11206444

Source:http://linkedlifedata.com/resource/pubmed/id/11206444

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002584, umls-concept:C0007732, umls-concept:C0178499, umls-concept:C0733755, umls-concept:C1527178
pubmed:issue	2
pubmed:dateCreated	2001-2-5
pubmed:abstractText	Incorporation of a basic aminopyridine into the C-7 position of 3-(amine-substituted arylthio)-3-norcephalosporins, as in 3, afforded high potency against MRSA and acceptable solubility for intravenous administration.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107377
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Aminopyridines, http://linkedlifedata.com/resource/pubmed/chemical/Cephalosporins, http://linkedlifedata.com/resource/pubmed/chemical/RWJ 54428
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0960-894X
pubmed:author	pubmed-author:DJOBB, pubmed-author:FanA TAT, pubmed-author:GlinkaT WTW, pubmed-author:HeckerS JSJ, pubmed-author:LudwikowMM, pubmed-author:WangMM
pubmed:issnType	Print
pubmed:day	22
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	137-40
pubmed:meshHeading	pubmed-meshheading:11206444-Aminopyridines, pubmed-meshheading:11206444-Cephalosporins, pubmed-meshheading:11206444-Combinatorial Chemistry Techniques, pubmed-meshheading:11206444-Methicillin Resistance, pubmed-meshheading:11206444-Microbial Sensitivity Tests, pubmed-meshheading:11206444-Solubility, pubmed-meshheading:11206444-Staphylococcus aureus, pubmed-meshheading:11206444-Structure-Activity Relationship
pubmed:year	2001
pubmed:articleTitle	New anti-MRSA cephalosporins with a basic aminopyridine at the C-7 position.
pubmed:affiliation	Microcide Pharmaceuticals, Inc., Mountain View, CA 94043, USA. acho@microcide.com
pubmed:publicationType	Journal Article