Phytochemical Name : Xanthone V

Properties Information
PhytoCAT-ID PhytoCAT-1991
Phytochemical name or plant extracts Xanthone V
PMID 21886765
Literature evidence In the present work, we carried out a preliminary screening of six natural compounds, xanthone V(1) (1); 2-acetylfuro-1,4-naphthoquinone (2); physcion (3); bisvismiaquinone (4); vismiaquinone (5); 1,8-dihydroxy-3-geranyloxy-6-methylQuinone (6) against MiaPaCa-2 pancreatic and CCRF-CEM leukemia cells and their multidrug-resistant subline, CEM/ADR5000.
IUPAC name methanol;5,9,10-trihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
Phytochemicals’ class or type of plant extracts Xanthone
Source of phytochemicals or plant Extracts Vismia laurentii
Geographical availability Cameroon, Central African Repu, Congo, Zaïre
Plant parts NA
Other cancers Breast cancer
Target gene or protein Caspase 3, Caspase 7
Gene or Protein evidence Caspase 3/7 was activated by xanthone V(1)
Target pathways NA
IC50 0.56±0.06 µg/ml against MCF-7
Potency The overall results of the present study provided evidence for the cytotoxicity of compounds xanthone V(1) and 2-acetylfuro-1,4-naphthoquinone, and bring supportive data for future investigations that will lead to their use in cancer therapy.
Cell line/ mice model CCRF-CEM, CEM/ADR5000, PF-382, HL-60, MiaPaCa-2, Capan-1, MCF-7, SW-680, 786-0, U87MG, A549, Colo-38, HeLa, Caski
Additional information  The most sensitive cancer cell lines to xanthone V1 and 2-acetylfuro-1,4-naphthoquinone were Colo-38 (melanoma), HeLa and Caski (cervix cancer) with IC50 values being closer or lower those obtained with doxorubicin. In addition, MCF-7 (breast cancer) and PF-382 (leukemia) also showed high sensitivity to xanthone V1 and 2-acetylfuro-1,4-naphthoquinone respectively.
PubChem ID 139068057
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:77185673-1
Safety NA