ML339 is a selective CXCR6 antagonist with an IC 50 of 140 nM. ML339 antagonizes β-arrestin recruitment and cAMP signaling pathway of human CXCR6 receptor induced by CXCL16, with IC 50 of 0.3 μM and 1.4 μM, respectively. ML339 shows weaker activity against the recruitment of β-arrestin in mouse CXCR6 receptors, with an IC 50 of 18 μM. ML339 has no inhibitory effect on CXCR5 , CXCR4 , CXCR6 and apelin receptor (APJ) , with IC 50 >79 μM. ML339 has the potential to promote the development of prostate cancer research.
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