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39303

Supelco

[6]-Shogaol

analytical standard

Synonyma:

1-(4-Hydroxy-3-methoxyphenyl)-4-decen-3-one

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About This Item

Empirický vzorec (Hillův zápis):
C17H24O3
Číslo CAS:
555-66-8
Molekulová hmotnost:
276.37
Beilstein/REAXYS Number:
2056098
MDL number:
MFCD01736094
UNSPSC Code:
85151701
PubChem Substance ID:
329755838
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

CCCCC\C=C\C(=O)CCc1ccc(O)c(OC)c1

InChI

1S/C17H24O3/c1-3-4-5-6-7-8-15(18)11-9-14-10-12-16(19)17(13-14)20-2/h7-8,10,12-13,19H,3-6,9,11H2,1-2H3/b8-7+

InChI key

OQWKEEOHDMUXEO-BQYQJAHWSA-N

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General description

[6]-Shogaol is a pungent and one of the most abundant dehydrated form of gingerols present in the fresh ginger roots or dried and thermally treated roots. It may serve as a potential anti-inflammatory agent.

Application

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: zingiber

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Vyberte jednu z posledních verzí:

Osvědčení o analýze (COA)

Lot/Batch Number
WXBF4194V
BCCJ9075
WXBF1851V
BCCG8779
BCCF8038

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Potřebujete-li konkrétní verzi, můžete vyhledat daný certifikát podle čísla dávky nebo čísla šarže.

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Zákazníci si také prohlíželi

Slide 1 of 8

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[6]-Gingerol, Zingiber officinale An antitumor, apoptosis-inducing compound of the ginger family that blocks EGF-induced cell transformation by inhibiting the activation of Activator Protein-1 (AP-1).

Sigma-Aldrich

345868

[6]-Gingerol, Zingiber officinale

6-Gingerol phyproof® Reference Substance

PHL89201

6-Gingerol

10-Shogaol phyproof® Reference Substance

PHL83911

10-Shogaol

10-Gingerol phyproof® Reference Substance

PHL89203

10-Gingerol

Zingerone analytical standard

Supelco

88787

Zingerone

Vanillylacetone ≥96%, FG

Sigma-Aldrich

W312401

Vanillylacetone

Sigma-Aldrich

Sigma-Aldrich

W252204

Ginger oil

Zerumbone ≥98% (HPLC)

Sigma-Aldrich

Z3902

Zerumbone

6-Shogaol reduced chronic inflammatory response in the knees of rats treated with complete Freund's adjuvant
Levy SAA, et al.
BioMed Central Pharmacology, 6, 12-12 (2006)
Yanke Yu et al.
The AAPS journal, 13(3), 417-426 (2011-06-04)
Ginger extracts have been studied in various clinical trials for different indications. However, the pharmacokinetics of the ginger active constituents in human biological matrices is not well investigated. This study aims to develop a LC-MS/MS method for simultaneous measurement of
Heinz H Pertz et al.
Planta medica, 77(10), 973-978 (2011-02-10)
The herbal drug ginger (Zingiber officinale Roscoe) may be effective for treating nausea, vomiting, and gastric hypomotility. In these conditions, cholinergic M (3) receptors and serotonergic 5-HT (3) and 5-HT (4) receptors are involved. The major chemical constituents of ginger
Huadong Chen et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 907, 126-139 (2012-10-04)
Ginger is frequently consumed as a spice and has numerous medicinal properties. Extensive research has characterized the anti-inflammatory, antioxidant, and antitumor activities of ginger. Previously, we reported the mercapturic acid pathway as a major metabolic route of [6]-shogaol in mice
Pharmacokinetics of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol and conjugate metabolites in healthy human subjects
Zick.MS, et al.
Cancer Epidemiology, Biomarkers & Prevention, 17, 1930-1936 (2008)
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