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Merck

A3145

Sigma-Aldrich

Apigenin

≥97% (TLC), from parsley, powder

Synonym(e):

4′,5,7-Trihydroxy-flavon, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyron

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About This Item

Empirische Formel (Hill-System):
C15H10O5
CAS-Nummer:
Molekulargewicht:
270.24
Beilstein:
262620
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:

Biologische Quelle

parsley

Assay

≥97% (TLC)

Form

powder

Farbe

yellow

mp (Schmelzpunkt)

>300 °C (lit.)

Löslichkeit

DMSO: 27 mg/mL
1 M KOH: 50 mg/mL

Lagertemp.

−20°C

SMILES String

Oc1ccc(cc1)C2=CC(=O)c3c(O)cc(O)cc3O2

InChI

1S/C15H10O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,16-18H

InChIKey

KZNIFHPLKGYRTM-UHFFFAOYSA-N

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Biochem./physiol. Wirkung

A plant flavonoid that has been found to inhibit cell proliferation by arresting the cell cycle at the G2/M phase. Inhibition of growth through cell cycle arrest and induction of apoptosis appear to be related to induction of p53. Inhibitory effects on tumor promotion may also be due to inhibition of kinase activity and the resulting suppression of oncogene expression. It has also been reported to inhibit topoisomerase I catalyzed DNA religation and enhance gap junctional intercellular communication.
A plant flavonoid that has been found to inhibit cell proliferation by arresting the cell cycle at the G2/M phase. Inhibition of growth through cell cycle arrest and induction of apoptosis appear to be related to induction of p53. Inhibits PMA-mediated tumor promotion by inhibiting protein kinase C and the resulting suppression of oncogene expression. It has also been reported to inhibit topoisomerase I-catalyzed DNA re-ligation and enhance gap junctional intercellular communication.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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