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Synthesis of novel nitro-substituted triaryl pyrazole derivatives as potential estrogen receptor ligands

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dc.contributor.author Naoum, F en
dc.contributor.author Kasiotis, KM en
dc.contributor.author Magiatis, P en
dc.contributor.author Haroutounian, SA en
dc.date.accessioned 2014-06-06T06:48:02Z
dc.date.available 2014-06-06T06:48:02Z
dc.date.issued 2007 en
dc.identifier.issn 14203049 en
dc.identifier.uri http://dx.doi.org/10.3390/12071259 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/3925
dc.subject Estrogen receptor binding affinity en
dc.subject Pyrazoles en
dc.subject SERMs en
dc.subject.other estrogen receptor alpha en
dc.subject.other estrogen receptor beta en
dc.subject.other ligand en
dc.subject.other nitro derivative en
dc.subject.other pyrazole en
dc.subject.other pyrazole derivative en
dc.subject.other article en
dc.subject.other chemistry en
dc.subject.other human en
dc.subject.other metabolism en
dc.subject.other synthesis en
dc.subject.other Estrogen Receptor alpha en
dc.subject.other Estrogen Receptor beta en
dc.subject.other Humans en
dc.subject.other Ligands en
dc.subject.other Nitro Compounds en
dc.subject.other Pyrazoles en
dc.title Synthesis of novel nitro-substituted triaryl pyrazole derivatives as potential estrogen receptor ligands en
heal.type journalArticle en
heal.identifier.primary 10.3390/12071259 en
heal.publicationDate 2007 en
heal.abstract Novel tetrasubstituted pyrazole derivatives bearing a nitro substituent on their A-phenol ring were synthesized and their binding affinity towards the estrogen receptor (ER) subtypes ERα and ERβ was determined. Among compounds tested, the 2-nitrophenol derivative 5c was found to bind satisfactorily to both estrogen receptor subtypes (RBAα=5.17 and RBAβ=3.27). In general, the introduction of a nitro group into the A ring of these compounds was found to benefit their ERβ binding abilities. © 2007 by MDPI. en
heal.journalName Molecules en
dc.identifier.issue 7 en
dc.identifier.volume 12 en
dc.identifier.doi 10.3390/12071259 en
dc.identifier.spage 1259 en
dc.identifier.epage 1273 en


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