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Phenols antifungal action

The fungitoxic effect of phenols can be increased by the introduction of nitro groups. Even the introduction of a single nitro group strengthens the antifungal action, but dinitrophenols have been applied most widely as fungicides. Dinitro-... [Pg.321]

Detailed analyses of the change in antifungal activity with chemical modification have appeared.3°>39 Naphthlomate-N is very active, but the other three naphthalene isomer combinations are inert. Various substituted phenols may be used in place of the p-naphthol moiety. Of the N-methyl (essential for activity) anilines tried, hydrogen, methyl, methoxyl, and halogen containing compounds were active whereas nltro, di-methylamino, carboxyl, etc., derivatives were inactive. The carbamates still retained some activity but other variations of the thiocarbamate system, such as the dithiocarbamate derivatives, were devoid of antifungal action. [Pg.140]

FIG. 10.15 Comparatively small effect of pH on the antifungal action of some phenolic ethers on Trichoderma viride. (Simon and Blackman,... [Pg.379]


See other pages where Phenols antifungal action is mentioned: [Pg.174]    [Pg.131]    [Pg.69]    [Pg.268]    [Pg.443]    [Pg.1118]    [Pg.222]    [Pg.268]    [Pg.325]    [Pg.327]    [Pg.335]    [Pg.471]    [Pg.255]    [Pg.544]    [Pg.918]    [Pg.268]    [Pg.131]    [Pg.220]   
See also in sourсe #XX -- [ Pg.422 ]

See also in sourсe #XX -- [ Pg.220 , Pg.374 , Pg.378 , Pg.380 ]




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Antifungal action

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