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dc.creatorArsić, Biljana
dc.creatorBarber, Jill
dc.creatorČikoš, Ana
dc.creatorKadirvel, Manikandan
dc.creatorKostić, Emilija
dc.creatorMcBain, Andrew J.
dc.creatorMilićević, Jelena S.
dc.creatorOates, Angela
dc.creatorRegan, Andrew
dc.date.accessioned2022-11-22T12:14:39Z
dc.date.available2022-11-22T12:14:39Z
dc.date.issued2022
dc.identifier.issn1420-3049
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/10502
dc.description.abstractAlthough many antibiotics are active against Gram-positive bacteria, fewer also show activity against Gram-negative bacteria. Here, we present a combination of in silico (electron ion-interaction potential, molecular docking, ADMET), NMR, and microbiological investigations of selected macrolides (14-membered, 15-membered, and 16-membered), aiming to discover the pattern of design for macrolides active against Gram-negative bacteria. Although the conformational studies of 14-membered and 15-membered macrolides are abundant in the literature, 16-membered macrolides, and their most prominent representative tylosin A, have received relatively little research attention. We therefore report the complete 1H and 13C NMR assignment of tylosin A in deuterated chloroform, as well as its 3D solution structure determined through molecular modelling (conformational search) and 2D ROESY NMR. Additionally, due to the degradation of tylosin A in deuterated chloroform, other species were also detected in 1D and 2D NMR spectra. We additionally studied the anti-bacterial activity of tylosin A and B against selected Gram-positive and Gram-negative bacteria.en
dc.languageen
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200124/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200017/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceMolecules
dc.subject2D ROESY NMRen
dc.subjectbacteriaen
dc.subjectmacrolidesen
dc.titleComputational Studies on Selected Macrolides Active against Escherichia coli Combined with the NMR Study of Tylosin A in Deuterated Chloroformen
dc.typearticleen
dc.rights.licenseBY
dc.citation.volume27
dc.citation.issue21
dc.citation.spage7280
dc.identifier.wos000881594700001
dc.identifier.doi10.3390/molecules27217280
dc.citation.rankM21
dc.identifier.pmid36364103
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85141563511
dc.identifier.fulltexthttp://vinar.vin.bg.ac.rs/bitstream/id/27360/molecules-27-07280-v2.pdf


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