Chemical Structure : PFM046
货号: PC-23680Not For Human Use, Lab Use Only.
PFM046 is a potent antagonist of liver X receptors (LXRs) with IC50 of 2.04 μM for LXRα and 1.58 μM for LXRβ.
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PFM046 is a potent antagonist of liver X receptors (LXRs) with IC50 of 2.04 μM for LXRα and 1.58 μM for LXRβ.
PFM046 does not induce SREBP-1c activation and inhibited the activation of SCD1 and FASN.
PFM046 is able to significantly increase the expression of ABCA1 gene.
PFM046 shows a remarkable antitumor activity in two both in vitro-and in-vivo mouse models.
分子量 | 422.65 | |
分子式 | C29H42O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Lorenzo Pontini, et al. Eur J Med Chem. 2025 Feb 5:283:117136.
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