Phytochemical Name : Kaempferol 3-O-α-l-rhamnopyranosyl-(1→6)-β-d-glucopyranoside

Properties Information
PhytoCAT-ID PhytoCAT-12
Phytochemical name or plant extracts Kaempferol 3-O-α-l-rhamnopyranosyl-(1→6)-β-d-glucopyranoside
PMID 28951762
Literature evidence Ethanol extracts of the three parts of C. procera were evaluated for their antiulcer activity and we found that the leaf extract possessed a powerful antiulcer activity which could be considered as a promising drug candidate.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Flavonoid glycoside
Source of phytochemicals or plant Extracts Calotropis procera
Geographical availability Afghanistan, Algeria, Assam, Bangladesh, Benin, Burkina, Cambodia, Cameroon, Canary Is., Cape Verde, Central African Repu, Chad, Congo, Djibouti, East Himalaya, Egypt, Eritrea, Ethiopia, Gambia, Ghana, Guinea, Guinea-Bissau, Gulf of Guinea Is., Gulf States, India, Iran, Ivory Coast, Kenya, Kuwait, Lebanon-Syria, Libya, Malawi, Mali, Mauritania, Morocco, Mozambique, Myanmar, Nepal, Niger, Nigeria, Oman, Pakistan, Palestine, Saudi Arabia, Senegal, Sierra Leone, Sinai, Socotra, Somalia, Sudan, Tanzania, Thailand, Tunisia, Uganda, Vietnam, Western Sahara, Yemen, Zambia, Zaïre, Zimbabwe
Plant parts Fruits
Other cancers Breast cancer, Colorectal cancer, Lung cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 18.0 ± 3.40 µg/mL against MCF-7
Potency NA
Cell line/ mice model MCF-7, HCT-116, HepG-2, A-549, SK-LU-1, KB
Additional information  Compound 2 was highly active on all the cell lines, whereas compounds 5 and 11 were more selective on colon and liver cell lines. Compound 10 demonstrated a significant activity on liver and lung cancer cell lines. Compound 11 is Kaempferol 3-O-α-l-rhamnopyranosyl-(1→6)-β-d-glucopyranoside
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:1004515-2
Safety NA