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. 2008 Mar 31;79(1):6–11. doi: 10.1016/j.antiviral.2008.01.160

Table 1.

Effects of GL derivatives on EBV replication in superinfected Raji cells

Compound EC50 (μM)a CC50 (μM)b Therapeutic indexc
(I) >1000 >8000 NDd
(II) >1000 >8000 ND
(III) >1000 >8000 ND
(IV) >1000 >1000 ND
(V) >1000 >8000 ND
(VI) 75 ± 15 (90 ± 20) 1500 ± 100 20
(VII) 65 ± 10 (75 ± 10) 1200 ± 60 18
(VIII) 30 ± 5 (50 ± 5) 4800 ± 180 160
(IX) >1000 >8000 ND
(X) 95 ± 25 (130 ± 20) 1400 ± 100 15
(XI) >1000 >8000 ND
(XII) 30 ± 5 (45 ± 5) 2000 ± 80 67
(XIII) 135 ± 35 (175 ± 20) 4000 ± 160 30
(XIV) >1000 >8000 ND
(XV) 25 ± 5 (42 ± 6) 5000 ± 150 200
GL (18β-GL) 30 ± 5 (38 ± 4) 4500 ± 160 150
GA (18β-GA) 4 ± 1 (5 ± 1) 75 ± 10 19
a

EC50, effective concentration of the compound needed to inhibit EBV genome copy numbers and, in parentheses, EA/VCA expression to 50% of untreated cells.

b

CC50, cytotoxic concentration of the compound that decreased cell viability to 50% of untreated cells determined by MTT. Results represent mean values ± S.D. of three independent experiments.

c

Therapeutic index is defined as the ratio of CC50 to EC50.

d

ND, not determined.