化学信息:
中文名 | 甘草苷 |
英文名 | Liquiritin |
中文别名 | - |
英文别名 | Liquiritoside |
来源 | 甘草Glycyrrhiza uralensis Fisch |
化合物类型 | 黄酮类(Flavonoids)>黄酮>二氢黄酮 |
化学式 | C21H22O9 |
分子量 | 418.39 |
CAS号 | 551-15-5 |
纯度 | 98%, HPLC |
溶剂/溶解度 | DMSO: 150 mg/ml (358.52 mM) |
溶液配制 | 5mg加入1.20ml DMSO,或者每4.18mg加入1ml DMSO,配制成10mM溶液。 |
生物信息
产品描述 | 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 vivo1. Liquiritin acts as an antioxidant and has neuroprotective, anti-cancer and anti-inflammatory activity. | ||||
信号通路 | - | ||||
靶点 | AKR1C1 | AKR1C2 | AKR1C3 | - | - |
IC50 | 0.62 μM | 0.61 μM | 3.72 μM | - | - |
体外研究 | Liquiritin can target the residues Ala-27, Val-29, Ala-25, and Asn-56 of AKR1C1. Liquiritin (50 μM; 6 hours) results in 85.00% of reduction in progesterone metabolism, which is mediated by Aldo-keto reductase family 1 member C1 (AKR1C1) enzymatic activity in HEC-1-B cells. Liquiritin (100 µM) increases glucose-6-phosphate dehydrogenase expression on B65 neuroblastoma cells. | ||||
体内研究 | N/A | ||||
临床实验 | N/A |
1. Zeng C, et al. Front Physiol. 2019,10:833.
2. Nakatani Y, et al. Eur J Pharmacol. 2017,815:381-390.
包装清单:产品编号 | 产品名称 | 包装 |
SM2097-10mM | 甘草苷(98%, HPLC) | 10mM×0.2ml |
SM2097-5mg | 甘草苷(98%, HPLC) | 5mg |
SM2097-25mg | 甘草苷(98%, HPLC) | 25mg |
SM2097-100mg | 甘草苷(98%, HPLC) | 100mg |
- | 说明书 | 1份 |
-20℃保存,至少一年有效。固体粉末4℃保存,至少一个月有效。如果溶于非DMSO溶剂,建议分装后-80℃保存,预计6个月内有效。
注意事项:本产品可能对人体有一定的毒害作用,请注意适当防护,以避免直接接触人体或吸入体内。
本产品仅限于专业人员的科学研究用,不得用于临床诊断或治疗,不得用于食品或药品,不得存放于普通住宅内。
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