Phytochemical Name : (6E,10E) Isopolycerasoidol Methyl Ester

Properties Information
PhytoCAT-ID PhytoCAT-772
Phytochemical name or plant extracts (6E,10E) Isopolycerasoidol Methyl Ester
PMID 25946039
Literature evidence Taken together, our data demonstrate that (1) and (2) induce intrinsic mitochondrial-mediated apoptosis in human breast cancer cells, which provides the first pharmacological evidence for their future development as anticancer agents.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Benzopyran derivative
Source of phytochemicals or plant Extracts Pseuduvaria monticola
Geographical availability Malaya, Thailand
Plant parts Leaves
Other cancers Breast cancer
Target gene or protein Caspase 3, Caspase 7, Caspase 9, Bcl-2, p38 MAPK
Gene or Protein evidence These effects occurred concomitantly with a dose-dependent activation of caspase 3/7 and 9, a down-regulation of the anti-apoptotic gene BCL2 and the accumulation of p38 MAPK in the nucleus.
Target pathways BCL2 and p38 MAPK signaling pathways
IC50 43 ± 2.4μM against MCF-7 58 ± 2.6μM against MDA-MB-231
Potency MTT results revealed both (1) and (2) were efficient in reducing cell viability of breast cancer cells. Flow cytometry analysis demonstrated that (1) and (2) induced cell death via apoptosis, as demonstrated by an increase in phosphotidylserine exposure. Both compounds elevated ROS production, leading to reduced mitochondrial membrane potential and increased plasma membrane permeability in breast cancer cells.
Cell line/ mice model MCF-7,MDA-MB-231
Additional information  Collectively, our data demonstrate that both (1) and (2) increase membrane permeability, decrease MMP and activate caspases involved in the intrinsic apoptosis pathway in breast cancer cells by modulating BCL2 and p38 MAPK signaling molecules
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:74957-1
Safety NA