SPD304 is a selective TNF-α inhibitor, which promotes dissociation of TNF trimers and therefore blocks the interaction of TNF and its receptor. SPD304 has an IC50 of 22 µM for inhibiting in vitro TNF receptor 1 (TNFR1) binding to TNF-α.
IC50&Target
IC50: 22 µM (TNFα).
体外研究
SPD304 (2 μM) significantly rescues the survivability of aHSCs, reduces the production of lipid hydroxides, and increased intracellular GSH. The co-treatment of GA (75 μM) and SPD304 (2 μM), down-regulate TRADD almost 2-fold (w/o inhibitor vs. w/ inhibitor) and p−RIP3 1.4−fold compared to GA alone, and promotes caspase 8 activation.
体内研究
SPD304 cannot be used in vivo due to its high toxicity.
分子式
C32H32F3N3O2
分子量
547.61
CAS号
869998-49-2
运输条件
Room temperature in continental US; may vary elsewhere.