Eriocitrin and Apigenin as New Carbonic Anhydrase VA Inhibitors from a Virtual Screening of Calabrian Natural Products

被引:32
作者
Gidaro, Maria Concetta [1 ]
Alcaro, Francesca [1 ]
Carradori, Simone [2 ]
Costa, Giosue [1 ]
Vullo, Daniela [3 ]
Supuran, Claudiu T. [3 ]
Alcaro, Stefano [1 ]
机构
[1] Magna Graecia Univ Catanzaro, Dipartimento Sci Salute, I-88100 Catanzaro, Italy
[2] Univ Roma La Sapienza, Dipartimento Chim & Tecnol Farmaco, I-00185 Rome, Italy
[3] Univ Florence, Lab Chim Bioinorgan, Polo Sci, Florence, Italy
关键词
Citrus bergamia; Rutaceae; Allium cepa var; Tropea; Liliaceae; flavonoids; docking; structure-based virtual screening; human carbonic anhydrase inhibition; OF-THE-ART; THERAPEUTIC APPLICATIONS; IDENTIFICATION; FLAVONOIDS; BERGAMOT; TARGETS; DESIGN; LIGAND; ONIONS; TOOL;
D O I
10.1055/s-0034-1396139
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In this work, we performed a structure-based virtual screening against five carbonic anhydrase isoforms using, as a ligand library, natural components of Citrus bergamia (Bergamot) and Allium cepa var. Tropea (red onion) sources, which are some typical Calabrian products. The most relevant Bergamot and red onion components, identified as potentially new hits by means of the computational work, were submitted to in vitro tests in order to confirm the ability to exert the predicted biological activity. Apigenin and eriocitrin were identified as new potent inhibitors of human carbonic anhydrase VA isozyme.
引用
收藏
页码:533 / 540
页数:8
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