Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits

Molecules. 2023 Apr 21;28(8):3621. doi: 10.3390/molecules28083621.

Abstract

High-performance liquid chromatography (HPLC) analysis of three commercial tomatine samples and another isolated from green tomatoes revealed the presence of two small peaks in addition to those associated with the glycoalkaloids dehydrotomatine and α-tomatine. The present study investigated the possible structures of the compounds associated with the two small peaks using HPLC-mass spectrophotometric (MS) methods. Although the two peaks elute much earlier on chromatographic columns than the elution times of the known tomato glycoalkaloids dehydrotomatine and α-tomatine, isolation of the two compounds by preparative chromatography and subsequent analysis by MS shows the two compounds have identical molecular weights, tetrasaccharide side chains, and MS and MS/MS fragmentation patterns to dehydrotomatine and α-tomatine. We suggest the two isolated compounds are isomeric forms of dehydrotomatine and α-tomatine. The analytical data indicate that widely used commercial tomatine preparations and those extracted from green tomatoes and tomato leaves consist of a mixture of α-tomatine, dehydrotomatine, an α-tomatine isomer, and a dehydrotomatine isomer in an approximate ratio of 81:15:4:1, respectively. The significance of the reported health benefits of tomatine and tomatidine is mentioned.

Keywords: LC-(Q) TOF/MS analysis; LC/MS analysis; dehydrotomatine; dehydrotomatine isomer; health benefits; research needs; tomato glycoalkaloids; tomatoes; α-tomatine; α-tomatine isomer.

MeSH terms

  • Solanum lycopersicum*
  • Tandem Mass Spectrometry
  • Tomatine* / chemistry

Substances

  • dehydrotomatine
  • alpha-tomatine
  • Tomatine

Grants and funding

This research received no external funding.