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产品名称 | lipoxygenase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Zileuton | ✔ | 97% | |||||||||||||||||
Nordihydroguaiaretic acid | ✔ | 99%+ | |||||||||||||||||
MK-886 | ✔ | 99%+ | |||||||||||||||||
Esculetin | ✔ | 98% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | ThioLox is a competitive inhibitor of 15-lipoxygenase-1 (15-LOX-1) with a Ki of 3.30 μM, displaying anti-inflammatory and neuroprotective effects. It competes for the active site of 15-LOX-1, indicating a non-covalent interaction [1]. |
体内研究 | ThioLox, with a logP of 3, exhibits properties that are well-aligned with BBB permeability [1]. |
体外研究 | ThioLox demonstrates competitive inhibition, indicating a non-covalent interaction with the active site of 15-LOX-1 [1]. ThioLox (50 μM; 24 h) reduces expression of interleukins (IL-1β, IL-6, IL-8, IL-12b, TNFα, and iNOS) in precision-cut lung slices (PCLS) [1]. ThioLox (10 μM; 16 hours) inhibits both lipid peroxidation and mitochondrial superoxide formation in neuronal cells [1]. ThioLox protects HT-22 cells from glutamate toxicity and significantly reduces neuronal cell death at concentrations of 5-20 μM over 14-16 hours [1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.64mL 0.73mL 0.36mL |
18.22mL 3.64mL 1.82mL |
36.45mL 7.29mL 3.64mL |
CAS号 | 1202193-89-2 |
分子式 | C15H18N2OS |
分子量 | 274.381 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,2-8°C |
溶解度 |
DMSO: 105 mg/mL(382.68 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |