SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 6, 2013, Pages 956-966

MAO Inhibitory Activity of 2-Arylbenzofurans versus 3-Arylcoumarins: Synthesis, invitro Study, and Docking Calculations

(13) Ferino, Giulio a Cadoni, Enzo a Matos, Maria João b Quezada, Elias b Uriarte, Eugenio b Santana, Lourdes b Vilar, Santiago c Tatonetti, Nicholas P c Yáñez, Matilde d Viña, Dolores d Picciau, Carmen e Serra, Silvia e Delogu, Giovanna e

a University of Cagiari (Italy)

b UNIVERSITY OF SANTIAGO DE COMPOSTELA (Spain)

c Department of Medicine (United States)

d Universidade de Santiago de Compostela and Instituto de Investigación Sanitaria de Santiago de Compostela (Spain)

e UNIVERSITY OF CAGLIARI (Italy)

Author keywords

2 arylbenzofurans; 3 arylcoumarins; Docking; Inhibitors; Monoamine oxidase; Reversibility

Indexed keywords

3 (4' METHOXYPHENYL) 6 NITRO COUMARIN; 3 PHENYLCOUMARIN; 5 NITRO 2 (4 METHOXYPHENYL)BENZOFURAN; BENZOFURAN DERIVATIVE; COUMARIN DERIVATIVE; MONOAMINE OXIDASE B INHIBITOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING SITE; COMPARATIVE STUDY; CONTROLLED STUDY; CRYSTAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME INHIBITOR INTERACTION; IC 50; IN VITRO STUDY; INSECT CELL; MASS SPECTROMETRY; MOLECULAR DOCKING; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN TARGETING; WITTIG REACTION;

BENZOFURANS; COUMARINS; DOSE-RESPONSE RELATIONSHIP, DRUG; ENZYME INHIBITORS; HUMANS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; MONOAMINE OXIDASE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84878358843 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.201300048 Document Type: Article

Times cited : (46)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.