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An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study

BACKGROUND: This study aims to synthesise and characterise novel compounds containing 2-amino-1,3,4-thiadiazole and their acyl derivatives and to investigate antifungal activities. Similarity search, molecular dynamics and molecular docking were also studied to find out a potential target and enligh...

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Autores principales: Er, Mustafa, Abounakhla, Abdulati Miftah, Tahtaci, Hakan, Bawah, Ali Hasin, Çınaroğlu, Süleyman Selim, Onaran, Abdurrahman, Ece, Abdulilah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768040/
https://www.ncbi.nlm.nih.gov/pubmed/30470928
http://dx.doi.org/10.1186/s13065-018-0485-3
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author Er, Mustafa
Abounakhla, Abdulati Miftah
Tahtaci, Hakan
Bawah, Ali Hasin
Çınaroğlu, Süleyman Selim
Onaran, Abdurrahman
Ece, Abdulilah
author_facet Er, Mustafa
Abounakhla, Abdulati Miftah
Tahtaci, Hakan
Bawah, Ali Hasin
Çınaroğlu, Süleyman Selim
Onaran, Abdurrahman
Ece, Abdulilah
author_sort Er, Mustafa
collection PubMed
description BACKGROUND: This study aims to synthesise and characterise novel compounds containing 2-amino-1,3,4-thiadiazole and their acyl derivatives and to investigate antifungal activities. Similarity search, molecular dynamics and molecular docking were also studied to find out a potential target and enlighten the inhibition mechanism. RESULTS: As a first step, 2-amino-1,3,4-thiadiazole derivatives (compounds 3 and 4) were synthesised with high yields (81 and 84%). The target compounds (6a–n and 7a–n) were then synthesised with moderate to high yields (56–87%) by reacting 3 and 4 with various acyl chloride derivatives (5a–n). The synthesized compounds were characterized using the IR, (1)H-NMR, (13)C-NMR, Mass, X-ray (compound 7n) and elemental analysis techniques. Later, the in vitro antifungal activities of the synthesised compounds were determined. The inhibition zones exhibited by the compounds against the tested fungi, their minimum fungicidal activities, minimum inhibitory concentration and the lethal dose values (LD(50)) were determined. The compounds exhibited moderate to high levels of activity against all tested pathogens. Finally, in silico modelling was used to enlighten inhibition mechanism using ligand and structure-based methods. As an initial step, similarity search was carried out and the resulting proteins that belong to Homo sapiens were used as reference in sequence similarity search to find the corresponding amino acid sequences in target organisms. Homology modelling was used to construct the protein structure. The stabilised protein structure obtained from molecular dynamics simulation was used in molecular docking. CONCLUSION: The overall results presented here might be a good starting point for the identification of novel and more active compounds as antifungal agents. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13065-018-0485-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-67680402019-10-03 An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study Er, Mustafa Abounakhla, Abdulati Miftah Tahtaci, Hakan Bawah, Ali Hasin Çınaroğlu, Süleyman Selim Onaran, Abdurrahman Ece, Abdulilah Chem Cent J Research Article BACKGROUND: This study aims to synthesise and characterise novel compounds containing 2-amino-1,3,4-thiadiazole and their acyl derivatives and to investigate antifungal activities. Similarity search, molecular dynamics and molecular docking were also studied to find out a potential target and enlighten the inhibition mechanism. RESULTS: As a first step, 2-amino-1,3,4-thiadiazole derivatives (compounds 3 and 4) were synthesised with high yields (81 and 84%). The target compounds (6a–n and 7a–n) were then synthesised with moderate to high yields (56–87%) by reacting 3 and 4 with various acyl chloride derivatives (5a–n). The synthesized compounds were characterized using the IR, (1)H-NMR, (13)C-NMR, Mass, X-ray (compound 7n) and elemental analysis techniques. Later, the in vitro antifungal activities of the synthesised compounds were determined. The inhibition zones exhibited by the compounds against the tested fungi, their minimum fungicidal activities, minimum inhibitory concentration and the lethal dose values (LD(50)) were determined. The compounds exhibited moderate to high levels of activity against all tested pathogens. Finally, in silico modelling was used to enlighten inhibition mechanism using ligand and structure-based methods. As an initial step, similarity search was carried out and the resulting proteins that belong to Homo sapiens were used as reference in sequence similarity search to find the corresponding amino acid sequences in target organisms. Homology modelling was used to construct the protein structure. The stabilised protein structure obtained from molecular dynamics simulation was used in molecular docking. CONCLUSION: The overall results presented here might be a good starting point for the identification of novel and more active compounds as antifungal agents. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13065-018-0485-3) contains supplementary material, which is available to authorized users. Springer International Publishing 2018-11-23 /pmc/articles/PMC6768040/ /pubmed/30470928 http://dx.doi.org/10.1186/s13065-018-0485-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Er, Mustafa
Abounakhla, Abdulati Miftah
Tahtaci, Hakan
Bawah, Ali Hasin
Çınaroğlu, Süleyman Selim
Onaran, Abdurrahman
Ece, Abdulilah
An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title_full An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title_fullStr An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title_full_unstemmed An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title_short An integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
title_sort integrated approach towards the development of novel antifungal agents containing thiadiazole: synthesis and a combined similarity search, homology modelling, molecular dynamics and molecular docking study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768040/
https://www.ncbi.nlm.nih.gov/pubmed/30470928
http://dx.doi.org/10.1186/s13065-018-0485-3
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