PMC:7291971 / 10752-10968
Annnotations
LitCovid-PMC-OGER-BB
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T212 | 37-44 | CHEBI:33543;CHEBI:33543 | denotes | sulfone |
T213 | 50-65 | CHEBI:50728;CHEBI:50728 | denotes | methylene group |
T214 | 101-108 | CHEBI:33543;CHEBI:33543 | denotes | sulfone |
T215 | 163-176 | CHEBI:23447;CHEBI:23447 | denotes | dinucleosides |
T216 | 192-193 | CHEBI:7586;CHEBI:7586 | denotes | N |
T217 | 193-194 | CHEBI:75508;CHEBI:75508 | denotes | - |
T218 | 194-209 | CHEBI:57472;CHEBI:57472 | denotes | arylsulfonamide |
LitCovid-PubTator
Id | Subject | Object | Predicate | Lexical cue | tao:has_database_id |
---|---|---|---|---|---|
198 | 37-44 | Chemical | denotes | sulfone | MESH:D013450 |
199 | 101-108 | Chemical | denotes | sulfone | MESH:D013450 |
200 | 163-176 | Chemical | denotes | dinucleosides | |
201 | 192-209 | Chemical | denotes | N-arylsulfonamide |
LitCovid-PD-CLO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T75 | 48-49 | http://purl.obolibrary.org/obo/CLO_0001020 | denotes | a |
T76 | 140-148 | http://purl.obolibrary.org/obo/CLO_0001658 | denotes | activity |
LitCovid-PD-CHEBI
Id | Subject | Object | Predicate | Lexical cue | chebi_id |
---|---|---|---|---|---|
T143 | 37-44 | Chemical | denotes | sulfone | http://purl.obolibrary.org/obo/CHEBI_35850 |
T144 | 50-65 | Chemical | denotes | methylene group | http://purl.obolibrary.org/obo/CHEBI_50728 |
T145 | 50-59 | Chemical | denotes | methylene | http://purl.obolibrary.org/obo/CHEBI_29357|http://purl.obolibrary.org/obo/CHEBI_29358 |
T147 | 60-65 | Chemical | denotes | group | http://purl.obolibrary.org/obo/CHEBI_24433 |
T148 | 101-108 | Chemical | denotes | sulfone | http://purl.obolibrary.org/obo/CHEBI_35850 |
LitCovid-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T71 | 0-216 | Sentence | denotes | In addition, we chose to replace the sulfone by a methylene group in 15–16 (Scheme 4 ) to assess the sulfone contribution to the inhibitory activity obtained with dinucleosides containing the N-arylsulfonamide motif. |