PMC:7291971 / 10752-10968 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T212","span":{"begin":37,"end":44},"obj":"CHEBI:33543;CHEBI:33543"},{"id":"T213","span":{"begin":50,"end":65},"obj":"CHEBI:50728;CHEBI:50728"},{"id":"T214","span":{"begin":101,"end":108},"obj":"CHEBI:33543;CHEBI:33543"},{"id":"T215","span":{"begin":163,"end":176},"obj":"CHEBI:23447;CHEBI:23447"},{"id":"T216","span":{"begin":192,"end":193},"obj":"CHEBI:7586;CHEBI:7586"},{"id":"T217","span":{"begin":193,"end":194},"obj":"CHEBI:75508;CHEBI:75508"},{"id":"T218","span":{"begin":194,"end":209},"obj":"CHEBI:57472;CHEBI:57472"}],"text":"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."}

{"project":"LitCovid-PubTator","denotations":[{"id":"198","span":{"begin":37,"end":44},"obj":"Chemical"},{"id":"199","span":{"begin":101,"end":108},"obj":"Chemical"},{"id":"200","span":{"begin":163,"end":176},"obj":"Chemical"},{"id":"201","span":{"begin":192,"end":209},"obj":"Chemical"}],"attributes":[{"id":"A198","pred":"tao:has_database_id","subj":"198","obj":"MESH:D013450"},{"id":"A199","pred":"tao:has_database_id","subj":"199","obj":"MESH:D013450"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"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."}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T75","span":{"begin":48,"end":49},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T76","span":{"begin":140,"end":148},"obj":"http://purl.obolibrary.org/obo/CLO_0001658"}],"text":"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."}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T143","span":{"begin":37,"end":44},"obj":"Chemical"},{"id":"T144","span":{"begin":50,"end":65},"obj":"Chemical"},{"id":"T145","span":{"begin":50,"end":59},"obj":"Chemical"},{"id":"T147","span":{"begin":60,"end":65},"obj":"Chemical"},{"id":"T148","span":{"begin":101,"end":108},"obj":"Chemical"}],"attributes":[{"id":"A143","pred":"chebi_id","subj":"T143","obj":"http://purl.obolibrary.org/obo/CHEBI_35850"},{"id":"A144","pred":"chebi_id","subj":"T144","obj":"http://purl.obolibrary.org/obo/CHEBI_50728"},{"id":"A145","pred":"chebi_id","subj":"T145","obj":"http://purl.obolibrary.org/obo/CHEBI_29357"},{"id":"A146","pred":"chebi_id","subj":"T145","obj":"http://purl.obolibrary.org/obo/CHEBI_29358"},{"id":"A147","pred":"chebi_id","subj":"T147","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"},{"id":"A148","pred":"chebi_id","subj":"T148","obj":"http://purl.obolibrary.org/obo/CHEBI_35850"}],"text":"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."}

{"project":"LitCovid-sentences","denotations":[{"id":"T71","span":{"begin":0,"end":216},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"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."}