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dc.contributor.author
Ding, Derong  
dc.contributor.author
Boudreau, Marc A.  
dc.contributor.author
Leemans, Erika J.  
dc.contributor.author
Spink, Edward  
dc.contributor.author
Yamaguchi, Takao  
dc.contributor.author
Testero, Sebastian Andres  
dc.contributor.author
O'Daniel, Peter I.  
dc.contributor.author
Lastochkin, Elena  
dc.contributor.author
Chang, Mayland  
dc.contributor.author
Mobashery, Shahriar  
dc.date.available
2016-06-02T18:29:51Z  
dc.date.issued
2015-06  
dc.identifier.citation
Ding, Derong; Boudreau, Marc A.; Leemans, Erika J.; Spink, Edward; Yamaguchi, Takao; et al.; Exploration of the Structure-Activity Relationship of 1,2,4-Oxadiazole Antibiotics; Elsevier; Bioorganic & Medicinal Chemistry Letters; 25; 21; 6-2015; 4854-4857  
dc.identifier.issn
0960-894X  
dc.identifier.uri
http://hdl.handle.net/11336/6004  
dc.description.abstract
We have recently disclosed the discovery of the class of 1,2,4-oxadiazole antibiotics, which emerged from in silico docking and scoring efforts. This class of antibacterials exhibits Gram-positive activity, particularly against Staphylococcus aureus. We define the structure–activity relationship (SAR) of this class of antibiotics with the synthesis and evaluation of a series of 59 derivatives with variations in the C ring or C and D rings. A total of 17 compounds showed activity against S. aureus. Four derivatives were evaluated against a panel of 16 Gram-positive strains, inclusive of several methicillin-resistant S. aureus strains. These compounds are broadly active against Gram-positive bacteria.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
1,2,4-Oxadiazoles  
dc.subject
Structureactivity Relationship  
dc.subject
Antibiotics  
dc.subject.classification
Química Orgánica  
dc.subject.classification
Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Exploration of the Structure-Activity Relationship of 1,2,4-Oxadiazole Antibiotics  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-06-01T13:48:38Z  
dc.journal.volume
25  
dc.journal.number
21  
dc.journal.pagination
4854-4857  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Ding, Derong. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Boudreau, Marc A.. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Leemans, Erika J.. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Spink, Edward. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Yamaguchi, Takao. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Testero, Sebastian Andres. University Of Notre Dame-indiana; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina  
dc.description.fil
Fil: O'Daniel, Peter I.. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Lastochkin, Elena. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Chang, Mayland. University Of Notre Dame-indiana; Estados Unidos  
dc.description.fil
Fil: Mobashery, Shahriar. University Of Notre Dame-indiana; Estados Unidos  
dc.journal.title
Bioorganic & Medicinal Chemistry Letters  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0960894X1500637X  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.bmcl.2015.06.044  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bmcl.2015.06.044