| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-105 |
Sentence |
denotes |
A strong inhibition of HIV-induced cytopathic effects by synthetic (1----6)-alpha-D-mannopyranan sulfate. |
| TextSentencer_T2 |
106-255 |
Sentence |
denotes |
The anti-HIV effects of mannopyranan sulfate (1) were investigated by using MT-4 cells, namely, an HTLV-I-carrying CD-4 positive cell-line, in vitro. |
| TextSentencer_T3 |
256-453 |
Sentence |
denotes |
Stereoregular (1----6)-alpha-D-mannopyranan, which had been synthesized by ring-opening polymerization of a 1,6-anhydromannose derivative, was sulfated with piperidine-N-sulfonic acid to provide 1. |
| TextSentencer_T4 |
454-588 |
Sentence |
denotes |
N.m.r. analysis of 1 indicated that the reactivity of hydroxyl groups was in the order, 3-OH greater than 2-OH much greater than 4-OH. |
| TextSentencer_T5 |
589-766 |
Sentence |
denotes |
Mannopyranan sulfate having degree of substitution (d.s.) of 1.19-1.83 effectively inhibited HIV-induced cytopathic effects at a concentration of greater than 3.3 micrograms/mL. |
| TextSentencer_T6 |
767-928 |
Sentence |
denotes |
The anticoagulant activity and the adsorption on concanavalin A of 1 indicated the possibility of selective binding of 1 having d.s. of 1.19-1.83 to HIV-protein. |
| T1 |
0-105 |
Sentence |
denotes |
A strong inhibition of HIV-induced cytopathic effects by synthetic (1----6)-alpha-D-mannopyranan sulfate. |
| T2 |
106-255 |
Sentence |
denotes |
The anti-HIV effects of mannopyranan sulfate (1) were investigated by using MT-4 cells, namely, an HTLV-I-carrying CD-4 positive cell-line, in vitro. |
| T3 |
256-453 |
Sentence |
denotes |
Stereoregular (1----6)-alpha-D-mannopyranan, which had been synthesized by ring-opening polymerization of a 1,6-anhydromannose derivative, was sulfated with piperidine-N-sulfonic acid to provide 1. |
| T4 |
454-588 |
Sentence |
denotes |
N.m.r. analysis of 1 indicated that the reactivity of hydroxyl groups was in the order, 3-OH greater than 2-OH much greater than 4-OH. |
| T5 |
589-766 |
Sentence |
denotes |
Mannopyranan sulfate having degree of substitution (d.s.) of 1.19-1.83 effectively inhibited HIV-induced cytopathic effects at a concentration of greater than 3.3 micrograms/mL. |
| T6 |
767-928 |
Sentence |
denotes |
The anticoagulant activity and the adsorption on concanavalin A of 1 indicated the possibility of selective binding of 1 having d.s. of 1.19-1.83 to HIV-protein. |
