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槲皮素 3-β-D-葡萄糖甙_分子结构_CAS_482-35-9)
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槲皮素 3-β-D-葡萄糖甙

产品号 17793 公司名称 Sigma Aldrich
CAS号 482-35-9 公司网站 http://www.sigmaaldrich.com
分子式 C21H20O12 电 话 1-800-521-8956
分子量 464.3763 传 真
纯 度 ≥90% (HPLC) 电子邮件
保 存 Chembase数据库ID: 155969

产品价格信息

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产品别名

标题
Quercetin 3-β-D-glucoside
IUPAC标准名
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
IUPAC传统名
isoquercitin
别名
3,3′,4′,5,7-Pentahydroxyflavone 3-β-glucoside
Isoquercitrin
3,3′,4′,5,7-五羟基黄酮 3-β-葡萄糖甙
异栎素

产品登记号

CAS号 482-35-9
Beilstein号 100989
MDL号 MFCD00017746
PubChem SID 24850700

产品性质

Empirical Formula (Hill Notation) C21H20O12
纯度 ≥90% (HPLC)
相关基因信息 mouse ... Hexa(15211)
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS编号 DJ2982500
保存温度 -20°C
德国WGK号 3

产品详细信息

详细说明 (简体中文)
Application
Quercetin 3-β-D-glucoside can be used to study cell biology, bioactive small molecules, biochemicals found in plants and nutrition. Quercetin-3-β-d-glucoside, a glucoside form of quercetin, significantly reduced the replication of influenza viruses in vitro and in vivo. Quercetin-3-β-d-glucoside has been used in a study to compare the anti-proliferative activities of quercetin derivatives using six different cancer cell lines (colon, breast, hepatocellular and lung cancer).
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 17793.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Protocols & Applications
Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references
详细说明 (English)
Application
Quercetin 3-β-D-glucoside can be used to study cell biology, bioactive small molecules, biochemicals found in plants and nutrition. Quercetin-3-β-d-glucoside, a glucoside form of quercetin, significantly reduced the replication of influenza viruses in vitro and in vivo. Quercetin-3-β-d-glucoside has been used in a study to compare the anti-proliferative activities of quercetin derivatives using six different cancer cell lines (colon, breast, hepatocellular and lung cancer).
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 17793.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Protocols & Applications
Ginkgo (Ginkgo biloba) Plant Profile: bioactives, mechanism of action, references

参考文献