Phytochemical Name : Embelin

Properties Information
PhytoCAT-ID PhytoCAT-1098
Phytochemical name or plant extracts Embelin
PMID 23425971
Literature evidence In our previous studies, we have demonstrated that embelin is able to induce the apoptosis of MCF-7 breast cancer cells in a dose-dependent manner.
IUPAC name 2,5-dihydroxy-3-undecylcyclohexa-2,5-diene-1,4-dione
Phytochemicals’ class or type of plant extracts Quinone
Source of phytochemicals or plant Extracts Embelia ribes
Geographical availability Assam, Bangladesh, Borneo, Cambodia, China South-Central, China Southeast, East Himalaya, Hainan, India, Jawa, Laos, Malaya, Myanmar, Nicobar Is., Philippines, Sri Lanka, Sulawesi, Sumatera, Thailand, Tibet, Vietnam
Plant parts Fruits
Other cancers Breast cancer
Target gene or protein SOD1, ERK1, ERK2, Bax, Bcl-2, XIAP
Gene or Protein evidence Embelin treatment resulted in activation of extracellular signal-regulated kinase (ERK)1/2 and ROS accumulation, which correlated with downregulation of antioxidant protein SOD1 and consumption of redox modulator reduced glutathione in the XIAP-overexpressing cells. Moreover, embelin was demonstrated to promote mitochondrial release of cytochrome C via regulation of Bax and Bcl-2, resulting in the activation of caspase-3 and -9, while no significant changes in the level of caspase-8 were observed. Embelin primes IBC cells for TRAIL-mediated apoptosis by its direct action on the anti-caspase activity of XIAP and by shifting the cellular redox balance toward oxidative stress-mediated apoptosis.
Target pathways The results have demonstrated that embelin-induced apoptosis of MCF-7 breast cancer cells involves the mitochondrial pathway.
IC50 NA
Potency Moreover, embelin has the potent effect of restraining the cell cycle transition of breast cancer cells to blockade the cell cycle in G2/M phase, therefore altering the progression of the cell cycle to induce apoptosis.
Cell line/ mice model MCF-7, 4T1
Additional information  Embelin, an inhibitor of RANKL-induced NF-κB activation has great potential as a therapeutic agent for osteoporosis and cancer-linked bone loss.
PubChem ID 3218
Additional PMIDs 20826545 23425971 22508521 34282169 33069102 12419914 25336399
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:588451-1
Safety NA