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Merck

00017

Acacetin

≥97.0% (HPLC)

Synonym(e):

4′-Methylapigenin, 5,7-Dihydroxy-4′-methoxy-flavon, Apigenin-4′-methylether, Buddleoflavonol, Linarigenin

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Über diesen Artikel

Empirische Formel (Hill-System):
C16H12O5
CAS-Nummer:
Molekulargewicht:
284.26
PubChem Substance ID:
eCl@ss:
32150233
UNSPSC Code:
12352200
NACRES:
NA.47
EC Number:
207-552-3
MDL number:
Beilstein/REAXYS Number:
277879
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Quality Segment

assay

≥97.0% (HPLC)

form

powder or crystals

mp

260-265 °C (lit.)

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

2-8°C

SMILES string

COc1ccc(cc1)C2=CC(=O)c3c(O)cc(O)cc3O2

InChI

1S/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3

InChI key

DANYIYRPLHHOCZ-UHFFFAOYSA-N

General description

Acacetin belongs to the category of naturally occurring plant pigments called flavonoids found in vascular plants. It was first reported to be extracted from the leaves of Robinia pseuducacia. It has been used as an active component of traditional Chinese medicine Xuelianhua.

Biochem/physiol Actions

Flavonoid with anti-peroxidative and anti-inflammatory properties. Used in traditional Chinese medicine.
Flavonoid with anti-peroxidative and anti-inflammatory properties. Used in traditional Chinese medicine. It has been recognized as an antiproliferative agent on cancer cell lines by inducing apoptosis and blocking cell cycle progression in the G1 phase.
Acacetin has been noted to exhibit anti-peroxidative, anti-inflammatory, and anti-plasmodial properties. It has been posited to prevent the proliferation of Hep G2 cells, thereby causing cell apoptosis and subsequent anti-cancer action. It has antiarrhythmic properties and can be used in the treatment of Atrial fibrillation.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.


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Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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