<HashMap><database>biostudies-literature</database><scores/><additional><submitter>De Gregorio E</submitter><funding>Fondazione per la Ricerca sulla Fibrosi Cistica</funding><pagination>E362</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7344813</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(6)</volume><pubmed_abstract>Staphylococcus aureus is one of the major causes of hospital- and community-associated bacterial infections throughout the world, which are difficult to treat due to the rising number of drug-resistant strains. New molecules displaying potent activity against this bacterium are urgently needed. In this study, d- and l-deoxynojirimycin (DNJ) and a small library of their N-alkyl derivatives were screened against S. aureus ATCC 29213, with the aim to identify novel candidates with inhibitory potential. Among them, N-nonyloxypentyl-l-DNJ (l-NPDNJ) proved to be the most active compound against S. aureus ATCC 29213 and its clinical isolates, with the minimum inhibitory concentration (MIC) value of 128 μg/mL. l-NPDNJ also displayed an additive effect with gentamicin and oxacillin against the gent</pubmed_abstract><journal>Antibiotics (Basel, Switzerland)</journal><pubmed_title>N-Nonyloxypentyl-l-Deoxynojirimycin Inhibits Growth, Biofilm Formation and Virulence Factors Expression of Staphylococcus aureus.</pubmed_title><pmcid>PMC7344813</pmcid><funding_grant_id>FFC #20/2019</funding_grant_id><pubmed_authors>Iula VD</pubmed_authors><pubmed_authors>Esposito A</pubmed_authors><pubmed_authors>Migliaccio A</pubmed_authors><pubmed_authors>Zarrilli R</pubmed_authors><pubmed_authors>De Gregorio E</pubmed_authors><pubmed_authors>De Fenza M</pubmed_authors><pubmed_authors>D'Alonzo D</pubmed_authors><pubmed_authors>Guaragna A</pubmed_authors><pubmed_authors>Vollaro A</pubmed_authors></additional><is_claimable>false</is_claimable><name>N-Nonyloxypentyl-l-Deoxynojirimycin Inhibits Growth, Biofilm Formation and Virulence Factors Expression of Staphylococcus aureus.</name><description>Staphylococcus aureus is one of the major causes of hospital- and community-associated bacterial infections throughout the world, which are difficult to treat due to the rising number of drug-resistant strains. New molecules displaying potent activity against this bacterium are urgently needed. In this study, d- and l-deoxynojirimycin (DNJ) and a small library of their N-alkyl derivatives were screened against S. aureus ATCC 29213, with the aim to identify novel candidates with inhibitory potential. Among them, N-nonyloxypentyl-l-DNJ (l-NPDNJ) proved to be the most active compound against S. aureus ATCC 29213 and its clinical isolates, with the minimum inhibitory concentration (MIC) value of 128 μg/mL. l-NPDNJ also displayed an additive effect with gentamicin and oxacillin against the gent</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-04-22T19:37:11.35Z</modification><creation>2025-04-06T02:47:26.12Z</creation></dates><accession>S-EPMC7344813</accession><cross_references><pubmed>32604791</pubmed><doi>10.3390/antibiotics9060362</doi></cross_references></HashMap>