Properties |
Information |
PhytoCAT-ID |
PhytoCAT-120 |
Phytochemical name or plant extracts |
Acacetin |
PMID |
19666078 |
Literature evidence |
Cotreatment of the CYP1 family inhibitor acacetin reversed the antiproliferative activity noticed for the two flavones in MDA-MB-468 cells to 13 and 14 microM respectively. |
IUPAC name |
5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one |
Phytochemicals’ class or type of plant extracts |
Flavonoid |
Source of phytochemicals or plant Extracts |
Calea urticifolia |
|
Geographical availability |
Belize, Costa Rica, El Salvador, Guatemala, Honduras, Mexico Central, Mexico Gulf, Mexico Northeast, Mexico Northwest, Mexico Southeast, Mexico Southwest, Nicaragua, Panamá |
Plant parts |
Leaves |
Other cancers |
Breast cancer |
Target gene or protein |
STAT-3, CYP1A1, CYP1B1 |
Gene or Protein evidence |
Sudachitin, chrysoeriol, and acacetin also exerted significantly cytotoxicity, clearly suppressed constitutive STAT3 activation, and induced apoptosis, although hesperetin did not show any significant effect in DU145 cells. The intracellular CYP1-mediated bioconversion of the flavone was reduced in the presence of the CYP1A1 and CYP1B1-selective inhibitors α-napthoflavone and acacetin. |
Target pathways |
PI3K/AKT/mTOR/p70S6K/ULK signaling pathway |
IC50 |
NA |
Potency |
These findings indicate that both acacetin and pinostrobin may serve as potential therapeutic options to target breast tumor cell migration during late-stage tumor progression. |
Cell line/ mice model |
MDA-MB-231, MCF-7, T47D |
Additional information |
Naturally occurring flavonoids, such as acacetin and pinostrobin, disrupt a wide range of processes during tumor progression, such as cell proliferation, apoptosis, and angiogenesis.
Two of the flavones, 3',4',7-trimethoxyflavone and acacetin, showed only low anti-P-gp activity, with the remainder displaying no suppressive effects against P-gp. |
PubChem ID |
5280442 |
Additional PMIDs |
28539711 22438130 9492340 15202555 32493139 |
Additional sources of information |
https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:187796-1 |
Safety |
NA |