rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
|
pubmed:dateCreated |
2002-6-11
|
pubmed:abstractText |
The 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.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0968-0896
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2625-33
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:12057651-Animals,
pubmed-meshheading:12057651-Blood,
pubmed-meshheading:12057651-Carbamates,
pubmed-meshheading:12057651-Cattle,
pubmed-meshheading:12057651-Cell Death,
pubmed-meshheading:12057651-Drug Delivery Systems,
pubmed-meshheading:12057651-Drug Stability,
pubmed-meshheading:12057651-Enzymes,
pubmed-meshheading:12057651-Humans,
pubmed-meshheading:12057651-Melanocytes,
pubmed-meshheading:12057651-Monophenol Monooxygenase,
pubmed-meshheading:12057651-Prodrugs,
pubmed-meshheading:12057651-Urea
|
pubmed:year |
2002
|
pubmed:articleTitle |
Synthesis and analysis of urea and carbamate prodrugs as candidates for melanocyte-directed enzyme prodrug therapy (MDEPT).
|
pubmed:affiliation |
Department of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|