frangula purshiana/antimikotično

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Antifungal activity of Rubia tinctorum, Rhamnus frangula and Caloplaca cerina.

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The results of a preliminary antifungal screening of the methanol extracts and the major anthraquinone aglycones, alizarin and emodin, of Rubia tinctorum and Rhamnus frangula in comparison with the antifungal activity of the anthraquinone-containing lichen Caloplaca cerina and its main secondary

Purification and characterization of a newly serine protease inhibitor from Rhamnus frangula with potential for use as therapeutic drug.

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Protease inhibitors from plants are well known to be potent inhibitors of the growth of bacteria, fungi, and even certain viruses which make them excellent candidates for use as the lead compounds for the development of novel antimicrobial agents for applications in medicine. In this study, Rhamnus

Vaccinium myrtillus leaves and Frangula alnus bark derived extracts as potential antistaphylococcal agents.

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Due to constantly increasing antibiotic resistance of pathogens and participation of the biofilms they make in various types of infections, a development of alternative therapeutic strategies becomes an urgent need. Taking advantage of the biological activity of plant-derived compounds can solve

Fusarium head blight control and prevention of mycotoxin contamination in wheat with botanicals and tannic acid.

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Suspensions or solutions with 1% of Chinese galls (Galla chinensis, GC) or 1% of tannic acid (TA), inhibited germination of conidia or mycelium growth of Fusarium graminearum (FG) by 98%-100% or by 75%-80%, respectively, whereas dried bark from buckthorn (Frangula alnus, FA) showed no effect at this

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