ML355

ML355是一高效、选择性12-LOX抑制剂,IC50值为0.34uM,对其他脂氧化酶和环氧化酶有很好的选择性,具有较好的药物动力学特征。

信号通路 >> 代谢酶/蛋白酶 >> 5脂氧合酶

研究领域 >> 炎症/免疫

[1]. Luci DK, et al. Synthesis and structure-activity relationship studies of 4-((2-hydroxy-3-methoxybenzyl)amino)benzenesulfonamide derivatives as potent and selective inhibitors of 12-lipoxygenase. J Med Chem. 2014 Jan 23;57(2):495-506.

[2]. Zhang XJ, et al. An ALOX12-12-HETE-GPR31 signaling axis is a key mediator of hepatic ischemia-reperfusion injury. Nat Med. 2018 Jan;24(1):73-83.

U型73122 | 齐留通 | 去甲二氢愈创木酸 | 靛玉红-3'-单肟 | 咖啡酸 | 异紫花前胡内酯 | 马洛替酯 | 5,4'-二羟基黄酮 | 依那扎群 | LY 178002 | RWJ 63556 | S-2474 | 1-ethyl-3-(4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)-5,5-dimethyl-2-thioxoimidazolidin-4-one | N-1-(Fur-3-ylethyl)-N-hydroxyurea | AZD 4407