Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.

This research aims to build a mathematical quantitative structure-activity relationship (QSAR) model, which could relate the relationship between newly-synthesized carbonyl thiourea derivatives with their anti-amoebic activities. Therefore, in this study, inhibition concentration of 50% cells popu...

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Main Authors: Ibrahim, Maizatul Akma, Zakaria, Nor Hafizah, Mohd Yusof, Mohd Sukeri
Format: Article
Language:English
Published: Faculty of Science and Technology, Universiti Kebangsaan Malaysia 2022
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Online Access:http://irep.iium.edu.my/98532/7/98532_Quantitative%20structure-activity%20relationship.pdf
http://irep.iium.edu.my/98532/
https://mjas.analis.com.my/mjas/v26_n3/pdf/Akma_26_3_3.pdf
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spelling my.iium.irep.985322022-06-27T02:49:48Z http://irep.iium.edu.my/98532/ Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp. Ibrahim, Maizatul Akma Zakaria, Nor Hafizah Mohd Yusof, Mohd Sukeri Q Science (General) QD Chemistry QR Microbiology This research aims to build a mathematical quantitative structure-activity relationship (QSAR) model, which could relate the relationship between newly-synthesized carbonyl thiourea derivatives with their anti-amoebic activities. Therefore, in this study, inhibition concentration of 50% cells population (IC50) was evaluated for 44 carbonyl thiourea derivatives on pathogenic Acanthamoeba sp. (Hospital Kuala Lumpur isolate). QSAR analysis was conducted using the obtained IC50 data with additional 4 thiourea compounds of the same group from our previous work by applying three linear regression techniques namely stepwise-MLR, GA-MLR, and GA-PLS. Results showed that these thiourea derivatives are positively active against the tested Acanthamoeba sp. with IC50 values ranging from 2.56 to 7.81 μg/mL. From the evaluation of the obtained models, the GAPLS technique is found to be the best model due to its best predictive ability. The final equation of GA-PLS model gave good statistical output with values of r2 = 0.827, r2 cv = 0.682 RMSEC=0.047, RMSECV=0.064, and r2 test =0.790 and RMSEP=0.051. Y-randomization test has confirmed that the model did not occur from the chance of correlation with r2 = 0.015- 0.372. Small residual with values less than 0.25 from the prediction in the test set proves the robustness of the model. The information generated from this study will provide an insight into designing a new lead compound from carbonyl thiourea containing highly potential anti-amoebic properties. Faculty of Science and Technology, Universiti Kebangsaan Malaysia 2022-06-22 Article PeerReviewed application/pdf en http://irep.iium.edu.my/98532/7/98532_Quantitative%20structure-activity%20relationship.pdf Ibrahim, Maizatul Akma and Zakaria, Nor Hafizah and Mohd Yusof, Mohd Sukeri (2022) Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp. Malaysian Journal of Analytical Sciences, 26 (3). pp. 457-477. ISSN 1394-2506 https://mjas.analis.com.my/mjas/v26_n3/pdf/Akma_26_3_3.pdf
institution Universiti Islam Antarabangsa Malaysia
building IIUM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider International Islamic University Malaysia
content_source IIUM Repository (IREP)
url_provider http://irep.iium.edu.my/
language English
topic Q Science (General)
QD Chemistry
QR Microbiology
spellingShingle Q Science (General)
QD Chemistry
QR Microbiology
Ibrahim, Maizatul Akma
Zakaria, Nor Hafizah
Mohd Yusof, Mohd Sukeri
Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
description This research aims to build a mathematical quantitative structure-activity relationship (QSAR) model, which could relate the relationship between newly-synthesized carbonyl thiourea derivatives with their anti-amoebic activities. Therefore, in this study, inhibition concentration of 50% cells population (IC50) was evaluated for 44 carbonyl thiourea derivatives on pathogenic Acanthamoeba sp. (Hospital Kuala Lumpur isolate). QSAR analysis was conducted using the obtained IC50 data with additional 4 thiourea compounds of the same group from our previous work by applying three linear regression techniques namely stepwise-MLR, GA-MLR, and GA-PLS. Results showed that these thiourea derivatives are positively active against the tested Acanthamoeba sp. with IC50 values ranging from 2.56 to 7.81 μg/mL. From the evaluation of the obtained models, the GAPLS technique is found to be the best model due to its best predictive ability. The final equation of GA-PLS model gave good statistical output with values of r2 = 0.827, r2 cv = 0.682 RMSEC=0.047, RMSECV=0.064, and r2 test =0.790 and RMSEP=0.051. Y-randomization test has confirmed that the model did not occur from the chance of correlation with r2 = 0.015- 0.372. Small residual with values less than 0.25 from the prediction in the test set proves the robustness of the model. The information generated from this study will provide an insight into designing a new lead compound from carbonyl thiourea containing highly potential anti-amoebic properties.
format Article
author Ibrahim, Maizatul Akma
Zakaria, Nor Hafizah
Mohd Yusof, Mohd Sukeri
author_facet Ibrahim, Maizatul Akma
Zakaria, Nor Hafizah
Mohd Yusof, Mohd Sukeri
author_sort Ibrahim, Maizatul Akma
title Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
title_short Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
title_full Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
title_fullStr Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
title_full_unstemmed Quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
title_sort quantitative structure-activity relationship (qsar) study of newly synthesized carbonyl thiourea derivatives on acanthamoeba sp.
publisher Faculty of Science and Technology, Universiti Kebangsaan Malaysia
publishDate 2022
url http://irep.iium.edu.my/98532/7/98532_Quantitative%20structure-activity%20relationship.pdf
http://irep.iium.edu.my/98532/
https://mjas.analis.com.my/mjas/v26_n3/pdf/Akma_26_3_3.pdf
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score 13.188404