Charles Cantrell

Charles Cantrell

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 May 2012 in Journal of Natural Products
Verified
Journal Article
Closed access
CCCharles Cantrell
Charles Cantrell
FDFranck Dayan
Franck Dayan
SDStephen O. Duke
Stephen O. Duke

29 July 2010 in Toxins
Verified
Journal Article
Open access
PDF file
SDStephen Duke
Stephen Duke
CCCharles Cantrell
Charles Cantrell
KMKumudini Meepagala
Kumudini Meepagala
DWDavid E. Wedge
David E. Wedge
NTNurhayat Tabanca
Nurhayat Tabanca
KSKevin Schrader
Kevin Schrader
Natural toxins are a source of new chemical classes of pesticides, as well as environmentally and toxicologically safer molecules than many of the currently used pesticides. Furthermore, they often have molecular target sites that are not exploited by currently marketed pesticides. There are highly successful products based on natural compounds in the major pesticide classes. These include the herbicide glufosinate (synthetic phosphinothricin), the spinosad insecticides, and the strobilurin fungicides. These and other examples of currently marketed natural product-based pesticides, as well as natural toxins that show promise as pesticides from our own research are discussed.

15 July 2010 in Chemistry & Biodiversity
Verified
Journal Article
Closed access
PDF file
CCCharles Cantrell
Charles Cantrell
JPJulia W. Pridgeon
Julia W. Pridgeon
FFFrank R. Fronczek
Frank R. Fronczek
JBJames J. Becnel
James J. Becnel

28 January 2020 in Molecules
Verified
Journal Article
Open access
PDF file
Mohamed Ali IbrahimMohamed Ali Ibrahim
Mohamed Ali Ibrahim
CCCharles Cantrell
Charles Cantrell
EJEkaterina A. Jeliazkova
Ekaterina A. Jeliazkova
TATess Astatkie
Tess Astatkie
Valtcho ZheljazkovValtcho Zheljazkov
Valtcho Zheljazkov
The intent of this study was to utilize distillation timeframes (DT) of nutmeg (Myristica fragrans) essential oil (EO) to generate fractions with differential chemical compositions and bioactivity. Ten fractions were captured at the following distillation timeframes: 0.0–0.5, 0.5–1.0, 1.0–2.5, 2.5–5.0, 5.0–10, 10–30, 30–60, 60–90, 90–120, and 120–240 min. In addition, a control EO was collected from a straight 0–240 min non-stop distillation. ANOVA and advanced regression modeling revealed that the produced EO fractions possess substantial variation in the concentration of potentially desired compounds. The concentrations (%) of α-phellandrene, 3-carene, p-cymene, limonene, α-thujene, α-pinene, camphene, sabinene, β-pinene, and myrcene decreased, while the concentrations (%) of α-terpinene, γ-terpinene, terpinolene, and myristicin increased in later DT fractions. Nutmeg EO showed some antimalarial activity against Plasmodium falciparum D6, but did not exhibit significant antifungal activity. In general, nutmeg seed oil yields increased with an increase of DT. These results may be utilized by industries using nutmeg EO.

29 January 2024 in Journal of Agricultural and Food Chemistry
Verified
Journal Article
Closed access
NSNa-Bo Sun
Na-Bo Sun
LMLi-Jing Min
Li-Jing Min
XSXin-Peng Sun
Xin-Peng Sun
ZZZhi-Wen Zhai
Zhi-Wen Zhai
JBJoanna Bajsa-Hirschel
Joanna Bajsa-Hirschel
XLXing-Hai Liu
Xing-Hai Liu

29 November 2023 in Journal of Agricultural and Food Chemistry
Verified
Journal Article
Closed access
XSXin-Peng Sun
Xin-Peng Sun
CYChen-Sheng Yu
Chen-Sheng Yu
LMLi-Jing Min
Li-Jing Min
CCCharles Cantrell
Charles Cantrell
XHXuewen Hua
Xuewen Hua
XLXing-Hai Liu
Xing-Hai Liu