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160162-42-5

中文名称 SR 11302
英文名称 SR 11302
CAS 160162-42-5
分子式 C26H32O2
分子量 376.53
MOL 文件 160162-42-5.mol
更新日期 2024/07/24 18:26:20
160162-42-5 结构式 160162-42-5 结构式

基本信息

中文别名
化合物SR 11302
英文别名
SR 11302
RQANARBNMTXCDM-DKOHIBGUSA-N
(E,E,Z,E)-3-Methyl-7-(4-methylphenyl)-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenoicacid
2,4,6,8-Nonatetraenoic acid, 3-methyl-7-(4-methylphenyl)-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6Z,8E)-

物理化学性质

沸点541.6±30.0 °C(Predicted)
密度1.048±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度溶于二甲基亚砜
酸度系数(pKa)4.67±0.33(Predicted)
形态结晶固体
颜色Light yellow to yellow
SR 11302价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/05/22HY-15870SR 11302160162-42-51 mg990元
2025/05/22HY-15870SR 11302
SR 11302
160162-42-55mg1800元
2025/05/22HY-15870SR 11302
SR 11302
160162-42-510mM * 1mLin DMSO1980元

常见问题列表

生物活性
SR 11302 是激活蛋白-1 (AP-1) 转录因子抑制剂。SR 11302 是一种类视黄醇,可特异性抑制 AP-1 活性,而不会激活视黄酸反应元件 (RARE) 的转录。
靶点

AP-1

体外研究

SR 11302 (SR11302) show strong anti-AP-1 activity with selective binding with RARα and RARγ, but not with RARβ and RXRα.
SR 11302 (SR-11302; 1 μM) inhibits AP-1 transcription factor activity and decreases aldosterone levels by 61.9% in hypoxia-treated cells.
SR 11302 (SR-11302; 2 µM; 48 hours) inhibits Helicobacter pylori ( H. pylori )-induced cell proliferation in adenocarcinoma gastric (AGS) cells.
SR 11302 (2 µM; 24 hours) inhibits H. pylori -induced expression of β-catenin and c-myc in AGS cells.

体内研究

SR 11302 (SR11302; low dose 0.5 mg/kg and high dose 1 mg/kg body weight; orally gavaged daily) treatment reduces the total vascular lesion number and lesion size in Vldlr -/- mice in a dose-dependent manner.

Animal Model: Vldlr -/- mice
Dosage: Low dose 0.5 mg/kg and high dose 1 mg/kg body weight
Administration: Orally gavaged daily from P5 to P15
Result: High-dose from P5 to P15 reduced the total vascular lesion number by 48% and decreased the lesion size by 40%, without detectable signs of toxicity in mice, including no change in body weight.
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