BW-A 78U is a PDE4 inhibitor with an IC 50 of 3 μM.
性状
Solid
IC50 & Target[1][2]
PDE4 3 μM (IC50)
体外研究(In Vitro)
BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM. BW-A 78U fails to significantly inhibit arachidonate release. BW-A 78U is ineffective to inhibit the lipopolysaccharide (LPS)-induced TNF-α release. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Boichot E, et al. Anti-inflammatory activities of a new series of selective phosphodiesterase 4 inhibitors derivedfrom 9-benzyladenine. J Pharmacol Exp Ther. 2000 Feb;292(2):647-53.
溶解度数据
In Vitro: DMSO : 150 mg/mL (583.05 mM; Need ultrasonic)配制储备液