Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches

Matrix metalloproteinase (MMP-2 and MMP-8) have been found to be promising targets for the discovery and development for of novel wound healing drugs candidate. However, there are currently no MMP-2 or MMP-8 inhibitors that are therapeutically helpful for treating wound healing. Therefore, the goal...

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Main Authors: Forid, Md Shaekh, Roney, Miah, Uddin, Md. Nazim, Huq, A. K.M.Moyeenul, Mohd Hamzah, Mohd Nasir, Mohd Fadhlizil Fasihi, Mohd Aluwi, Muhammad Saupi, Azuri, Wan Maznah, Wan Ishak
Format: Article
Language:English
Published: International Scientific Organization 2024
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Online Access:http://umpir.ump.edu.my/id/eprint/40525/
http://umpir.ump.edu.my/id/eprint/40525/1/Wound%20Healing%20Activity%20of%20Pyrazole-thiazole%20Derivatives%20of%20Curcumin%20Through%20the%20Docking%2C%20Pharmacokinetics%2C%20MD%20Simulation%20and%20MM%20GBSA%20Approaches.pdf
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author Forid, Md Shaekh
Roney, Miah
Uddin, Md. Nazim
Huq, A. K.M.Moyeenul
Mohd Hamzah, Mohd Nasir
Mohd Fadhlizil Fasihi, Mohd Aluwi
Muhammad Saupi, Azuri
Wan Maznah, Wan Ishak
author_facet Forid, Md Shaekh
Roney, Miah
Uddin, Md. Nazim
Huq, A. K.M.Moyeenul
Mohd Hamzah, Mohd Nasir
Mohd Fadhlizil Fasihi, Mohd Aluwi
Muhammad Saupi, Azuri
Wan Maznah, Wan Ishak
author_sort Forid, Md Shaekh
building UMP Institutional Repository
collection Online Access
description Matrix metalloproteinase (MMP-2 and MMP-8) have been found to be promising targets for the discovery and development for of novel wound healing drugs candidate. However, there are currently no MMP-2 or MMP-8 inhibitors that are therapeutically helpful for treating wound healing. Therefore, the goal of this study was to investigate the wound healing potential of novel pyrazole-thiazole derivatives of curcumin using a series of computational studies. We first utilized the physicochemical and ADMET to screen the eight curcumin analogs and the outcomes from showed that compound C2 is potential favorable compound for further exploration. The docking analysis showed that compound C2 has strong binding affinity with the MMP-2 and MMP-8 compared to reference drug. Furthermore, MD simulation result indicated C2/MMP-2 complex is more stable than C2/MMP-8 complex. Likewise, MM/GBSA results suggest that binding stability of C2/MMP-2 complex is more stable as they showed most negative binding free energy (ΔGbind -24.434 kcal/mol) compared to C2/MMP-8 complex (ΔGbind -12.347). Furthermore, PCA and FEL analysis revealed that C2/MMP-2 complex displayed stable complex formation compared to C2/MMP8 complex in 100 ns molecular dynamics simulation trajectory. Hence, C2 could be considered a potent MMP-2 inhibitor and could be experimentally verified as a lead compound for the search for MMP-2 inhibitors for the treatment of wound healing.
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institution Universiti Malaysia Pahang
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language English
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publisher International Scientific Organization
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spelling ump-405252024-02-28T00:29:36Z http://umpir.ump.edu.my/id/eprint/40525/ Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches Forid, Md Shaekh Roney, Miah Uddin, Md. Nazim Huq, A. K.M.Moyeenul Mohd Hamzah, Mohd Nasir Mohd Fadhlizil Fasihi, Mohd Aluwi Muhammad Saupi, Azuri Wan Maznah, Wan Ishak T Technology (General) TP Chemical technology Matrix metalloproteinase (MMP-2 and MMP-8) have been found to be promising targets for the discovery and development for of novel wound healing drugs candidate. However, there are currently no MMP-2 or MMP-8 inhibitors that are therapeutically helpful for treating wound healing. Therefore, the goal of this study was to investigate the wound healing potential of novel pyrazole-thiazole derivatives of curcumin using a series of computational studies. We first utilized the physicochemical and ADMET to screen the eight curcumin analogs and the outcomes from showed that compound C2 is potential favorable compound for further exploration. The docking analysis showed that compound C2 has strong binding affinity with the MMP-2 and MMP-8 compared to reference drug. Furthermore, MD simulation result indicated C2/MMP-2 complex is more stable than C2/MMP-8 complex. Likewise, MM/GBSA results suggest that binding stability of C2/MMP-2 complex is more stable as they showed most negative binding free energy (ΔGbind -24.434 kcal/mol) compared to C2/MMP-8 complex (ΔGbind -12.347). Furthermore, PCA and FEL analysis revealed that C2/MMP-2 complex displayed stable complex formation compared to C2/MMP8 complex in 100 ns molecular dynamics simulation trajectory. Hence, C2 could be considered a potent MMP-2 inhibitor and could be experimentally verified as a lead compound for the search for MMP-2 inhibitors for the treatment of wound healing. International Scientific Organization 2024 Article PeerReviewed pdf en http://umpir.ump.edu.my/id/eprint/40525/1/Wound%20Healing%20Activity%20of%20Pyrazole-thiazole%20Derivatives%20of%20Curcumin%20Through%20the%20Docking%2C%20Pharmacokinetics%2C%20MD%20Simulation%20and%20MM%20GBSA%20Approaches.pdf Forid, Md Shaekh and Roney, Miah and Uddin, Md. Nazim and Huq, A. K.M.Moyeenul and Mohd Hamzah, Mohd Nasir and Mohd Fadhlizil Fasihi, Mohd Aluwi and Muhammad Saupi, Azuri and Wan Maznah, Wan Ishak (2024) Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches. International Journal of Chemical and Biochemical Sciences, 25 (18). pp. 83-109. ISSN 2226-9614. (Published) https://www.iscientific.org/wp-content/uploads/2024/02/8-IJCBS-24-25-18-8.pdf
spellingShingle T Technology (General)
TP Chemical technology
Forid, Md Shaekh
Roney, Miah
Uddin, Md. Nazim
Huq, A. K.M.Moyeenul
Mohd Hamzah, Mohd Nasir
Mohd Fadhlizil Fasihi, Mohd Aluwi
Muhammad Saupi, Azuri
Wan Maznah, Wan Ishak
Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title_full Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title_fullStr Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title_full_unstemmed Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title_short Wound Healing Activity of Pyrazole-thiazole Derivatives of Curcumin Through the Docking, Pharmacokinetics, MD Simulation and MM/GBSA Approaches
title_sort wound healing activity of pyrazole-thiazole derivatives of curcumin through the docking, pharmacokinetics, md simulation and mm/gbsa approaches
topic T Technology (General)
TP Chemical technology
url http://umpir.ump.edu.my/id/eprint/40525/
http://umpir.ump.edu.my/id/eprint/40525/
http://umpir.ump.edu.my/id/eprint/40525/1/Wound%20Healing%20Activity%20of%20Pyrazole-thiazole%20Derivatives%20of%20Curcumin%20Through%20the%20Docking%2C%20Pharmacokinetics%2C%20MD%20Simulation%20and%20MM%20GBSA%20Approaches.pdf