Quinoxapeptins: Novel chromodepsipeptide inhibitors of HIV-1 and HIV-2 reverse transcriptase .1. The producing organism and biological activity

RB Lingham, AHM Hsu, JA OBrien, JM Sigmund,M Sanchez,MM Gagliardi,BK Heimbuch,O Genilloud,I Martin,MT Diez, CF Hirsch, DL Zink, JM Liesch, GE Koch,SE Gartner,GM Garrity,NN Tsou,GM Salituro

JOURNAL OF ANTIBIOTICS(1996)

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摘要
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-I 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-land HIV-2 reverse transcriptase.
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