GSK494581A is a selective ligand for the human GPR55 receptor, exhibiting a pEC50 value of 6.8, and serves as an inhibitor of glycine transporter subtype 1 (GlyT1). This compound is implicated in various biological processes, including the modulation of pain signaling, promotion of bone morphogenesis, and enhancement of vascular endothelial cell formation through its action on GPR55. Its specificity and dual activity make GSK494581A a valuable tool for research in pain management and vascular biology.
GSK494581A is a selective ligand for the human GPR55 receptor, exhibiting a pEC50 value of 6.8, and serves as an inhibitor of glycine transporter subtype 1 (GlyT1). This compound is implicated in various biological processes, including the modulation of pain signaling, promotion of bone morphogenesis, and enhancement of vascular endothelial cell formation through its action on GPR55. Its specificity and dual activity make GSK494581A a valuable tool for research in pain management and vascular biology.
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