Phytochemical Name : (E)-resveratrol 3-O-rutinoside

Properties Information
PhytoCAT-ID PhytoCAT-1942
Phytochemical name or plant extracts (E)-resveratrol 3-O-rutinoside
PMID 30346066
Literature evidence In addition, compounds 1-3 showed low toxicity against normal human prostate cell line, with selectivity indices greater than five across the carcinoma cells, indicating that the compounds possess potential in the development of low-toxicity chemotherapeutic agents.
IUPAC name (2S,3R,4S,5S,6R)-2-{3-hydroxy-5-[(1E)-2-(4-hydroxyphenyl)ethenyl]phenoxy}-6-({[(1R,2R,3R,4S,5R)-2,3,4-trihydroxy-5-methylcyclohexyl]oxy}methyl)oxane-3,4,5-triol
Phytochemicals’ class or type of plant extracts Resveratrol derivative
Source of phytochemicals or plant Extracts Commiphora africana
Geographical availability Angola, Benin, Botswana, Burkina, Cameroon, Caprivi Strip, Chad, Djibouti, Eritrea, Ethiopia, Gambia, Ghana, Ivory Coast, Kenya, KwaZulu-Natal, Malawi, Mali, Mauritania, Mozambique, Namibia, Niger, Nigeria, Northern Provinces, Rwanda, Senegal, Somalia, Sudan, Swaziland, Tanzania, Togo, Uganda, Zambia, Zaïre, Zimbabwe
Plant parts Stem
Other cancers NA
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 16.80 μM against MCF7
Potency Displayed the highest antiproliferative effect on the cell lines, with IC50 values of 16.80, 21.74, 17.89, and 17.44 μM, against MCF7, A549, PC3, and HepG2 human cancer cell lines, respectively.
Cell line/ mice model MCF-7, A549, PC3, and HepG2
Additional information  NA
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:127576-1
Safety compounds 1-3 showed low toxicity against normal human prostate cell line, with selectivity indices greater than five across the carcinoma cells, indicating that the compounds possess potential in the development of low-toxicity chemotherapeutic agents.