Source:http://linkedlifedata.com/resource/pubmed/id/13129581
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
20
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pubmed:dateCreated |
2003-9-17
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pubmed:abstractText |
For a series of monosubstituted arylguanidines, 5-HT3 receptor affinity was found generally related to the electron withdrawing nature of the substituent at the aryl 3-position and the lipophilicity of the 4-position substituent. A broader examination of 35 arylguanidines and arylbiguanides revealed that affinity could be described by molecular polarizability, a Chi index term (8chiP), and the sum of all (-Cl) E-State values (SsCl) in the molecule.
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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 |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4449-54
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:13129581-Animals,
pubmed-meshheading:13129581-Electrons,
pubmed-meshheading:13129581-Guanidines,
pubmed-meshheading:13129581-Humans,
pubmed-meshheading:13129581-Ligands,
pubmed-meshheading:13129581-Protein Binding,
pubmed-meshheading:13129581-Quantitative Structure-Activity Relationship,
pubmed-meshheading:13129581-Radioligand Assay,
pubmed-meshheading:13129581-Serotonin 5-HT3 Receptor Antagonists,
pubmed-meshheading:13129581-Serotonin Antagonists
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pubmed:year |
2003
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pubmed:articleTitle |
Arylguanidine and arylbiguanide binding at 5-HT3 serotonin receptors: a QSAR study.
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pubmed:affiliation |
Department of Medicinal Chemistry, School of Pharmacy, Virginia Commonwealth University, Richmond, VA 23298, USA. glennon@hsc.vcu.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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