Source:http://linkedlifedata.com/resource/pubmed/id/19665385
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2009-8-21
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pubmed:abstractText |
A series of bis(alkylpyridinium)alkanes with a twelve carbon spacer between the positive charges was synthesised and their antifungal activity has been investigated. Compounds with 2-pentyl, 4-pentyl, 4-hexyl, 4-octyl, 4-propylbenzene, 3,4-dipentyl, 4-(5'-nonyl) and 3-methyl,4-pentyl head groups were the most potent antifungal agents with MICs in the range of 1.4-2.7 microM against reference strains of both Cryptococcus neoformans and Candida albicans.
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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 |
Sep
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pubmed:issn |
1464-3391
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6329-39
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pubmed:meshHeading |
pubmed-meshheading:19665385-Animals,
pubmed-meshheading:19665385-Antifungal Agents,
pubmed-meshheading:19665385-Candida albicans,
pubmed-meshheading:19665385-Cryptococcus neoformans,
pubmed-meshheading:19665385-Hemolysis,
pubmed-meshheading:19665385-Lysophospholipase,
pubmed-meshheading:19665385-Microbial Sensitivity Tests,
pubmed-meshheading:19665385-Phospholipases A2,
pubmed-meshheading:19665385-Pyridinium Compounds,
pubmed-meshheading:19665385-Swine
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pubmed:year |
2009
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pubmed:articleTitle |
Synthesis, antifungal, haemolytic and cytotoxic activities of a series of bis(alkylpyridinium)alkanes.
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pubmed:affiliation |
School of Chemistry, The University of Sydney, 2006 NSW, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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