Liquiritin

別名：Liquiritoside, Liquiritigenin-4'-O-glucoside

製品コード：S3930 純度：99.85%

Liquiritin (LIQ, Liquiritoside, Liquiritigenin-4'-O-glucoside) is a main component among the licorice flavonoids, and possesses anti-inflammatory and anti-cancer abilities.

CAS No. 551-15-5

サイズ	価格(税別)	在庫状況
5mg	JPY 22000	国内在庫あり
25mg	JPY 44500	国内在庫あり

代表番号: 045-509-1970\|電子メール：[email protected] よく尋ねられる質問

製品安全説明書

現在のバッチを見る： S393001 DMSO] 100 mg/mL] false] ] ] false] ] ] false 純度： 99.85%

99.85

Liquiritin関連製品

関連ターゲット	AKR1C1 AKR1C2 AKR1C3 AKR1C4	もっと見る
関連化合物ライブラリー	Kinase Inhibitor Library FDA-approved Drug Library Natural Product Library Bioactive Compound Library-I Highly Selective Inhibitor Library	もっと見る

AKR1C阻害剤の選択性比較

生物活性

製品説明	Liquiritin (LIQ, Liquiritoside, Liquiritigenin-4'-O-glucoside) is a main component among the licorice flavonoids, and possesses anti-inflammatory and anti-cancer abilities.

In Vitro
In vitro	Liquiritin exerts neuroprotective and neurotrophic effects on primary cultured hippocampal cells^[1]. Liquiritin may enhance cell survival by increasing the protein expression level of glucose-6 phosphate dehydrogenase. Liquiritin potentiates neurite outgrowth induced by nerve growth factor in PC12 cells. It affects particular types of cells such as neurons in the central nervous system. Liquiritin increases the proliferation of B65 neuroblastoma cells^[2].
細胞実験	細胞株	B65 neuroblastoma cells
	濃度	--
	反応時間	24, 48 and 72 h
	実験の流れ	The proliferation of B65 neuroblastoma cells was investigated by a WST-8 assay using a Cell Counting Kit-8. Once cells became confluent, they were plated into 96-well microplates at a density of 5×10⁴/mL (5×10³/well) and incubated with glycyrrhizin, isoliquiritin and liquiritin, which were first dissolved in dimethyl sulfoxide (DMSO). When cells were treated with these compounds, the final concentration of DMSO was set at 0.1% in the culture medium. When cells were treated with various cytotoxic reagents, such as hydrogen peroxide, monosodium glutamate, or menadione sodium bisulfate, these agents were directly dissolved in culture media following the description in each experiment. In general, this assay was performed after cells were cultured with each compound or reagent for 24, 48 and 72 h. After culture, the cells were incubated with WST-8 solution at 37℃ for 2 h, and the spectrophotometric absorbance of WST-8-formazan produced by dehydrogenase activity in the living cells at 450 nm.

In Vivo
In Vivo	Liquiritin at doses of 50-100 mg/kg significantly improves the cognitive ability, restores the abnormal activities of glutathione peroxidase and superoxide dismutase, and decreases the levels of malondialdehyde，8-hydroxy-2′-deoxyguanosine and protein carbonyl in the hippocampus of rats with Alzheimer's disease. Liquiritin can significantly ameliorate Aβ1-42-induced spatial learning and memory impairment by inhibiting oxidative stress and neural apoptosis. It is also frequently used to treat injury or swelling owing to its life-enhancing properties, as well as detoxification in traditional oriental medicine. It exerts significant antidepressant-like effects on the forced swimming and tail suspension tests in mice. It can also produce obvious neuroprotective effects on focal cerebral ischemia/reperfusion induced by middle cerebral artery occlusion. Liquiritin can protect neurons from Aβ-induced neurotoxicity. This ability probably involves the suppression of oxidative stress and neuron apoptosis in a rat model of Alzheimer disease (AD) induced by subsequent bilateral intrahippocampal (IH) injections of aggregated soluble oligomeric Aβ_1-42. Liquiritin provides beneficial effects on the cognitive impairments observed in an Aβ_1-42-induced model of AD. The neuroprotective effects of liquiritin are closely associated with its effects of inhibiting oxidative stress and neuronal apoptosis^[1].
動物実験	動物モデル	Adult male Sprague-Dawley rats
	投与量	100, 50, or 25 mg/kg
	投与経路	orally administered

参考
[1] Jia SL, et al. J Asian Nat Prod Res. 2016, 18(12):1186-1199. [2] Nakatani Y, et al. Eur J Pharmacol. 2017, 815:381-390.

参考

化学情報

分子量	418.39	化学式	C₂₁H₂₂O₉
CAS No.	551-15-5	SDF	Download Liquiritin SDFをダウンロードする
Smiles	C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	1年-80°Cin solvent
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	1个月-20°Cin solvent

In vitro
Batch:

DMSO : 100 mg/mL ( (239.01 mM)；吸湿したDMSOは溶解度を減少させます。新しいDMSOをご使用ください。)

モル濃度計算器

in vivo
Batch:

Add solvents to the product individually and in order.

投与溶液組成計算機

実験計算

モル濃度計算器

質量	濃度	体積	分子量
=	×	×

希釈計算器分子量計算器

投与溶液組成計算機(クリア溶液)

ステップ１：実験データを入力してください。（実験操作によるロスを考慮し、動物数を1匹分多くして計算・調製することを推奨します）

投与量 mg/kg 動物平均体重 g 投与体積（動物毎）μL 動物数匹

ステップ２：投与溶媒の組成を入力してください。（ロット毎に適した溶解組成が異なる場合があります。詳細については弊社までお問い合わせください）

% DMSO + % + % Tween 80 + % ddH₂O

%DMSO+ %

計算結果：

投与溶媒濃度： mg/ml;

DMSOストック溶液調製方法： mg 試薬を μL DMSOに溶解する（濃度 mg/mL, 注：濃度が当該ロットのDMSO溶解度を超える場合はご連絡ください。 )

投与溶媒調製方法：Take μL DMSOストック溶液に μL PEG300，を加え、完全溶解後μL Tween 80，を加えて完全溶解させた後 μL ddH₂O，を加え完全に溶解させます。

投与溶媒調製方法：μL DMSOストック溶液に μL Corn oil，を加え、完全溶解。

注意：１.ストック溶液に沈殿、混濁などがないことをご確認ください；
２.順番通りに溶剤を加えてください。次のステップに進む前に溶液に沈殿、混濁などがないことを確認してから加えてください。ボルテックス、ソニケーション、水浴加熱など物理的な方法で溶解を早めることは可能です。

技術サポート

ストックの作り方、阻害剤の保管方法、細胞実験や動物実験の際に注意すべき点など、製品を取扱う時に問い合わせが多かった質問に対しては取扱説明書でお答えしています。

Handling Instructions

他に質問がある場合は、お気軽にお問い合わせください。

* 必須

* 大学・企業名 大学・企業名を記入してください

* 名前 名前を記入してください

* 電子メール 電子メール・アドレスを記入してください 有効なメールアドレスを入力してください

電話番号

* 内容 お問い合わせ内容をご入力ください

C1=C0/X	C1:	LOG(C1):
C2=C1/X	C2:	LOG(C2):
C3=C2/X	C3:	LOG(C3):
C4=C3/X	C4:	LOG(C4):
C5=C4/X	C5:	LOG(C5):
C6=C5/X	C6:	LOG(C6):
C7=C6/X	C7:	LOG(C7):
C8=C7/X	C8:	LOG(C8):