Source:http://linkedlifedata.com/resource/pubmed/id/17582660
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-2-15
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pubmed:abstractText |
Nucleoside hydrolase (NH) is a key enzyme in the purine salvage pathway. The purine specificity of the IAG-NH from Trypanosoma vivax is at least in part due to cation-pi-stacking interactions. Guanidinium ions can be involved in cation-pi-stacking interactions, therefore a series of guanidino-alkyl-ribitol derivatives were synthesized in order to examine the binding affinity of these compounds towards the target enzyme. The compounds show moderate to good inhibiting activity towards the IAG-NH from T. vivax.
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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 |
Feb
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pubmed:issn |
0223-5234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
315-26
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pubmed:meshHeading |
pubmed-meshheading:17582660-Animals,
pubmed-meshheading:17582660-Drug Evaluation, Preclinical,
pubmed-meshheading:17582660-Enzyme Inhibitors,
pubmed-meshheading:17582660-Magnetic Resonance Spectroscopy,
pubmed-meshheading:17582660-Models, Molecular,
pubmed-meshheading:17582660-N-Glycosyl Hydrolases,
pubmed-meshheading:17582660-Spectrometry, Mass, Electrospray Ionization,
pubmed-meshheading:17582660-Trypanosoma vivax
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pubmed:year |
2008
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pubmed:articleTitle |
Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors.
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pubmed:affiliation |
Department of Medicinal Chemistry, University of Antwerp, Universiteitsplein 1, B-2610 Antwerp, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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