2017
DOI: 10.1016/j.bioorg.2017.10.014
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Synthetic and medicinal perspective of thiazolidinones: A review

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Cited by 138 publications
(74 citation statements)
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“…Releases in the public media, however, revealed reported commercial concerns with regard to success criteria, and it has since been shelved. Variants of thiazolidinones (a class of small molecule that has been very useful in drug discovery [67]) have been used clinically for unrelated purposes (rosiglitazone and pioglitazone, which are both insulin sensitizers); however, it is clear that the structure of these molecules can to be optimized for effect in inhibiting type III secretion systems in both bacteria from the genus Salmonella and Yersinia [68]. With regard to compounds that can inhibit type II fatty acid synthesis, Anthranilic acid has been used clinically previously [69] and has chemistry associated with other clinically used products.…”
Section: Therapeutics To Prevent Host Cell Subversionmentioning
confidence: 99%
“…Releases in the public media, however, revealed reported commercial concerns with regard to success criteria, and it has since been shelved. Variants of thiazolidinones (a class of small molecule that has been very useful in drug discovery [67]) have been used clinically for unrelated purposes (rosiglitazone and pioglitazone, which are both insulin sensitizers); however, it is clear that the structure of these molecules can to be optimized for effect in inhibiting type III secretion systems in both bacteria from the genus Salmonella and Yersinia [68]. With regard to compounds that can inhibit type II fatty acid synthesis, Anthranilic acid has been used clinically previously [69] and has chemistry associated with other clinically used products.…”
Section: Therapeutics To Prevent Host Cell Subversionmentioning
confidence: 99%
“…7,8 Among others, derivatives of ve-membered heterocyclic systems based on the core of 1,3-thiazolidine or imidazolidine have been studied due to their broad biological activity. 9,10 Of particular interest are their derivatives containing exocyclic sulfur and oxygen atoms, such as rhodanine (2-sulfanylidene-1,3-thiazolidin-4-one) 11 or 2thiohydantoin (2-sulfanylidene-1,3-diazolidin-4-one). 12 The presence of these double-bonded atoms with other functional groups results in particularly high density of binding sites for polar interactions and hydrogen bonds, which are responsible for their interesting biological properties.…”
Section: Introductionmentioning
confidence: 99%
“…The intrinsic versatility and unique physicochemical properties of the heterocycles make them a true cornerstone in the medicinal chemistry research area . Among various types of heterocyclic compounds, indole and its derivatives have been established as important medicinal agents, possessing various biological activities such as anticholinesterase , antinociceptive , antiproliferative, tuberculostatic , antiviral, antidiabetic , and antidepressant . Indole has been already seeking the attention of many researchers; as a result, wide variety of newer synthetic strategies are continuously being explored to prepare a huge number of new derivatives with better pharmacological activity as compared with existing ones.…”
Section: Introductionmentioning
confidence: 99%