2021
DOI: 10.1080/10406638.2021.1887295
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Design, Synthesis, and Molecular Docking of Novel Hybrids of Coumarin-Dithiocarbamate Alpha-Glucosidase Inhibitors Targeting Type 2 Diabetes Mellitus

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Cited by 12 publications
(13 citation statements)
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“…A hydrolyzing enzyme (α-Glucosidase), which is important in the breaking down of starch and carbohydrate to glucose, is usually a target enzyme in the treatment of diabetes mellitus [100,101]. Among the compounds that has been used for the inhibition of this enzyme, coumarin-dithiocarbamate scaffold has proven to be very effective and this has made it a useful compound in the treatment of type 2 diabetes.…”
Section: Application Of Dithiocarbamate Compounds As Enzyme Inhibitormentioning
confidence: 99%
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“…A hydrolyzing enzyme (α-Glucosidase), which is important in the breaking down of starch and carbohydrate to glucose, is usually a target enzyme in the treatment of diabetes mellitus [100,101]. Among the compounds that has been used for the inhibition of this enzyme, coumarin-dithiocarbamate scaffold has proven to be very effective and this has made it a useful compound in the treatment of type 2 diabetes.…”
Section: Application Of Dithiocarbamate Compounds As Enzyme Inhibitormentioning
confidence: 99%
“…Coumarin-dithiocarbamate is a competitive inhibitor of α-glucosidase since it binds to its active site as evidenced by results obtained from molecular docking [101]. Specifically, there is formation of a hydrogen bond between the amino acid (His279) and coumarin moiety [100]. Pyrrolidine dithiocarbamate has also been used as an effective inhibitor of enzymes, specifically the nuclear factor kappa B [102].…”
Section: Application Of Dithiocarbamate Compounds As Enzyme Inhibitormentioning
confidence: 99%
“…3‐(Bromoacetyl)coumarin has gained a reputation as a crucial structural class that is able to take part in the synthesis of diverse bioactive scaffolds [10,11] . Accumulated studies showed a broad range of 3‐(bromoacetyl)coumarin biological activity including anti‐proliferative, antimicrobial, [12] and type 2 diabetes mellitus inhibitory activities [13] . A comprehensive review on different aspects on bi‐heterocyclic coumarins was published by Anand [14] …”
Section: Introductionmentioning
confidence: 99%
“…Among these compounds, 3-(bromoacetyl)coumarin 1 and its derivatives are a prominent structural class in the synthesis of various bioactive heterocyclic scaffolds, 17,18 they also are important components in drug discovery on account of their biological activities such as antiproliferative, antimicrobial activities, 19 and are promising inhibitors of type 2 diabetes mellitus. 20 In addition, numerous chemosensors are based on polyfunctional coumarin platforms used to detect multianalyte detection, such as different bioactive elements and various environmental pollutants. 21,22 There is no survey available on the biological and chemical applications achieved since the discovery of 3-(bromoacetyl)coumarins.…”
Section: Introductionmentioning
confidence: 99%