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Salicylic acid水杨酸,69-72-7

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  • ¥400 - 600
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-B0167
  • 2025年12月06日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, protect from light

    • 英文名

      2-Hydroxybenzoic acid

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      69-72-7

    • 规格

      10 mM * 1 mL/500 mg/10 g/50 g

    规格:10 mM * 1 mL产品价格:¥500.0
    规格:500 mg产品价格:¥400.0
    规格:10 g产品价格:¥500.0
    规格:50 g产品价格:¥600.0

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    Salicylic acid

    CAS No. : 69-72-7

    MCE 国际站:Salicylic acid

    产品活性:Salicylic acid (2-Hydroxybenzoic acid) 抑制 COX-2 活性,抑制作用与转录因子 (NF-κB) 激活无关。

    研究领域:Immunology/Inflammation | Autophagy | Apoptosis | Metabolic Enzyme/Protease

    作用靶点:COX | Autophagy | Mitophagy | Apoptosis | Endogenous Metabolite

    结构分类:酚类 | 单酚类 | 酮、醛、酸

    来源:植物 | 其他科

    In Vitro: Salicylic acid is an effective inhibitor of COX-2 activity at concentrations far below those required to inhibit NF-κB (20 mg/mL) activation. Salicylic acid inhibits prostaglandin E2 release when add together with interleukin 1β for 24 hr with an IC50 value of 5 μg/mL, an effect that is independent of NF-κB activation or COX-2 transcription or translation. Salicylic acid acutely (30 min) also causes a concentration-dependent inhibition of COX-2 activity measured in the presence of 0, 1, or 10 μM exogenous arachidonic acid. In contrast, when exogenous arachidonic acid is increased to 30 μM, Salicylic acid is a very weak inhibitor of COX-2 activity with an IC50 of >100 μg/mL. When added together with IL-1β for 24 hr, Salicylic acid causes a concentration-dependent inhibition of PGE2 release with an apparent IC50 value of approximately 5 μg/mL. The ability of Salicylic acid to directly inhibit COX-2 activity in A549 cells is tested after a 30-min exposure period, followed by the addition of different concentrations of exogenous arachidonic acid (1, 10, and 30 μM). Salicylic acid causes a concentration-dependent inhibition of COX-2 activity in the absence of added arachidonic acid or in the presence of 1 or 10 μM exogenous substrate with an apparent IC50 value of approximately 5 μg/mL. However, when the same experiments are performed using 30 μM arachidonic acid, Salicylic acid is an ineffective inhibitor of COX-2 activity, with an apparent IC50 value of more than 100 μg/mL, and achieves a maximal inhibition of less than 50%.

    In Vivo: In C57Bl/6 DIO mice, Salicylic acid decreases both fasting and postprandial plasma glucose levels. Furthermore, there is a trend to reduce plasma triglyceride levels after Salicylic acid treatment in C57Bl/6 DIO mice (P=0.059). Salicylic acid significantly reduces 11β-HSD1 mRNA in omental adipose tissue in C57Bl/6 DIO mice, with a similar trend in mesenteric adipose (P=0.057). In mesenteric adipose of C57Bl/6 DIO mice, Salicylic acid also reduces 11β-HSD1 enzyme activity.

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