Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents

Hypertension has emerged as one of the leading risk factors responsible for global burden and mortality. Among the hypertensive patients, there is a segment of patients who are suffering from resistant hypertension, whose blood pressure cannot be controlled despite concurrently taking three or more...

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Main Author: Lee, Fong Kai
Format: Thesis (University of Nottingham only)
Language:English
Published: 2020
Subjects:
Online Access:https://eprints.nottingham.ac.uk/60469/
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author Lee, Fong Kai
author_facet Lee, Fong Kai
author_sort Lee, Fong Kai
building Nottingham Research Data Repository
collection Online Access
description Hypertension has emerged as one of the leading risk factors responsible for global burden and mortality. Among the hypertensive patients, there is a segment of patients who are suffering from resistant hypertension, whose blood pressure cannot be controlled despite concurrently taking three or more classes of antihypertensive drugs. The adverse effects associated with the common classes of antihypertensive agents used have limited the combinations available to be used in treating resistant hypertension. Natural products play a vital role in drug discovery and development as they represent promising sources of useful lead molecules, in which they might be able to address the resistant hypertension issue. Our group has recently isolated from a previously uninvestigated Ficus species (F. schwarzii) a series of nine new phenethylamine alkaloids, namely, schwarzinicines A–G (142–148) and schwarzificusines A (149) and B (150). Schwarzinicine A (142), being the most abundant alkaloid of this series, was found to exhibit pronounced vasorelaxant effects in rat isolated aorta. In this study, we have successfully developed the total syntheses of schwarzinicines A (142), B (143) and F (147). In order to explore the active pharmacophore of schwarzinicine A (142) as a lead compound for vasorelaxation, several series of analogues were designed, synthesized and evaluated for their vasorelaxant activity for structure-activity relationship (SAR) analysis. In addition to the discovery of 13 synthetic analogues that were shown to be promising for further development, the SAR study revealed a few structural features that are associated with enhancement of vasorelaxant effects. These structural features could be useful to design better vasorelaxant agents in the future.
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spelling nottingham-604692025-02-28T14:53:50Z https://eprints.nottingham.ac.uk/60469/ Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents Lee, Fong Kai Hypertension has emerged as one of the leading risk factors responsible for global burden and mortality. Among the hypertensive patients, there is a segment of patients who are suffering from resistant hypertension, whose blood pressure cannot be controlled despite concurrently taking three or more classes of antihypertensive drugs. The adverse effects associated with the common classes of antihypertensive agents used have limited the combinations available to be used in treating resistant hypertension. Natural products play a vital role in drug discovery and development as they represent promising sources of useful lead molecules, in which they might be able to address the resistant hypertension issue. Our group has recently isolated from a previously uninvestigated Ficus species (F. schwarzii) a series of nine new phenethylamine alkaloids, namely, schwarzinicines A–G (142–148) and schwarzificusines A (149) and B (150). Schwarzinicine A (142), being the most abundant alkaloid of this series, was found to exhibit pronounced vasorelaxant effects in rat isolated aorta. In this study, we have successfully developed the total syntheses of schwarzinicines A (142), B (143) and F (147). In order to explore the active pharmacophore of schwarzinicine A (142) as a lead compound for vasorelaxation, several series of analogues were designed, synthesized and evaluated for their vasorelaxant activity for structure-activity relationship (SAR) analysis. In addition to the discovery of 13 synthetic analogues that were shown to be promising for further development, the SAR study revealed a few structural features that are associated with enhancement of vasorelaxant effects. These structural features could be useful to design better vasorelaxant agents in the future. 2020-07-24 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/60469/1/Thesis%20Submission%20Lee%20Fong%20Kai%20%28Final%29.pdf Lee, Fong Kai (2020) Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents. PhD thesis, University of Nottingham. synthesis alkaloids organic compounds vasorelaxant hypertension schwarzinicines structure-activity relationship
spellingShingle synthesis
alkaloids
organic compounds
vasorelaxant
hypertension schwarzinicines
structure-activity relationship
Lee, Fong Kai
Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title_full Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title_fullStr Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title_full_unstemmed Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title_short Syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
title_sort syntheses and structure-activity relationship studies of schwarzinicine alkaloids as vasorelaxant agents
topic synthesis
alkaloids
organic compounds
vasorelaxant
hypertension schwarzinicines
structure-activity relationship
url https://eprints.nottingham.ac.uk/60469/