Phytochemical Name : 23-O-acetylcimigenol-3-O-β-D-xylopyranoside

Properties Information
PhytoCAT-ID PhytoCAT-4
Phytochemical name or plant extracts 23-O-acetylcimigenol-3-O-β-D-xylopyranoside
PMID 20564500
Literature evidence The present study was carried out to investigate the antitumor activity of five cycloartane triterpenoids isolated from Cimicifuga yunnanensis on the breast cancer cell line MCF7 and its corresponding drug resistant subline R-MCF7, including cimigenol-3-O-β-D-xylopyranoside (compound 1), 25-O-acetylcimigenol-3-O-β-D-xylopyranoside (compound 2), 25-chlorodeoxycimigenol-3-O-β-D-xylopyranoside (compound 3), 25-O-acetylcimigenol-3-O-α-L-arabinopyranoside (compound 4) and 23-O-acetylcimigenol-3-O-β-D-xylopyranoside (compound 5).
IUPAC name NA
Phytochemicals’ class or type of plant extracts Cycloartane triterpenoid
Source of phytochemicals or plant Extracts Cimicifuga yunnanensis
Geographical availability China North-Central, China South-Central
Plant parts Rhizome
Other cancers Breast cancer
Target gene or protein p53, Bax, Caspase 7
Gene or Protein evidence The results of RT-PCR showed that compounds 2-5 increased the expression of p53 and bax, which led to the loss of mitochondrial potential and then resulted in the activation of caspase-7.
Target pathways p53-dependent mitochondrial pathway.
IC50 39.13 ± 1.52 µg/mL against MCF-7 59.75 ± 1.13 µg/mL against R-MCF-7
Potency The results showed that compounds 2-5 have relatively high antitumor activity on both MCF7 and R-MCF7 cells. Compound 5 is 23-O-acetylcimigenol-3-O-β-D-xylopyranoside.
Cell line/ mice model MCF-7, R-MCF-7
Additional information  Compound 2 and compound 5 have been reported to have anti-liver cancer activity, and this study displayed that they also have anti-breast cancer activity. Compound 5 is 23-O-acetylcimigenol-3-O-β-D-xylopyranoside. These findings collectively demonstrated that compounds 2-5 induced apoptosis of MCF7 via p53-dependent mitochondrial pathway.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:1002882-1
Safety NA