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Ginsenoside Rh2

analytical standard

Synonym(s):

(3β,12β)-12,20-Dihydroxydammar-24-en-3-yl-β-D-glucopyranoside, 20(S)-Ginsenoside-Rh2

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About This Item

Empirical Formula (Hill Notation):
C36H62O8
CAS Number:
78214-33-2
Molecular Weight:
622.87
MDL number:
MFCD00800712
UNSPSC Code:
85151701
PubChem Substance ID:
329765120
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥97.0% (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(C)=C/CC[C@](C)(O)[C@H]1CC[C@]2(C)[C@@H]1[C@H](O)C[C@@H]3[C@@]4(C)CC[C@H](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)C(C)(C)[C@@H]4CC[C@@]23C

InChI

1S/C36H62O8/c1-20(2)10-9-14-36(8,42)21-11-16-35(7)27(21)22(38)18-25-33(5)15-13-26(32(3,4)24(33)12-17-34(25,35)6)44-31-30(41)29(40)28(39)23(19-37)43-31/h10,21-31,37-42H,9,11-19H2,1-8H3/t21-,22+,23+,24-,25+,26-,27-,28+,29-,30+,31-,33-,34+,35+,36-/m0/s1

InChI key

CKUVNOCSBYYHIS-IRFFNABBSA-N

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General description

Ginsenoside Rh2 is an active component of Red P. ginseng. It is reported to be obtained as a metabolite of ginsenoside Rg3, when anaerobically incubated with human fecal microflora.

Application

Ginsenoside Rh2 may be used as an analytical reference standard for the quantification of the analyte in plasma samples using high-performance liquid chromatography technique.[24]
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

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH1115
BCCG0514
BCBV9500
BCCB2967
BCBT0133

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Chunjing Zhang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 36(12), 1670-1674 (2011-10-20)
To evaluate and explore the effects of 20(S)-ginsenoside Rh2 and 20(R)-ginsenoside Rh2 on the cytotoxicity, proliferation and the apoptosis of human lung adenocarcinoma A549 cells, and to illustrate the structure-activity relationship and possible mechanisms of anti-tumor active ingredients of ginseng.
Yong-Sheng Jiang et al.
International journal of molecular medicine, 26(6), 787-793 (2010-11-03)
Herbal remedies containing root extracts of Panax ginseng are commonly used for complementary or alternative therapies. Ginsenosides, the major components of root extracts, are responsible for ginseng's pharmacological and biological effects; however, their mechanisms of action are unclear. We examined
Y Wang et al.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 44(1), 33-40 (2011-12-30)
The present study was designed to determine the antihyperglycemic function of ginsenoside Rh2 (GS-Rh2) by the regeneration of β-cells in mice that underwent 70% partial pancreatectomy (PPx), and to explore the mechanisms of GS-Rh2-induced β-cell proliferation. Adult C57BL/6J mice were
In-Sook An et al.
Oncology reports, 29(2), 523-528 (2012-11-16)
Non-small cell lung cancer (NSCLC) is the most common type of lung cancer insensitive to chemotherapy. Efforts are, therefore, directed toward understanding the molecular mechanisms of chemotherapy insensitivity and the development of new anticancer drugs. Ginsenoside Rh2, one of the
High performance liquid chromatographic?mass spectrometric determination of ginsenoside Rg3 and its metabolites in rat plasma using solid-phase extraction for pharmacokinetic studies
Xie T-H, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 818(2), 167-173 (2005)
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