CJ-13,610 是一种具有口服活性的非氧化还原型 5-脂氧合酶 (5-LOX) 抑制剂。 CJ-13,610 抑制白三烯 B4 的生物合成并调节巨噬细胞中 IL-6 mRNA 的表达。

CJ-13,610 is an orally active and nonredox-type inhibitor of 5-lipoxygenase (5-LOX). CJ-13,610 inhibits the biosynthesis of leukotriene B4 and regulates the expression of IL-6 mRNA in macrophages.

CJ-13,610 dose-dependently suppresses 5-LOX product formation in ionophore A23187-stimulated polymorphonuclear in the absence of exogenous arachidonic acid with an IC50 of about 70 nM[1].

179420-17-8

C22H23N3O2S

393.5

CJ-13610;CJ 13610

(< 1 mg/ml refers to the product slightly soluble or insoluble )
Powder: -20°C for 3 years
In solvent: -80°C for 2 years