| In vitro: |
| Front Microbiol. 2014 Mar 7;5:87. | | Use of benzo analogs to enhance antimycotic activity of kresoxim methyl for control of aflatoxigenic fungal pathogens.[Pubmed: 24639673] | The aim of this study was to examine two benzo analogs, octylgallate (OG) and Veratraldehyde (VT), as antifungal agents against strains of Aspergillus parasiticus and A.flavus (toxigenic or atoxigenic).
METHODS AND RESULTS:
Both toxigenic and atoxigenic strains used were capable of producing kojic acid, another cellular secondary product. A. fumigatus was used as a genetic model for this study. When applied independently, OG exhibits considerably higher antifungal activity compared to Veratraldehyde. The minimum inhibitory concentrations (MICs) of OG were 0.3-0.5 mM, while that of Veratraldehyde were 3.0-5.0 mM in agar plate-bioassays. OG or Veratraldehyde in concert with the fungicide kresoxim methyl (Kre-Me; strobilurin) greatly enhanced sensitivity of Aspergillus strains to Kre-Me. The combination with OG also overcame the tolerance of A. fumigatus mitogen-activated protein kinase (MAPK) mutants to Kre-Me. The degree of compound interaction resulting from chemosensitization of the fungi by OG was determined using checkerboard bioassays, where synergistic activity greatly lowered MICs or minimum fungicidal concentrations. However, the control chemosensitizer benzohydroxamic acid, an alternative oxidase inhibitor conventionally applied in concert with strobilurin, did not achieve synergism. The level of antifungal or chemosensitizing activity was also "compound-strain" specific, indicating differential susceptibility of tested strains to OG or Veratraldehyde, and/or heat stress. Besides targeting the antioxidant system, OG also negatively affected the cell wall-integrity pathway, as determined by the inhibition of Saccharomyces cerevisiae cell wall-integrity MAPK pathway mutants.
CONCLUSIONS:
We concluded that certain benzo analogs effectively inhibit fungal growth. They possess chemosensitizing capability to increase efficacy of Kre-Me and thus, could reduce effective dosages of strobilurins and alleviate negative side effects associated with current antifungal practices. OG also exhibits moderate antiaflatoxigenic activity. | | Der Pharma Chemica, 2010,2(6):295. | | Veratraldehyde as Corrosion Inhibitor for Zinc in Different Acid Mediu[Reference: WebLink] |
METHODS AND RESULTS:
The corrosion inhibition of zinc in 0.1 M HCl and 0.05 M H2SO4 was studied separately by using Veratraldehyde as a corrosion inhibitor. Mass loss and electrochemical studies were part of the investigations. The Inhibition efficiencies were evaluated at different concentrations of the inhibitor at different temperature. The inhibition efficiency increased with increase in inhibitor concentration and decreased with increase in temperature in both the medium. The inhibitor was more active in HCl than in H2SO4. The maximum inhibition efficiency approached at 1000 ppm in both HCl and H2SO4 medium.
CONCLUSIONS:
Electrochemical studies show that inhibitor acts a mixed type inhibitor. The inhibitor was found to adsorb on the zinc surface according to the Langmuir adsorption isotherm. |
|
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.IF=36.216(2019)
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.IF=22.415(2019)
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.IF=14.548(2019)
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.IF=13.903(2019)
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.IF=13.297(2019)
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.IF=12.804(2019)
