Articles with "enzyme inhibition" as a keyword



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Biologically active phthalocyanine metal complexes: Preparation, evaluation of α‐glycosidase and anticholinesterase enzyme inhibition activities, and molecular docking studies

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Published in 2021 at "Journal of Biochemical and Molecular Toxicology"

DOI: 10.1002/jbt.22765

Abstract: In this study, preparation, as well as investigation of α‐glycosidase and cholinesterase (ChE) enzyme inhibition activities of furan‐2‐ylmethoxy‐substituted compounds 1–7, are reported. Peripherally, tetra‐substituted copper and manganese phthalocyanines (5 and 6) were synthesized for the… read more here.

Keywords: glycosidase; enzyme inhibition; inhibition activities; metal complexes ... See more keywords
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Irreversible Enzyme Inhibition Kinetics and Drug-Drug Interactions.

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Published in 2021 at "Methods in molecular biology"

DOI: 10.1007/978-1-0716-1554-6_3

Abstract: This chapter describes the types of irreversible inhibition of drug-metabolizing enzymes and the methods commonly employed to quantify the irreversible inhibition and subsequently predict the extent and time course of clinically important drug-drug interactions. read more here.

Keywords: drug interactions; enzyme inhibition; inhibition; irreversible enzyme ... See more keywords
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Evaluation of herb-drug interaction of a polyherbal Ayurvedic formulation through high throughput cytochrome P450 enzyme inhibition assay.

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Published in 2017 at "Journal of ethnopharmacology"

DOI: 10.1016/j.jep.2016.07.061

Abstract: ETHNOPHARMACOLOGICAL RELEVANCE Arishtas are Ayurvedic formulation made with decoction of herbs. Arjunarishta formulation is being used in Ayurveda for cardio-protective activity. Ashwagandharishta formulation possesses antioxidant, anti-atherosclerotic and anti-stress properties. Ridayarishta, a novel empirical formulation was… read more here.

Keywords: enzyme inhibition; inhibition; formulation; inhibition assay ... See more keywords
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Synthesis, crystal structure and Hirschfeld surface analyses of an alkyl amine based salt, [C5H16N2][ZnCl4] and its enzyme inhibition activity

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Published in 2017 at "Journal of Saudi Chemical Society"

DOI: 10.1016/j.jscs.2016.12.002

Abstract: Abstract A novel ionic zinc salt based on alkyl amine is reported. The structure of the studied salt is established by crystal X-ray crystallography, FT-IR and NMR spectroscopy. Furthermore, Hirschfeld surface analyses of the studied… read more here.

Keywords: surface analyses; inhibition activity; enzyme inhibition; salt ... See more keywords
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Metal based triazole compounds: Their synthesis, computational, antioxidant, enzyme inhibition and antimicrobial properties

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Published in 2018 at "Journal of Molecular Structure"

DOI: 10.1016/j.molstruc.2018.05.036

Abstract: Abstract The present research work was aimed to synthesize biologically active Schiff base compound, 2-{(E)-[(3-{[(Z)-(2-hydroxyphenyl)methylidene]amino}-1H-1,2,4-triazol-5-yl)imino]methyl}phenol (L) by condensation reaction of 2-hydroxybenzaldehyde with 3,5-diamino-1,2,4-triazole. In order to evaluate the effect of metal ions on the biological… read more here.

Keywords: metal ions; antioxidant enzyme; metal based; enzyme inhibition ... See more keywords
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Sulfonamide hybrid schiff bases of anthranilic acid: Synthesis, characterization and their biological potential

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Published in 2019 at "Journal of Molecular Structure"

DOI: 10.1016/j.molstruc.2019.02.056

Abstract: Abstract In the present work, the novel Schiff bases (03–20) of 4-chloro-N-[2-(hydrazinocarbonyl) phenyl]benzenesulfonamide (02) were synthesized by reacting it with various aldehydes. 4-Chloro-N-[2-(hydrazinocarbonyl) phenyl]benzenesulfonamide (02) was synthesized by reacting methyl 2-{[(4-chlorophenyl)sulfonyl]amino}benzoate (01) with hydrazine. All… read more here.

Keywords: synthesized compounds; sulfonamide hybrid; inhibition; schiff bases ... See more keywords
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Enzyme inhibition and antioxidant potential of new synthesized sulfonamides; synthesis, single crystal and molecular docking

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Published in 2021 at "Journal of Molecular Structure"

DOI: 10.1016/j.molstruc.2021.130608

Abstract: Abstract This study describes the synthesis of four (1-4) new phenylalanine based sulfonamides from benzene sulfonyl chlorides. The progress of the reaction was monitored on TLC and after completion; the products were subjected to various… read more here.

Keywords: synthesis; single crystal; inhibition antioxidant; inhibition ... See more keywords
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Indole Chloropyridinyl Ester-Derived SARS-CoV-2 3CLpro Inhibitors: Enzyme Inhibition, Antiviral Efficacy, Structure–Activity Relationship, and X-ray Structural Studies

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Published in 2021 at "Journal of Medicinal Chemistry"

DOI: 10.1021/acs.jmedchem.1c01214

Abstract: Here, we report the synthesis, structure–activity relationship studies, enzyme inhibition, antiviral activity, and X-ray crystallographic studies of 5-chloropyridinyl indole carboxylate derivatives as a potent class of SARS-CoV-2 chymotrypsin-like protease inhibitors. Compound 1 exhibited a SARS-CoV-2… read more here.

Keywords: enzyme inhibition; cov 3clpro; activity relationship; structure activity ... See more keywords
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Synthesis, Characterization, and Enzyme Inhibition Properties of 1,2,4-Triazole Bearing Azinane Analogues

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Published in 2022 at "ACS Omega"

DOI: 10.1021/acsomega.2c03779

Abstract: Considering the importance of acetylcholine esterase (AChE, BchE) and α-glucosidase in the treatment of Alzheimer’s disease and diabetes mellitus, the synthesis of novel azinane triazole-based derivatives as effective acetylcholinesterase (AchE), α-glucosidase, urease, lipoxygenase (LOX), and… read more here.

Keywords: inhibition; enzyme inhibition; azinane; glucosidase ... See more keywords
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A novel method to engineer proteases for selective enzyme inhibition.

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Published in 2019 at "Chemical communications"

DOI: 10.1039/c9cc08085f

Abstract: In this work, we have proposed a new strategy to expand the function of a protein. By taking a protease as an example, it can be engineered to make up the shortcoming of natural proteases,… read more here.

Keywords: proteases selective; selective enzyme; novel method; enzyme inhibition ... See more keywords
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The use of dimethylsulfoxide as a solvent in enzyme inhibition studies: the case of aldose reductase

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Published in 2017 at "Journal of Enzyme Inhibition and Medicinal Chemistry"

DOI: 10.1080/14756366.2017.1363744

Abstract: Abstract Aldose reductase (AR) is an enzyme devoted to cell detoxification and at the same time is strongly involved in the aetiology of secondary diabetic complications and the amplification of inflammatory phenomena. AR is subjected… read more here.

Keywords: aldose reductase; inhibition studies; inhibition; enzyme inhibition ... See more keywords