Chemical Structure : IACS-9439
货号: PC-24734Not For Human Use, Lab Use Only.
IACS-9439 is a potent, highly selective, and orally bioavailable CSF1R inhibitor with IC50 of 1.7 nM, and cellular IC50 of 7 nM in the MNSF-60 cell phenotypical assay.
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
IACS-9439 is a potent, highly selective, and orally bioavailable CSF1R inhibitor with IC50 of 1.7 nM, and cellular IC50 of 7 nM in the MNSF-60 cell phenotypical assay.
IACS-9439 is high selective against a panel of kinases (ScanEdge, 97-member kinase panel, DiscoverX) at 1 uM.
IACS-9439 has IC50 of 17 in pCSF1R cellular target engagement assay.
IACS-9439 depletes tumor macrophages, promotes M1 macrophage, and inhibits tumor growth.
分子量 | 516.02 | |
分子式 | C23H26ClN7O3S | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Barbara Czako, et al. J Med Chem. 2020 Sep 10;63(17):9888-9911.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright