Dimeric anthracenones were isolated from toxic plants of the genus Kar
winskia (Rhamnaceae). T 514 or peroxisomicine A(1) is one of these tox
ic compounds which produces an irreversible and selective damage on th
e peroxisomes of yeast cells in vivo. In this paper we now report the
inhibitory effect in vitro of peroxisomicine Al and other structurally
related anthracenones on liver catalase activity. The peroxisomicine
A(1) produces a non-competitive inhibition with respect to H2O2 on bov
ine, dog, and mouse liver catalases. In the three cases V-max was decr
eased whereas K-m was unaffected. Other dimeric anthracenones of natur
al origin were also found to be inhibitors of bovine liver catalase. T
here is a relationship between structure and degree of inhibition of a
ll anthracenonic compounds tested. Peroxisomicine A(1) and peroxisomic
ine A(2) caused the highest degree of inhibition (IC50 = 3.34 and 3.64
mu M, respectively).