Potent and selective PXR agonist. (EC50=200 nM for human PXR). A weak activator of rat and mouse PXR. Inhibits cholesterol biosynthesis in a number of species.
Molecular Weight:
504.5
Source:
Synthetic.
Purity:
98% (TLC)
CAS Number:
[126411-39-0]
Formula:
C24H42O7P2
Target:
PXR
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