Phytochemical Name : Methyl antcinate A

Properties Information
PhytoCAT-ID PhytoCAT-1784
Phytochemical name or plant extracts Methyl antcinate A
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 methyl (6R)-6-[(6S,11aR)-6,11a-dimethyl-7,10-dioxo-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]-2-methyl-3-methylideneheptanoate
Phytochemicals’ class or type of plant extracts Triterpenoid
Source of phytochemicals or plant Extracts Antrodia camphorata, Antrodia cinnamomea
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 Bax, Bak, PUMA.
Gene or Protein evidence MAA can also up-regulate Bax, Bak, PUMA, and mitochondrial translocation of cofilin, activate caspase-3 and lead to cell death
Target pathways Exerts cell death through the caspase-dependent cascade and the Bax-mediated mitochondrial apoptotic pathway Suppresses the expression of heat shock protein 27 and increases the expression of IkBα and p53 3. MAA induces apoptosis in human liver and oral cancer cells through the mitochondrial-dependent pathway .
IC50 29.0 μM against BT474
Potency Our previous study in a liver cancer model showed that MAA, compound 11, which has more potent cytotoxic effects than Ant A and Ant C, may exert its anticancer capability via inducing ROS generation and NADPH oxidase activation
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  Shows good inhibitory effects on the self-renewal capability and cell migration ability of MCF7 sphere cells
PubChem ID NA
Additional PMIDs 23442930
Additional sources of information https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095428/
Safety NA