| Autor: |
Jumina, Kurniawan, Yehezkiel Steven, Sari, Ratna, Purba, Sri Nessy Handayani Br, Radean, Hesti, Priatmoko, Pranowo, Deni, Purwono, Bambang, Julianus, Jeffry, Zulkarnain, Abdul Karim, Sholikhah, Eti Nurwening |
| Předmět: |
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| Zdroj: |
Indonesian Journal of Pharmacy / Majalah Farmasi Indonesia; 2022, Vol. 33 Issue 3, p422-433, 12p |
| Abstrakt: |
In the present work, a successful synthesis and high antioxidant activity of C-alkylcalix[4]resorcinarene and C-alkylcalix[4]pyrogallolarene derivatives were reported. The C-alkylcalix[4]resorcinarenes were prepared from a cyclization reaction of resorcinol and either pentanaldehyde or octanaldehyde under acidic conditions. Meanwhile, the Calkylcalix[ 4]pyrogallolarenes were prepared from a cyclization reaction of pyrogallol with pentanaldehyde or octanaldehyde. Four synthesized products, i.e., nBu-CR, nHep-CR, nBu-CP, and nHep-CP, were successfully prepared in 92.4-96.4% yield. Their chemical structure was elucidated by Fourier transform infrared (FTIR), liquid chromatography-mass spectrometry (LC-MS), and proton nuclear magnetic resonance (1H-NMR) analysis. The antioxidant activity assay of these compounds was evaluated through an in vitro assay employing 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals. The DPPH assay showed that the half-maximal inhibitory concentration (IC50) values of nBu-CR, nHep-CR, nBu-CP, and nHep-CP compounds were 25.1, 22.9, 11.5, and 21.9 µg mL-1, respectively. The IC50 value of the synthesized compounds was 2.0-4.3 times lower than the positive standard of butylated hydroxytoluene (BHT, IC50 = 49.9 µg mL-1), which was remarkable. This finding demonstrates that both Calkylcalix[ 4]resorcinarenes and C-alkylcalix[4]pyrogallolarenes are better antioxidant agents than BHT. The nHep-CR compound was found as the best antioxidant agent among the other compounds due to weaker intramolecular and intermolecular hydrogen bondings and a longer alkyl chain. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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