| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-117 |
Sentence |
denotes |
Bioactivity screening of partially desulfated low-molecular-weight heparins: a structure/activity relationship study. |
| T1 |
0-117 |
Sentence |
denotes |
Bioactivity screening of partially desulfated low-molecular-weight heparins: a structure/activity relationship study. |
| T1 |
0-117 |
Sentence |
denotes |
Bioactivity screening of partially desulfated low-molecular-weight heparins: a structure/activity relationship study. |
| TextSentencer_T2 |
118-284 |
Sentence |
denotes |
A series of size-defined low-molecular-weight heparins were generated by regioselective chemical modifications and profiled for their in vitro and in vivo activities. |
| T2 |
118-284 |
Sentence |
denotes |
A series of size-defined low-molecular-weight heparins were generated by regioselective chemical modifications and profiled for their in vitro and in vivo activities. |
| T2 |
118-284 |
Sentence |
denotes |
A series of size-defined low-molecular-weight heparins were generated by regioselective chemical modifications and profiled for their in vitro and in vivo activities. |
| TextSentencer_T3 |
285-673 |
Sentence |
denotes |
The compounds displayed reduced anti-coagulant activity, demonstrated varying affinities toward angiogenic growth factors (fibroblast growth factor-2, vascular endothelial growth factor and stromal cell-derived factor-1α), inhibited the P-selectin/P-selectin glycoprotein ligand-1 interaction and, notably, exhibited anti-tumor efficacy in a murine melanoma experimental metastasis model. |
| T3 |
285-673 |
Sentence |
denotes |
The compounds displayed reduced anti-coagulant activity, demonstrated varying affinities toward angiogenic growth factors (fibroblast growth factor-2, vascular endothelial growth factor and stromal cell-derived factor-1α), inhibited the P-selectin/P-selectin glycoprotein ligand-1 interaction and, notably, exhibited anti-tumor efficacy in a murine melanoma experimental metastasis model. |
| T3 |
285-673 |
Sentence |
denotes |
The compounds displayed reduced anti-coagulant activity, demonstrated varying affinities toward angiogenic growth factors (fibroblast growth factor-2, vascular endothelial growth factor and stromal cell-derived factor-1α), inhibited the P-selectin/P-selectin glycoprotein ligand-1 interaction and, notably, exhibited anti-tumor efficacy in a murine melanoma experimental metastasis model. |
| TextSentencer_T4 |
674-908 |
Sentence |
denotes |
Our results demonstrate that modulating specific sequences, especially the N-domains (-NS or -NH(2) or -NHCOCH(3)) in these polysaccharide sequences, has a major impact on the participation in a diverse range of biological activities. |
| T4 |
674-908 |
Sentence |
denotes |
Our results demonstrate that modulating specific sequences, especially the N-domains (-NS or -NH(2) or -NHCOCH(3)) in these polysaccharide sequences, has a major impact on the participation in a diverse range of biological activities. |
| T4 |
674-908 |
Sentence |
denotes |
Our results demonstrate that modulating specific sequences, especially the N-domains (-NS or -NH(2) or -NHCOCH(3)) in these polysaccharide sequences, has a major impact on the participation in a diverse range of biological activities. |
| TextSentencer_T5 |
909-1154 |
Sentence |
denotes |
These results also suggest that the 6-O-sulfates, but not the 2-O-sulfates, critically affect the binding of a desulfated derivative to certain angiogenic proteins as well as its ability to inhibit P-selectin-mediated B16F10 melanoma metastases. |
| T5 |
909-1154 |
Sentence |
denotes |
These results also suggest that the 6-O-sulfates, but not the 2-O-sulfates, critically affect the binding of a desulfated derivative to certain angiogenic proteins as well as its ability to inhibit P-selectin-mediated B16F10 melanoma metastases. |
| T5 |
909-1154 |
Sentence |
denotes |
These results also suggest that the 6-O-sulfates, but not the 2-O-sulfates, critically affect the binding of a desulfated derivative to certain angiogenic proteins as well as its ability to inhibit P-selectin-mediated B16F10 melanoma metastases. |
| TextSentencer_T6 |
1155-1327 |
Sentence |
denotes |
Furthermore, N-desulfation followed by N-acetylation regenerates the affinity/inhibition properties to different extents in all the compounds tested in the in vitro assays. |
| T6 |
1155-1327 |
Sentence |
denotes |
Furthermore, N-desulfation followed by N-acetylation regenerates the affinity/inhibition properties to different extents in all the compounds tested in the in vitro assays. |
| T6 |
1155-1327 |
Sentence |
denotes |
Furthermore, N-desulfation followed by N-acetylation regenerates the affinity/inhibition properties to different extents in all the compounds tested in the in vitro assays. |
| TextSentencer_T7 |
1328-1549 |
Sentence |
denotes |
This systematic study lays a conceptual foundation for detailed structure function elucidation and will facilitate the rational design of targeted heparan sulfate proteoglycan-based anti-metastatic therapeutic candidates. |
| T7 |
1328-1549 |
Sentence |
denotes |
This systematic study lays a conceptual foundation for detailed structure function elucidation and will facilitate the rational design of targeted heparan sulfate proteoglycan-based anti-metastatic therapeutic candidates. |
| T7 |
1328-1549 |
Sentence |
denotes |
This systematic study lays a conceptual foundation for detailed structure function elucidation and will facilitate the rational design of targeted heparan sulfate proteoglycan-based anti-metastatic therapeutic candidates. |