The relative amounts of protein in the detected bands were quantified by Image J software. The anti-β-actin antibody was used as a control for total protein loading. Potential synergistic effects of ON-01910 molecular weight MI-S in combination with ACV was evaluated by plaque reduction assay, according to experimental design proposed by Chou (2006). Therefore, each drug alone or in combination was tested at an equipotency ratio, based on its corresponding IC50 value. The degree of interaction between MI-S and ACV was calculated

through combination index (CI) equation, based on the median-effect principle of the mass-action law, using Calcusyn software (version 2.1, Biosoft®). According to the CI theorem, CI values <1, =1, and >1 indicate synergism, additive effect, and antagonism, respectively. Assignment of 13C NMR spectrum (Fig. 1) was selleck kinase inhibitor based on the previously published spectrum by Mizuno and colleagues (1999). Anomeric signals (C1) at δ 105.1 and 101.9 ppm were assigned to β-glucopyranosyl and β-mannopyranosyl residues, respectively. The signals at δ 98.1 and 94.3 ppm were assigned to the

corresponding reducing end-groups. The characteristic resonances of C2, C3, C4, C5, and C6 of β-(1 → 2)-linked components were observed at δ 78.2, 73.7, 71.8, 77.9, and 62.9 ppm, respectively. The signals of β-(1 → 3)-linked components were assigned as C2 (75.0), C3 (86.6), C4 (71.9), C5 (76.3), and C6 (62.9). This result suggested that MI is a glucomannan with a main chain of β-1,2-linked d-mannopyranosyl residues and β-d-glucopyranosyl-3-O-β-d-glucopyranosyl residues as side chains. A symmetric single tuclazepam peak was

obtained by gel permeation chromatography of MI-S, suggesting that the polymer is homogeneous. Based on calibration curves with standard dextrans, the apparent Mw of MI-S was 86 kDa. In the MI-S spectrum, obtained by FTIR analyses, two new absorption bands appeared at 1253 and 810 cm−1 (data not shown). These bands are related to S O and C–S–O sulfate groups respectively, confirming that sulfation had actually occurred ( Silverstein et al., 2005). In addition, the content of sulfur determined by elemental analyses was 14.77% and 10.72% for MI-S and DEX-S, respectively. The cytotoxicity and antiviral activity results were used to calculate the selectivity index of each sample (SI = CC50/IC50) (Table 1). The data show that MI presented no antiviral activity, whereas MI-S inhibited both HSV-1 and HSV-2 replication, indicating that chemical sulfation was required for the antiviral activity. Since the simultaneous treatment was more efficient than the p.i. treatment, a direct inactivation of viral particles or inhibition of virus replication at the initial phases of the viral replication cycle could be involved.