BMS-986020 (AM152) is a high-affinity and selective lysophosphatidic acid receptor 1 (LPA1) antagonist[1]. BMS-986020 inhibits bile acid and phospholipid transporters with IC50s of 4.8 µM, 6.2 µM, and 7.5 µM for BSEP, MRP4, and MDR3, respectively[2]. BMS
Molecular Weight:
482.53
Purity:
99.91
CAS Number:
[1257213-50-5]
Formula:
C29H26N2O5
Target:
LPL Receptor
Application Notes:
Reference compound
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