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. 2012 Jan;56(1):341–351. doi: 10.1128/AAC.05537-11

Fig 1.

Fig 1

Activity of F18 against HIV-1NL4-3 wild-type strains and five major subtypes in PBMCs. (A) Structure of 10-chloromethyl-11-demethyl-12-oxo-calanolide A (F18). (B and C) Serially diluted F18, NVP, and (+)-calanolide A were added to PBMCs infected with wild-type HIV-1NL4-3 (B) or five major subtypes (C). The p24 level was measured 7 days PI. Each drug was tested in three PHA-stimulated fresh healthy donor PBMCs. All results are means ± standard errors of the means from three independent experiments.