Phytochemical Name : Tomatine

Properties Information
PhytoCAT-ID PhytoCAT-244
Phytochemical name or plant extracts Tomatine
PMID 25466288
Literature evidence Upon emergence of modern anticancer therapy, medical community is divided into two opposite camps, one of them claiming absolute necessity of using isolated or synthesized chemical compounds for efficient patient treatment and another one advocating alternative cancer therapies, in particular those based on natural sources, including extracts from plants.
IUPAC name (2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6S,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-piperidine]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Phytochemicals’ class or type of plant extracts Alkaloid
Source of phytochemicals or plant Extracts Solanum lycopersicum
Geographical availability Peru
Plant parts Leaves
Other cancers Breast cancer
Target gene or protein MMP2, MMP9, MMP9\NGAL
Gene or Protein evidence Activation of MMP-2, MMP-9 and MMP-9\NGAL has been shown to decrease significantly in cells treated with tomatine by gelatin zymography compared to the control.
Target pathways NA
IC50 7.07 μM against MCF-7
Potency As a result, matrix metalloproteinase activity and cell proliferation were suppressed by tomatine and this may provide support in treatment methods.
Cell line/ mice model MCF-7
Additional information  NA
PubChem ID 28523
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:316947-2
Safety NA