Phytochemical Name : Glycybridin D (4)

Properties Information
PhytoCAT-ID PhytoCAT-443
Phytochemical name or plant extracts Glycybridin D (4)
PMID 28140583
Literature evidence A number of compounds significantly activate Nrf2, inhibit tyrosinase or PTP1B, inhibit LPS-induced NO production and NF-κB transcription, and inhibit the proliferation of human cancer cells (HepG2, SW480, A549, MCF7).
IUPAC name 8-(7-hydroxy-2H-chromen-3-yl)-2,2-dimethyl-3-(3-methylbut-2-enyl)chromen-5-ol
Phytochemicals’ class or type of plant extracts Phenolic compound
Source of phytochemicals or plant Extracts Glycyrrhiza glabra
Geographical availability Afghanistan, Albania, Bulgaria, Central European Rus, China North-Central, Cyprus, East Aegean Is., East European Russia, Greece, Iran, Iraq, Italy, Kazakhstan, Kirgizstan, Krym, Lebanon-Syria, Mongolia, North Caucasus, Pakistan, Palestine, Romania, Sardegna, Saudi Arabia, Sicilia, South European Russi, Tadzhikistan, Transcaucasus, Turkey, Turkmenistan, Ukraine, Uzbekistan, West Siberia, Xinjiang, Yugoslavia
Plant parts Root and Rhizome
Other cancers Breast cancer, Liver cancer, Lung cancer, Colon cancer
Target gene or protein PTP1B
Gene or Protein evidence The two new compounds 4 and 8 and the six known compounds 16, 35, 37, 39, 47, and 52, all bearing an isoprenyl and an ortho-hydroxy group, dose-dependently inhibited PTP1B with IC50 values ranging from 5.0 to 7.9 μM.
Target pathways NA
IC50 4.6 to 6.6 μM
Potency Glycybridin D (4) showed moderate cytotoxic activities against the four cancer cell lines, with IC50 values ranging from 4.6 to 6.6 μM. 90.7 ± 1.0 % cytotoxic activity against MCF-7
Cell line/ mice model HepG2, SW480, A549, MCF-7
Additional information  Further studies indicated that 4 (10 mg/kg, ip) decreased tumor mass by 39.7% on an A549 human lung carcinoma xenograft mice model, but showed little toxicity.
PubChem ID 132504088
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:496941-1
Safety NA