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Sulfonylhydrazones: Design, synthesis and investigation of ectonucleotidase (ALP & e5'NT) inhibition activities.

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TLDR
The potent compounds 5a, 7, and 9d against different ectonucleotidases (h-ecto 5'-NT, h-TNAP, h -IAP) could potentially serve as lead for the development of new therapeutic agents.
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This article is published in Bioorganic Chemistry.The article was published on 2020-07-01. It has received 10 citations till now.

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The bioactivity of benzenesulfonyl hydrazones: A short review.

TL;DR: The synthesis and biological activity evaluation of benzenesulfonyl hydrazones is quite frequently encountered in scientific literature as discussed by the authors, which is very interesting due to the wide spectrum of potential applications in the field of medicinal chemistry.
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Development of New Antimycobacterial Sulfonyl Hydrazones and 4-Methyl-1,2,3-thiadiazole-Based Hydrazone Derivatives

TL;DR: The 4-methyl-1,2,3-thiadiazole-based hydrazone derivatives and sulfonyl hydrazones proved to be new classes of lead compounds having the potential of novel candidate antituberculosis drugs.
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Synthesis, Characterization, and In Silico Studies of Novel Spirooxindole Derivatives as Ecto-5'-Nucleotidase Inhibitors.

TL;DR: An efficient, environment friendly route for the synthesis of non-nucleotide based small molecules is reported, i.e., substituted spirooxindole derivatives 9a-9l and in silico studies were carried out to assess binding interactions of potent compounds within enzyme active sites and demonstrated excellent correlation with the experimental findings.
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Targeting ecto-5'-nucleotidase: A comprehensive review into small molecule inhibitors and expression modulators.

TL;DR: In this article , the authors highlight important biochemical and structural features of ecto-5'NT, highlight its expression profile in normal and cancer cell lines detailing compounds which may act as expression regulators and to review the several classes of ectoe-5'-NT inhibitors developed in the past 12 years, in order to build a general structure-activity relationship model to guide further compound design.
References
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Journal ArticleDOI

The role of alkaline phosphatase in mineralization

TL;DR: The mechanism with which this enzyme carries out its function is not complete and it is appropriate to review the current status of this important enzyme.
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Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO(2) capture.

TL;DR: Novel drug design strategies have been reported principally based on the tail approach for obtaining all these types of CAIs, which exploit more external binding regions within the enzyme active site (in addition to coordination to the metal ion), leading thus to isoformselective compounds.
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Diuretics: from classical carbonic anhydrase inhibitors to novel applications of the sulfonamides.

TL;DR: It has been proposed that the recently observed beneficial effect of indapamide for the treatment of patients with hypertension and type 2 diabetes might be due to its potent inhibition of CA isoforms present in kidneys and blood vessels, which would explain both the blood pressure lowering effects as well as organ-protective activity of the drug.
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Novel Inhibitors of Alkaline Phosphatase Suppress Vascular Smooth Muscle Cell Calcification

TL;DR: Three novel inhibitors of the physiological pyrophosphatase activity of alkaline phosphatase are reported and it is shown that these compounds are capable of reducing calcification in two models of vascular calcification.
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Ecto-5'-nucleotidase: Structure function relationships.

TL;DR: The currently available structural information on ecto-5’NT is reviewed in relation to the catalytic properties and enzyme function.
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