PMC:7291971 / 23818-24118 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T524","span":{"begin":24,"end":32},"obj":"CHEBI:33910;CHEBI:33910"},{"id":"T525","span":{"begin":33,"end":37},"obj":"CHEBI:33250;CHEBI:33250"},{"id":"T526","span":{"begin":63,"end":74},"obj":"CHEBI:29785;CHEBI:29785"},{"id":"T527","span":{"begin":221,"end":226},"obj":"CHEBI:53325;CHEBI:53325"},{"id":"T528","span":{"begin":264,"end":269},"obj":"CHEBI:24433;CHEBI:24433"}],"text":"Remarkably 13 bearing a chlorine atom in “para” position and a nitro group in “meta” position displayed the best inhibition which was 6.5–9.5 fold more potent than the derivatives 10 and 12, respectively that contain the nitro in “ortho” position and a lipophilic group CF3 or MeO in “para” position."}

{"project":"LitCovid-PubTator","denotations":[{"id":"428","span":{"begin":24,"end":32},"obj":"Chemical"},{"id":"429","span":{"begin":63,"end":68},"obj":"Chemical"},{"id":"430","span":{"begin":221,"end":226},"obj":"Chemical"}],"attributes":[{"id":"A428","pred":"tao:has_database_id","subj":"428","obj":"MESH:D002713"}],"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":"Remarkably 13 bearing a chlorine atom in “para” position and a nitro group in “meta” position displayed the best inhibition which was 6.5–9.5 fold more potent than the derivatives 10 and 12, respectively that contain the nitro in “ortho” position and a lipophilic group CF3 or MeO in “para” position."}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T196","span":{"begin":22,"end":23},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T197","span":{"begin":61,"end":62},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T198","span":{"begin":251,"end":252},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"}],"text":"Remarkably 13 bearing a chlorine atom in “para” position and a nitro group in “meta” position displayed the best inhibition which was 6.5–9.5 fold more potent than the derivatives 10 and 12, respectively that contain the nitro in “ortho” position and a lipophilic group CF3 or MeO in “para” position."}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T407","span":{"begin":24,"end":37},"obj":"Chemical"},{"id":"T408","span":{"begin":24,"end":32},"obj":"Chemical"},{"id":"T409","span":{"begin":33,"end":37},"obj":"Chemical"},{"id":"T410","span":{"begin":63,"end":74},"obj":"Chemical"},{"id":"T411","span":{"begin":69,"end":74},"obj":"Chemical"},{"id":"T412","span":{"begin":221,"end":226},"obj":"Chemical"},{"id":"T413","span":{"begin":264,"end":269},"obj":"Chemical"}],"attributes":[{"id":"A407","pred":"chebi_id","subj":"T407","obj":"http://purl.obolibrary.org/obo/CHEBI_23116"},{"id":"A408","pred":"chebi_id","subj":"T408","obj":"http://purl.obolibrary.org/obo/CHEBI_29310"},{"id":"A409","pred":"chebi_id","subj":"T409","obj":"http://purl.obolibrary.org/obo/CHEBI_33250"},{"id":"A410","pred":"chebi_id","subj":"T410","obj":"http://purl.obolibrary.org/obo/CHEBI_29785"},{"id":"A411","pred":"chebi_id","subj":"T411","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"},{"id":"A412","pred":"chebi_id","subj":"T412","obj":"http://purl.obolibrary.org/obo/CHEBI_29785"},{"id":"A413","pred":"chebi_id","subj":"T413","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"}],"text":"Remarkably 13 bearing a chlorine atom in “para” position and a nitro group in “meta” position displayed the best inhibition which was 6.5–9.5 fold more potent than the derivatives 10 and 12, respectively that contain the nitro in “ortho” position and a lipophilic group CF3 or MeO in “para” position."}

{"project":"LitCovid-sentences","denotations":[{"id":"T165","span":{"begin":0,"end":300},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Remarkably 13 bearing a chlorine atom in “para” position and a nitro group in “meta” position displayed the best inhibition which was 6.5–9.5 fold more potent than the derivatives 10 and 12, respectively that contain the nitro in “ortho” position and a lipophilic group CF3 or MeO in “para” position."}