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
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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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Title
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
Creators - without role
Mpho Mankone Makola
Contributors - without role
N .E. Madala
I. A. Dubery
P. A. Steenkamp
M. M. Kabanda
Awarding Institution
University of Johannesburg; Master of Science (MSc)
Theses and Dissertations
Master of Science (MSc), University of Johannesburg
Identifiers
9910086807691
Copyright
University of Johannesburg
Academic Unit
Department of Biochemistry
Resource Type
Thesis
Details
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