Saltar al contenido
Merck

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
RESUMEN

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.

MATERIALES
Número de producto
Marca
Descripción del producto

Sigma-Aldrich
Deoxynivalenol
Supelco
Deoxynivalenol solution, 100 μg/mL in acetonitrile, analytical standard
Sigma-Aldrich
T-2 Toxin, from Fusarium sp., powder, ≥98% (HPLC)
Supelco
T2-Toxin solution, 100 μg/mL in acetonitrile, analytical standard
Sigma-Aldrich
15-O-Acetyl-4-deoxynivalenol from Fusarium graminearum
Supelco
Nivalenol solution, 100 μg/mL in acetonitrile, analytical standard
4-Deoxynivalenol in acetonitrile, IRMM®, certified reference material
Supelco
15-Acetyldeoxynivalenol solution, ~100 μg/mL in acetonitrile, analytical standard
Supelco
Fusarenon X solution, 100 μg/mL in acetonitrile, analytical standard
Nivalenol in acetonitrile, IRMM®, certified reference material