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Preferential alkali metal adduct formation by cis geometrical isomers of dicaffeoylquinic acids allows for efficient discrimination from their trans isomers during ultra-high-performance liquid chromatography/quadrupole time-of-flight mass spectrometry

Makola, MM; Steenkamp, Paul A; Dubery, IA; Kabanda, MM; Madala, NE (Wiley, 2016-03)
Effect of geometrical isomerism of 3,5-dicaffeoylquinic acid on its binding affinity to HIV-integrase enzyme: a molecular docking study

Makola, MM; Dubery, IA; Koorsen, G; Steenkamp, Paul A; Kabanda, MM; Du Preez, LL; Madala, NE (Hindawi, 2016)
Influence of the geometric isomers on the radical scavenging properties of 3,5-dica®eoylquinic acid: A DFT study in vacuo and in solution

Makola, MM; Madala, NE; Dubery, IA; Steenkamp, Paul A; Kabanda, MM (World Scientific Publishing, 2016-09)

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