| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-115 |
Sentence |
denotes |
Artificial N-functionalized UDP-glucosamine analogues as modified substrates for N-acetylglucosaminyl transferases. |
| TextSentencer_T2 |
116-324 |
Sentence |
denotes |
Analogues of UDP-GlcNAc modified at the 2-acetamido group of the GlcNAc moiety were prepared in order to study their role in the mechanism of N-acetylglucosaminyl transferase mediated glycosylation reactions. |
| TextSentencer_T3 |
325-653 |
Sentence |
denotes |
The structural analogues with N-formyl-, N-propionyl-, N-butyryl- and N-isobutyryl-groups were synthesized, utilizing the morpholidate coupling method starting from d-glucosaminyl-1-phosphate after selective N-acylation of its amino group with the appropriate N-acyloxysuccinimide esters as well as a chlorinated formylformiate. |
| T1 |
0-115 |
Sentence |
denotes |
Artificial N-functionalized UDP-glucosamine analogues as modified substrates for N-acetylglucosaminyl transferases. |
| T2 |
116-324 |
Sentence |
denotes |
Analogues of UDP-GlcNAc modified at the 2-acetamido group of the GlcNAc moiety were prepared in order to study their role in the mechanism of N-acetylglucosaminyl transferase mediated glycosylation reactions. |
| T3 |
325-653 |
Sentence |
denotes |
The structural analogues with N-formyl-, N-propionyl-, N-butyryl- and N-isobutyryl-groups were synthesized, utilizing the morpholidate coupling method starting from d-glucosaminyl-1-phosphate after selective N-acylation of its amino group with the appropriate N-acyloxysuccinimide esters as well as a chlorinated formylformiate. |
