The in vitro anticandidal properties of six chlorinated 8-quinolinols
(3-chloro-, 5-chloro-, 6-chloro-, 7-chloro-, 3,6-dichloro-, and 5,7-di
chloro-8-quinolinols) were evaluated. Various concentrations of these
compounds were added to cultures of Candida albicans and C. tropicalis
grown in Sabouraud dextrose broth with and without bovine serum. The
5-chloro- and 6-chloro-8-quinolinols proved to be most effective at in
hibiting the growth of C. albicans while 3,6-dichloro-8-quinolinol was
most effective at controlling the growth of C. tropicalis. Cytotoxici
ty tests on baby hamster kidney (BHK) cells, however, demonstrated tha
t the compounds tested were cytotoxic at their minimum inhibitory conc
entrations except for 3,6-dichloro-8-quinolinol which proved effective
at inhibiting the growth of C. tropicalis at about one half the cytot
oxic dose. Because this compound showed antifungal properties at conce
ntrations that do not suppress mammalian cell growth, it merits furthe
r investigation as a possible topical or systemic anticandidal agent.