Ribaudo Giovanni, Memo Maurizio, Gianoncelli Alessandra
Department of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.
Pharmaceuticals (Basel). 2021 Jan 13;14(1):58. doi: 10.3390/ph14010058.
As life expectancy increases, dementia affects a growing number of people worldwide. Besides current treatments, phosphodiesterase 9 (PDE9) represents an alternative target for developing innovative small molecules to contrast neurodegeneration. PDE inhibition promotes neurotransmitter release, amelioration of microvascular dysfunction, and neuronal plasticity. This review will provide an update on natural and nature-inspired PDE9 inhibitors, with a focus on the structural features of PDE9 that encourage the development of isoform-selective ligands. The expression in the brain, the presence within its structure of a peculiar accessory pocket, the asymmetry between the two subunits composing the protein dimer, and the selectivity towards chiral species make PDE9 a suitable target to develop specific inhibitors. Additionally, the world of natural compounds is an ideal source for identifying novel, possibly asymmetric, scaffolds, and xanthines, flavonoids, neolignans, and their derivatives are currently being studied. In this review, the available literature data were interpreted and clarified, from a structural point of view, taking advantage of molecular modeling: 3D structures of ligand-target complexes were retrieved, or built, and discussed.
随着预期寿命的增加,痴呆症在全球影响着越来越多的人。除了现有的治疗方法外,磷酸二酯酶9(PDE9)是开发用于对抗神经退行性变的创新小分子的另一个靶点。PDE抑制可促进神经递质释放、改善微血管功能障碍和神经元可塑性。本综述将提供关于天然和天然灵感的PDE9抑制剂的最新信息,重点关注PDE9的结构特征,这些特征有助于开发亚型选择性配体。PDE9在大脑中的表达、其结构中独特辅助口袋的存在、构成蛋白质二聚体的两个亚基之间的不对称性以及对手性物种的选择性,使其成为开发特异性抑制剂的合适靶点。此外,天然化合物领域是识别新型、可能不对称的支架的理想来源,目前正在研究黄嘌呤、黄酮类化合物、新木脂素及其衍生物。在本综述中,利用分子建模从结构角度对现有文献数据进行了解释和阐明:检索、构建并讨论了配体-靶点复合物的3D结构。