dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorScience and Technology of Maranhão-IFMA
dc.date.accessioned2020-12-12T01:30:16Z
dc.date.accessioned2022-12-19T20:48:32Z
dc.date.available2020-12-12T01:30:16Z
dc.date.available2022-12-19T20:48:32Z
dc.date.created2020-12-12T01:30:16Z
dc.date.issued2020-01-01
dc.identifierNatural Product Research.
dc.identifier1478-6427
dc.identifier1478-6419
dc.identifierhttp://hdl.handle.net/11449/199081
dc.identifier10.1080/14786419.2020.1786824
dc.identifier2-s2.0-85087636834
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5379715
dc.description.abstractInga edulis is traditionally used as anti-inflammatory and antidiarrheal and has been investigated as potential sources of biologically active natural products. In this study, dereplication strategy using HPLC-SPE-TT, RP-HPLC-PDA and NMR spectroscopy was employed, and this resulted in the identification of sixteen compounds from the leaves extract of I. edulis, including four triterpenes (lupeol, α-amirin, olean-18-ene acid and frideline), three flavonoids, eight phenolic acids, an anthocyanin derived from delphinidin-3-glycoside and a mixture of five acylated anthocyanins. The chemical identification was performed based on NMR data, chemosystematics aspects, UV spectra and by comparison with the retention time and UV spectra of authentic standards. The metabolic profile of the species indicated the presence of phenolic compounds as major constituents justifying its strong antioxidant potential performed in β-carotene test. The techniques used have shown effective strategies for the early detection of active natural products from plant extracts, as these approaches are still crucially absent. (Figure presented.).
dc.languageeng
dc.relationNatural Product Research
dc.sourceScopus
dc.subjectdereplication
dc.subjectHPLC-SPE-TT
dc.subjectInga edulis
dc.subjectMedicinal plants
dc.subjectNMR
dc.subjectRP-HPLC-PDA
dc.titleDereplication of terpenes and phenolic compounds from Inga edulis extracts using HPLC-SPE-TT, RP-HPLC-PDA and NMR spectroscopy
dc.typeArtículos de revistas


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