H. Laatsch et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF PHENYLPYRROLES AND BENZOYLPYRROLES, Chemical and Pharmaceutical Bulletin, 43(4), 1995, pp. 537-546
Antitumor, antimicrobial, and phytotoxic activities of the marine anti
biotic pentabromopseudilin (1a) and related phenyl-, benzyl- and benzo
yl pyrroles were compared. All activities depended strongly on the sub
stituent pattern, with the natural compound la being the most active o
ne, As judged from model reactions, a covalent bond of nucleophiles to
the pyrrole system may be involved in the inhibition of macromolecula
r syntheses.