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Merck
CN

I3766

Sigma-Aldrich

异甘草素

powder

别名:

(E)-1-(2,4-二羟基苯基)-3-(4-羟基苯基)-2-丙烯-1-酮, 4,2′,4′-三羟基查尔酮

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关于此项目

经验公式(希尔记法):
C15H12O4
化学文摘社编号:
分子量:
256.25
Beilstein:
1914296
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.77
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表单

powder

质量水平

颜色

yellow to orange

溶解性

H2O: <0.1 mg/mL
methanol: 10 mg/mL
DMSO: 20 mg/mL

储存温度

2-8°C

SMILES字符串

Oc1ccc(cc1)\C=C\C(=O)c2ccc(O)cc2O

InChI

1S/C15H12O4/c16-11-4-1-10(2-5-11)3-8-14(18)13-7-6-12(17)9-15(13)19/h1-9,16-17,19H/b8-3+

InChI key

DXDRHHKMWQZJHT-FPYGCLRLSA-N

基因信息

rat ... Alox5(25290)

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一般描述

异甘草素是一种芳香族酮,属于查耳酮化合物类。它来源于甘草,是药品和食品中的一种成分。

应用

异甘草素已被用于:
  • 作为斑马鱼胚胎中的骨形态发生蛋白(BMP)激动剂
  • 作为斑马鱼胚胎中的鸟苷酸环化酶激活剂
  • 用于测试其对Epstein-Barr病毒相关胃癌的抗肿瘤和抗病毒作用

生化/生理作用

异甘草素是一种可溶性鸟苷酸环化酶激活剂,具有抗肿瘤活性。它还具有抗氧化、抗血小板和雌激素特性。

特点和优势

这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

免责声明

光敏性、吸湿性

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Isoliquiritigenin (ISL), a licorice chalconoid, is a bioactive agent with chemopreventive potential that has been patented for tumor treatment in China. This study investigated the mechanisms of ISL-induced apoptosis in ovarian carcinoma SKOV-3 cells. Cell viability was evaluated using a
Lei Yang et al.
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An ionic liquid-based ultrasonic-assisted extraction (ILUAE) method had been used for the effective extraction of isoliquiritigenin (IQ), liquiritin (LQ) and glycyrrhizic acid (GA) from licorice. The ionic liquids with different cations and anions were investigated in this work and 0.5
S Yamamoto et al.
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A topical application of a chalcone derivative, 4,2',4'-trihydroxychalcone (isoliquiritigenin) inhibited epidermal ornithine decarboxylase (ODC) induction and ear edema formation, i.e. inflammation, caused by a topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA) in CD-1 mice. In addition, isoliquiritigenin potently inhibited 7,12-dimethylbenz[alpha]anthracene (DMBA)-initiated and
M Tawata et al.
European journal of pharmacology, 212(1), 87-92 (1992-02-25)
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