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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
质子供体 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
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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