2017
DOI: 10.1016/j.arabjc.2014.05.029
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Synthesis of coumarin derivatives containing pyrazole and indenone rings as potent antioxidant and antihyperglycemic agents

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Cited by 60 publications
(32 citation statements)
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“…Actually, all newly synthesized coumarin derivatives expressed considerable radical scavenging or antioxidant activity with IC 50 range (1.49-18.79) µg/ml. Our inding came in agreement with Kenchappa et al they found that the presence of electron-withdrawing functional groups have promising antioxidant activities (Kenchappa et al, 2017).…”
Section: Antioxidant Activitysupporting
confidence: 91%
“…Actually, all newly synthesized coumarin derivatives expressed considerable radical scavenging or antioxidant activity with IC 50 range (1.49-18.79) µg/ml. Our inding came in agreement with Kenchappa et al they found that the presence of electron-withdrawing functional groups have promising antioxidant activities (Kenchappa et al, 2017).…”
Section: Antioxidant Activitysupporting
confidence: 91%
“…The spectral characteristics correspond to the literature data. [43] (10). Hydroquinone (1 mmol) and camphene (1 mmol) were placed in a two-necked flask equipped with a thermometer and a condenser.…”
Section: Synthesis Of Alkylphenolsmentioning
confidence: 99%
“…It has been recognized that hydroxycoumarins are effective metal chelators, free radical scavengers and powerful chain breaking antioxidants. [10] Thus, 4hydroxycoumarins used to treat deep venous thrombosis and some cardiovascular diseases [11] demonstrate the anti-inflammatory properties, which have also been associated with their antioxidant activities. [12] A comparative study of the antioxidant activity of several coumarins against liver toxicity induced by carbon tetrachloride showed that 4-methylumbelliferone was completely inactive, whereas other C-6 and C-7 disubstituted coumarins significantly prevented oxidative stress induced by carbon tetrachloride.…”
Section: Introductionmentioning
confidence: 99%
“…3-(4-((Z)-(5,6-Dimethoxy-1-oxo-1H-inden-2(3H)-ylidene)-methyl)-1-p-tolyl-1H-pyrazol-3-yl)-2Hchromen-2-one and 3-(4-((Z)-(5,6-dimethoxy-1-oxo-1H-inden-2(3H)-ylidene)-methyl)-1-(4-methoxy phenyl)-1H-pyrazol-3-yl)-2H-chromen-2-one have shown the greatest activity. Furthermore, fraxidin, by inhibiting the formation of inductible nitric oxide synthase, can down-regulate the blood glucose level [38,40] Anti-inflammatory activity:…”
Section: Biological Properties Of Volatile Phenylpropanoidsmentioning
confidence: 99%