Castanospermine was identified as an inhibitor of the Rho/Ras-glucosylating
Clostridium sordellii lethal toxin and Clostridium difficile toxin B.
Microinjection of castanospermine into embryonic bovine lung cells prevented the
cytotoxic effects of toxins. The crystal structure of the glucosyltransferase
domain of C. sordellii lethal toxin in complex with castanospermine, UDP and a
calcium ion was solved at a resolution of 2.3A. The inhibitor binds in a
conformation that brings its four hydroxyl groups and its N-atom almost exactly
in the positions of the four hydroxyls and of the ring oxygen of the glucosyl
moiety of UDP-glucose, respectively.