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Synthesis and Modeling Study of Some Potential Pyrimidine Derivatives as HIV Inhibitors

  • Najim A. Al-Masoudi EMAIL logo , Yossra A. Marich , Niran J. Al-Salihi und Bahjat Saeed
Veröffentlicht/Copyright: 2. Juni 2014
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A new series of 2-amino-6-((4-aryldiazenyl)benzyloxy)-4-chloropyrimidine derivatives 4 - 13 and 2,6-diamino-5-arylazo-4-chloro-pyrimidine analogs 15 - 20 were synthesized from the pyrimidine scaffolds 3 and 14, respectively, via diazotization with various amines. Nucleophilic displacement at the 2,4-diamino-5-arylazo-6-chloro-pyrimidine 16 by different amines afforded the 4-alkylamino analogs 21 - 27. All new compounds were evaluated for their in vitro anti-HIV activity in MT-4 cells as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that 10 and 11 were found to be the only compounds in the series inhibiting HIV-1 replication in cell cultures with EC50 of >1:23 and >2:92 μg mL-1 of a CC50 of 12.30 and 17.52 μg mL-1, resulting in a selectivity index of 10 and 6, respectively. In addition, preliminary structure-activity relationships and molecular modeling of these new analogs are detailed in this manuscript.

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 Synthesis and Modeling Study of Some Potential Pyrimidine Derivatives as HIV Inhibitors

Synthesis and Modeling Study of Some Potential Pyrimidine Derivatives as HIV Inhibitors

Received: 2014-5-20
Published Online: 2014-6-2
Published in Print: 2014-8-1

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