Petasis adducts of tryptanthrin – synthesis, biological activity evaluation and druglikeness assessment,

dc.contributor.authorBurke, Anthony
dc.contributor.authorMarques, Carolina
dc.contributor.authorBrandão, Pedro
dc.contributor.authorPineiro, Marta
dc.contributor.authorEugenia, Pinto
dc.contributor.editorGérard, Jean-François
dc.date.accessioned2022-01-31T15:20:36Z
dc.date.available2022-01-31T15:20:36Z
dc.date.issued2021-07-01
dc.description.abstractTryptanthrin is a valuable tetracyclic alkaloid, which displays a wide variety of biological activities. The application of this type of scaffold as a starting material for the discovery of new drug candidates is of major importance in medicinal chemistry. In this work, we report one of the few examples of tryptanthrin-based multicomponent reaction approaches for drug discovery, and the first using the Petasis reaction. The optimized BINOL-catalyzed reaction conditions allowed the synthesis of a library of new tryptanthrin derivatives bearing considerable structural diversity. An asymmetric version was also established, achieving the desired enantiomerically pure derivative with 99% ee and 71% yield. The resulting library was screened against one Gram-positive and one Gram-negative bacteria, two yeasts, and three filamentous and four dermatophyte fungal strains with clinical relevance, with compound 5bea displaying moderate fungicidal activity.por
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dc.identifier.doi10.1039/D1NJ02079Jpor
dc.identifier.pagina, 14633-14649
dc.identifier.revistaNew Journal of Chemistry
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2021/NJ/D1NJ02079J
dc.identifier.urihttp://hdl.handle.net/10174/30934
dc.identifier.volume45
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherRoyal Society of Chemistry/CNRS Francepor
dc.rightsrestrictedAccesspor
dc.subjectPetasis Reactionpor
dc.subjectSynthesispor
dc.subjectanti-microbialpor
dc.titlePetasis adducts of tryptanthrin – synthesis, biological activity evaluation and druglikeness assessment,por
dc.typearticle

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