SCREENING OF UNSUBSTITUTED CYCLIC-COMPOUNDS AS INHIBITORS OF MONOAMINE OXIDASES

Authors
Citation
U. Thull et B. Testa, SCREENING OF UNSUBSTITUTED CYCLIC-COMPOUNDS AS INHIBITORS OF MONOAMINE OXIDASES, Biochemical pharmacology, 47(12), 1994, pp. 2307-2310
Citations number
20
Categorie Soggetti
Pharmacology & Pharmacy",Biology
Journal title
ISSN journal
00062952
Volume
47
Issue
12
Year of publication
1994
Pages
2307 - 2310
Database
ISI
SICI code
0006-2952(1994)47:12<2307:SOUCAI>2.0.ZU;2-P
Abstract
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.