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Papers of the Week


Papers: 30 Jul 2022 - 5 Aug 2022


Pharmacology/Drug Development


2022 Jul 06


RSC Adv


12


31

Selectivity profile comparison for certain γ-butyrolactone and oxazolidinone-based ligands on a sigma 2 receptor over sigma 1: a molecular docking approach.

Authors

Abstract

Sigma receptors (σ R and σ R) are pharmacologically characterized membrane-bound receptors that bind a wide range of chemical compounds. Alzheimer's disease, traumatic brain injury, schizophrenia, and neuropathic pain have all been associated with abnormal σ activity. The σ receptor has recently been identified as a potential therapeutic target for inhibiting the formation of amyloid plaques. Numerous laboratories are now investigating the potential of σ ligands. Small molecule discovery is the focus of current research, with the goal of using target-based action to treat a variety of illnesses and ailments. Functionalized γ-butyrolactone and oxazolidinone-based ligands, in particular, are pharmacologically important scaffolds in drug discovery research and have been thoroughly examined for σ receptor efficacy. The purpose of this study was to evaluate the pharmacophoric features of different σ receptor ligands using techniques. This study used a library of 58 compounds having a γ-butyrolactone and oxazolidinone core. To investigate the binding characteristics of the ligands with the σ receptor, a 3D homology model was developed. To understand the binding pattern of the γ-butyrolactone and oxazolidinone based ligands, molecular docking studies were performed on both σ and σ receptors. Furthermore, MM/GBSA binding energy calculations were used to confirm the binding of ligands on the σ over σ receptor. These findings will aid in the discovery of selective σ ligands with good pharmacophoric properties and potency in the future.