Phytochemical Name : 7β-(3-Ethyl-cis-crotonoyloxy)-1α-(2-methylbutyryloxy)-3,14-dehydro-Z-notonipetranone (ECN)

Properties Information
PhytoCAT-ID PhytoCAT-168
Phytochemical name or plant extracts 7β-(3-Ethyl-cis-crotonoyloxy)-1α-(2-methylbutyryloxy)-3,14-dehydro-Z-notonipetranone (ECN)
PMID 31337063
Literature evidence Therefore, research on searching for promising compounds with metabolism that suppress phosphorylation or transcription of STAT3 in TNBC cells is important.
IUPAC name NA
Phytochemicals’ class or type of plant extracts Sesquiterpene
Source of phytochemicals or plant Extracts Tussilago farfara
Geographical availability Afghanistan, Albania, Algeria, Altay, Austria, Baltic States, Belarus, Belgium, Bulgaria, Buryatiya, Central European Rus, China North-Central, China South-Central, China Southeast, Corse, Cyprus, Czechoslovakia, Denmark, East Aegean Is., East European Russia, East Himalaya, Egypt, Finland, France, Føroyar, Germany, Great Britain, Greece, Hainan, Hungary, Iceland, Inner Mongolia, Iran, Ireland, Irkutsk, Italy, Kazakhstan, Kirgizstan, Krasnoyarsk, Kriti, Krym, Lebanon-Syria, Libya, Manchuria, Morocco, Nepal, Netherlands, North Caucasus, North European Russi, Northwest European R, Norway, Pakistan, Poland, Qinghai, Romania, Sardegna, Sicilia, South European Russi, Spain, Sweden, Switzerland, Tadzhikistan, Tibet, Transcaucasus, Tunisia, Turkey, Turkey-in-Europe, Turkmenistan, Ukraine, Uzbekistan, West Himalaya, West Siberia, Western Sahara, Xinjiang, Yakutskiya, Yugoslavia
Plant parts Flowers
Other cancers Breast cancer
Target gene or protein STAT-3
Gene or Protein evidence ECN inhibited JAK-STAT3 signaling and suppressed the expression of STAT3 target genes.
Target pathways JAK-STAT3 signaling
IC50 NA
Potency Therefore, ECN can be an effective chemotherapeutic agent for breast cancer treatment.
Cell line/ mice model MDA-MB-231
Additional information  Here, 7β-(3-Ethyl-cis-crotonoyloxy)-1α-(2-methylbutyryloxy)-3,14-dehydro-Z-notonipetranone (ECN), a compound isolated from Farfarae Flos showed a potent cytotoxic effect on MDA-MB-231 cells.
PubChem ID NA
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:256904-1
Safety NA