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59870-68-7 分子结构
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4-[(3R)-8,8-dimethyl-2H,3H,4H,8H-pyrano[2,3-f]chromen-3-yl]benzene-1,3-diol

ChemBase编号:127561
分子式:C20H20O4
平均质量:324.3704
单一同位素质量:324.13615912
SMILES和InChIs

SMILES:
O1c2c3C=CC(Oc3ccc2C[C@H](c2ccc(O)cc2O)C1)(C)C
Canonical SMILES:
Oc1ccc(c(c1)O)[C@@H]1COc2c(C1)ccc1c2C=CC(O1)(C)C
InChI:
InChI=1S/C20H20O4/c1-20(2)8-7-16-18(24-20)6-3-12-9-13(11-23-19(12)16)15-5-4-14(21)10-17(15)22/h3-8,10,13,21-22H,9,11H2,1-2H3/t13-/m0/s1
InChIKey:
LBQIJVLKGVZRIW-ZDUSSCGKSA-N

引用这个纪录

CBID:127561 http://www.chembase.cn/molecule-127561.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
4-[(3R)-8,8-dimethyl-2H,3H,4H,8H-pyrano[2,3-f]chromen-3-yl]benzene-1,3-diol
4-[(5R)-12,12-dimethyl-3,11-dioxatricyclo[8.4.0.02,7]tetradeca-1,7,9,13-tetraen-5-yl]benzene-1,3-diol
IUPAC传统名
glabridin
4-[(5R)-12,12-dimethyl-3,11-dioxatricyclo[8.4.0.02,7]tetradeca-1,7,9,13-tetraen-5-yl]benzene-1,3-diol
别名
4-[3,4-Dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b']dipyran-3-yl]-1,3-benzenediol
4-[(3R)-3,4-Dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b′]dipyran-3-yl]-1,3-benzenediol
(R)-4-(3,4-Dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b′]dipyran-3-yl)-1,3-benzenediol
Glabridin
Glabridin
Glabridin
CAS号
59870-68-7
MDL号
MFCD03427694
Beilstein号
7141956
PubChem SID
162221880
PubChem CID
124052
CHEMBL
480477
Chemspider ID
110560
维基百科标题
Glabridin

数据来源

数据来源

所有数据来源 商品来源 非商品来源

理论计算性质

理论计算性质

JChem
Acid pKa 9.516527  质子受体 4 
质子供体 2  LogD (pH = 5.5) 4.09226 
LogD (pH = 7.4) 4.0890117  Log P 4.0923014 
摩尔折射率 93.3536 cm3 极化性 35.4321 Å3
极化表面积 58.92 Å2 可自由旋转的化学键 1 
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
DMSO: ≥14 mg/mL expand 查看数据来源
外观
white to tan powder expand 查看数据来源
Yellowish-brown powder expand 查看数据来源
熔点
156 - 158°C expand 查看数据来源
闪点
267 °C expand 查看数据来源
512.6 °F expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
GHS危险声明
H413 expand 查看数据来源
保存温度
room temp expand 查看数据来源
生物活性机理
Human cytochrome P450S 3A4, 2B6, 2C9 inhibitor expand 查看数据来源
Melanogenesis inhibitor expand 查看数据来源
Tyrosinase inhibitor expand 查看数据来源
纯度
≥98% (HPLC) expand 查看数据来源
≥98.0% (HPLC) expand 查看数据来源
级别
analytical standard expand 查看数据来源
生物来源
Isol. from Glycyrrhiza glabra expand 查看数据来源
有效期
(limited shelf life, expiry date on the label) expand 查看数据来源
应用领域
Anti-inflammatory expand 查看数据来源
Antimicrobial expand 查看数据来源
Anti-proliferative expand 查看数据来源
Cytotoxic expand 查看数据来源
Estrogenic expand 查看数据来源
Empirical Formula (Hill Notation)
C20H20O4 expand 查看数据来源

详细说明

详细说明

Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich
Sigma Aldrich -  G9548 external link
Biochem/physiol Actions
Glabridin is a bio-available isoflavan isolated from licorice (Glycyrrhiza glabra L.) root extract. Glabridin has been reported to posses varies biological activities including strong antioxidant activity, antioxidant against LDL oxidation, anti-Helicobacter pylori properties, estrogen-like activity and antinephritic and radical scavenging activities. Also it appears to inhibit serotonin re-uptake, melanogenesis, inflammation and cytochrome P450 3A4, 2B6, and 2C9.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • 1. T. Fukai, H. Sakagami, M. Toguchi, F. Takayama, I. Iwakura and T. Atsumi, Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines,
  • Anticancer Res 20 (2000), pp. 2525?536.
  • 2. T. Fukai, A. Marumo, K. Kaitou, T. Kanda, S. Terada and T. Nomura, Anti-Helicobacter pylori flavonoids from licorice extract, Life Sci 71 (2002), pp. 1449?463
  • 3. S. Tamir, M. Eizenberg, D. Somjen, S. Izrael and J. Vaya, Estrogen-like activity of glabrene and other constituents isolated from licorice root, J Steroid Biochem Mol Biol 78 (2001), pp. 291?98.
  • 4. T. Yokota, H. Nishio, Y. Kubota and M. Mizoguchi, The inhibitory effect of glabridin from licorice extracts on melanogenesis and inflammation, Pigment Cell Res 11 (1998), pp. 355?61.
  • 5. O. Nerya, J. Vaya, R. Musa, S. Izrael, R. Ben-Arie and S. Tamir, Glabrene and isoliquiritigenin as tyrosinase inhibitors from licorice roots, J Agric Food Chem 51 (2003), pp. 1201?207.
  • 6. U.M. Kent, M. Aviram, M. Rosenblat and P.F. Hollenberg, The licorice root derived isoflavan glabridin inhibits the activities of human cytochrome P450S 3A4, 2B6, and 2C9,
  • Drug Metab Dispos 30 (2002), pp. 709?15.
  • 7. Choi, E. The licorice root derived isoflavan glabridin increases the function of osteoblastic
  • MC3T3-E1 cells. Biochem. Pharm. 2005, 70, 363-368.
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专利

专利

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