Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4178
DC FieldValueLanguage
dc.contributor.authorCampiani, Giuseppeen_us
dc.contributor.authorCappelli, Andreaen_us
dc.contributor.authorNacci, Vitoen_us
dc.contributor.authorAnzini, Maurizioen_us
dc.contributor.authorVomero, Salvatoreen_us
dc.contributor.authorM., Hamonen_us
dc.contributor.authorA., Cagnottoen_us
dc.contributor.authorC., Fracassoen_us
dc.contributor.authorC., Uboldien_us
dc.contributor.authorS., Cacciaen_us
dc.contributor.authorS., Consoloen_us
dc.contributor.authorT., Menninien_us
dc.date.accessioned2021-03-30T14:42:16Z-
dc.date.available2021-03-30T14:42:16Z-
dc.date.issued1997-
dc.identifier.issn0022-2623en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/4178-
dc.description20356en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofJOURNAL OF MEDICINAL CHEMISTRYen_US
dc.titleNovel and Highly Potent 5-HT3 Receptor Agonists Based on a Pyrroloquinoxaline Structureen_US
dc.typeArticleen_US
dc.identifier.scopus2-s2.0-9844234810en_US
dc.identifier.isiWOS:A1997YD59900023en_US
dc.relation.volume40en_US
dc.relation.issue22en_US
dc.description.firstpage3670en_US
dc.description.lastpage3678en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0001-5295-9529-
crisitem.author.orcid0000-0003-4140-3028-
crisitem.author.orcid0000-0002-7481-5566-
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