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. 2006 May 6;71(2):227–236. doi: 10.1016/j.antiviral.2006.04.008

Table 1.

Antibacterial and antiviral activities of glycopeptide aglycons and their derivatives (Printsevskaya et al., 2005) (See Fig. 4)

Compound MICa (μg/ml)
IC50b (μM)
EC50c (μM)
533 S. epider-midis 559 E. faecalis (GSE) 560 E. faecalis (GRE) L1210 MOLT-4/C8 CEM HIV-1 HIV-2
Vancomycin aglycon and its amide
 11 4 2 >64 >500 >500 >500 65 ≥250
 11a 2 1 16 ≥250 72 ≥250 3.0 9.5



Eremomycin aglycon and its amide
 12 32 16 >128 >500 >500 >500 50.6 ≥250
 12a 8 4 8 94 126 148 1.6 7
Des-(N-d-MeLeu)-vancomycin aglycon and its amide
 13 >128 >128 >128 ≥250 ≥250 >250 ≥125 ≥125
 13a >32 >64 >64 ≥250 178 ≥250 20 30



Des-(N-d-MeLeu)-eremomycin aglycon and its amide
 14 >128 >128 >128 >250 >250 >250 115.2 >250
 14a >32 >64 >64 175 >250 >250 5.5 3.5
a

Minimum inhibitory concentration of the compound. As MWs of all compounds are in the interval ∼1000–1400 Da and MICs values given in “μg/ml” are very close to those calculated in “μM”.

b

Inhibitory concentration, or compound concentration required to inhibit cell proliferation by 50%.

c

Effective concentration or concentration required to protect cells against the cytopathicity of the different HIV strains by 50%.