New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study
A series of thiazole derivatives 1-4 were synthesized employing simple one-pot reaction pathway and characterized via Fourier Transform Infrared (FTIR), Proton Nuclear Magnetic Resonance (1H NMR), Ultraviolet-Visible (UV-Vis) and Gas Chromatography-Mass Spectrometry (GC-MS). The newly synthesized co...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English English |
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Universiti Teknologi Malaysia
2020
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| Online Access: | http://irep.iium.edu.my/80658/ http://irep.iium.edu.my/80658/1/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives.pdf http://irep.iium.edu.my/80658/2/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives_WOS.pdf |
| _version_ | 1848788999640973312 |
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| author | Abdullah Ripain, Iswatun Hasanah Darnis, Deny Susanti Muhamad Bunnori, Noraslinda Ngah, Nurziana |
| author_facet | Abdullah Ripain, Iswatun Hasanah Darnis, Deny Susanti Muhamad Bunnori, Noraslinda Ngah, Nurziana |
| author_sort | Abdullah Ripain, Iswatun Hasanah |
| building | IIUM Repository |
| collection | Online Access |
| description | A series of thiazole derivatives 1-4 were synthesized employing simple one-pot reaction pathway and characterized via Fourier Transform Infrared (FTIR), Proton Nuclear Magnetic Resonance (1H NMR), Ultraviolet-Visible (UV-Vis) and Gas Chromatography-Mass Spectrometry (GC-MS). The newly synthesized compounds were evaluated for their in vitro antimicrobial properties against several bacterial strains including Gram-positive and Gram-negative as well as fungus using broth microdilution method. The results revealed that all of the compounds exhibited good activity with a range of MIC values between 1.25-5.0 mg/mL. From the MIC and MBC results, compound 1 exhibited good activities with same MIC value of 1.25 mg/mL and MBC value of 5 mg/mL against B. cereus and S. flexneri. In order to support antimicrobial results, the molecular docking studies were carried out for inhibition of the GlcN-6-P synthase as the target. Out of four compounds underwent for molecular docking studies, 5-acetyl-4-methyl-2-(4-aminobiphenyl)-1,3- thiazole (1) shows the lowest minimum binding energy at -7.32 kcal/mol as compared to 2, 3 and 4 with -7.31, -7.20 and -6.76 kcal/mol, respectively which are in agreement with antimicrobial assay results. In conclusion, 2, 4, 5-trisubstituted- 1,3- thiazole derivatives could be considered as promising antimicrobial in drug discovery candidates.
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Satu siri terbitan tiazol 1-4 telah disintesis menggunakan tindak balas mudah ‘one-pot’ dan
dicirikan dengan kaedah spektroskopi Transformasi Fourier-Inframerah (FTIR), Proton
Resonans Magnetik Nukleus (1H NMR) dan Sinar tampak ultraviolet (UV-Vis) serta
Kromatografi Jisim Gas-Spektrometer (GC-MS). Sebatian baru yang disintesis ini telah diuji
sebagai sebatian yang bercirikan antimikrob secara ‘in-vitro’. Ciri antimikrob ini telah diuji
terhadap beberapa strain bakteria iaitu Gram-positif dan Gram-negatif serta fungus
menggunakan kaedah kaldu mikrocairan. Keputusan mendapati kesemua sebatian yang
diuji (1-4) mempunyai aktiviti di dalam julat nilai MIC diantara 1.25-5.0 mg/mL. Daripada
nilai bacaan MIC dan MBC, sebatian 1 menunjukkan aktiviti yang bagus dengan nilai MIC
pada 1.25 mg/mL dan MBC pada 5 mg/mL terhadap B. cereus dan S. flexneri. Seterusnya,
kajian penyatuan molekul dilakukan ke atas semua sebatian (1-4) untuk merencat GlcN6-P sintase yang digunakan sebagai sebatian sasaran. Diantara empat molekul yang diuji,
5-asetil-4-metil-2-(4-aminobifenil)-1,3-tiazol (1) menunjukkan tenaga pengikatan minimum yang paling rendah iaitu -7.32 kcal/mol berbanding dengan sebatian 2, 3 dan 4 dengan
nilai masing-masing iaitu -7.31, -7.20 dan -6.76 kcal/mol selari dengan keputusan ujian
antimikrobial. Kesimpulannya, ujian selanjutnya boleh dilakukan ke atas sebatian terbitan
1,3-tiazo berpenggantian-2, 4, 5 di dalam mencari sebatian baru dalam bidang
penemuan ubatan baru. |
| first_indexed | 2025-11-14T17:49:45Z |
| format | Article |
| id | iium-80658 |
| institution | International Islamic University Malaysia |
| institution_category | Local University |
| language | English English |
| last_indexed | 2025-11-14T17:49:45Z |
| publishDate | 2020 |
| publisher | Universiti Teknologi Malaysia |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | iium-806582020-06-18T03:19:47Z http://irep.iium.edu.my/80658/ New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study Abdullah Ripain, Iswatun Hasanah Darnis, Deny Susanti Muhamad Bunnori, Noraslinda Ngah, Nurziana QD Chemistry A series of thiazole derivatives 1-4 were synthesized employing simple one-pot reaction pathway and characterized via Fourier Transform Infrared (FTIR), Proton Nuclear Magnetic Resonance (1H NMR), Ultraviolet-Visible (UV-Vis) and Gas Chromatography-Mass Spectrometry (GC-MS). The newly synthesized compounds were evaluated for their in vitro antimicrobial properties against several bacterial strains including Gram-positive and Gram-negative as well as fungus using broth microdilution method. The results revealed that all of the compounds exhibited good activity with a range of MIC values between 1.25-5.0 mg/mL. From the MIC and MBC results, compound 1 exhibited good activities with same MIC value of 1.25 mg/mL and MBC value of 5 mg/mL against B. cereus and S. flexneri. In order to support antimicrobial results, the molecular docking studies were carried out for inhibition of the GlcN-6-P synthase as the target. Out of four compounds underwent for molecular docking studies, 5-acetyl-4-methyl-2-(4-aminobiphenyl)-1,3- thiazole (1) shows the lowest minimum binding energy at -7.32 kcal/mol as compared to 2, 3 and 4 with -7.31, -7.20 and -6.76 kcal/mol, respectively which are in agreement with antimicrobial assay results. In conclusion, 2, 4, 5-trisubstituted- 1,3- thiazole derivatives could be considered as promising antimicrobial in drug discovery candidates. ************************************************************************************** Satu siri terbitan tiazol 1-4 telah disintesis menggunakan tindak balas mudah ‘one-pot’ dan dicirikan dengan kaedah spektroskopi Transformasi Fourier-Inframerah (FTIR), Proton Resonans Magnetik Nukleus (1H NMR) dan Sinar tampak ultraviolet (UV-Vis) serta Kromatografi Jisim Gas-Spektrometer (GC-MS). Sebatian baru yang disintesis ini telah diuji sebagai sebatian yang bercirikan antimikrob secara ‘in-vitro’. Ciri antimikrob ini telah diuji terhadap beberapa strain bakteria iaitu Gram-positif dan Gram-negatif serta fungus menggunakan kaedah kaldu mikrocairan. Keputusan mendapati kesemua sebatian yang diuji (1-4) mempunyai aktiviti di dalam julat nilai MIC diantara 1.25-5.0 mg/mL. Daripada nilai bacaan MIC dan MBC, sebatian 1 menunjukkan aktiviti yang bagus dengan nilai MIC pada 1.25 mg/mL dan MBC pada 5 mg/mL terhadap B. cereus dan S. flexneri. Seterusnya, kajian penyatuan molekul dilakukan ke atas semua sebatian (1-4) untuk merencat GlcN6-P sintase yang digunakan sebagai sebatian sasaran. Diantara empat molekul yang diuji, 5-asetil-4-metil-2-(4-aminobifenil)-1,3-tiazol (1) menunjukkan tenaga pengikatan minimum yang paling rendah iaitu -7.32 kcal/mol berbanding dengan sebatian 2, 3 dan 4 dengan nilai masing-masing iaitu -7.31, -7.20 dan -6.76 kcal/mol selari dengan keputusan ujian antimikrobial. Kesimpulannya, ujian selanjutnya boleh dilakukan ke atas sebatian terbitan 1,3-tiazo berpenggantian-2, 4, 5 di dalam mencari sebatian baru dalam bidang penemuan ubatan baru. Universiti Teknologi Malaysia 2020-02-27 Article PeerReviewed application/pdf en http://irep.iium.edu.my/80658/1/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives.pdf application/pdf en http://irep.iium.edu.my/80658/2/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives_WOS.pdf Abdullah Ripain, Iswatun Hasanah and Darnis, Deny Susanti and Muhamad Bunnori, Noraslinda and Ngah, Nurziana (2020) New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study. Jurnal Teknologi, 82 (2). pp. 61-69. ISSN 0127-9696 E-ISSN 2180–3722 https://doi.org/10.11113/jt.v82.13666 |
| spellingShingle | QD Chemistry Abdullah Ripain, Iswatun Hasanah Darnis, Deny Susanti Muhamad Bunnori, Noraslinda Ngah, Nurziana New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title | New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title_full | New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title_fullStr | New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title_full_unstemmed | New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title_short | New 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| title_sort | new 2,4,5-trisubstituted-1,3-thiazole derivatives: synthesis, in vitro antimicrobial activity and in silico study |
| topic | QD Chemistry |
| url | http://irep.iium.edu.my/80658/ http://irep.iium.edu.my/80658/ http://irep.iium.edu.my/80658/1/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives.pdf http://irep.iium.edu.my/80658/2/80685_New%202%2C4%2C5-trisubstituted-1%2C3-thiazole%20derivatives_WOS.pdf |