Design and synthesis of an antitumor prodrug released by the reaction with sulfhydryl compounds

Bioorganic & Medicinal Chemistry Letters
1995.0

Abstract

The design and synthesis of --dalmolnycin prodrug 11 that lxll rehsc free daunomycin by the reaction with sulfhydryl compounds is described The compound 11 is more sensitive to adriamycinresistant L1210 cell line than free daunomycin with relative resistance of3.7 and 9.2, respectively.

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