Ugrás a tartalomra
Merck

SMB00702

Sigma-Aldrich

Apigenin

≥97% (TLC), from citrus

Szinonimák:

4′,5,7-Trihydroxyflavone, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Tapasztalati képlet (Hill-képlet):
C15H10O5
CAS-szám:
Molekulatömeg:
270.24
Beilstein:
262620
EC-szám:
MDL-szám:
UNSPSC kód:
12352212
NACRES:
NA.79

Minőségi szint

Teszt

≥97% (TLC)

Forma

powder

mp

>300 °C (lit.)

oldhatóság

DMSO: 27 mg/mL
1 M KOH: 50 mg/mL

alkalmazás(ok)

metabolomics
vitamins, nutraceuticals, and natural products

tárolási hőmérséklet

−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

Nemzetközi kémiai azonosító kulcs

KZNIFHPLKGYRTM-UHFFFAOYSA-N

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Általános leírás

Apigenin (ApI) is also called as 5,7,4′-trihydroxyflavone. It is a natural compound, found in several fruits and herbs, like, oranges, onions and parsley.

Alkalmazás

Apigenin has been used:
  • to test its anti-cancer effects as a reference agent to treat various digestive track and liver cancer cells in in vitro studies
  • as stimuli and inhibitor to test its anti-inflammatory effects on in vitro inflammatory responses due to dietary and metabolic changes of rural- and urban-living Tanzanians
  • as a reference standard to identify the phenolic compounds in olive mill wastewater and pomace

Biokémiai/fiziológiai hatások

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.
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.
Apigenin (ApI) blocks the development of thyroid cancer cells by attenuating epidermal growth factor receptor (EGF-R) tyrosine phosphorylation and phosphorylation of ERK mitogen-activated protein (MAP) kinase. Apigenin participates in the modulation of different signaling cascades. It possesses several functions such as, antiapoptosis, anti-inflammation, anticancer, antibacterial and antioxidant effects.

Tárolási osztály kódja

11 - Combustible Solids

WGK

WGK 3


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Dokumentumtár megtekintése

Az ügyfelek ezeket is megtekintették

Apigenin inhibits growth and induces G2/M arrest by modulating cyclin-CDK regulators and ERK MAP kinase activation in breast carcinoma cells.
Yin F, et al.
Anticancer Research, 21(1A), 413-420 (2001)
Apigenin as an effective anticancer natural product: Spotlight on TRAIL, WNT beta-catenin, JAK-STAT pathways, and microRNAs
Ozbey U, et al.
Journal of Cellular Biochemistry (2018)
Apigenin, a component of Matricaria recutita flowers, is a central benzodiazepine receptors-ligand with anxiolytic effects
Viola H, et al.
Planta Medica, 61(03), 213-216 (1995)
Effect of apigenin on apoptosis induced by renal ischemia reperfusion injury in vivo and in vitro
Wang Xiao, et al.
Renal Failure, 40(1), 498-505 (2018)
Lukasz Szoka et al.
Journal of cellular and molecular medicine, 25(24), 11085-11096 (2021-11-11)
Flavonoids are bioactive secondary metabolites of plants, which exert anti-cancer effects. However, metabolism in enterocytes and the liver can influence the biological activity of flavonoids contained in the diet. Therefore, results from in vitro studies on cancer cells from the

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