Source:http://linkedlifedata.com/resource/pubmed/id/17074492
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-12-15
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pubmed:abstractText |
Comparative molecular field analysis (CoMFA) was performed on a set of 1H-benzimidazole derivatives. Molecular modeling and 3D-QSAR were employed to determine the tautomeric form that would probably fit a target receptor in Entamoeba histolytica. CoMFA results suggest that the antiamoebic activity is favored with steric bulk at position 5 of the benzimidazole ring and low electron density on the group at position 2. To the best of our knowledge this is the first 3D-QSAR study performed for benzimidazoles as antiamoebic agents. The CoMFA models derived will be very valuable to design new and more potent compounds against E. histolytica.
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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 |
Jan
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pubmed:issn |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1117-26
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pubmed:meshHeading |
pubmed-meshheading:17074492-Algorithms,
pubmed-meshheading:17074492-Amebicides,
pubmed-meshheading:17074492-Animals,
pubmed-meshheading:17074492-Benzimidazoles,
pubmed-meshheading:17074492-Entamoeba histolytica,
pubmed-meshheading:17074492-Least-Squares Analysis,
pubmed-meshheading:17074492-Ligands,
pubmed-meshheading:17074492-Models, Molecular,
pubmed-meshheading:17074492-Quantitative Structure-Activity Relationship,
pubmed-meshheading:17074492-Reproducibility of Results
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pubmed:year |
2007
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pubmed:articleTitle |
Molecular modeling of some 1H-benzimidazole derivatives with biological activity against Entamoeba histolytica: a comparative molecular field analysis study.
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pubmed:affiliation |
Departamento de Farmacia, Facultad de Química, UNAM, CU, D.F. 04510, Mexico.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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