SCOPUS 정보 검색 플랫폼

Volumn 7, Issue 3, 2012, Pages 464-470

8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies

(8) Viña, Dolores c Matos, Maria J a,c Ferino, Giulio b Cadoni, Enzo b Laguna, Reyes c Borges, Fernanda a Uriarte, Eugenio c Santana, Lourdes c

a UNIVERSITY OF PORTO (Portugal)

b UNIVERSITY OF CAGLIARI (Italy)

c UNIVERSITY OF SANTIAGO DE COMPOSTELA (Spain)

Author keywords

Coumarins; Heterocycles; Molecular modeling; Monoamine oxidase; Perkin reaction

Indexed keywords

3 (4' BROMOPHENYL) 8 METHOXYCOUMARIN; 3 (4' BROMOPHENYL) 8 METHYLCOUMARIN; 3 (4' METHOXYPHENYL) 8 METHYLCOUMARIN; 3 (4' METHYLPHENYL) 8 METHYLCOUMARIN; 3 ARYLCOUMARIN; 8 ETHOXY 3 (4' METHOXYPHENYL)COUMARIN; 8 ETHOXY 3 (4' METHYLPHENYL)COUMARIN; 8 ETHOXY 3 PHENYLCOUMARIN; AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B; COUMARIN DERIVATIVE; MONOAMINE OXIDASE B INHIBITOR; SELEGILINE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; CRYSTAL STRUCTURE; DRUG POTENCY; DRUG SCREENING; DRUG SELECTIVITY; DRUG SYNTHESIS; ENZYME INHIBITOR INTERACTION; IN VITRO STUDY; MOLECULAR DOCKING; NONHUMAN; PRIORITY JOURNAL;

ALZHEIMER DISEASE; COUMARINS; HUMANS; MODELS, MOLECULAR; MONOAMINE OXIDASE; MONOAMINE OXIDASE INHIBITORS; PARKINSON DISEASE; PROTEIN BINDING; PROTEIN ISOFORMS; SELEGILINE; SOLUTIONS;

EID: 84857718412 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.201100538 Document Type: Article

Times cited : (59)

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