Source:http://linkedlifedata.com/resource/pubmed/id/20627739
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
2011-3-25
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pubmed:abstractText |
A compact synthesis of 15 new binaphthyl-based dicationic tripeptoids and one biphenyl based dicationic tripeptoid is described. Fourteen of these tripeptoids resulted from variation of the C-2' ether substituent of the binaphthyl unit. An O-iso-butyl ether binaphthyl derivative was found to be the most active against Staphylococcus aureus (MIC 1.95 ?g/mL). The biphenyl analogue also showed good activity against S. aureus (MIC 1.95 ?g/mL). These compounds, however, were less active against four vancomycin-resistant strains of enterococci (VRE) than some of our previously developed compounds that had an O-iso-pentyl ether substituent on the binaphthyl unit and a C-2 L-Leu moiety.
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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 |
Jul
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pubmed:issn |
1464-3391
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pubmed:author |
pubmed-author:BoyleTimothy PTP,
pubmed-author:BremnerJohn BJB,
pubmed-author:BrkicZinkaZ,
pubmed-author:CoatesJonathan AJA,
pubmed-author:DeadmanJohnJ,
pubmed-author:KellerPaul APA,
pubmed-author:MorganJodyJ,
pubmed-author:PyneStephen GSG,
pubmed-author:RhodesDavid IDI,
pubmed-author:SompholKittiyaK
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pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4793-800
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pubmed:meshHeading |
pubmed-meshheading:20627739-Anti-Bacterial Agents,
pubmed-meshheading:20627739-Enterococcus,
pubmed-meshheading:20627739-Microbial Sensitivity Tests,
pubmed-meshheading:20627739-Naphthalenes,
pubmed-meshheading:20627739-Peptoids,
pubmed-meshheading:20627739-Staphylococcus aureus,
pubmed-meshheading:20627739-Vancomycin Resistance
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pubmed:year |
2010
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pubmed:articleTitle |
Synthesis and antibacterial studies of binaphthyl-based tripeptoids. Part 2.
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pubmed:affiliation |
School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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