Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities
Diabetes mellitus type II (T2DM) is a global public health crisis that can lead to death and disability if poorly treated. T2DM patients are usually prescribed antidiabetic drugs, including α-glucosidase inhibitors (AGIs), but their use can lead to complications. Epidemiological studies have already...
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Malaysian Institute of Chemistry
2023
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my.upm.eprints.1093392024-08-05T04:06:04Z http://psasir.upm.edu.my/id/eprint/109339/ Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities Adam, Faruk Auwal Md Razali, Mohammad Aidiel Rukayardi, Yaya Mastuki, Siti Nurulhuda Wei, Leong Sze Mad Nasir, Nadiah Mohd Faudzi, Siti Munirah Diabetes mellitus type II (T2DM) is a global public health crisis that can lead to death and disability if poorly treated. T2DM patients are usually prescribed antidiabetic drugs, including α-glucosidase inhibitors (AGIs), but their use can lead to complications. Epidemiological studies have already shown that antioxidant compounds are able to scavenge reactive species and alleviate oxidative stress in T2DM patients. With the main objective of improving the quality of life of T2DM patients, a series of diarylpentadienones (3a-j) and their new pyrazoline derivatives (4a-i) were synthesized and evaluated for their α-glucosidase inhibition and anti-oxidant abilities. The results showed that 5-(4-methoxyphenyl)-1-(5-methylthiophen-2-yl)penta- 2,4-dien-1-one (3h) exhibited significant α-glucosidase inhibition (IC50 40.52 ± 2.0 µM) compared to the standard drug acarbose (IC50 543.80 ± 3.0 µM). While 1-(2,4-dimethoxyphenyl)-5-(4-methoxyphenyl)penta-2,4-dien-1-one (3d) and 1-(3-(3-fluorophenyl)-5-(4-methoxystyryl)-4,5-dihydro-1H-pyrazol-1-yl)ethenone (4f) showed promising radical scavenging potentials of DPPH (96-97) and NO (8-74), which were comparable to the control compounds, quercetin and gallic acid. Molecular docking simulations were then performed to reveal several significant binding interactions of the active molecules with the corresponding protein crystals. It can be concluded that diaryl pentadienone and its pyrazoline derivatives are molecules with potential anti-α-glucosidase and antioxidant properties, but not as dual active compounds, suitable for possible chemical modification according to pharmaceutical requirements in the future. Malaysian Institute of Chemistry 2023-03-09 Article PeerReviewed Adam, Faruk Auwal and Md Razali, Mohammad Aidiel and Rukayardi, Yaya and Mastuki, Siti Nurulhuda and Wei, Leong Sze and Mad Nasir, Nadiah and Mohd Faudzi, Siti Munirah (2023) Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities. Malaysian Journal of Chemistry, 25 (2). 13 - 31. ISSN 2550-1658 https://ikm.org.my/publications/malaysian-journal-of-chemistry/view-abstract.php?abs=J0043-cc1b612 10.55373/mjchem.v25i2.13 |
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Diabetes mellitus type II (T2DM) is a global public health crisis that can lead to death and disability if poorly treated. T2DM patients are usually prescribed antidiabetic drugs, including α-glucosidase inhibitors (AGIs), but their use can lead to complications. Epidemiological studies have already shown that antioxidant compounds are able to scavenge reactive species and alleviate oxidative stress in T2DM patients. With the main objective of improving the quality of life of T2DM patients, a series of diarylpentadienones (3a-j) and their new pyrazoline derivatives (4a-i) were synthesized and evaluated for their α-glucosidase inhibition and anti-oxidant abilities. The results showed that 5-(4-methoxyphenyl)-1-(5-methylthiophen-2-yl)penta- 2,4-dien-1-one (3h) exhibited significant α-glucosidase inhibition (IC50 40.52 ± 2.0 µM) compared to the standard drug acarbose (IC50 543.80 ± 3.0 µM). While 1-(2,4-dimethoxyphenyl)-5-(4-methoxyphenyl)penta-2,4-dien-1-one (3d) and 1-(3-(3-fluorophenyl)-5-(4-methoxystyryl)-4,5-dihydro-1H-pyrazol-1-yl)ethenone (4f) showed promising radical scavenging potentials of DPPH (96-97) and NO (8-74), which were comparable to the control compounds, quercetin and gallic acid. Molecular docking simulations were then performed to reveal several significant binding interactions of the active molecules with the corresponding protein crystals. It can be concluded that diaryl pentadienone and its pyrazoline derivatives are molecules with potential anti-α-glucosidase and antioxidant properties, but not as dual active compounds, suitable for possible chemical modification according to pharmaceutical requirements in the future. |
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Adam, Faruk Auwal Md Razali, Mohammad Aidiel Rukayardi, Yaya Mastuki, Siti Nurulhuda Wei, Leong Sze Mad Nasir, Nadiah Mohd Faudzi, Siti Munirah |
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Adam, Faruk Auwal Md Razali, Mohammad Aidiel Rukayardi, Yaya Mastuki, Siti Nurulhuda Wei, Leong Sze Mad Nasir, Nadiah Mohd Faudzi, Siti Munirah Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
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Adam, Faruk Auwal Md Razali, Mohammad Aidiel Rukayardi, Yaya Mastuki, Siti Nurulhuda Wei, Leong Sze Mad Nasir, Nadiah Mohd Faudzi, Siti Munirah |
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Adam, Faruk Auwal |
title |
Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
title_short |
Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
title_full |
Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
title_fullStr |
Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
title_full_unstemmed |
Synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
title_sort |
synthesis of diarylpentadienones and pyrazoline derivatives as potential α-glucosidase inhibitor and their antioxidant activities |
publisher |
Malaysian Institute of Chemistry |
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2023 |
url |
http://psasir.upm.edu.my/id/eprint/109339/ https://ikm.org.my/publications/malaysian-journal-of-chemistry/view-abstract.php?abs=J0043-cc1b612 |
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