Source:http://linkedlifedata.com/resource/pubmed/id/20207048
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2010-4-20
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pubmed:abstractText |
A series of 3-benzyloxy-1-aza-9-oxafluorenes has been synthesized and biologically evaluated as novel MDR modulators. The concentration dependent inhibition of the efflux pump ABCB1 (P-glycoprotein) has been characterized and is discussed in relation to calculated lipophilicity data. Instead of the molecular lipophilicity the exact positioning of functional groups was found decisive for the biological activities.
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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 |
Jun
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pubmed:issn |
1768-3254
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pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2010 Elsevier Masson SAS. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2683-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:20207048-Animals,
pubmed-meshheading:20207048-Cell Line, Tumor,
pubmed-meshheading:20207048-Drug Discovery,
pubmed-meshheading:20207048-Drug Resistance, Multiple,
pubmed-meshheading:20207048-Fluorenes,
pubmed-meshheading:20207048-Hydrophobic and Hydrophilic Interactions,
pubmed-meshheading:20207048-Mice,
pubmed-meshheading:20207048-Neoplasms,
pubmed-meshheading:20207048-P-Glycoproteins,
pubmed-meshheading:20207048-Structure-Activity Relationship
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pubmed:year |
2010
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pubmed:articleTitle |
First biological evaluation of developed 3-benzyloxyfluorenes as novel class of MDR modulators.
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pubmed:affiliation |
Institute of Pharmacy, Martin-Luther University Halle-Wittenberg, Wolfgang-Langenbeck Str. 4, D-06120 Halle, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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