Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1978-2-18
|
pubmed:abstractText |
1-(Tetrahydro-2-furanyl)-5-fluorouracil (Thf-FU), which is named Ftorafur or FT-207 and is used clinically as an antitumor agent, was conveniently synthesized by condensation of the trimethylsilyl derivative of 5-fluorouracil with 2-acetoxytetrahydrofuran using NaI as a catalyst. This optically inactive Thf-FU was resolved into optically active (R)-(+)- and (S)-(-)-Thf-FU in high optical purity and excellent yield by formation of diastereoisomers with brucine. 13C NMR data were obtained on Thf-FU and related compounds and the antibacterial activities and in vivo antitumor activities of these isomers were tested. The degradations of these isomers to 5-fluorouracil by liver microsomes were also examined. No significant differences were found in any of these properties of these isomers.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0022-2623
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
20
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1592-4
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:338900-Animals,
pubmed-meshheading:338900-Bacteria,
pubmed-meshheading:338900-Fluorouracil,
pubmed-meshheading:338900-Male,
pubmed-meshheading:338900-Mice,
pubmed-meshheading:338900-Microsomes, Liver,
pubmed-meshheading:338900-Neoplasms, Experimental,
pubmed-meshheading:338900-Rats,
pubmed-meshheading:338900-Stereoisomerism,
pubmed-meshheading:338900-Structure-Activity Relationship,
pubmed-meshheading:338900-Tegafur
|
pubmed:year |
1977
|
pubmed:articleTitle |
Studies of antitumor agents. 1. Resolution of racemic 1-(tetrahydro-2-furanyl)-k-fluorouracil into the R and S isomers and examination of the biological activities of the isomers.
|
pubmed:publicationType |
Journal Article,
In Vitro
|