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Number of results
2007 | 54 | 4 | 863-868

Article title

Synthesis and anti-HIV properties of novel 6-phenylselenenyl-5-propyluracils

Content

Title variants

Languages of publication

EN

Abstracts

EN
Novel 6-phenylselenenyl-5-propyluracils were synthesized from 5-propyluracil with the use of regioselective synthesis to give 1-[(2-hydroxyethoxy)-methyl]-6-phenylselenenyl-5-propyluracil (6), 1-ethoxymethyl-6-phenylselenenyl-5-propyluracil (9) and 1-benzyloxymethyl-6-phenylselenenyl-5-propyluracil (10). Interaction of these compounds with recombinant HIV-1 reverse transcriptase (RT) was evaluated using a non-isotopic colorimetric method. Compounds 9 and 10 exerted potent HIV RT inhibition (IC50 0.06 and 0.05 µM respectively) while compound 6 showed moderate inhibition (IC50 = 3.5 µM). Potent anti-HIV-1 activity in MT-2 cells inoculated by a syncythia-inducing HIV-1 (cat #3 strain) laboratory isolate was exerted by compounds 9 and 10 (EC50 0.62 µM and 0.025 µM, respectively), while compound 6 showed only moderate activity (IC50 = 4.1 µM). In addition, compound 10 showed very good in vitro therapeutic index (TI > 2046), indicating that it is a potential anti-HIV/AIDS drug.

Year

Volume

54

Issue

4

Pages

863-868

Physical description

Dates

published
2007
received
2007-08-08
revised
2007-09-03
accepted
2007-09-04
(unknown)
2007-12-08

Contributors

  • Institute of Biochemistry and Biophysics, PAS, Warszawa, Poland
  • Institute of Biochemistry and Biophysics, PAS, Warszawa, Poland
  • Institute of Biochemistry and Biophysics, PAS, Warszawa, Poland
  • Medical Research Center PAS, Warszawa, Poland
  • National Medicines Institute, Warszawa, Poland
  • Institute of Biochemistry and Biophysics, PAS, Warszawa, Poland

References

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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv54p863kz
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