with subsequent destruction of tumor cells. The compound is also nontoxic in dosages well exceeding anticipated human dosages.</p> |
