Phytochemical Name : Arachidin-1

Properties Information
PhytoCAT-ID PhytoCAT-250
Phytochemical name or plant extracts Arachidin-1
PMID 35163062
Literature evidence Investigating alternative therapies to increase survival rates for this disease is essential.
IUPAC name 5-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-2-[(E)-3-methylbut-1-enyl]benzene-1,3-diol
Phytochemicals’ class or type of plant extracts Stilbenoid
Source of phytochemicals or plant Extracts Arachis hypogaea
Geographical availability Bolivia
Plant parts Root
Other cancers Breast cancer
Target gene or protein Caspase 9, PARP, Survivin
Gene or Protein evidence Furthermore, A-1 induced caspase-dependent apoptosis through the intrinsic pathway by activating caspase-9 and PARP cleavage, and inhibiting survivin.
Target pathways NA
IC50 For 24h, 48h and 72h: 2.68 µM against MDA-MB-231, 7.82 µM against MDA-MB-231, 2.51 µM against MDA-MB-231 11.95 µM against MDA-MB-436, 6.20 µM against MDA-MB-436, 2.09 µM against MDA-MB-436
Potency In conclusion, A-1 merits further research as a potential lead molecule for the treatment of TNBC.
Cell line/ mice model MDA-MB-231, MDA-MB-435, MCF-10A
Additional information  A-1 did not show significant cytotoxicity in the non-cancerous cell line MCF-10A. While A-1 blocked cell division in G2-M phases in the TNBC cells, it did not affect cell division in MCF-10A cells.
PubChem ID 11220670
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:318562-2
Safety A-1 did not show significant cytotoxicity in the non-cancerous cell line MCF-10A.