Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase

Tuberculosis, which is caused by the pathogenic bacterium Mycobacteria tuberculosis (MTB), is an infectious disease that remains a significant worldwide health threat. Galactofuranose (Galf) residues play an imperative role in the growth of MTB as it is an essential component in the cell wall of thi...

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Main Author: Tie, Ding Yee
Format: Thesis (University of Nottingham only)
Language:English
Published: 2013
Online Access:https://eprints.nottingham.ac.uk/13796/
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author Tie, Ding Yee
author_facet Tie, Ding Yee
author_sort Tie, Ding Yee
building Nottingham Research Data Repository
collection Online Access
description Tuberculosis, which is caused by the pathogenic bacterium Mycobacteria tuberculosis (MTB), is an infectious disease that remains a significant worldwide health threat. Galactofuranose (Galf) residues play an imperative role in the growth of MTB as it is an essential component in the cell wall of this bacterium. UDP-Galactopyranose mutase UGM) is a flavoenzyme that involved in Galf biosynthesis. It catalyzes the reversible conversion of UDP-galactopyranose (UDP-Galp) to UDP-galactofuranose (UDP-Galf). The absence of both UGM and Galf residues in humans make UGM a target for new TB therapeutic drugs. This has also brought us to an interest in UGM. Fourteen potential inhibitors of UGM were identified by alternating the R groups of the structure found computationally, and successfully synthesised in this project. Besides, HPLC assay was carried out to determine the purity of these inhibitors. Subsequently, docking experiments were performed to dock these compounds into the X-ray structure of Deinococcus radiodurans UGM. Further insight of the docking result is evaluated.
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institution University of Nottingham Malaysia Campus
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spelling nottingham-137962025-02-28T11:27:05Z https://eprints.nottingham.ac.uk/13796/ Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase Tie, Ding Yee Tuberculosis, which is caused by the pathogenic bacterium Mycobacteria tuberculosis (MTB), is an infectious disease that remains a significant worldwide health threat. Galactofuranose (Galf) residues play an imperative role in the growth of MTB as it is an essential component in the cell wall of this bacterium. UDP-Galactopyranose mutase UGM) is a flavoenzyme that involved in Galf biosynthesis. It catalyzes the reversible conversion of UDP-galactopyranose (UDP-Galp) to UDP-galactofuranose (UDP-Galf). The absence of both UGM and Galf residues in humans make UGM a target for new TB therapeutic drugs. This has also brought us to an interest in UGM. Fourteen potential inhibitors of UGM were identified by alternating the R groups of the structure found computationally, and successfully synthesised in this project. Besides, HPLC assay was carried out to determine the purity of these inhibitors. Subsequently, docking experiments were performed to dock these compounds into the X-ray structure of Deinococcus radiodurans UGM. Further insight of the docking result is evaluated. 2013-12-10 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/13796/1/TDY_MSc_thesis_FINAL_VERSION.pdf Tie, Ding Yee (2013) Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase. MSc(Res) thesis, University of Nottingham.
spellingShingle Tie, Ding Yee
Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title_full Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title_fullStr Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title_full_unstemmed Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title_short Design and synthesis of indole-thiazole based inhibitors of UDP-galactopyranose mutase
title_sort design and synthesis of indole-thiazole based inhibitors of udp-galactopyranose mutase
url https://eprints.nottingham.ac.uk/13796/