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pubmed-article:12057651pubmed:abstractTextThe suitability of 4-di(2-chloroethyl)aminoanilino-4-hydroxyphenethylaminomethanone 2 to act as a prodrug for melanocyte-directed enzyme prodrug therapy (MDEPT) is assessed. Thus its synthesis, ability to generate a cytotoxic agent upon exposure to tyrosinase, and stability within different sera are reported. A comparison is made to illustrate that the new urea prodrug 2 is a more suitable candidate for MDEPT than the corresponding carbamate prodrug 1.lld:pubmed
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pubmed-article:12057651pubmed:articleTitleSynthesis and analysis of urea and carbamate prodrugs as candidates for melanocyte-directed enzyme prodrug therapy (MDEPT).lld:pubmed
pubmed-article:12057651pubmed:affiliationDepartment of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, UK.lld:pubmed
pubmed-article:12057651pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12057651pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed