Abstract
3′-Azido-3′-deoxythymidine-5′-phosphate diglyceride ( 16:0 18:1ω9), 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 A2 hydrolyzes it to the lysophosphatidic acid conjugate. © 1990.
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CITATION STYLE
Steim, J. M., Neto, C. C., Sarin, P. S., Sun, D. K., Sehgal, R. K., & Turcotte, J. G. (1990). Lipid conjugates of antiretroviral agents. I. Azidothymidine-monophosphate-diglyceride: Anti-HIV activity, physical properties, and interaction with plasma proteins. Biochemical and Biophysical Research Communications, 171(1), 451–457. https://doi.org/10.1016/0006-291X(90)91414-N
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