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SML3610

Sigma-Aldrich

Gingerenone A

≥95% (HPLC)

Synonym(s):

(4E)​-1,​7-​bis(4-​hydroxy-​3-​methoxyphenyl)​-4-​Hepten-​3-​one, (E)-1,7-Bis(4-hydroxy-3-methoxyphenyl)hept-4-en-3-one

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About This Item

Empirical Formula (Hill Notation):
C21H24O5
CAS Number:
Molecular Weight:
356.41
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77

Quality Level

Assay

≥95% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

Biochem/physiol Actions

Gingerenone A is a potent anticancer agent isolated from Ginger (Zingiber officinale) that exhibits minimal toxicity toward normal cells. Gingerenone A potently inhibits JAK2 (Janus Kinase 2) and S6K1 (p70 ribosomal S6 kinase). Gingerenone A significantly suppressed tumor growth in vivo. Also, it exhibits promising senolytic properties. Gingerenone A selectively eliminate senescent cells in WI-38 human fibroblasts rendered senescent by exposure to ionizing radiation.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sanguine Byun et al.
The Journal of biological chemistry, 290(39), 23553-23562 (2015-08-06)
Bioactive phytochemicals can suppress the growth of malignant cells, and investigation of the mechanisms responsible can assist in the identification of novel therapeutic strategies for cancer therapy. Ginger has been reported to exhibit potent anti-cancer effects, although previous reports have
Tzu-Jung Yu et al.
Antioxidants (Basel, Switzerland), 11(3) (2022-03-26)
Ginger is a popular spice and consists of several bioactive antioxidant compounds. Gingerenone A (Gin A), a novel compound isolated from Zingiber officinale, is rarely investigated for its anti-breast-cancer properties. Some ginger extracts have been reported to initiate senescence, an
Identification of gingerenone A as a novel senolytic compound
PLoS ONE, 17(3), e0266135-e0266135 (2022)

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