Molecules (May 2016)

Regioselective Palmitoylation of 9-(2,3-Dihydroxy- propyl)adenine Catalyzed by a Glycopolymer-enzyme Conjugate

  • Jana Brabcová,
  • Jiří Blažek,
  • Marcela Krečmerová,
  • Jiří Vondrášek,
  • Jose M. Palomo,
  • Marie Zarevúcka

DOI
https://doi.org/10.3390/molecules21050648
Journal volume & issue
Vol. 21, no. 5
p. 648

Abstract

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The enzymatic regioselective monopalmitoylation of racemic 9-(2,3-dihydroxypropyl)- adenine (DHPA), an approved antiviral agent, has been performed by an immobilized form of Candida antarctica B lipase (CAL-B) using a 4:1 DMF/hexane mixture as the reaction medium. To improve the chemical yield of the desired monopalmitoylation reaction, solid-phase chemical modifications of the lipase were evaluated. The reaction yield was successfully increased obtaining 100% product after a second treatment of the product solution with fresh immobilised chemically glycosylated-CAL-B.

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