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dc.contributor.authorLam, Jennifer D.-
dc.date.accessioned2023-11-30T02:43:09Z-
dc.date.available2023-11-30T02:43:09Z-
dc.date.issued2023-
dc.identifier.otherOER000002748vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/23612-
dc.description.abstractAngiotensin-converting enzyme inhibitors (ACEI) such as Moexipril, Trandolapril, Ramipril, and Perindopril are used to treat hypertension. However, these drugs have undesired side effects. Using computational studies, two new novel drug candidates were designed with improved molecular interactions, ADMET properties, and docking scores compared to Moexipril. Homology analysis was done to determine the best animal model for preclinical studies, and it revealed that Pan troglodytes (chim-panzees) and Mus musculus (house mouse) were the best candidates.vi
dc.description.urihttps://www.biorxiv.org/content/10.1101/2022.04.27.489637v1.full.pdf+htmlvi
dc.formatPDFvi
dc.language.isoenvi
dc.publisherbioRxivvi
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Vietnam*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/vn/*
dc.subjectchất ức chếvi
dc.subjectenzymevi
dc.subjectAngiotensin mớivi
dc.subjectThiết kếvi
dc.subjectchuyển đổivi
dc.subject.lccTP248.27vi
dc.titleComputationally Guided Design of Novel Angiotensin Converting Enzyme Inhibitorsvi
dc.typeJournal articlevi
dc.description.noteCC BY-NC-ND 4.0vi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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