Literature DB >> 25467681

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

Khalid Abu Khadra1, Shehadeh Mizyed2, Deeb Marji3, Salim F Haddad4, Muhammad Ashram5, Ayat Foudeh3.   

Abstract

Some p-tert-butylcalix[4]arene Schiff base crown ethers were synthesized, characterized using (1)H, (13)C-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.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  C(60); Calix[4]aren Schiff bases; Complexes; HIV-Protease inhibitors

Year:  2014        PMID: 25467681     DOI: 10.1016/j.saa.2014.10.100

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  1 in total

1.  Optical Sensing Properties of Pyrene-Schiff Bases toward Different Acids.

Authors:  Bandar A Babgi; Asma Alzahrani
Journal:  J Fluoresc       Date:  2016-05-25       Impact factor: 2.217

  1 in total

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