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Qualitative structure-activity relationship (QSAR) studies of 3,5-dicaffeoylquinic acid geometrical isomers with the aid of density functional theory (DFT), liquid chromatography mass spectrometry (LC-MS) and HIV-1 integrase docking studies
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Qualitative structure-activity relationship (QSAR) studies of 3,5-dicaffeoylquinic acid geometrical isomers with the aid of density functional theory (DFT), liquid chromatography mass spectrometry (LC-MS) and HIV-1 integrase docking studies

Mpho Mankone Makola
Master of Science (MSc), University of Johannesburg
2016
Handle:
https://hdl.handle.net/10210/124743

Abstract

Plant metabolites Phytochemicals Plant extracts - Therapeutic use Alkali metals Inductively coupled plasma mass spectrometry
Please refer to full text to view abstract M.Sc. (Biochemistry)
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Qualitative Structure-Activity Relationship (QSAR) studies of 3,5-dicaffeoylquinic acid geometrical isomers with the aid of Density Functional Theory (DFT), Liquid Chromatography Mass Spectrometry (LC-MS) and HIV-1 Integrase docking studiesDownloadView
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