Malotilate is hepatotrophic drug which can selectively inhibit the 5-lipoxygenase, whereas both the 12- and the 15-lipoxygenase pathways were stimulated, with antifibrotic and hepatoprotective properties.
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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 | Malotilate is a hepatoprotective agent that selectively inhibits 5-lipoxygenase with an IC50 value of 4.7μM[3]. Malotilate at concentrations of 0.1 – 100μM increased collagenase secretion in the multilayered cultures of normal human dermal fibroblasts, but not in the monolayers[4]. Pretreatment of rat lung endothelial (RLE) cells with malotilate (10 and 20ng/mL) for 24 h markedly inhibited the invasion of the RLE monolayer by c-SST-2 cells. In SHR rats inoculated with c-SST-2 tumors, administration with malotilate (300mg/kg/day), which started 7 days before or after c-SST-2 cell inoculation, significantly suppressed pulmonary metastatic compared with non-treated or vehicle control rats[5]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.47mL 0.69mL 0.35mL |
17.34mL 3.47mL 1.73mL |
34.68mL 6.94mL 3.47mL |
CAS号 | 59937-28-9 |
分子式 | C12H16O4S2 |
分子量 | 288.38 |
别名 | NKK 105 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 105 mg/mL(364.1 mM),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 |