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基于药效团的新型胞质型磷脂酶 A2α抑制剂的发现。

Pharmacophore-based discovery of a novel cytosolic phospholipase A(2)α inhibitor.

机构信息

Institute of Pharmacy/Pharmaceutical Chemistry, Computer-Aided Molecular Design (CAMD) Group and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innrain 80/82, AT-6020 Innsbruck, Austria.

出版信息

Bioorg Med Chem Lett. 2012 Jan 15;22(2):1202-7. doi: 10.1016/j.bmcl.2011.11.093. Epub 2011 Nov 30.

Abstract

The release of arachidonic acid, a precursor in the production of prostaglandins and leukotrienes, is achieved by activity of the cytosolic phospholipase A(2)α (cPLA(2)α). Signaling mediated by this class of bioactive lipids, which are collectively referred to as eicosanoids, has numerous effects in physiological and pathological processes. Herein, we report the development of a ligand-based pharmacophore model and pharmacophore-based virtual screening of the National Cancer Institute (NCI) database, leading to the identification of 4-(hexadecyloxy)-3-(2-(hydroxyimino)-3-oxobutanamido)benzoic acid (NSC 119957) as cPLA(2)α inhibitor in cell-free and cell-based in vitro assays.

摘要

花生四烯酸的释放,是前列腺素和白三烯生成的前体,通过胞质型磷脂酶 A(2)α(cPLA(2)α)的活性来实现。由这一类生物活性脂质介导的信号转导,通常被称为类二十烷酸,在生理和病理过程中具有多种作用。在此,我们报告了基于配体的药效团模型的开发和国家癌症研究所(NCI)数据库的药效团筛选,导致 4-(十六烷氧基)-3-(2-(羟亚氨基)-3-氧代丁酰胺基)苯甲酸(NSC 119957)作为细胞游离和基于细胞的体外测定中 cPLA(2)α抑制剂的鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/097b/3268354/c13750d8b456/fx1.jpg

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