PMC:7291971 / 16058-16258 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T365","span":{"begin":70,"end":82},"obj":"CHEBI:23447;CHEBI:23447"},{"id":"T366","span":{"begin":112,"end":121},"obj":"CHEBI:36357;CHEBI:36357"},{"id":"T367","span":{"begin":144,"end":149},"obj":"CHEBI:29337;CHEBI:29337"}],"text":"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)."}

{"project":"LitCovid-PubTator","denotations":[{"id":"330","span":{"begin":53,"end":82},"obj":"Chemical"},{"id":"331","span":{"begin":141,"end":143},"obj":"Chemical"},{"id":"332","span":{"begin":144,"end":149},"obj":"Chemical"}],"attributes":[{"id":"A331","pred":"tao:has_database_id","subj":"331","obj":"MESH:D009584"},{"id":"A332","pred":"tao:has_database_id","subj":"332","obj":"MESH:D000577"}],"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":"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)."}

{"project":"LitCovid-PD-MONDO","denotations":[{"id":"T36","span":{"begin":141,"end":143},"obj":"Disease"}],"attributes":[{"id":"A36","pred":"mondo_id","subj":"T36","obj":"http://purl.obolibrary.org/obo/MONDO_0009735"}],"text":"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)."}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T293","span":{"begin":141,"end":143},"obj":"Chemical"},{"id":"T295","span":{"begin":144,"end":149},"obj":"Chemical"},{"id":"T297","span":{"begin":177,"end":188},"obj":"Chemical"},{"id":"T298","span":{"begin":183,"end":188},"obj":"Chemical"}],"attributes":[{"id":"A293","pred":"chebi_id","subj":"T293","obj":"http://purl.obolibrary.org/obo/CHEBI_33349"},{"id":"A294","pred":"chebi_id","subj":"T293","obj":"http://purl.obolibrary.org/obo/CHEBI_33355"},{"id":"A295","pred":"chebi_id","subj":"T295","obj":"http://purl.obolibrary.org/obo/CHEBI_29337"},{"id":"A296","pred":"chebi_id","subj":"T295","obj":"http://purl.obolibrary.org/obo/CHEBI_32988"},{"id":"A297","pred":"chebi_id","subj":"T297","obj":"http://purl.obolibrary.org/obo/CHEBI_51102"},{"id":"A298","pred":"chebi_id","subj":"T298","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"}],"text":"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)."}

{"project":"LitCovid-sentences","denotations":[{"id":"T100","span":{"begin":0,"end":200},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"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)."}