Design and discovery of tyrosinase inhibitors based on a coumarin scaffold

RSC Advances - Tập 5 Số 114 - Trang 94227-94235
María João Matos1,2,3,4,5, Carla Varela6,7,8,9,10, Santiago Vilar11,12,3,8,13, George Hripcsak14,12,15, Fernanda Borges1,2,16,4,5, Lourdes Santana11,3,8,13,17, Eugenio Uriarte11,3,8,13,17, Antonella Fais18,19,20,21, Amalia Di Petrillo18,19,20,21, Francesca Pintus18,19,20,21, Benedetta Era18,19,20,21
14169-007 Porto
2CIQUP/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal
3Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain
4Portugal
5University of Porto
63000-548 Coimbra
7CNC-IBILI, Pharmaceutical Chemistry Group, Faculty of Pharmacy, University of Coimbra,3000-548 Coimbra,Portugal
8Faculty of Pharmacy
9Pharmaceutical Chemistry Group
10University of Coimbra
1115782 Santiago de Compostela
12Department of Biomedical Informatics, Columbia University Medical Center, New York, NY 10032, USA
13Spain
14Columbia University Medical Center
15New York
16Faculty of Sciences
17University of Santiago de Compostela
1809042 Monserrato
19Department of Life Science and Environment, University of Cagliari, 09042 Monserrato, Cagliari, Italy
20Italy
21University of Cagliari

Tóm tắt

A novel series of 3-aryl and 3-heteroarylcoumarins displaying tyrosinase inhibitory activity.

Từ khóa


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