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Merck
CN

56805

人参皂苷Rh1

analytical standard

别名:

(3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl-β-D-glucopyranoside, Prosapogenin A2, Sanchinoside B2, Sanchinoside Rh1

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关于此项目

经验公式（希尔记法）:
C36H62O9
化学文摘社编号:
63223-86-9
分子量:
638.87
NACRES:
NA.24
PubChem Substance ID:
329758240
UNSPSC Code:
85151701
MDL number:
MFCD09951797

主要文件

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产品名称

人参皂苷Rh1, analytical standard

InChI key

RAQNTCRNSXYLAH-RFCGZQMISA-N

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(C)(C)[C@@H]4[C@H](C[C@@]23C)O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O

InChI

1S/C36H62O9/c1-19(2)10-9-13-36(8,43)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(39)32(3,4)30(33)22(17-35(24,34)7)44-31-29(42)28(41)27(40)23(18-37)45-31/h10,20-31,37-43H,9,11-18H2,1-8H3/t20-,21+,22-,23+,24+,25-,26-,27+,28-,29+,30-,31+,33+,34+,35+,36-/m0/s1

grade

analytical standard

assay

≥90.0% (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

Quality Level

100

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相关类别

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN8369
BCCK6974
BCCJ8219
BCCG3836
BCCD4244

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Ji-Hae Yoon et al.
European journal of pharmacology, 679(1-3), 24-33 (2012-02-09)
Invasion and metastasis are the major causes of treatment failure in patients with cancer. Here, we investigated the effects of ginsenoside Rh1 on tumor invasion and metastasis in human hepatocellular carcinoma HepG2 cells and its possible mechanism of action. Rh1
Hua Zheng et al.
International immunopharmacology, 11(4), 511-518 (2011-01-18)
In the present study, we examined the inhibitive effect of ginsenoside Rh1 on oxazolone-induced atopic dermatitis-like skin lesions in hairless mice. Oral administration of ginsenoside Rh1 improved clinical symptoms, and it was confirmed by histophathological analysis. In ginsenoside Rh1 (20mg/kg)
Li Lai et al.
Planta medica, 75(8), 797-802 (2009-03-07)
20(S)-Ginsenoside Rh1 is one of the important protopanaxatriol ginsenosides and has been reported to be the main hydrolysis product reaching the systemic circulation after oral ingestion of ginseng. However, its pharmacokinetic characteristics and metabolic fate have never been reported. The
Keiichi Samukawa et al.
Biorheology, 45(6), 689-700 (2008-12-10)
The extract from Panax ginseng has been reported to improve the microcirculation in various organs. However, the mechanisms underlying this phenomenon are still poorly understood. In the present study, using the rheological properties of erythrocytes as an index, we have
Jingang Hou et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 34(23), 3030-3033 (2010-03-13)
To obtain 20(S)-ginsenoside Rh1 by the method of enzymolysis with the protopananxtriol saponins, and to provide the theory for large-scale preparation of 20(S)-ginsenoside Rh1. AB-8 macroporous resin was used to isolate the total saponins of the stems and leaves from
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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.

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