Phytochemical Name : Cichorin E

Properties Information
PhytoCAT-ID PhytoCAT-131
Phytochemical name or plant extracts Cichorin E
PMID 32932909
Literature evidence Moreover compounds 1-3 did not show any promising anthelmintic effects.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Naphthalane derivative
Source of phytochemicals or plant Extracts Cichorium intybus
Geographical availability Afghanistan, Albania, Algeria, Austria, Azores, Baleares, Baltic States, Belarus, Belgium, Bulgaria, Cape Verde, Central European Rus, Corse, Cyprus, Czechoslovakia, Denmark, East Aegean Is., East European Russia, Egypt, Finland, France, Germany, Greece, Hungary, Iran, Iraq, Italy, Kazakhstan, Kirgizstan, Kriti, Krym, Lebanon-Syria, Morocco, Netherlands, North Caucasus, North European Russia, Northwest European Russia, Norway, Pakistan, Palestine, Poland, Portugal, Romania, Sardegna, Sicilia, Sinai, South European Russia, Spain, Sweden, Switzerland, Tadzhikistan, Transcaucasus, Tunisia, Turkey, Turkey-in-Europe, Turkmenistan, Ukraine, Uzbekistan, West Himalaya, Yugoslavia
Plant parts Whole plant
Other cancers Breast cancer, Ewing's sarcoma, Prostate cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 MTT assay IC50 =85.9 µM against MDA-MB-468 CV assay IC50 = 80.0 µM against MDA-MB-468 MTT assay IC50 = >100 µM against MDA-MB-231 CV assay IC50 = >100 µM against MDA-MB-231
Potency Whereas Cichorins D was not active (IC50s > 100 µM) in all tested cell lines, Cichorins E exhibited anti-proliferative effects in the triple-negative breast cancer (TNBC) cell line MDA-MB-468 (IC50 = 85.9 µM and 80.0 µM when determined by MTT and CV assay, respectively) and the Ewing’s sarcoma cell line SK-N-MC (IC50 = 71.1 µM and 56.4 µM using MTT and CV assay, respectively)
Cell line/ mice model MDA-MB-468, MDA-MB-231, SK-N-MC, PC-3
Additional information  Phytochemical investigations of C. intybus provided two new naphthalane derivatives viz., cichorins D (1) and E (2) along with one new Quinone, cichorin F (3).
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:194533-1
Safety NA