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67530

Supelco

Pseudoginsenoside F11

analytical standard

Synonym(s):

(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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About This Item

Empirical Formula (Hill Notation):
C42H72O14
CAS Number:
69884-00-0
Molecular Weight:
801.01
UNSPSC Code:
85151701
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥85% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

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

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General description

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.

Application

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.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCC6136
BCBZ5125
BCBW5999
BCBS5958V
BCBR3831V

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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)
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)
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

Articles

High-Performance Thin-Layer Chromatography: A Fast and Efficient Fingerprint Analysis Method for Medicinal Plants

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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