460745

Aldrich

 

Apigenin

95%

Synonym:4′,5,7-Trihydroxyflavone
CAS Number:520-36-5
Linear Formula:C15H10O5
Molecular Weight:270.24
Beilstein Registry Number:262620
EC Number:208-292-3
MDL number:MFCD00006831

Description

Biochem/physiol ActionsA 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.
Packaging5, 25, 100 mg in glass btl

Properties

assay95%
total impurities<5% acetic acid
mp>300 °C(lit.)

Safety

Hazard CodesXi
Risk Statements36/37/38
Safety Statements26-36
WGK Germany3
RTECSLK9276000

Related Products

Comparable productA3145, Apigenin

References

referenceSato, F., et al., Apigenin induces morphological differentiation and G2-M arrest in rat neuronal cells. Biochem. Biophys. Res. Commun. 204, 578-584, (1994)
 Plaumann, B., et al., Flavonoids activate wild-type p53. Oncogene 13, 1605-1614, (1996)
 Way, T.D., et al., Degradation of HER2/neu by apigenin induces apoptosis through cytochrome c release and caspase-3 activation in HER2/neu-overexpressing breast cancer cells. FEBS Lett. 579, 145-152, (2005)
 Huang, Y.T., et al., Inhibition of protein kinase C and proto-oncogene expression in NIH 3T3 cells by apigenin. Eur. J. Cancer 32A, 146-151, (1996)
 Snyder, R.D., and Gillies, P.J., Evaluation of the clastogenic, DNA intercalative, and topoisomerase II-interactive properties of bioflavonoids in Chinese hamster V79 cells. Environ. Mol. Mutagen. 40, 266-276, (2002)
 Czyz, J., et al., Hierarchy of carcinoma cell responses to apigenin: gap junctional coupling versus proliferation. Oncol. Rep. 11, 739-744, (2004)
MerckMerck 13,737
BeilsteinBeil. 18,V,4,574