Calcium channel antagonists discovered by a multidisciplinary approach

被引:61
作者
Carosati, Emanuele
Cruciani, Gabriele
Chiarini, Alberto
Budriesi, Roberta
Ioan, Pierfranco
Spisani, Raffaella
Spinelli, Domenico
Cosimelli, Barbara
Fusi, Fabio
Frosini, Maria
Matucci, Rosanna
Gasparrini, Francesco
Ciogli, Alessia
Stephens, Philip J.
Devlin, Frank J.
机构
[1] Univ Perugia, Dipartimento Chim, I-06123 Perugia, Italy
[2] Univ Bologna, Dipartimento Sci Farmaceut, I-40126 Bologna, Italy
[3] Univ Bologna, Dipartimento Chim Organ A Mangini, I-40126 Bologna, Italy
[4] Univ Naples Federico II, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy
[5] Univ Siena, Dipartimento Sci Biomed, I-53100 Siena, Italy
[6] Univ Florence, Dipartimento Farmacol Preclin & Clin, I-50139 Florence, Italy
[7] Univ Roma La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biol At, I-00185 Rome, Italy
[8] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
关键词
D O I
10.1021/jm0604373
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A multidisciplinary project has led to the discovery of novel, structurally diverse, L-type calcium entry blockers (CEBs). The absolute configuration of a recently reported CEB has been determined by vibrational circular dichroism spectroscopy, to assign the stereospecificity of the ligand-channel interaction. Thereafter, a virtual screening procedure was performed with the aim of identifying novel chemotypes for CEBs, starting from a database of purchasable compounds; 340 000 molecules were screened in silico in order to prioritize structures of interest for bioscreening. As a result, 20 compounds were tested in vitro, and functional and binding assays revealed several hits with promising behavior as CEBs.
引用
收藏
页码:5206 / 5216
页数:11
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