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Lipid conjugates of antiretroviral agents. I. Azidothymidine-monophosphate-diglyceride: Anti-HIV activity, physical properties, and interaction with plasma proteins
Journal article   Peer reviewed

Lipid conjugates of antiretroviral agents. I. Azidothymidine-monophosphate-diglyceride: Anti-HIV activity, physical properties, and interaction with plasma proteins

Joseph M. Steim, Catherine Neto, Prem S. Sarin, Daisy K. Sun, Raj K. Sehgal and Joseph G. Turcotte
Biochemical and biophysical research communications, Vol.171(1), pp.451-457
08/31/1990
PMID: 2393400

Abstract

PBS HDL PC AZT AZTMPDG LDL
3′-Azido-3′-deoxythymidine-5′-phosphate diglyceride ( 16:0 18:1 ω9 ), a phosphatic acid conjugate of AZT, is active against HIV replication in H9 cells and syncytia formation in MOLT-3 cells. The activities rank as AZT > pure conjugate > conjugate in mixed liposomes, with the pure conjugate having about one-third the activity of free AZT. The compound binds very rapidly to serum lipoproteins, but not to serum albumin, α and β globulins, or red cells. Pancreatic phospholipase A 2 hydrolyzes it to the lysophosphatidic acid conjugate.

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