Chemical Structure : HEC72702
货号: PC-63328Not For Human Use, Lab Use Only.
HEC72702 is a novel potent, orally active inhibitor of HBV capsid assembly, inhibits HBV-DNA levels in HepG.2.2.15 cells with IC50 of 39 nM.
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
HEC72702 is a novel potent, orally active inhibitor of HBV capsid assembly, inhibits HBV-DNA levels in HepG.2.2.15 cells with IC50 of 39 nM.
HEC72702 displays no induction of the CYP1A2, CYP3A4, or CYP2B6 enzyme at 10 uM.
HEC72702 demonstrates a good systemic exposure and high oral bioavailability and achieves a viral-load reduction greater than 2 log in a hydrodynamic-injected (HDI) HBV mouse model.
分子量 | 581.457 | |
分子式 | C24H26BrFN4O5S | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Ren Q, et al. J Med Chem. 2018 Feb 8;61(3):1355-1374.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright