Phytochemical Name : Dehydroeburicoic acid

Properties Information
PhytoCAT-ID PhytoCAT-1786
Phytochemical name or plant extracts Dehydroeburicoic acid
PMID 22753732
Literature evidence In addition to MAA, methyl antcinate B, dehydroeburicoic acid, and 15α-acetyl-dehydrosulfurenic acid also exhibited significant selective cytotoxic effects to respective cancer cells.
IUPAC name (2R)-2-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoic acid
Phytochemicals’ class or type of plant extracts Triterpenoid
Source of phytochemicals or plant Extracts Antrodia camphorata
Geographical availability Taiwan
Plant parts NA
Other cancers Breast cancer, Oral cancer, Epithelioid cancer, Prostate cancer, Ovarian cancer, Cervical cancer, Bone cancer, Stomach cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways Deregulates the PI3K/Akt/mTOR signaling pathway and key cell-cycle mediators, and induces apoptosis
IC50 NA
Potency NA
Cell line/ mice model KB, TSCCa, GNM, OC-2, and OEC-M1 , Panc-1 , BT-474, PC-3, OVCAR-3, HeLa, and U2OS, ER+ T47D
Additional information  Exhibits significant selective cytotoxic effects on the cell lines Inhibits tube-like structures of endothelial cells, blood vessel branching and microvessel formation ex vivo and in vivo. 3. DeEA exhibited non-cytotoxic effects towards human stomach cancer NUGC-3 cells , here it had significant cytotoxic effects on various cancer types, especially on head and neck cancer. Moreover, it has been reported that DeEA induced calcium- and calpain-dependent necrosis but not apoptosis in human U87MG glioblastomas .
PubChem ID 15250826
Additional PMIDs 28160860
Additional sources of information https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095428/
Safety NA