CID16020046 has been used as an antagonist of G-protein coupled receptor (GPR55) to test its effect on nociceptive behavior in rats induced with formalin.[1]
Biochem./physiol. Wirkung
CID16020046 is a potent and a selective GPR55 antagonist that inhibits GPR55-mediated ERK1/2 phosphorylation. CID16020046 inhibits LPI-induced Ca2+ signaling in HEK-GPR55 cells.
CID16020046 is a potent and a selective GPR55 antagonist.
The G-protein coupled receptor, GPR55, modulates nociceptive processing. Given the expression of GPR55 in the anterior cingulate cortex (ACC), a key brain region involved in the cognitive and affective dimensions of pain, the present study tested the hypothesis that GPR55
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