2016
DOI: 10.1007/s40242-016-6047-0
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Design and synthesis of 1,4-dihydropyridine and cinnamic acid esters and their antioxidant properties

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Cited by 8 publications
(1 citation statement)
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“…The results indicated the radical scavenging ability of 1,4-DHP rings as a hydrogen donor, which could be further enhanced by vanillin moieties. 76,77 The visual results agreed well with the quantitative data obtained by monitoring the absorbance at 734 nm of each solution (Figure S3). The half-maximal value of the inhibitory concentration (IC 50 ) of PVA-vanillin to ABTS +• was calculated as 56.8 μM, which is lower than that of PVA-ph (150.0 μM) (Figure S4a,b).…”
mentioning
confidence: 99%
“…The results indicated the radical scavenging ability of 1,4-DHP rings as a hydrogen donor, which could be further enhanced by vanillin moieties. 76,77 The visual results agreed well with the quantitative data obtained by monitoring the absorbance at 734 nm of each solution (Figure S3). The half-maximal value of the inhibitory concentration (IC 50 ) of PVA-vanillin to ABTS +• was calculated as 56.8 μM, which is lower than that of PVA-ph (150.0 μM) (Figure S4a,b).…”
mentioning
confidence: 99%