Phytochemical Name : Icaritin

Properties Information
PhytoCAT-ID PhytoCAT-1245
Phytochemical name or plant extracts Icaritin
PMID 28529129
Literature evidence Our results thus indicated that icaritin has a potential to be developed into a novel therapeutic agent for human TNBC.
IUPAC name 3,5,7-trihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
Phytochemicals’ class or type of plant extracts Flavonoid
Source of phytochemicals or plant Extracts Epimedium diphyllum
Geographical availability Japan
Plant parts NA
Other cancers Breast cancer, Prostate cancer, Liver cancer, Kidney cancer
Target gene or protein EGFR, GPER1
Gene or Protein evidence Our study demonstrated that icartin decreased both ER-?36 and EGFR protein expression, and induced apoptosis in TNBC MDA-MB-231 and MDA-MB-453 cells. To the best of our knowledge, our current findings demonstrate for the first time that ICA and ICT promote the progression of ER-negative breast cancer through the activation of membrane GPER1.
Target pathways We also found that icaritin inhibited ER-?36-mediated MAPK/ERK pathway and cyclin D1 induction by estrogen. Icariin and icaritin stimulate the proliferation of SKBr3 cells through the GPER1-mediated modulation of the EGFR-MAPK signaling pathway. An anticancer agent icaritin induces sustained activation of the extracellular signal-regulated kinase (ERK) pathway and inhibits growth of breast cancer cells.
IC50 NA
Potency Our results thus indicated that icaritin has a potential to be developed into a novel therapeutic agent for human TNBC.
Cell line/ mice model MDA-MB-231, MCF-7, MDA-MB-453 , 4T1,SKBR-3
Additional information  Icaritin has been used in trials studying the treatment of Solid Tumors, Metastatic Breast Cancer, and Hepatocellular Carcinoma (HCC).
PubChem ID 5318980
Additional PMIDs 23977023 24718680 26079090 32003229 32762483 25531867 21376032 28529129
Additional sources of information https://www.drugbank.ca/drugs/DB12672 https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:107274-1
Safety NA