XAX-162 is a highly selective sphingosine 1-phosphate receptor 2 (S1PR2) agonist with a human EC50 of 0.55 µM. XAX-162 does not activate other S1P receptors. XAX-162 exhibits noncompetitive inhibition of activity by S1PR2 antagonist JTE-013 (HY-100675)[1].
Molecular Weight:
349.49
CAS Number:
[883053-48-3]
Formula:
C16H15NO2S3
Target:
LPL Receptor
Application Notes:
MCE Product type: Reference compound
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