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苯并咪唑类作为 NOD2 拮抗剂的结构特征和功能活性。

Structural features and functional activities of benzimidazoles as NOD2 antagonists.

机构信息

Faculty of Pharmacy, University of Ljubljana, Aškerčeva 7, 1000, Ljubljana, Slovenia.

Laboratory of Toxicology, Department of Environmental Science and Policy, University of Milan, Via Balzaretti 9, 20133, Milan, Italy.

出版信息

Eur J Med Chem. 2020 Mar 15;190:112089. doi: 10.1016/j.ejmech.2020.112089. Epub 2020 Jan 24.

Abstract

NOD1 and NOD2 are pattern recognition receptors that have important roles in innate immune responses. Although their overactivation has been linked to a number of diseases, NOD2 in particular remains a virtually unexploited target in this respect, with only one structural class of antagonist reported. To gain insight into the structure-activity relationships of NOD2 antagonists, a series of novel analogs was designed and synthesized, and then screened for antagonist activity versus NOD2, and counter-screened versus NOD1. Compounds 32 and 38 were identified as potent and moderately selective NOD2 antagonists, and 33 and 42 as dual NOD1/NOD2 antagonists, with balanced activities against both targets in the low micromolar range. These data enable in-depth exploration of their structure-activity relationships and provide deeper understanding of the structural features required for NOD2 antagonism.

摘要

NOD1 和 NOD2 是模式识别受体,在先天免疫反应中具有重要作用。虽然它们的过度激活与许多疾病有关,但 NOD2 在这方面仍然是一个几乎未被开发的靶点,仅报道了一种结构类型的拮抗剂。为了深入了解 NOD2 拮抗剂的结构-活性关系,设计并合成了一系列新型类似物,然后对其针对 NOD2 的拮抗剂活性进行筛选,并针对 NOD1 进行反向筛选。化合物 32 和 38 被鉴定为强效且中度选择性的 NOD2 拮抗剂,而化合物 33 和 42 则为 NOD1/NOD2 双重拮抗剂,对两个靶点的活性在低微摩尔范围内平衡。这些数据使我们能够深入探索它们的结构-活性关系,并深入了解 NOD2 拮抗作用所需的结构特征。

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