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In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins

AIM: To evaluate the inhibitory interaction of thymohydroquinone against blood–brain barrier (BBB)-associated neuropsychiatric and neurodegenerative disorders. MATERIALS & METHODS: An elaborated in silico study was designed to evaluate the interaction of thymohydroquinone with BBB-disrupting pro...

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Autores principales: Shah, Fahad Hassan, Salman, Saad, Idrees, Jawaria, Idrees, Fariha, Akbar, Muhammad Yasir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720366/
https://www.ncbi.nlm.nih.gov/pubmed/33312701
http://dx.doi.org/10.2144/fsoa-2020-0115
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author Shah, Fahad Hassan
Salman, Saad
Idrees, Jawaria
Idrees, Fariha
Akbar, Muhammad Yasir
author_facet Shah, Fahad Hassan
Salman, Saad
Idrees, Jawaria
Idrees, Fariha
Akbar, Muhammad Yasir
author_sort Shah, Fahad Hassan
collection PubMed
description AIM: To evaluate the inhibitory interaction of thymohydroquinone against blood–brain barrier (BBB)-associated neuropsychiatric and neurodegenerative disorders. MATERIALS & METHODS: An elaborated in silico study was designed to evaluate the interaction of thymohydroquinone with BBB-disrupting proteins and to highlight its pharmacokinetic and safety attributes. RESULTS: Thymohydroquinone demonstrated stable interaction with BBB-disrupting protein active site with Ki (inhibition constant) ranges of (2.71 mM–736.15 μM), binding energy (-4.3 to 5.6 Kcal/mol), ligand efficiency (-0.36 to 0.42 Kcal/mol) and root mean square deviation value of (0.80–2.59 Å). CONCLUSION: Further pharmacokinetic analysis revealed that thymohydroquinone is BBB and central nervous system (CNS) permeant with high acute toxicity and could be a candidate drug for the treatment of these neurological conditions.
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spelling pubmed-77203662020-12-11 In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins Shah, Fahad Hassan Salman, Saad Idrees, Jawaria Idrees, Fariha Akbar, Muhammad Yasir Future Sci OA Research Article AIM: To evaluate the inhibitory interaction of thymohydroquinone against blood–brain barrier (BBB)-associated neuropsychiatric and neurodegenerative disorders. MATERIALS & METHODS: An elaborated in silico study was designed to evaluate the interaction of thymohydroquinone with BBB-disrupting proteins and to highlight its pharmacokinetic and safety attributes. RESULTS: Thymohydroquinone demonstrated stable interaction with BBB-disrupting protein active site with Ki (inhibition constant) ranges of (2.71 mM–736.15 μM), binding energy (-4.3 to 5.6 Kcal/mol), ligand efficiency (-0.36 to 0.42 Kcal/mol) and root mean square deviation value of (0.80–2.59 Å). CONCLUSION: Further pharmacokinetic analysis revealed that thymohydroquinone is BBB and central nervous system (CNS) permeant with high acute toxicity and could be a candidate drug for the treatment of these neurological conditions. Future Science Ltd 2020-09-25 /pmc/articles/PMC7720366/ /pubmed/33312701 http://dx.doi.org/10.2144/fsoa-2020-0115 Text en © 2020 Fahad Hassan Shah This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Shah, Fahad Hassan
Salman, Saad
Idrees, Jawaria
Idrees, Fariha
Akbar, Muhammad Yasir
In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title_full In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title_fullStr In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title_full_unstemmed In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title_short In silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
title_sort in silico study of thymohydroquinone interaction with blood–brain barrier disrupting proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720366/
https://www.ncbi.nlm.nih.gov/pubmed/33312701
http://dx.doi.org/10.2144/fsoa-2020-0115
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