Phytochemical Name : α-eleostearic acid (α-ESA)

Properties Information
PhytoCAT-ID PhytoCAT-1818
Phytochemical name or plant extracts α-eleostearic acid (α-ESA)
PMID 24425042
Literature evidence China. α-eleostearic acid (α-ESA) has been shown to possess antitumor activity in cancer cells.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Trienoic fatty acid
Source of phytochemicals or plant Extracts Momordica charantia
Geographical availability Angola, Assam, Bangladesh, Benin, Borneo, Burkina, Burundi, Cameroon, Cape Verde, Central African Repu, Chad, Christmas I., Congo, East Himalaya, Ethiopia, Fiji, Gabon, Gambia, Ghana, Guinea, Guinea-Bissau, Gulf of Guinea Is., India, Ivory Coast, Jawa, Kenya, KwaZulu-Natal, Laos, Lesser Sunda Is., Liberia, Malawi, Malaya, Mali, Maluku, Mozambique, Namibia, Nepal, New Guinea, Niger, Nigeria, Northern Provinces, Northern Territory, Pakistan, Philippines, Queensland, Rwanda, Senegal, Sierra Leone, Society Is., Solomon Is., Sri Lanka, Sudan, Sulawesi, Sumatera, Tanzania, Thailand, Togo, Tonga, Uganda, Vanuatu, Vietnam, West Himalaya, Western Australia, Zambia, Zaïre, Zimbabwe
Plant parts Seeds
Other cancers Breast cancer
Target gene or protein Bcl-2, BAD, HER2, PTEN, HER3
Gene or Protein evidence Overall, these data suggest that a decreased Bcl-2 expression and increased BAD binding to Bcl-2 mediate α-ESA-induced apoptosis. Overall, these results suggest that decreased HER2/HER3 expression along with activation of PTEN upon α-ESA treatment may lead to decreased Akt phosphorylation.
Target pathways Akt/BAD/Bcl-2 apoptotic pathway, Akt/GSK-3β survival pathway, PI3K/Akt/GSK-3β pathway
IC50 NA
Potency Therefore, α-ESA may be considered a beneficial dietary factor for the prevention and treatment of invasive breast cancer in cells overexpressing HER2.
Cell line/ mice model SKBR-3, T47D, MCF-7
Additional information  α-linolenic acid and α-eleostearic acid could serve as cost-effective and natural phytochemical preparation to protect against the adverse effects caused by organic mercury in human.
PubChem ID NA
Additional PMIDs 22269903
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:293413-1
Safety NA