Quinoxapeptins: Novel Chromodepsipeptide Inhibitors of HIV-1 and HIV-2 Reverse Transcriptase. I. The Producing Organism and Biological Activity.

Russell B. Lingham, Amy Hsu, JULIE A. O' BRIEN, J Sigmund, Manuel Almagro Sánchez, MAGDA M. GAGLIARDI, Brian K. Heimbuch, Olga Genilloud, I. Martín, C. F. Hirsch,

The Journal of Antibiotics · 1996 · 52 citations · 19 references

Concepts

Abstract

Quinoxapeptin A and B are novel chromodepsipeptides which were isolated from a nocardioform actinomycete with indeterminant morphology. Quinoxapeptins A and B are potent inhibitors of HIV-1 and HIV-2 reverse transcriptase and almost equally active against two single mutants forms as well as a double mutant form of HIV-1 reverse transcriptase. Quinoxapeptin A and B are specific inhibitors of HIV-1 and HIV-2 reverse transcriptase because they did not inhibit human DNA polymerase alpha, beta, gamma and delta. Quinoxapeptin A and B are structurally similar to luzopeptin A which was also active against HIV-1 and HIV-2 reverse transcriptase.

References

19