天然产物 糖类和糖苷 Saccharides and Glycosides
Liquiritin;(Synonyms: 甘草苷) 纯度: 99.68%
Liquiritin 是一种从甘草中分离出的类黄酮,是一种有效的和竞争性的 AKR1C1 抑制剂,对 AKR1C1,AKR1C2 和 AKR1C3 的 IC50 分别为 0.62 μM,0.61 μM 和 3.72μM。Liquiritin 在体内有效抑制 AKR1C1 介导的孕酮代谢。Liquiritin 是抗氧化剂,具有神经保护、抗癌、抗炎的活性。
Liquiritin Chemical Structure
CAS No. : 551-15-5
规格 | 价格 | 是否有货 | 数量 |
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10;mM;*;1 mL in DMSO | ¥660 | In-stock | |
5 mg | ¥600 | In-stock | |
10 mg | ¥900 | In-stock | |
25 mg | ¥1800 | In-stock | |
50 mg | ¥2800 | In-stock | |
100 mg | ¥4500 | In-stock | |
200 mg | ; | 询价 | ; |
500 mg | ; | 询价 | ; |
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Liquiritin 相关产品
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生物活性 |
Liquiritin, a flavonoid isolated from Glycyrrhiza, is a potent and competitive AKR1C1 inhibitor with IC50s of 0.62 μM, 0.61 μM, and 3.72μM for AKR1C1, AKR1C2 and AKR1C3, respectively. Liquiritin efficiently inhibits progesterone metabolism mediated by AKR1C1 in vivo[1]. Liquiritin acts as an antioxidant and has neuroprotective, anti-cancer and anti-inflammatory activity[2]. |
IC50 Target |
IC50: 0.62 μM (AKR1C1), 0.61 μM (AKR1C2) and 3.72μM (AKR1C3)[1] |
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体外研究 (In Vitro) |
Liquiritin can target the residues Ala-27, Val-29, Ala-25, and Asn-56 of AKR1C1[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
418.39 |
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Formula |
C21H22O9 |
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CAS 号 |
551-15-5 |
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中文名称 |
甘草苷 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:;
DMSO : 150 mg/mL (358.52 mM; Need ultrasonic) H2O : < 0.1 mg/mL (ultrasonic) (insoluble) 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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