Rb. Lingham et al., QUINOXAPEPTINS - NOVEL CHROMODEPSIPEPTIDE INHIBITORS OF HIV-1 AND HIV-2 REVERSE-TRANSCRIPTASE .1. THE PRODUCING ORGANISM AND BIOLOGICAL-ACTIVITY, Journal of antibiotics, 49(3), 1996, pp. 253-259
Quinoxapeptin A and B are novel chromodepsipeptides which were isolate
d from a nocardioform actinomycete with indeterminant morphology. Quin
oxapeptins a and B are potent inhibitors of HIV-1 and HIV-2 reverse tr
anscriptase and almost equally active against two single mutants forms
as well as a double mutant form of HIV-1 reverse transcriptase. Quino
xapeptin A and B are specific inhibitors of HIV-I and HIV-2 reverse tr
anscriptase because they did not inhibit human DNA polymerase alpha, b
eta, gamma, and delta. Quinoxapeptin A and B are structurally similar
to luzopeptin A which was also active against HIV-land HIV-2 reverse t
ranscriptase.