Phytochemical Name : Livistona chinensis extract

Properties Information
PhytoCAT-ID PhytoCAT-677
Phytochemical name or plant extracts Livistona chinensis extract
PMID 16919867
Literature evidence In conclusion, the active components with both antitumor and protein kinases inhibitor activities were highly purified from LC, which can inhibit the EGF signaling events mainly through EGFR modification.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Ethanolic extract
Source of phytochemicals or plant Extracts Livistona chinensis
Geographical availability China Southeast, Hainan, Japan, Nansei-shoto, Taiwan
Plant parts Seeds
Other cancers Breast cancer, Nasopharyngeal cancer
Target gene or protein PAK2, PKA, PKC, GSK-3alpha, CK2, MAPK, JNK1, EGF
Gene or Protein evidence LC-X inhibited the activities of various protein kinases in vitro, including PAK2, PKA, PKC, GSK-3alpha, CK2, mitogen-activated protein kinase (MAPK), and JNK1, with IC(50) between approximately 1 and 40microg/ml. In conclusion, the active components with both antitumor and protein kinases inhibitor activities were highly purified from LC, which can inhibit the EGF signaling events mainly through EGFR modification.
Target pathways EGF/EGFR-mediated MAPK signaling pathway
IC50 NA
Potency In conclusion, the active components with both antitumor and protein kinases inhibitor activities were highly purified from LC, which can inhibit the EGF signaling events mainly through EGFR modification. Blockage of the functions of EGFR may account for the antitumor activity of these active components.
Cell line/ mice model HeLa, A431, MCF-7, NPC-TW02 and -TW04
Additional information  The proliferation of two NPC (NPC-TW02 and -TW04) and one breast cancer (MCF-7) cell lines, but not the epidermoid (A431) and cervical (HeLa) carcinoma cell lines, were significantly blocked by LC-X at the dose of >50microg/ml.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:668021-1
Safety NA