2014
DOI: 10.5935/0103-5053.20140115
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Leishmanicidal Galloylquinic Acids are Noncompetitive Inhibitors of Arginase

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Cited by 7 publications
(8 citation statements)
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“…Given that our study was focused on hydromethanolic extract compared to other extracts, galloylquinic acid derivatives were described in TG for the first time. They have already been reported as metabolites with biological properties that include antioxidant, leishmanicidal, anti-HSV-1, and anti-allergy bioactivities [41,42]. Our work also highlights the presence of isorhamnetin for the first time.…”
Section: Discussionsupporting
confidence: 62%
“…Given that our study was focused on hydromethanolic extract compared to other extracts, galloylquinic acid derivatives were described in TG for the first time. They have already been reported as metabolites with biological properties that include antioxidant, leishmanicidal, anti-HSV-1, and anti-allergy bioactivities [41,42]. Our work also highlights the presence of isorhamnetin for the first time.…”
Section: Discussionsupporting
confidence: 62%
“…Darora residents regularly use the two Byrsonima species as medicinal products for digestive disorders, such as diarrhea and dysentery. This finding is in accordance with an extensive scientific documentation about the medicinal use of Byrsonima spp., including their anti-inflammatory, antimicrobial and Use and traditional knowledge of Byrsonima crassifolia and B. coccolobifolia (Malpighiaceae) in a Makuxi community of the Roraima savanna, northern Brazil ACTA AMAZONICA antioxidant activities (Sannomiya et al 2005;Michelin et al 2008;Sousa et al 2014). Some specific examples are the molluscidal action of Byrsonima coccolobifolia against Biomphalaria glabrata, and its effective bactericidal action against Staphylococcus aureus, Bacillus cereus, Pseudomonas aeruginosa, and Escherichia coli (Alves et al 2000;Pereira 2011).…”
Section: Discussionmentioning
confidence: 99%
“…The chemical shifts are given as δ (ppm) using TMS as an internal standard. The isolated compounds were identified by comparing 1 H NMR data (Table S1) with literature data (Gottlieb et al, 1991;Motta et al, 2017;Nishimura et al, 1984;Souza et al, 2014;Nishizawa et al, 1989;Neszmélyi et al, 1993;Srinivasan et al, 2008).…”
Section: Chemical Characterizationmentioning
confidence: 99%