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PMC:7291971 / 16058-16258 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T365 70-82 CHEBI:23447;CHEBI:23447 denotes dinucleoside
T366 112-121 CHEBI:36357;CHEBI:36357 denotes compounds
T367 144-149 CHEBI:29337;CHEBI:29337 denotes amide

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
330 53-82 Chemical denotes nosyl-containing dinucleoside
331 141-143 Chemical denotes Ns MESH:D009584
332 144-149 Chemical denotes amide MESH:D000577

LitCovid-PD-MONDO

Id Subject Object Predicate Lexical cue mondo_id
T36 141-143 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T293 141-143 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T295 144-149 Chemical denotes amide http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988
T297 177-188 Chemical denotes nosyl group http://purl.obolibrary.org/obo/CHEBI_51102
T298 183-188 Chemical denotes group http://purl.obolibrary.org/obo/CHEBI_24433

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T100 0-200 Sentence denotes The same synthetic route used for the preparation of nosyl-containing dinucleoside 9 was followed to synthesize compounds 10–13 with diverse Ns-amide moieties as analogs of the nosyl group (Scheme 3).