| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-145 |
Sentence |
denotes |
Design of new benzoxazole-2-thione-derived inhibitors of Streptococcus pneumoniae hyaluronan lyase: structure of a complex with a 2-phenylindole. |
| T1 |
0-145 |
Sentence |
denotes |
Design of new benzoxazole-2-thione-derived inhibitors of Streptococcus pneumoniae hyaluronan lyase: structure of a complex with a 2-phenylindole. |
| TextSentencer_T2 |
146-296 |
Sentence |
denotes |
The bacterial hyaluronan lyases (Hyals) that degrade hyaluronan, an important component of the extracellular matrix, are involved in microbial spread. |
| T2 |
146-296 |
Sentence |
denotes |
The bacterial hyaluronan lyases (Hyals) that degrade hyaluronan, an important component of the extracellular matrix, are involved in microbial spread. |
| TextSentencer_T3 |
297-489 |
Sentence |
denotes |
Inhibitors of these enzymes are essential in investigation of the role of hyaluronan and Hyal in bacterial infections and constitute a new class of antibiotics against Hyal-producing bacteria. |
| T3 |
297-489 |
Sentence |
denotes |
Inhibitors of these enzymes are essential in investigation of the role of hyaluronan and Hyal in bacterial infections and constitute a new class of antibiotics against Hyal-producing bacteria. |
| TextSentencer_T4 |
490-607 |
Sentence |
denotes |
Recently, we identified 1,3-diacetylbenzimidazole-2-thione and related molecules as inhibitors of streptococcal Hyal. |
| T4 |
490-607 |
Sentence |
denotes |
Recently, we identified 1,3-diacetylbenzimidazole-2-thione and related molecules as inhibitors of streptococcal Hyal. |
| TextSentencer_T5 |
608-785 |
Sentence |
denotes |
One of such compounds, 1-decyl-2-(4-sulfamoyloxyphenyl)-1-indol-6-yl sulfamate, was co-crystallized in a complex with Streptococcus pneumoniae Hyal and its structure elucidated. |
| T5 |
608-785 |
Sentence |
denotes |
One of such compounds, 1-decyl-2-(4-sulfamoyloxyphenyl)-1-indol-6-yl sulfamate, was co-crystallized in a complex with Streptococcus pneumoniae Hyal and its structure elucidated. |
| TextSentencer_T6 |
786-964 |
Sentence |
denotes |
The resultant X-ray structure demonstrates that this inhibitor fits in the enzymatic active site via interactions resembling the binding mode of the natural hyaluronan substrate. |
| T6 |
786-964 |
Sentence |
denotes |
The resultant X-ray structure demonstrates that this inhibitor fits in the enzymatic active site via interactions resembling the binding mode of the natural hyaluronan substrate. |
| TextSentencer_T7 |
965-1112 |
Sentence |
denotes |
X-ray structural analysis also indicates binding interactions with the catalytic residues and those of a catalytically essential hydrophobic patch. |
| T7 |
965-1112 |
Sentence |
denotes |
X-ray structural analysis also indicates binding interactions with the catalytic residues and those of a catalytically essential hydrophobic patch. |
| TextSentencer_T8 |
1113-1286 |
Sentence |
denotes |
An IC50 value of 11 microM for Hyal from Streptococcus agalactiae (strain 4755) qualifies this phenylindole compound as one of the most potent Hyal inhibitors known to date. |
| T8 |
1113-1286 |
Sentence |
denotes |
An IC50 value of 11 microM for Hyal from Streptococcus agalactiae (strain 4755) qualifies this phenylindole compound as one of the most potent Hyal inhibitors known to date. |
| TextSentencer_T9 |
1287-1387 |
Sentence |
denotes |
The structural data suggested a similar binding mode for N-(3-phenylpropionyl)-benzoxazole-2-thione. |
| T9 |
1287-1387 |
Sentence |
denotes |
The structural data suggested a similar binding mode for N-(3-phenylpropionyl)-benzoxazole-2-thione. |
| TextSentencer_T10 |
1388-1518 |
Sentence |
denotes |
This new compound's inhibitory properties were confirmed resulting in discovery of yet another Hyal inhibitor (IC50 of 15 microM). |
| T10 |
1388-1518 |
Sentence |
denotes |
This new compound's inhibitory properties were confirmed resulting in discovery of yet another Hyal inhibitor (IC50 of 15 microM). |
| TextSentencer_T11 |
1519-1710 |
Sentence |
denotes |
These benzoxazole-2-thiones constitute a new class of inhibitors of bacterial Hyals and are well suited for further optimization of their selectivity, potency, and pharmacokinetic properties. |
| T11 |
1519-1710 |
Sentence |
denotes |
These benzoxazole-2-thiones constitute a new class of inhibitors of bacterial Hyals and are well suited for further optimization of their selectivity, potency, and pharmacokinetic properties. |