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Merck
CN

67530

Supelco

拟人参皂苷F11

analytical standard

别名:

(3β,6α,12β,24R)-20,24-Epoxy-3,12,25-trihydroxydammaran-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside, Ginsenoside A1

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关于此项目

经验公式(希尔记法):
C42H72O14
化学文摘社编号:
分子量:
801.01
UNSPSC代码:
85151701
NACRES:
NA.24
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等级

analytical standard

质量水平

方案

≥85% (HPLC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

food and beverages

包装形式

neat

储存温度

2-8°C

SMILES字符串

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2O[C@H]3C[C@]4(C)[C@H](C[C@@H](O)[C@@H]5[C@H](CC[C@@]45C)[C@]6(C)CC[C@@H](O6)C(C)(C)O)[C@@]7(C)CC[C@H](O)C(C)(C)[C@H]37)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C42H72O14/c1-19-28(46)30(48)32(50)35(52-19)55-33-31(49)29(47)23(18-43)54-36(33)53-22-17-41(8)24(39(6)13-11-25(45)37(2,3)34(22)39)16-21(44)27-20(10-14-40(27,41)7)42(9)15-12-26(56-42)38(4,5)51/h19-36,43-51H,10-18H2,1-9H3/t19?,20-,21+,22-,23?,24?,25-,26+,27-,28?,29?,30?,31?,32?,33?,34?,35?,36?,39+,40+,41+,42-/m0/s1

InChI key

JBGYSAVRIDZNKA-GSXRAQGCSA-N

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一般描述

Pseudoginsenoside F11 is a natural product and ocotillol-type saponin, isolated from Panax quinquefolius L. It is found to exhibit pharmacological effects related to immune systems, endocrine, central nervous, and cardiovascular systems.

应用

Pseudoginsenoside F11 may be used as an analytical reference standard for the quantification of the analyte in human plasma samples using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

其他说明

This compound is commonly found in plants of the genus: panax

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Ultra-performance liquid chromatography and time-of-flight mass spectrometry analysis of ginsenoside metabolites in human plasma
Wang Z-C, et al.
American Journal of Chinese Medicine, 39(06), 1161-1171 (2011)
Protective effects of pseudoginsenoside-F11 on methamphetamine-induced neurotoxicity in mice
Wu FC, et al.
Macedonian pharmaceutical bulletin, 39(06), 39-44 (2012)
Cirsilineol inhibits proliferation of cancer cells by inducing apoptosis via mitochondrial pathway
Sheng X, et al.
Pharmacology, Biochemistry, and Behavior, 76(1), 103-109 (2003)
Jiali Chen et al.
Chemical & pharmaceutical bulletin, 67(8), 839-848 (2019-08-02)
Panacis Japonici Rhizoma (PJR) contains various kinds of saponins, which possesses extensive pharmacological activities, but studies of comprehensive analysis of its saponins were limited. Thus, ultra-fast liquid chromatography coupled with triple quadrupole-time of flight tandem mass spectrometry (UFLC-Triple TOF-MS/MS) and

商品

In this article we present several HPTLC applications and analytical standards for ginsenosides.

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