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Mycotoxins are structurally diverse groups largely composed of small molecular weight chemicals, which are generally produced by the mycelial structure of filamentous fungi. These toxins are secondary metabolites mainly synthesized during the end of the mould exponential phase of growth. They appear to have no biological significance with respect to their growth/development or competitiveness, but when ingested by higher vertebrates and other animals they can cause diseases called mycotoxicoses (Kabak et al., 2006; MadrigalSantillan et al., 2010). Aflatoxin B1 (AFB1), in particular, is a tetrahydrofuran moiety fused to a coumarin ring and was chemically classified as cyclopenta[c]furo[3',2':4,5]furo[2,3h][1] benzopyran-1,11-dione,2,3,6a,9a-tetrahydro-4-methoxy-, (6aR,9aS) (Eaton et al., 1994; Hedayati et al., 2007) (Figure 1).

Aflatoxin B1 - Prevention of Its Genetic Damage by Means of Chemical Agents