Antifungal activity of cinnamic acid derivatives involves inhibition of benzoate 4-hydroxylase (CYP53)
Journal of Applied Microbiology2013Vol. 116(4), pp. 955–966
Citations Over TimeTop 10% of 2013 papers
Branka Korošec, Matej Sova, Samo Turk, Nada Kraševec, Metka Novak, Ljerka Lah, Jure Stojan, Barbara Podobnik, Sabina Berne, Neja Zupanec, Matjaž Bunc, Stanislav Gobec, Radovan Komel
Abstract
By identifying selected derivatives of cinnamic acid as possible antifungal drugs, and CYP53 family enzymes as their targets, we revealed a potential inhibitor-target system for antifungal drug development.
Related Papers
- → Microbial Transformations of 3-methoxyflavone by the Strains of Aspergillus niger(2014)10 cited
- → Mechanism of oxalic acid fermentation by Aspergillus niger.(1988)4 cited
- → GAMMA RAYS MUTAGENESIS OF ASPERGILLUS NIGER FOR HYPERPRODUCTION OF MUTAROTASE(2012)1 cited
- [Report on applications for use of three enzyme preparations [Aspergillus niger ; inulase (Novozym 280), betaglucanase (Novozym 188); Aspergillus niger var. niger, betaglucanase + hemicellulase (Viscozym 120 L)]]. [French](1991)
- → دراسة كفاءة مضادات الأكسدة المنتجة من الرز بواسطة عفن Aspergillus niger في بعض الزيوت(2014)