Phytochemical Name : Daidzin

Properties Information
PhytoCAT-ID PhytoCAT-1339
Phytochemical name or plant extracts Daidzin
PMID 15492830
Literature evidence Taken together, our results suggest that dietary soy isoflavones inhibit adhesion and motility of highly invasive breast cancer cells by distinct signaling pathways.
IUPAC name 3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Phytochemicals’ class or type of plant extracts Flavanoid
Source of phytochemicals or plant Extracts Glycine max
Geographical availability Amur, China North-Central, China South-Central, China Southeast, Hainan, Inner Mongolia, Japan, Khabarovsk, Korea, Laos, Manchuria, Nansei-shoto, Primorye, Qinghai, Taiwan, Thailand, Tibet, Vietnam, Xinjiang
Plant parts NA
Other cancers Breast cancer
Target gene or protein ER
Gene or Protein evidence Furthermore, in drug interaction studies daidzin-rich isoflavone extracts antagonized tamoxifen, an ER inhibitor.
Target pathways NF-kappaB/AP-1-dependent and -independent pathways
IC50 50 µg/mL against ZR-75-1
Potency NA
Cell line/ mice model ZR-75-1, MDA-MB-231, MCF-7
Additional information  Inhibits constitutively active NF-kappaB and AP-1 and suppresses secretion of uPA from breast cancer cells, reduces motility of MDA-MB-231 cells. Enhances the acetylcholinesterase (AChE) activity of the rat neuronal cell line PC12 at concentrations as low as 0.08 muM by binding to the estrogen receptor (ER). 2. significantly decreases 8-hydroxydeoxyguanosine content and increased superoxide dismutase level in normal rats and decreased malondialdehyde concentrations in ovariectomized rats
PubChem ID 107971
Additional PMIDs 19003112 18313242 12670155 27043076 15492830 8910911 4426188 2749004 17142977 26658676
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:60450240-2
Safety NA