Enzyme Inhibitory Kinetics and Molecular Docking Studies of Halo-Substituted Mixed Ester/Amide-Based Derivatives as Jack Bean Urease Inhibitors.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Enzyme Inhibitory Kinetics and Molecular Docking Studies of Halo-Substituted Mixed Ester/Amide-Based Derivatives as Jack Bean Urease Inhibitors.
Συγγραφείς: Rashid M; Department of Chemistry, Allama Iqbal Open University, Islamabad 44000, Pakistan., Rafique H; Department of Chemistry, University of Gujrat, Gujrat 50700, Pakistan., Roshan S; Department of Zoology, University of Gujrat, Gujrat 50700, Pakistan., Shamas S; Department of Zoology, University of Gujrat, Gujrat 50700, Pakistan., Iqbal Z; Department of Chemistry, Allama Iqbal Open University, Islamabad 44000, Pakistan., Ashraf Z; Department of Chemistry, Allama Iqbal Open University, Islamabad 44000, Pakistan., Abbas Q; Department of Physiology, University of Sindh, Jamshoro, Pakistan., Hassan M; Institute of Molecular Biology and Biotechnology, The University of Lahore, Lahore, Pakistan., Qureshi ZUR; Department of Pharmacy, SBK Women University, Quetta, Balochistan, Pakistan., Asad MHHB; Department of Pharmacy, COMSATS University Islamabad, Abbottabad Campus, Pakistan.; Institute of Fundamental Medicine, Department of Genetics, Kazan Federal University, Russia.
Πηγή: BioMed research international [Biomed Res Int] 2020 Dec 24; Vol. 2020, pp. 8867407. Date of Electronic Publication: 2020 Dec 24 (Print Publication: 2020).
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Wiley Country of Publication: United States NLM ID: 101600173 Publication Model: eCollection Cited Medium: Internet ISSN: 2314-6141 (Electronic) NLM ISO Abbreviation: Biomed Res Int Subsets: MEDLINE
Imprint Name(s): Publication: 2024- : [Hoboken, NJ] : Wiley
Original Publication: New York, NY : Hindawi Pub. Co.
Ιατρικοί όροι (MeSH): Benzoates*/chemistry , Benzoates*/metabolism , Benzoates*/pharmacology , Enzyme Inhibitors*/chemistry , Enzyme Inhibitors*/metabolism , Enzyme Inhibitors*/pharmacology, Canavalia/*enzymology , Plant Proteins/*antagonists & inhibitors , Urease/*antagonists & inhibitors, Amides/chemistry ; Amides/metabolism ; Esters/chemistry ; Esters/metabolism ; Plant Proteins/chemistry ; Plant Proteins/metabolism ; Urea/metabolism ; Urease/chemistry ; Urease/metabolism ; Binding Sites ; Hydrolysis ; Kinetics ; Molecular Docking Simulation
Περίληψη: A series of halo-substituted mixed ester/amide-based analogues 4a-l have been prepared as jack bean urease inhibitor, which showed good to excellent inhibition of enzyme activity. The role of halo-substituted benzoyl moieties and alkyl substituted anilines in urease inhibitory kinetics was also investigated. The alkyl-substituted anilines 1a-b reacted with chloroacetyl chloride to afford intermediates 2a-b, which were then reacted with different halo-substituted benzoic acids 3a-f to prepare the title compounds 4a-l. The chemical structures of final products 4a-l were ascertained by FTIR, 1H NMR, 13C NMR, and mass spectra. The compound 4b showed remarkable activity with IC501.6 ± 0.2 nM, better than the standard thiourea having IC50472.1 ± 135.1 nM. The 2-chloro-substituted phenyl ring on one side of compound 4b and 4-isopropyl-substituted benzene on the other side play an essential role in inhibition of urease activity. Lineweaver-Burk plots (kinetics study) indicated about 4b derivative as a mixed type of inhibitor. The virtual screening performed against urease enzyme (PDBID 4H9M) showed that compounds 4b and 4e have binding energies of -7.8 and -7.9 Kcal/mol, respectively. Based upon our results, it was found that derivative 4b is a highly potent urease inhibitor, better than the standard thiourea.
(Copyright © 2020 Muhammad Rashid et al.)
Competing Interests: The authors declare no conflicts of interest.
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Substance Nomenclature: 0 (Amides)
0 (Benzoates)
0 (Enzyme Inhibitors)
0 (Esters)
0 (Plant Proteins)
8W8T17847W (Urea)
EC 3.5.1.5 (Urease)
Entry Date(s): Date Created: 20210111 Date Completed: 20210524 Latest Revision: 20240330
Update Code: 20260130
PubMed Central ID: PMC7775144
DOI: 10.1155/2020/8867407
PMID: 33426080
Βάση Δεδομένων: MEDLINE