Properties | Information | |
---|---|---|
PhytoCAT-ID | PhytoCAT-54 | |
Phytochemical name or plant extracts | Kaempferide | |
PMID | 11525602 | |
Literature evidence | Further examination in HEK-293 cells transfected with ERalpha or ERbeta demonstrated potent antagonism with kaempferide and apigenin, while flavone was weakly antagonistic only toward ERP. | |
IUPAC name | 3,5,7-trihydroxy-2-(4-methoxyphenyl)chromen-4-one | |
Phytochemicals’ class or type of plant extracts | Flavonoid | |
Source of phytochemicals or plant Extracts | Azadirachta indica | |
Geographical availability | Assam, Bangladesh, Cambodia, Laos, Myanmar, Thailand, Vietnam | |
Plant parts | Flowers | |
Other cancers | Breast cancer, Prostate cancer, Gastric cancer, Lung cancer, Leukemia | |
Target gene or protein | ER | |
Gene or Protein evidence | We conclude that antiestrogenic activities of flavonoid phytochemicals may occur through ER binding-dependent and -independent mechanisms and that the binding-independent antiestrogen activity of certain flavonoids is biologically significant in regulation of breast cancer cell proliferation. | |
Target pathways | NA | |
IC50 | 81.2±8.0 μM against SKBR-3 | |
Potency | NA | |
Cell line/ mice model | HL60, A549, AZ521, SKBR-3, MCF-7,PC-3, T-47D | |
Additional information | Several flavonoids, including kaempferide, apigenin, and flavone, were distinct, in that their antiestrogenic activity did not appear to correlate with binding to ER, and therefore their suppression of estrogen-mediated gene transactivation and proliferation may occur independent of direct antagonism of the receptor. | |
PubChem ID | 5281666 | |
Additional PMIDs | 26047480 31493543 11525602 23123452 26345098 24443427 | |
Additional sources of information | https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:1213180-2 | |
Safety | NA |