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Atraric acid

(Synonyms: Methyl atrarate)
目录号: PC58679 纯度: ≥99%
Atraric acid (Methyl atrarate) 是一种特异的雄激素受体 (androgen receptor) 拮抗剂,具有抗炎和抗癌作用。Atraric acid 抑制 LNCaP 和 C4-2 细胞中内源性前列腺特异性抗原基因的表达。Atraric acid 还能抑制 NO 和细胞因子的合成,抑制 MAPK-NFκB 信号通路。Atraric acid 可用于前列腺疾病和炎症性疾病的研究。Atraric acid (Methyl atrarate) 是一种特异的雄激素受体 (androgen receptor) 拮抗剂,具有抗炎和抗癌作用。Atraric acid 抑制 LNCaP 和 C4-2 细胞中内源性前列腺特异性抗原基因的表达。Atraric acid 还能抑制 NO 和细胞因子的合成,抑制 MAPK-NFκB 信号通路。Atraric acid 可用于前列腺疾病和炎症性疾病的研究。
CAS No. :4707-47-5
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PC58679-100mg 100mg ¥259.00 请登录
PC58679-500mg 500mg ¥432.00 请登录
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中文名称
Atraric acid
中文别名
2,4-二羟基-3,6-二甲基苯甲酸甲酯;橡苔;阿彻瑞酸;甲基2,4-二羟基-3,6-二苯甲酸乙酯;2,4-二羟基-3,6-三甲基苯甲酸甲酯,橡苔;EVERNYL 2,4-二羟基-3,6-二甲基苯甲酸甲酯;二羟基二甲基苯甲酸甲酯
英文名称
Atraric acid
英文别名
Methyl 2,4-dihydroxy-3,6-dimethylbenzoate;Methyl atratate;Atraric acid;Benzoic acid,2,4-dihydroxy-3,6-dimethyl-, methyl ester;Veramoss;Methyl 3,6-dimethylresorcylate;Methyl .beta.-orcinolcarboxylate;[ "" ]
Cas No.
4707-47-5
分子式
C10H12O4
分子量
196.20
包装储存
4°C, stored under nitrogen;*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen);
详情描述
Atraric acid (Methyl atrarate) 是一种特异的雄激素受体 (androgen receptor) 拮抗剂,具有抗炎和抗癌作用。Atraric acid 抑制 LNCaP 和 C4-2 细胞中内源性前列腺特异性抗原基因的表达。Atraric acid 还能抑制 NO 和细胞因子的合成,抑制 MAPK-NFκB 信号通路。Atraric acid 可用于前列腺疾病和炎症性疾病的研究。Atraric acid (Methyl atrarate) 是一种特异的雄激素受体 (androgen receptor) 拮抗剂,具有抗炎和抗癌作用。Atraric acid 抑制 LNCaP 和 C4-2 细胞中内源性前列腺特异性抗原基因的表达。Atraric acid 还能抑制 NO 和细胞因子的合成,抑制 MAPK-NFκB 信号通路。Atraric acid 可用于前列腺疾病和炎症性疾病的研究。
生物活性
Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases.
性状
Solid
IC50 & Target[1][2]
Androgen receptor, NO synthesis, MAPK-NFκB pathway
体外研究(In Vitro)
Atraric acid (10 μM; CV1 cells) represses the transactivation function mediated by Dihydrotestosterone-induced human AR.
Atraric acid (10 μM; PCa cells) inhibits the expression of the PSA gene in both androgen-dependent and androgen-independent PCa cells.
Atraric acid (1-300 μM; 24 h) dose-dependently inhibits pro-inflammatory cytokine, nitric oxide, prostaglandin E2 in LPS-stimulated RAW264.7 cells, but does not influence the cell viability.
Atraric acid (100 and 300 μM; 18 h or 4 h) downregulates the expression of phosphorylated IκB, extracellular signal-regulated kinases (ERK) and nuclear factor kappa B (NFκB) signaling pathway to exhibit anti-inflammatory effects in LPS-stimulated RAW264.7 cells.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Atraric acid (10, 30 mg/kg; i.p.; single dosage) inhibits the production of pro-inflammatory cytokines and reduces pathological damages in LPS-induced endotoxin shock mice.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
运输条件
Room temperature or refrigerated transport.
储存方式
4°C, stored under nitrogen;*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen);
结构分类
Phenols
来源
Plants
溶解度数据
体外研究:
DMSO : 100 mg/mL(509.68 mM;Need ultrasonic)
配制储存液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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