Chemical Structure : PB151
货号: PC-28552Not For Human Use, Lab Use Only.
PB151 is a highly potent and isoform-selective HDAC11 inhibitor with IC50 of 59 nM, displays > 172-fold selectivity margin over all other class I, IIa, and IIb HDAC isoforms.
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
PB151 is a highly potent and isoform-selective HDAC11 inhibitor with IC50 of 59 nM, displays > 172-fold selectivity margin over all other class I, IIa, and IIb HDAC isoforms.
PB151 selectively engages HDAC11 in cells and inhibits its intracellular defatty-acylase activity.
PB151 suppresses HCC proliferation and induces apoptosis, inhibiting the growth of HepG2, MHCC97-L, and HuH-7 cells with IC50 values of 5.50 uM, 7.08 uM, and 6.67 uM respectively (72 h of exposure).
PB151 (30 mg/kg once daily, i.p.) suppresses tumor progression in an endogenous orthotopic HCC model.
PB151 treatment improves liver histology and downregulates Ki67 expression in orthotopic hepatocellular carcinoma model.
PB151 treatment alters fatty acid metabolism and reduces lipid accumulation in hepatocellular carcinoma.
PB151 restricts lipogenesis via activation of the LKB1-AMPK signaling axis.
| 分子量 | 515.65 | |
| 分子式 | C31H37N3O4 | |
| 外观性状 | Solid | |
| 储存条件 |
|
|
| Solubility |
10 mM in DMSO |
|
1. Wang W, et al. Eur J Med Chem. 2026 Oct 19;321(Pt 2):119430.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright