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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003286,
umls-concept:C0003299,
umls-concept:C0013227,
umls-concept:C0076829,
umls-concept:C0205314,
umls-concept:C0220781,
umls-concept:C0243072,
umls-concept:C0311404,
umls-concept:C0679622,
umls-concept:C0870883,
umls-concept:C1261322,
umls-concept:C1527178,
umls-concept:C1705938,
umls-concept:C1883254
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pubmed:issue |
1
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pubmed:dateCreated |
1998-3-3
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pubmed:abstractText |
To corroborate the structures of two monohydroxylated metabolites of topiramate (1), we synthesized four monosaccharide derivatives from D-fructose: 4,5-O-[(1R)- and 4,5-O-[(1S)-1-hydroxymethylethylidene]-2,3-O-isopropylidene-beta-D -fructopyranose sulfamates (2a and 2b); 2,3-O-[(1R)- and 2,3-O-[(1R)-1-hydroxymethylethylidene]-4,5-O-isopropylidene-beta-D -fructopyranose sulfamates (3a and 3b). The route to 2a and 2b was brief and straightforward, while that to 3a and 3b was more involved. In the latter case, the D-fructose bis-acetal 10 was benzylated and converted to a monoacetal dibenzoate (14) (50% yield), which was then transacetalized to give a mixture of 4,5-dibenzoyl-2,3-O-[(1R)- and 4,5-dibenzoyl-2,3-O-[(1S)-1-benzyloxymethylethylidene]- beta-D-fructopyranose (16a and 16b) (22%). The individual diastereomers were separated and processed via ester saponification, acetonation, sulfamoylation, and hydrogenolysis into 3a (36%) and 3b (27%). Structure 2b was confirmed for one oxidative metabolite, but the other metabolite was found not to correspond with either 2a, 3a, or 3b. On the basis of CI-MS and 1H NMR data, a (2-hydroxy-1,4-dioxano)pyran structure, 4, is proposed for this unidentified metabolite.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0008-6215
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
304
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
29-38
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9490196-Animals,
pubmed-meshheading:9490196-Anticonvulsants,
pubmed-meshheading:9490196-Dogs,
pubmed-meshheading:9490196-Fructose,
pubmed-meshheading:9490196-Humans,
pubmed-meshheading:9490196-Hydroxylation,
pubmed-meshheading:9490196-Magnetic Resonance Spectroscopy,
pubmed-meshheading:9490196-Mass Spectrometry,
pubmed-meshheading:9490196-Oxidation-Reduction,
pubmed-meshheading:9490196-Rats,
pubmed-meshheading:9490196-Stereoisomerism
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pubmed:year |
1997
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pubmed:articleTitle |
Synthesis of hydroxylated derivatives of topiramate, a novel antiepileptic drug based on D-fructose: investigation of oxidative metabolites.
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pubmed:affiliation |
The R.W. Johnson Pharmaceutical Research Institute, Spring House, PA 19477, USA.
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pubmed:publicationType |
Journal Article
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