| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-97 |
Sentence |
denotes |
Synthesis of N-acetylglucosamine derivatives as probes for specificity of chicken hepatic lectin. |
| T1 |
0-97 |
Sentence |
denotes |
Synthesis of N-acetylglucosamine derivatives as probes for specificity of chicken hepatic lectin. |
| TextSentencer_T2 |
98-149 |
Sentence |
denotes |
Syntheses of the following compounds are described: |
| T2 |
98-149 |
Sentence |
denotes |
Syntheses of the following compounds are described: |
| TextSentencer_T3 |
150-443 |
Sentence |
denotes |
6-(Trifluoroacetylamino)hexyl 2-acetamido-2,6-dideoxy-beta-D-glucopyranoside and 2-acetamido-2-deoxy-alpha-D-xylopyranoside, two allyl 2-acetamido-2-deoxy-alpha-D-glucopyranosiduronic acid derivatives, and several allyl 2-acylamido-2-deoxy-beta-D-glucopyranosides having different acyl groups. |
| T3 |
150-443 |
Sentence |
denotes |
6-(Trifluoroacetylamino)hexyl 2-acetamido-2,6-dideoxy-beta-D-glucopyranoside and 2-acetamido-2-deoxy-alpha-D-xylopyranoside, two allyl 2-acetamido-2-deoxy-alpha-D-glucopyranosiduronic acid derivatives, and several allyl 2-acylamido-2-deoxy-beta-D-glucopyranosides having different acyl groups. |
| TextSentencer_T4 |
444-579 |
Sentence |
denotes |
These and other compounds were used as inhibitors in the binding assay for the chicken hepatic lectin specific for N-acetylglucosamine. |
| T4 |
444-579 |
Sentence |
denotes |
These and other compounds were used as inhibitors in the binding assay for the chicken hepatic lectin specific for N-acetylglucosamine. |
| TextSentencer_T5 |
580-594 |
Sentence |
denotes |
We found that: |
| T5 |
580-594 |
Sentence |
denotes |
We found that: |
| TextSentencer_T6 |
595-944 |
Sentence |
denotes |
1) The inhibitory potency of N-acylglucosamine derivatives decreased progressively with increase in the size of acyl group, 2) absence of either 3- or 4-OH group of N-acetylglucosamine lowered the binding affinity more than 100-fold, and 3) the presence of a negatively charged group (carboxylic acid) at the C-6 position did not lower the affinity. |
| T6 |
595-944 |
Sentence |
denotes |
1) The inhibitory potency of N-acylglucosamine derivatives decreased progressively with increase in the size of acyl group, 2) absence of either 3- or 4-OH group of N-acetylglucosamine lowered the binding affinity more than 100-fold, and 3) the presence of a negatively charged group (carboxylic acid) at the C-6 position did not lower the affinity. |
| TextSentencer_T7 |
945-1110 |
Sentence |
denotes |
The first two items are similar to the mammalian hepatic galactose/N-acetylgalactosamine lectins, but the last item is in a strong contrast to the mammalian lectins. |
| T7 |
945-1110 |
Sentence |
denotes |
The first two items are similar to the mammalian hepatic galactose/N-acetylgalactosamine lectins, but the last item is in a strong contrast to the mammalian lectins. |