Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-122 |
Sentence |
denotes |
5a-Carba-glycopyranoside primers: potential building blocks for biocombinatorial synthesis of glycosphingolipid analogues. |
T1 |
0-122 |
Sentence |
denotes |
5a-Carba-glycopyranoside primers: potential building blocks for biocombinatorial synthesis of glycosphingolipid analogues. |
TextSentencer_T2 |
123-349 |
Sentence |
denotes |
Three ether-linked alkyl 5a-carba-glycopyranosides 1b,d, and 5b, and 5a'-carba-lactoside 7b were examined as potent primers in mouse B16 melanoma cells for their feasibility as building blocks for oligosaccharide biosynthesis. |
T2 |
123-349 |
Sentence |
denotes |
Three ether-linked alkyl 5a-carba-glycopyranosides 1b,d, and 5b, and 5a'-carba-lactoside 7b were examined as potent primers in mouse B16 melanoma cells for their feasibility as building blocks for oligosaccharide biosynthesis. |
TextSentencer_T3 |
350-659 |
Sentence |
denotes |
Uptake by B16 cells was first observed for all carba-glycoside primers, and, especially, the 5a-carba-sugar analogues of N-acetyl-beta-d-glucosaminide 1b and beta-d-glucoside 1d were shown to produce two-to-four-fold larger amounts of glycosylated products than the corresponding true sugar primers 1a and 1c. |
T3 |
350-659 |
Sentence |
denotes |
Uptake by B16 cells was first observed for all carba-glycoside primers, and, especially, the 5a-carba-sugar analogues of N-acetyl-beta-d-glucosaminide 1b and beta-d-glucoside 1d were shown to produce two-to-four-fold larger amounts of glycosylated products than the corresponding true sugar primers 1a and 1c. |
TextSentencer_T4 |
660-899 |
Sentence |
denotes |
The carba glycoside uptake by cells resulted in beta-galactosylation and subsequent sialylation of the incorporated galactose residues, giving rise to glycosylated products 3b and 3d having similar glycan structures as the ganglioside GM3. |
T4 |
660-899 |
Sentence |
denotes |
The carba glycoside uptake by cells resulted in beta-galactosylation and subsequent sialylation of the incorporated galactose residues, giving rise to glycosylated products 3b and 3d having similar glycan structures as the ganglioside GM3. |
TextSentencer_T5 |
900-1202 |
Sentence |
denotes |
According to efficient uptake in cells, in addition to stability of the ether-linked pseudo-reducing ends of the oligosaccharides that formed, the carba glycoside primers have been demonstrated to be versatile building blocks for these biocombinatorial syntheses of glycolipid oligosaccharide mimetics. |
T5 |
900-1202 |
Sentence |
denotes |
According to efficient uptake in cells, in addition to stability of the ether-linked pseudo-reducing ends of the oligosaccharides that formed, the carba glycoside primers have been demonstrated to be versatile building blocks for these biocombinatorial syntheses of glycolipid oligosaccharide mimetics. |
TextSentencer_T6 |
1203-1356 |
Sentence |
denotes |
On the other hand, uptake for 5a-carba-galactopyranoside residue was found to be decreased by one-third for dodecyl 5a-carba-beta-d-galactopyranoside 5b. |
T6 |
1203-1356 |
Sentence |
denotes |
On the other hand, uptake for 5a-carba-galactopyranoside residue was found to be decreased by one-third for dodecyl 5a-carba-beta-d-galactopyranoside 5b. |
TextSentencer_T7 |
1357-1536 |
Sentence |
denotes |
Observation of similar levels for 5a'-carba-beta-lactoside 7b under both cellular and cell-free conditions suggested that enzymes are likely to recognize the pyranose oxygen atom. |
T7 |
1357-1536 |
Sentence |
denotes |
Observation of similar levels for 5a'-carba-beta-lactoside 7b under both cellular and cell-free conditions suggested that enzymes are likely to recognize the pyranose oxygen atom. |