Synthesis and in silico screening of a library of β-carboline-containing compounds

被引:9
作者
Brummond, Kay M. [1 ]
Goodell, John R. [1 ]
LaPorte, Matthew G. [1 ]
Wang, Lirong [2 ,3 ,4 ,5 ]
Xie, Xiang-Qun [2 ,3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Dept Chem Chem Methodol & Lib Dev, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Sch Pharm, Computat Chem Genom Ctr, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Drug Discovery Inst, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Dept Computat Biol, Pittsburgh, PA 15260 USA
关键词
beta-carboline; biological activity; chemical diversity; diversity-oriented synthesis; in silico screening; DRUG DISCOVERY; SEARCH; ANTAGONISTS; INHIBITORS; MOLECULES; DOCKING; POTENT;
D O I
10.3762/bjoc.8.117
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of a library of tetrahydro- beta-carboline-containing compounds in milligram quantities is described. Among the unique heterocyclic frameworks are twelve tetrahydroindolizinoindoles, six tetrahydrocyclobutanindoloquinolizinones and three tetrahydrocyclopentenoneindolizinoindolones. These compounds were selected from a virtual combinatorial library of 11,478 compounds. Physical chemical properties were calculated and most of them are in accordance with Lipinski's rules. Virtual docking and ligand-based target evaluations were performed for the beta-carboline library compounds and selected synthetic intermediates to assess the therapeutic potential of these small organic molecules. These compounds have been deposited into the NIH Molecular Repository (MLSMR) and may target proteins such as histone deacetylase 4, endothelial nitric oxide synthase, 5-hydroxytryptamine receptor 6 and mitogen-activated protein kinase 1. These in silico screening results aim to add value to the beta-carboline library of compounds for those interested in probes of these targets.
引用
收藏
页码:1048 / 1058
页数:11
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