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      Antimicrobial and Antioxidant Activities of Coumarins from the Roots of Ferulago campestris (Apiaceae)

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          Abstract

          We report the isolation of several coumarins and the stereochemical assessment of some pyranocoumarins, as well as the antibacterial and antioxidant activities of the three most abundant ones (grandivittin, agasyllin and aegelinol benzoate) isolated from the roots of Ferulago campestris collected in Sicily and of the hydrolysis product (aegelinol). Aegelinol and agasyllin showed antibacterial activity against nine ATCC and the same clinically isolated Gram-positive and Gram-negative bacterial strains. At a concentration between 16 and 125 μg/mL both coumarins showed a significant antibacterial effect against both Gram-negative and Gram-positive bacteria. In particular the ATCC strains Staphylococcus aureus, Salmonella thypii, Enterobacter cloacae and Enterobacter earogenes (MIC = 16 and 32 μg/mL for aegelinol and agasyllin, respectively) were the most inhibited. Antibacterial activity was also found against Helicobacter pylori: a dose-dependent inhibition was shown between 5 and 25 μg/mL. The antioxidant activity of the coumarins was evaluated by their effects on human whole blood leukocytes (WB) and on isolated polymorphonucleate (PMN) chemiluminescence (CL), PMA-stimulated and resting.

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          Helicobacter pylori virulence and genetic geography.

          Isolated for the first time in 1982 from human gastric biopsy, Helicobacter pylori is responsible for gastritis, peptic ulcer, and gastric cancer. A pathogenicity island acquired by horizontal transfer, coding for a type IV secretion system, is a major determinant of virulence. The infection is now treated with antibiotics, and vaccines are in preparation. The geographic distribution suggests coevolution of man and Helicobacter pylori.
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            Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

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              Antibacterial activity of pure flavonoids isolated from mosses.

              Seven pure flavonoids were isolated and identified from five moss species. The flavonoids were the flavones apigenin, apigenin-7-O-triglycoside, lucenin-2, luteolin-7-O-neohesperidoside, saponarine and vitexin; and the biflavonoid bartramiaflavone. Some of these flavonoids were shown to have pronounced antibacterial effects against Enterobacter cloaceae, E. aerogenes and Pseudomonas aeruginosa (minimal bacteriostatic concentration MIC in the range of 4-2048 micrograms/ml). Because of their antibacterial spectrum mainly active against Gram negative bacterial strains, responsible for severe opportunistic infections and resistant to common antibacterial therapy, these flavonoids may be important tools in antibacterial strategies.
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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                Molecular Diversity Preservation International
                1420-3049
                27 February 2009
                March 2009
                : 14
                : 3
                : 939-952
                Affiliations
                [1 ]Dipartimento delle Scienze Biologiche, sezione di Biologia Vegetale, Università Federico II, via Foria 223, 80139 Napoli, Italy; E-mail: adbasile@ 123456unina.it (A.B.)
                [2 ]Centro Interdipartimentale di Servizio per la Microscopia Elettronica C.I.S.M.E., Università Federico II, via Foria 223, 80139 Napoli, Italy; E-mail: sersorbo@ 123456unina.it (S.S.)
                [3 ]Dipartimento di Scienze Botaniche, Università di Palermo, Via Archirafi, 38 - 90123 Palermo, Italy E-mail: vspadaro@ 123456unipa.it (V.S.)
                [4 ]Dipartimento di Chimica Organica, Università di Palermo, Viale delle Scienze, Parco d’Orleans II - 90128 Palermo, Italy; E-mails: antonellamaggio@ 123456unipa.it (A.M.), nic.far.ale@ 123456gmail.com (N.F.), rosselli@ 123456unipa.it (S.R.)
                Author notes
                [* ]Author to whom correspondence should be addressed. E-mail: bruno@ 123456dicpm.unipa.it
                Article
                molecules-14-00939
                10.3390/molecules14030939
                6253837
                19255552
                daba066e-87c6-4b80-a4b0-a38b106555b9
                © 2009 by the authors;

                licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 15 January 2009
                : 11 February 2009
                : 01 February 2009
                Categories
                Article

                ferulago campestris,coumarins,pyranocoumarins,absolute configuration,antibacterial activity,antioxidant activity

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