dc.contributor.author |
Masike, Keabetswe |
|
dc.contributor.author |
Mhlongo, Msizi I. |
|
dc.contributor.author |
Mudau, Shonisani P. |
|
dc.contributor.author |
Nobela, Ofentse |
|
dc.contributor.author |
Ncube, Efficient N. |
|
dc.contributor.author |
Tugizimana, Fidele |
|
dc.contributor.author |
George, Mosotho J. |
|
dc.contributor.author |
Madala, Ntakadzeni E. |
|
dc.date.accessioned |
2018-05-04T13:46:56Z |
|
dc.date.available |
2018-05-04T13:46:56Z |
|
dc.date.issued |
2017 |
|
dc.identifier.uri |
http://repository.tml.nul.ls/handle/20.500.14155/1419 |
|
dc.description.abstract |
Plants contain a myriad of metabolites which exhibit diverse biological activities. However, in-depth
analyses of these natural products with current analytical platforms remains an undisputed challenge due to the multidimensional chemo-diversity of these molecules, amplifid by both isomerization and conjugation. In this study, we
looked at molecules such as hydroxyl-cinnamic acids (HCAs), which are known to exist as positional and geometrical
isomers conjugated to diffrent organic acids namely quinic- and isocitric acid. |
en_ZA |
dc.description.sponsorship |
RCC |
en_ZA |
dc.language.iso |
en |
en_ZA |
dc.publisher |
Springer |
en_ZA |
dc.subject |
Amaranthus viridis, Hydroxyl-cinnamic acid, Hydroxycinnamoyl-isocitric acid, Hydroxycinnamoyl-quinic acid, Mass spectrometry, Moringa oleifera |
en_ZA |
dc.title |
Highlighting mass spectrometric fragmentation diffrences and similarities between hydroxycinnamoyl-quinic acids and hydroxycinnamoyl-isocitric acids |
en_ZA |
dc.type |
Article |
en_ZA |