GtoPdb v.2023.1中的GPR18, GPR55和GPR119

Stephen P. H. Alexander, A. Irving
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引用次数: 0

摘要

GPR18、GPR55和GPR119(临时命名)虽然与CB1和CB2大麻素受体在结构上没有什么相似之处,但它们对类似于内源性大麻素配体的内源性药物以及一些天然/合成大麻素受体配体有反应[104]。虽然有多篇报道表明GPR18、GPR55和GPR119分别可以在体外被n -花生四烯醇酰甘氨酸、溶磷脂酰肌醇和n -油基乙醇酰胺激活,但在体内缺乏这些脂质信使激活的证据。因此,这些受体保持孤儿状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GPR18, GPR55 and GPR119 in GtoPdb v.2023.1
GPR18, GPR55 and GPR119 (provisional nomenclature), although showing little structural similarity to CB1 and CB2 cannabinoid receptors, respond to endogenous agents analogous to the endogenous cannabinoid ligands, as well as some natural/synthetic cannabinoid receptor ligands [104]. Although there are multiple reports to indicate that GPR18, GPR55 and GPR119 can be activated in vitro by N-arachidonoylglycine, lysophosphatidylinositol and N-oleoylethanolamide, respectively, there is a lack of evidence for activation by these lipid messengers in vivo. As such, therefore, these receptors retain their orphan status.
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