kaempferide
CAS No. 491-54-3
kaempferide ( Kaempferide )
产品货号. M18646 CAS No. 491-54-3
Kaempferide trigluside 通过一种不由配体结合依赖性雌激素受体激活介导的机制抑制天然和雌激素受体β过度表达的结肠癌细胞的增殖。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
100MG | ¥2349 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
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生物学信息
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产品名称kaempferide
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Kaempferide trigluside 通过一种不由配体结合依赖性雌激素受体激活介导的机制抑制天然和雌激素受体β过度表达的结肠癌细胞的增殖。
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产品描述Kaempferide triglycoside inhibits the proliferation of native and estrogen receptor beta overexpressing colon cancer cells through a mechanism not mediated by ligand binding dependent estrogen receptor activation.
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体外实验Western Blot Analysis Cell Line:HepG2Concentration:5 μM, 10 μM, 20 μM . Before treatment with OA (HY-N1446) (0.5 mM; 48 h)Incubation Time:48 h Result:Lowered the expression of proteins related to fat production, including sterol regulatory element-binding protein 1 (SREBP1), fatty acid synthase (FAS), and stearoyl-CoA desaturase 1 (SCD-1).Reduced the expression of two adipogenic transcription factors, peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT enhancer-binding protein β (C/EBPβ).Enhanced the expression of heme oxygenase-1 (HO-1) and nuclear factor erythroid 2-related factor 2 (Nrf2).
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体内实验Animal Model:High-fat diet male C57BL/6J mice modelDosage:10 mg/kg Administration:Supplemented in daily diet, once daily for16 weeksResult:Reduced the weight, organ weight, and index of mice.Lowered the levels of glycolipids in mouse serum.Decreased the expression levels of inflammatory-related genes, including NF-κB, IL-6, ICAM-1, VCAM-1, and TNF-α.Animal Model:Ischemia/Reperfusion (I/R) SD rat model.Dosage:0.1 mg/kg, 0.3 mg/kg, 3 mg/kg Administration:Injection, Single dose. Before the I/R injury induced by Coronary Artery Ligation (CAL) in SD rats.Result:Significantly improved heart function, reduced myocardial injury by reducing myocardial enzyme levels, and dose-dependently reduced the area of myocardial infarction in rats.Significantly decreased serum levels of TNF-α, IL-6, C-reactive protein (CRP), MDA, and ROS, while increasing serum levels of SOD.Downregulated the expression levels of nuclear factor erythroid 2-related factor 2 (Nrf2) and cleaved caspase-3, and upregulated the phosphorylation expression levels of phospho-Akt (p-Akt) and phospho-glycogen synthase kinase-3β (p-GSK-3β).
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同义词Kaempferide
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通路Others
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靶点Other Targets
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受体ER
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研究领域Others-Field
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适应症——
化学信息
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CAS Number491-54-3
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分子量300.27
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分子式C16H12O6
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纯度>98% (HPLC)
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溶解度DMSO : 20 mg/mL 66.61 mM;
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SMILESCOc1ccc(cc1)c1c(c(=O)c2c(cc(cc2o1)O)O)O
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化学全称3,5,7-trihydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Song P,et al. [Comparison of effects of kaempferide and anhydroicaritin on biomineralization of cultured osteoblasts]. Yao Xue Xue Bao. 2012 Jul;47(7):890-6.
产品手册
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