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Rhapontigenin (Synonyms: 丹叶大黄素) 纯度: 99.66%
Rhapontigenin 是白藜芦醇的天然类似物,具有抗癌,抗氧化剂,抗真菌和抗菌活性。 Rhapontigenin 是强效选择性细胞色素 P450 1A1 抑制剂 (IC50=400 nM)。Rhapontigenin 对 P450 1A1 的选择性分别是 P450 1A2 和 P450 1B1 的 400 和 23 倍。
Rhapontigenin Chemical Structure
CAS No. : 500-65-2
规格 | 价格 | 是否有货 | 数量 |
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5 mg | ¥1190 | In-stock | |
10 mg | ¥2020 | In-stock | |
20 mg | ¥3430 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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Rhapontigenin 相关产品
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生物活性 |
Rhapontigenin is a natural analog of resveratrol with anticancer, antioxidant, antifungal and antibacterial activities. Rhapontigenin is amechanism-based, potent and selective cytochrome P450 1A1 inactivator (IC50 = 400 nM). Rhapontigenin exhibits 400-fold and 23-fold selectivity for P450 1A1 over P450 1A2 and P450 1B1, respectively[1]. |
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IC50 & Target[1] |
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体外研究 (In Vitro) |
Rhapontigenin (0-250 μM; 24 hours) demonstrates concentration-dependent anti-cancer activity with an IC50 115μM in HEP G2 cells[1]. Rhapontigenin (20 μM; 20 hours) pre-treatment decreases TGF-β triggered increased snail expression in diverse cancer cells[2]. Rhapontigenin (0-20 μM; 6 hours) inhibits TGF-β-induced expression of N-cadherin, vimentin, and CA9 in a dose-dependent manner[2]. Rhapontigenin inhibits ADP- and collagen-induced platelet aggregation with IC50 values of 4 and 70 μg/ml, respectively[3]. Rhapontigenin demonstrates a strong inhibitory activity on the 13-hexosaminidase release induced by DNP-BSA, it exhibits IC50 value of 0.03 mM in RBL 2H3 cells[3]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot Analysis[2]
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体内研究 (In Vivo) |
Rhapontigenin (intraperitoneal injection; 25mg/kg) shows significant protection from death due to pulmonary thrombosis in mice, those samples are orally administered 90 min before tail vein injection of epinephrine and collagen[3]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
258.27 |
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Formula |
C15H14O4 |
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CAS 号 |
500-65-2 |
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中文名称 |
丹叶大黄素 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:
DMSO : 125 mg/mL (483.99 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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