Screening of unsubstituted cyclic compounds as inhibitors of monoamine oxidases

التفاصيل البيبلوغرافية
العنوان: Screening of unsubstituted cyclic compounds as inhibitors of monoamine oxidases
المؤلفون: Ulrike Thull, Bernard Testa
المصدر: Biochemical pharmacology. 47(12)
سنة النشر: 1994
مصطلحات موضوعية: Monoamine Oxidase Inhibitors, Stereochemistry, Xanthones, Drug Evaluation, Preclinical, Biochemistry, Rats, Sprague-Dawley, chemistry.chemical_compound, Structure-Activity Relationship, Xanthone, Animals, Isoquinoline, Pharmacology, chemistry.chemical_classification, Flavonoids, Cyclic compound, Brain, Thioxanthone, Mitochondria, Rats, Dibenzofuran, Acridone, chemistry, Xanthenes, Heterocyclic compound, Chromones, Drug Design, Acridine
الوصف: A number of unsubstituted aromatic hydrocarbons, azaheterocycles, oxaheterocycles and cyclic ketones were screened for their inhibitory potency towards monoamine oxidases (MAO; EC 1.4.3.4.) A and B. Fair activities (IC50 10-100 microM) and selectivities were found for, e.g. naphthalene, anthracene, phenanthrene, isoquinoline and acridine. The most active inhibitors are oxygen-containing compounds (e.g. coumarin, flavone, dibenzofuran, xanthene, thioxanthone and acridone), with xanthone emerging as a potent (IC50 0.8 microM) and reversible MAO-A inhibitor. All tested inhibitors seem to act in a reversible and time-independent manner.
تدمد: 0006-2952
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af1b231e10238b7654169bd4a9d866d5
https://pubmed.ncbi.nlm.nih.gov/8031326
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....af1b231e10238b7654169bd4a9d866d5
قاعدة البيانات: OpenAIRE