大麻素受体
大麻素
化学
体外
酶
生物化学
受体
合成大麻素
兴奋剂
作者
Michael F. Santillo,Isabella Glenn,Lu Paris,Robert L. Sprando
标识
DOI:10.1021/acs.jnatprod.4c00608
摘要
There is limited information on interactions between cannabinoids and many pharmacologically and toxicologically relevant targets in humans (e.g., receptors, ion channels, enzymes, and transporters). To address this data gap, seven cannabinoids were screened against a panel of 44 safety-related biological targets in competitive ligand binding or enzymatic activity assays. Diverse binding profiles were observed among the cannabinoids; however, colloidal aggregates were detected by dynamic light scattering and a detergent-sensitive enzyme inhibition assay. These aggregates may nonspecifically inhibit targets, yielding false positives. Although screening identified aggregates, additional testing is required to confirm cannabinoid aggregation in individual
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