Phytochemical Name : Jatrorrhizine

Properties Information
PhytoCAT-ID PhytoCAT-730
Phytochemical name or plant extracts Jatrorrhizine
PMID 31302315
Literature evidence CONCLUSION: These findings provide an overall perspective that jatrorrhizine potentially restrains TNIK regulating Wnt/β-catenin signalling and EMT expression for mammary cancer targeted therapy.
IUPAC name 2,9,10-trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol
Phytochemicals’ class or type of plant extracts Alkaloid
Source of phytochemicals or plant Extracts Coptis chinensis
Geographical availability China North-Central, China South-Central, China Southeast, Vietnam
Plant parts Rhizome
Other cancers Breast cancer
Target gene or protein TNIK
Gene or Protein evidence The results showed that targeted knockout of TNIK that attenuated Wnt/β-catenin signalling and epithelial-mesenchymal transition (EMT) expression, the effects were potentiated by the addition of jatrorrhizine.
Target pathways TNIK regulating Wnt/β-catenin signalling and EMT expression
IC50 11.08 ± 1.19 μM against MDA-MB-231 17.11 ± 4.54 μM against MCF-7 22.14 ± 2.87 μM against 4T1
Potency These findings provide an overall perspective that jatrorrhizine potentially restrains TNIK regulating Wnt/β-catenin signalling and EMT expression for mammary cancer targeted therapy.
Cell line/ mice model MDA-MB-231, MCF-7 and 4T1
Additional information  Here, we found that JAT could ameliorate NLRP3-N-GSDMD-dependent pyroptosis induced by MNV infection through inhibiting the MAPKs/NF-κB signaling pathways and decrease MNV replication in RAW264.7 macrophages, suggesting that JAT has the potential to be a therapeutic agent for treating norovirus gastroenteritis.
PubChem ID 72323
Additional PMIDs 30963783 36680009
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:710313-1
Safety These results were further corroborated by the 4T1 tumour-bearing mice, which showed that jatrorrhizine significantly suppressed the proliferation and metastasis of mammary carcinoma cells without obvious toxicity.