Structural, Antioxidant and Antivarial Studies of C-3-nitrophenyl CALIX[4]resorcinarene
How to cite (IJASEIT) :
[1]
B. M Yamin, H. M Abosadiya, S. Aisah Hasbullah, and J. Jumina, “Structural, Antioxidant and Antivarial Studies of C-3-nitrophenyl CALIX[4]resorcinarene”, Int. J. Adv. Sci. Eng. Inf. Technol., vol. 4, no. 3, pp. 125–128, Jun. 2014.
Citation Format :
The calix[4]arene derivative C-3-nitrophenylcalix[4]resorcinarene was synthesized by using one-pot reaction of resorcinol with 3-nitrobenzaldehyde in the presence of concentrated HCl. The compound was characterized by IR, 1H and 13C NMR spectroscopy. X-ray crystallographic study showed that this compound crystallized in a triclinic system with space group of PÄ« and the unit cell dimensions, a = 10.6143(3) í… ,b = 13.6262(4) í…, c = 14.7971(5) í…, α = 102.813(3)°, β = 110.917(3)°, γ = 90.885(2)°. V= 1938.78(11) í…3 and Z =2. The biological Studies were also investigated. It has a stromg antioxidant property and high antiviral activity against HSV-1 . Cytotoxicity testing on Vero cells showed that it is non-toxic, with a CC50 of more than 0.4 mg/mL. Moderate antibacterial activity.
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