| Literature DB >> 7575986 |
M Azoulay1, J C Florent, C Monneret, J P Gesson, J C Jacquesy, F Tillequin, M Koch, K Bosslet, J Czech, D Hoffman.
Abstract
The two novel prodrugs 4 and 11 have been prepared from tetra-O-acetyl-D-galactopyranose and doxorubicin in three and six steps, respectively. Their low cytotoxicity, high stability in plasma and, in the case of 11, efficient hydrolysis in the presence of alpha-galactosidase, fulfill preliminary conditions for their use in combination with monoclonal antibody-enzyme conjugates.Entities:
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Year: 1995 PMID: 7575986
Source DB: PubMed Journal: Anticancer Drug Des ISSN: 0266-9536