Merck
CN

3D QSAR study of the toxicity of trichothecene mycotoxins.

European journal of medicinal chemistry (2009-07-10)
Wayne E Steinmetz, Cezar B Rodarte, Alvin Lin
ABSTRACT

Trichothecene mycotoxins, toxic natural products of fungi from the family Hypocreaceae, are potent inhibitors of protein synthesis. The application of 3D QSAR to these toxins explored the structural basis for their biological activities. A CoMFA (Q(2)=0.619, R(2)=0.921) model was developed for a set of 15 toxins with the trichothecene nucleus; CoMFA (Q(2)=0.518, R(2)=0.855) and CoMSIA (Q(2)=0.695, R(2)=0.960) models were developed for 31 toxins with the nucleus and a macrolide ring. The results show the role of electrostatics and steric factors in the activity of the toxins and indicate that the conformation of the macrolide ring influences the toxicity of the macrolide toxins.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
15-O-Acetyl-4-deoxynivalenol from Fusarium graminearum
Supelco
15-Acetyldeoxynivalenol solution, ~100 μg/mL in acetonitrile, analytical standard
Supelco
Nivalenol solution, 100 μg/mL in acetonitrile, analytical standard
Sigma-Aldrich
Deoxynivalenol
Nivalenol in acetonitrile, IRMM®, certified reference material
Supelco
T2-Toxin solution, 100 μg/mL in acetonitrile, analytical standard
Supelco
Deoxynivalenol solution, 100 μg/mL in acetonitrile, analytical standard