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Merck
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資料

安全性情報

03000590

Ginsenoside Re

primary reference standard

別名:

(3β,6α,12β)-20-(β-D-Glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside, Chikusetsusaponin IVc, Ginsenoside B2, NSC 308877, Panaxoside Re, Sanchinoside Re

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About This Item

実験式（ヒル表記法）:
C48H82O18
CAS番号:
52286-59-6
分子量:
947.15
UNSPSCコード:
85151701
NACRES:
NA.24

グレード

primary reference standard

シェルフライフ

limited shelf life, expiry date on the label

メーカー／製品名

HWI

アプリケーション

food and beverages

SMILES記法

CC1O[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@](C)(CC\C=C(/C)C)O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@@]7(C)CC[C@H](O)C(C)(C)[C@H]37)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C48H82O18/c1-21(2)11-10-14-48(9,66-42-38(60)35(57)32(54)26(19-49)63-42)23-12-16-46(7)30(23)24(51)17-28-45(6)15-13-29(52)44(4,5)40(45)25(18-47(28,46)8)62-43-39(36(58)33(55)27(20-50)64-43)65-41-37(59)34(56)31(53)22(3)61-41/h11,22-43,49-60H,10,12-20H2,1-9H3/t22-,23-,24+,25-,26+,27+,28?,29-,30+,31-,32+,33+,34+,35?,36-,37+,38+,39+,40-,41-,42-,43+,45+,46+,47+,48-/m0/s1

InChI Key

PWAOOJDMFUQOKB-QVPADXGFSA-N

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詳細

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

アプリケーション

Reference Standard in the analysis of herbal medicinal products

その他情報

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

ピクトグラム

Exclamation mark
GHS07

シグナルワード

Warning

危険有害性情報

H302

危険有害性の分類

Acute Tox. 4 Oral

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

03000590-10MG:

Choose from one of the most recent versions:

試験成績書（COA）

Lot/Batch Number
HWI02844-1
HWI02844
HWI01844-3
HWI01844-2
HWI01844-1

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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ジンセノサイドRg1 United States Pharmacopeia (USP) Reference Standard

USP

1291672

ジンセノサイドRg1

ジンセノサイドRg1 European Pharmacopoeia (EP) Reference Standard

Y0002096

ジンセノサイドRg1

ジンセノサイドRg1 analytical standard

Supelco

68317

ジンセノサイドRg1

Ginsenoside Rb2 analytical standard

Supelco

41868

Ginsenoside Rb2

Ginsenoside Rh1 analytical standard

Supelco

56805

Ginsenoside Rh1

ギンセノシド化合物K phyproof® Reference Substance

PHL80461

ギンセノシド化合物K

ギンセノシドRb1 European Pharmacopoeia (EP) Reference Standard

Y0001347

ギンセノシドRb1

ジンセノシド-Rc from Panax ginseng (Korean ginseng) root triterpenoid saponin, ≥98% (HPLC)

Sigma-Aldrich

G0902

ジンセノシド-Rc from Panax ginseng (Korean ginseng) root

ジンセノサイドRg3 analytical standard

Supelco

64139

ジンセノサイドRg3

Tiegui Nan et al.
Analytical chemistry, 84(10), 4327-4333 (2012-04-13)
Ginsenoside Re (GRe) is a major active component of the Chinese medicinal herb ginseng, Panax ginseng . A sensitive and specific monoclonal antibody (mAb), designated as mAb3D6, was generated with a GRe-bovine serum albumin conjugate as an immunogen. Microcantilever immunosensors
In-Ah Lee et al.
Journal of agricultural and food chemistry, 60(38), 9595-9602 (2012-08-02)
Ginseng (the root of Panax ginseng C.A. Meyer, family Araliaceae), which contains protopanaxadiol ginsenoside Rb1 and protopanaxatriol ginsenoside Re as main constituents, is frequently used to treat cancer, inflammation, and stress. In the preliminary study, protopanaxatriol ginsenoside Re inhibited NF-κB
Unyong Kim et al.
Food chemistry, 136(3-4), 1364-1369 (2012-12-01)
Following oral administration of ginsenoside Re, the compound and its metabolites were identified and quantified in rat urine and faeces by liquid chromatography coupled with triple quadrupole mass spectrometry (LC-MS/MS). Ginsenoside Re (200 mg/kg) was orally administered to rats by
Chang-Hao Cui et al.
Journal of microbiology (Seoul, Korea), 49(3), 393-398 (2011-07-01)
The Gram-negative, strictly aerobic, non-motile, non-spore-forming, rod shaped bacterial strain designated TR6-03(T) was isolated from compost, and its taxonomic position was investigated by using a polyphasic approach. Strain TR6-03(T) grew at 4-42°C and at pH 6.0-8.0 on R2A and nutrient
Kang-Woo Lee et al.
BMC complementary and alternative medicine, 12, 196-196 (2012-10-30)
Microglial activation plays an important role in neurodegenerative diseases by producing several pro-inflammatory enzymes and pro-inflammatory cytokines. Lipopolysaccharide (LPS)-induced inflammation leads to the activation of microglial cells in the central nervous system (CNS) and is associated with the pathological mechanisms
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関連コンテンツ

Ginsenosides

Ginsenosides Separation in Ginseng. The HPLC method was first optimized using a ginsenoside standard mixture, and was then applied to a sample of American Ginseng root.

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