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dc.creatorMueller, Jonas I.
dc.creatorKusserow, Kalina
dc.creatorHertrampf, Gesa
dc.creatorPavić, Aleksandar
dc.creatorNikodinović-Runić, Jasmina
dc.creatorGulder, Tobias A. M.
dc.date.accessioned2022-11-15T15:10:00Z
dc.date.available2022-11-15T15:10:00Z
dc.date.issued2019
dc.identifier.issn1477-0520
dc.identifier.urihttps://imagine.imgge.bg.ac.rs/handle/123456789/1290
dc.description.abstractThe myxocoumarins A and B from Stigmatella aurantiaca MYX-030 are natural products featuring unusual nitro-and long-chain alkyl substitution. While myxocoumarin A was shown to exhibit strong antifungal properties, the antifungal potential of myxocoumarin B was not yet assessed due to low production titers during initial isolation. We therefore developed a total synthesis of myxocoumarin B that involves a late-stage Pd-catalyzed nitration of the coumarin core. The availability of synthetic material facilitated the initial evaluation of the bioactivity of myxocoumarin B, which revealed a lack of activity against medically relevant Candida sp. and low cytotoxicity in vitro against human fibroblasts (MRC-5) and in vivo (zebrafish).en
dc.publisherRoyal Soc Chemistry, Cambridge
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173048/RS//
dc.relationDAAD (Deutscher Akademischer Austauschdienst)
dc.relationDFG [GU 1233/11]
dc.relationDFG (Center for Integrated Protein Science Munich CIPSM)
dc.rightsrestrictedAccess
dc.sourceOrganic & Biomolecular Chemistry
dc.titleSynthesis and initial biological evaluation of myxocoumarin Ben
dc.typearticle
dc.rights.licenseARR
dc.citation.epage1969
dc.citation.issue7
dc.citation.other17(7): 1966-1969
dc.citation.rankM21
dc.citation.spage1966
dc.citation.volume17
dc.identifier.doi10.1039/c8ob02273a
dc.identifier.pmid30357251
dc.identifier.scopus2-s2.0-85061515800
dc.identifier.wos000458679200055
dc.type.versionpublishedVersion


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