Phytochemical Name : 6-prenylnaringenin (6-PN)

Properties Information
PhytoCAT-ID PhytoCAT-1039
Phytochemical name or plant extracts 6-prenylnaringenin (6-PN)
PMID 25044854
Literature evidence METHODS AND RESULTS: ABCG2-inhibitory activity of xanthohumol (XN), isoxanthohumol (IX), 6-prenylnaringenin (6-PN), 8-prenylnaringenin (8-PN), and 6,8-diprenylnarigenin (6,8-diPN) was evaluated using mitoxantrone accumulation and vesicular transport assays.
IUPAC name (2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
Phytochemicals’ class or type of plant extracts Flavonoid
Source of phytochemicals or plant Extracts Humulus lupulus
Geographical availability Albania, Altay, Austria, Baltic States, Belarus, Belgium, Bulgaria, Buryatiya, Central European Rus, Chita, Corse, Czechoslovakia, Denmark, East European Russia, Finland, France, Germany, Great Britain, Greece, Hungary, Iran, Irkutsk, Italy, Kazakhstan, Krasnoyarsk, Krym, Morocco, Netherlands, North Caucasus, North European Russi, Northwest European R, Norway, Poland, Portugal, Romania, Sardegna, Sicilia, South European Russi, Spain, Sweden, Switzerland, Transcaucasus, Turkey, Turkey-in-Europe, Ukraine, West Siberia, Yugoslavia
Plant parts NA
Other cancers Breast cancer, Prostate cancer, Colon cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 NA
Potency 6-prenylnaringenin was stronger than cisplatin against breast cancer cell line T-47D.
Cell line/ mice model MDA-MB-231, T-47D, PC-3, HT-29, A-2780
Additional information  NA
PubChem ID 155094
Additional PMIDs 30423918
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:303502-2
Safety NA