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Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies

PURPOSE: The current work was designed to synthesize a bioactive derivative of succinimide and evaluate it for anti-Alzheimer, anticancer and anti-diabetic potentials. METHODS: The compound was synthesized by Michael addition of butyraldehyde with N-phenylmaleimide. The synthesized compound was scre...

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Autores principales: Ahmad, Ashfaq, Ullah, Farhat, Sadiq, Abdul, Ayaz, Muhammad, Rahim, Haroon, Rashid, Umer, Ahmad, Sajjad, Jan, Muhammad Saeed, Ullah, Riaz, Shahat, Abdelaaty A, Mahmood, Hafiz Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911349/
https://www.ncbi.nlm.nih.gov/pubmed/31849450
http://dx.doi.org/10.2147/DDDT.S226080
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author Ahmad, Ashfaq
Ullah, Farhat
Sadiq, Abdul
Ayaz, Muhammad
Rahim, Haroon
Rashid, Umer
Ahmad, Sajjad
Jan, Muhammad Saeed
Ullah, Riaz
Shahat, Abdelaaty A
Mahmood, Hafiz Majid
author_facet Ahmad, Ashfaq
Ullah, Farhat
Sadiq, Abdul
Ayaz, Muhammad
Rahim, Haroon
Rashid, Umer
Ahmad, Sajjad
Jan, Muhammad Saeed
Ullah, Riaz
Shahat, Abdelaaty A
Mahmood, Hafiz Majid
author_sort Ahmad, Ashfaq
collection PubMed
description PURPOSE: The current work was designed to synthesize a bioactive derivative of succinimide and evaluate it for anti-Alzheimer, anticancer and anti-diabetic potentials. METHODS: The compound was synthesized by Michael addition of butyraldehyde with N-phenylmaleimide. The synthesized compound was screened for biological potentials including anti-cholinesterase, in-vitro anti-diabetic, antioxidant and anthelmintic potentials. The anti-cholinesterase potential was evaluated against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), anti-diabetic potential against α-glucosidase, antioxidant potential against ABTS, DPPH and H(2)O(2) and anthelmintic potential against Perethima posthuma and Ascaridia galli respectively. RESULTS: The compound demonstrated significant AChE and BChE inhibition i.e., 71.34±1.92 and 73.42 ±1.92 at the concentration of 1000 µg/mL respectively. Other dilutions exhibited concentration-dependent inhibitory activity against both enzymes. In the MTT assay, the newly synthesized compound was found active against all of the cell lines viz, HCT-116, MDA-MB231, NIH/3T3 and MCF-7 and the highest cytotoxicity potential was observed against the colon cancer cell line (HCT-116) with an IC(50) value of 78 µg/mL exhibiting its highest potential. Moreover, the compound exhibited prominent α-glucosidase inhibitory potentials (79.86±2.54% at 1000 µg/mL) with IC(50) value of 156.23 µg/mL. Further, our test compound exhibited considerable scavenging activity against DPPH, ABTS and H(2)O(2) free radicals with percent inhibitions of 75.84±1.58, 72.85±1.17 and 54.82±1.82 and IC(50) values of 84.36, 139.74 and 752.21 µg/mL respectively. Our test sample exhibited significant anthelmintic potentials. It demonstrated significant paralysis and death of the test worms in an unbelievably short time in comparison with albendazole. CONCLUSION: Going into the detail of all observations, it may be deduced that the newly synthesized succinimide derivative could be an important drug candidate against neurodegenerative disorders like Alzheimer’s disease, cancer, diabetes mellitus and worms. Further detailed studies in animal models are required for in-vivo analysis of the compound.
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spelling pubmed-69113492019-12-17 Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies Ahmad, Ashfaq Ullah, Farhat Sadiq, Abdul Ayaz, Muhammad Rahim, Haroon Rashid, Umer Ahmad, Sajjad Jan, Muhammad Saeed Ullah, Riaz Shahat, Abdelaaty A Mahmood, Hafiz Majid Drug Des Devel Ther Original Research PURPOSE: The current work was designed to synthesize a bioactive derivative of succinimide and evaluate it for anti-Alzheimer, anticancer and anti-diabetic potentials. METHODS: The compound was synthesized by Michael addition of butyraldehyde with N-phenylmaleimide. The synthesized compound was screened for biological potentials including anti-cholinesterase, in-vitro anti-diabetic, antioxidant and anthelmintic potentials. The anti-cholinesterase potential was evaluated against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), anti-diabetic potential against α-glucosidase, antioxidant potential against ABTS, DPPH and H(2)O(2) and anthelmintic potential against Perethima posthuma and Ascaridia galli respectively. RESULTS: The compound demonstrated significant AChE and BChE inhibition i.e., 71.34±1.92 and 73.42 ±1.92 at the concentration of 1000 µg/mL respectively. Other dilutions exhibited concentration-dependent inhibitory activity against both enzymes. In the MTT assay, the newly synthesized compound was found active against all of the cell lines viz, HCT-116, MDA-MB231, NIH/3T3 and MCF-7 and the highest cytotoxicity potential was observed against the colon cancer cell line (HCT-116) with an IC(50) value of 78 µg/mL exhibiting its highest potential. Moreover, the compound exhibited prominent α-glucosidase inhibitory potentials (79.86±2.54% at 1000 µg/mL) with IC(50) value of 156.23 µg/mL. Further, our test compound exhibited considerable scavenging activity against DPPH, ABTS and H(2)O(2) free radicals with percent inhibitions of 75.84±1.58, 72.85±1.17 and 54.82±1.82 and IC(50) values of 84.36, 139.74 and 752.21 µg/mL respectively. Our test sample exhibited significant anthelmintic potentials. It demonstrated significant paralysis and death of the test worms in an unbelievably short time in comparison with albendazole. CONCLUSION: Going into the detail of all observations, it may be deduced that the newly synthesized succinimide derivative could be an important drug candidate against neurodegenerative disorders like Alzheimer’s disease, cancer, diabetes mellitus and worms. Further detailed studies in animal models are required for in-vivo analysis of the compound. Dove 2019-12-10 /pmc/articles/PMC6911349/ /pubmed/31849450 http://dx.doi.org/10.2147/DDDT.S226080 Text en © 2019 Ahmad et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Ahmad, Ashfaq
Ullah, Farhat
Sadiq, Abdul
Ayaz, Muhammad
Rahim, Haroon
Rashid, Umer
Ahmad, Sajjad
Jan, Muhammad Saeed
Ullah, Riaz
Shahat, Abdelaaty A
Mahmood, Hafiz Majid
Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title_full Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title_fullStr Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title_full_unstemmed Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title_short Pharmacological Evaluation of Aldehydic-Pyrrolidinedione Against HCT-116, MDA-MB231, NIH/3T3, MCF-7 Cancer Cell Lines, Antioxidant and Enzyme Inhibition Studies
title_sort pharmacological evaluation of aldehydic-pyrrolidinedione against hct-116, mda-mb231, nih/3t3, mcf-7 cancer cell lines, antioxidant and enzyme inhibition studies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911349/
https://www.ncbi.nlm.nih.gov/pubmed/31849450
http://dx.doi.org/10.2147/DDDT.S226080
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