The solvation structure of alprazolam

Alprazolam is a benzodiazepine that is commonly prescribed for the treatment of anxiety and other related disorders. Like other benzodiazepines, it is thought to exert its effect through interaction with GABAA receptors. However, it has also been described as a potent and selective protein interacti...

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Main Authors: Sridhar, A, Johnston, A, Varathan, L, McLain, S, Biggin, P
Format: Journal article
Language:English
Published: Royal Society of Chemistry 2016
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author Sridhar, A
Johnston, A
Varathan, L
McLain, S
Biggin, P
author_facet Sridhar, A
Johnston, A
Varathan, L
McLain, S
Biggin, P
author_sort Sridhar, A
collection OXFORD
description Alprazolam is a benzodiazepine that is commonly prescribed for the treatment of anxiety and other related disorders. Like other benzodiazepines, it is thought to exert its effect through interaction with GABAA receptors. However, it has also been described as a potent and selective protein interaction inhibitor of bromodomain and extra-terminal (BET) proteins. Indeed, the only crystal structure of alprazolam bound to a protein is a complex between alprazolam and the BRD4 bromodomain. The structure shows that the complex also involves many water interactions that mediate contacts between the drug and the protein, a scenario that exists in many drug-protein complexes. How such waters relate to solvation patterns of small molecules may improve our understanding of what dictates their appearance or absence in bridging positions within complexes and thus will be important in terms of future rational drug-design. Here, we use neutron diffraction in conjunction with molecular dynamics simulations to provide a detailed analysis of how water molecules interact with alprazolam in methanol/water mixtures. The agreement between the neutron diffraction and the molecular dynamics is extremely good. We discuss the results in the context of drug design.
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spelling oxford-uuid:21794a43-1726-4a96-8b8f-22fd0c108f2f2022-03-26T11:33:37ZThe solvation structure of alprazolamJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:21794a43-1726-4a96-8b8f-22fd0c108f2fEnglishSymplectic Elements at OxfordRoyal Society of Chemistry2016Sridhar, AJohnston, AVarathan, LMcLain, SBiggin, PAlprazolam is a benzodiazepine that is commonly prescribed for the treatment of anxiety and other related disorders. Like other benzodiazepines, it is thought to exert its effect through interaction with GABAA receptors. However, it has also been described as a potent and selective protein interaction inhibitor of bromodomain and extra-terminal (BET) proteins. Indeed, the only crystal structure of alprazolam bound to a protein is a complex between alprazolam and the BRD4 bromodomain. The structure shows that the complex also involves many water interactions that mediate contacts between the drug and the protein, a scenario that exists in many drug-protein complexes. How such waters relate to solvation patterns of small molecules may improve our understanding of what dictates their appearance or absence in bridging positions within complexes and thus will be important in terms of future rational drug-design. Here, we use neutron diffraction in conjunction with molecular dynamics simulations to provide a detailed analysis of how water molecules interact with alprazolam in methanol/water mixtures. The agreement between the neutron diffraction and the molecular dynamics is extremely good. We discuss the results in the context of drug design.
spellingShingle Sridhar, A
Johnston, A
Varathan, L
McLain, S
Biggin, P
The solvation structure of alprazolam
title The solvation structure of alprazolam
title_full The solvation structure of alprazolam
title_fullStr The solvation structure of alprazolam
title_full_unstemmed The solvation structure of alprazolam
title_short The solvation structure of alprazolam
title_sort solvation structure of alprazolam
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