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Fusarium equiseti

Phenylboronic acid reacts with equisetin, a toxin from Fusarium equiseti, to give a 1 1 adduct (30) (Equation (5)) <89JA8223>. The reaction occurs under mild conditions and was used in the structural assignment of equisetin. The H NMR of equisetin is poorly resolved, but that of the phenyl boronic ester (30) is well resolved and can be mapped out using two-dimensional techniques. [Pg.359]

Brian PW, Dawkins AW, Grove JF, Hemming HG, Lowe D, Norris GLF (1961) Phytotoxic Compounds Produced by Fusarium equiseti. J Exp Bot 12 1... [Pg.113]

In 1960, Brian et al. isolated anguidine (376) for the first time from Fusarium equiseti... [Pg.78]

Zearalenone (ZEA) Fusarium crookwellense, Fusarium culmorum, Fusarium equiseti, Fusarium graminearum, Fusarium semitectum Cereals and cereal products, other food commodities... [Pg.114]

Fusarium equiseti [1096], The product (ursodeoxycholic acid) is capable of dissolving cholesterol and thus can be used in the therapy of gallstones. [Pg.182]

Unlike other biological agents, T2 is quite toxic when applied to unprotected skin. But like other biologically derived toxins, related substances have been investigated for possible medical uses, including the treatment of some cancerous tumors. A mycotoxin from Fusarium equiseti (diacetoxyscirpenol, or DAS) was considered for an anti-tumor drug formulation called Anguidine, but it was found to be far too toxic for therapeutic use. [Pg.214]

Dawkins, A. W. Phytotoxic compounds produced by Fusarium equiseti II. The chemistry of diacetoxyscirpenol. J. Chem. Soc. (C) 1966, 116. [Pg.213]

Fusarium equiseti CGMCC 3.3658 [94] Penicillium lilacinum ACCC 31890 [94] Streptomyces griseus CGMCC 4.18 [94]... [Pg.706]


See other pages where Fusarium equiseti is mentioned: [Pg.405]    [Pg.223]    [Pg.121]    [Pg.122]    [Pg.277]    [Pg.280]    [Pg.362]    [Pg.387]    [Pg.49]    [Pg.322]    [Pg.96]    [Pg.249]    [Pg.691]    [Pg.182]    [Pg.374]    [Pg.445]    [Pg.952]    [Pg.783]    [Pg.221]    [Pg.701]    [Pg.74]   
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