U. Thull et B. Testa, SCREENING OF UNSUBSTITUTED CYCLIC-COMPOUNDS AS INHIBITORS OF MONOAMINE OXIDASES, Biochemical pharmacology, 47(12), 1994, pp. 2307-2310
A number of unsubstituted aromatic hydrocarbons, azaheterocycles, oxah
eterocycles and cyclic ketones were screened for their inhibitory pote
ncy towards monoamine oxidases (MAO; EC 1.4.3.4.) A and B. Fair activi
ties (IC50 10-100 mu M) and selectivities were found for, e.g. naphtha
lene, anthracene, phenanthrene, isoquinoline and acridine. The most ac
tive inhibitors are oxygen-containing compounds (e.g. coumarin, flavon
e, dibenzofuran, xanthene, thioxanthone and acridone), with xanthone e
merging as a potent (IC50 0.8 mu M) and reversible MAO-A inhibitor. Al
l tested inhibitors seem to act in a reversible and time-independent m
anner.