Hepatic toxicity of myclobutanil exacerbates fatty acid-induced steatosis.
Myclobutanil reduces viability of HepG2 cells to <50% at 100 ppm and to <10% at 500 ppm.
Myclobutanil modifies the function of enzymes such LDH and cytochrome c.
Analysis of biomarkers such as Bcl-xL/Bak and Mcl-1/Bak confirmed activation of cell death pathways at low doses of myclobutanil.