Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
23
pubmed:dateCreated
2007-11-6
pubmed:abstractText
A new and efficient method for the synthesis of PEG-6-mercaptopurine is described. The key feature of the proposed approach is the protection of the thiol group against metabolic inactivation. Preliminary in vivo and in vitro evaluations of the macromolecular prodrug have been carried out.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1464-3405
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6607-9
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
A simple method for the preparation of PEG-6-mercaptopurine for oral administration.
pubmed:affiliation
Department of Pharmaceutical Science, piazzale Europa 1, 34127 Trieste, Italy. zacchign@units.it
pubmed:publicationType
Journal Article, Comparative Study