Synthesis of novel p-tert-butylcalix[4]arene Schiff bases and their complexes with C60, potential HIV-Protease inhibitors

• We prepare eight p-tert-butylcalixarene Schiff bases using different aliphatic and aromatic diamines.
• We study the complexes of these p-tert-butylcalixarene Schiff bases with C60.
• The inhibition effect of these compounds on HIV-Protease is reported.

Some p-tert-butylcalix[4]arene Schiff base crown ethers were synthesized, characterized using 1H, 13C-NMR, DEPT 135 and Mass spectrometry. Their complexes with C60 were isolated and characterized. The inhibition effect of these complexes on HIVP was studied and found that complexes of 9 and 10 have comparable Ki values to Pepstatine which is known as HIVP inhibitor and used as a control. The synthesis of the ligands, complexes and the inhibition behavior are discussed in this article.

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