PMC:7461420 / 59874-60085 JSONTXT

{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T258","span":{"begin":178,"end":186},"obj":"Body_part"}],"attributes":[{"id":"A258","pred":"fma_id","subj":"T258","obj":"http://purl.org/sig/ont/fma/fma13478"}],"text":"162 Docking studies of compound 73 to the protease revealed that the indole amino hydrogen and the carbonyl group attached to the 2‐position formed H‐bond interactions with the backbone Glu166 (see Figure 23B)."}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T764","span":{"begin":0,"end":3},"obj":"http://purl.obolibrary.org/obo/CLO_0001002"}],"text":"162 Docking studies of compound 73 to the protease revealed that the indole amino hydrogen and the carbonyl group attached to the 2‐position formed H‐bond interactions with the backbone Glu166 (see Figure 23B)."}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T7771","span":{"begin":70,"end":76},"obj":"Chemical"},{"id":"T81173","span":{"begin":77,"end":82},"obj":"Chemical"},{"id":"T92675","span":{"begin":83,"end":91},"obj":"Chemical"},{"id":"T52035","span":{"begin":100,"end":114},"obj":"Chemical"},{"id":"T73981","span":{"begin":109,"end":114},"obj":"Chemical"}],"attributes":[{"id":"A4653","pred":"chebi_id","subj":"T7771","obj":"http://purl.obolibrary.org/obo/CHEBI_16881"},{"id":"A13880","pred":"chebi_id","subj":"T7771","obj":"http://purl.obolibrary.org/obo/CHEBI_35581"},{"id":"A9077","pred":"chebi_id","subj":"T81173","obj":"http://purl.obolibrary.org/obo/CHEBI_46882"},{"id":"A1425","pred":"chebi_id","subj":"T92675","obj":"http://purl.obolibrary.org/obo/CHEBI_49637"},{"id":"A66687","pred":"chebi_id","subj":"T52035","obj":"http://purl.obolibrary.org/obo/CHEBI_23019"},{"id":"A71321","pred":"chebi_id","subj":"T73981","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"}],"text":"162 Docking studies of compound 73 to the protease revealed that the indole amino hydrogen and the carbonyl group attached to the 2‐position formed H‐bond interactions with the backbone Glu166 (see Figure 23B)."}

{"project":"LitCovid-PubTator","denotations":[{"id":"1816","span":{"begin":83,"end":91},"obj":"Chemical"},{"id":"1817","span":{"begin":187,"end":193},"obj":"Chemical"}],"attributes":[{"id":"A1816","pred":"tao:has_database_id","subj":"1816","obj":"MESH:D006859"}],"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":"162 Docking studies of compound 73 to the protease revealed that the indole amino hydrogen and the carbonyl group attached to the 2‐position formed H‐bond interactions with the backbone Glu166 (see Figure 23B)."}

{"project":"LitCovid-sentences","denotations":[{"id":"T517","span":{"begin":0,"end":211},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"162 Docking studies of compound 73 to the protease revealed that the indole amino hydrogen and the carbonyl group attached to the 2‐position formed H‐bond interactions with the backbone Glu166 (see Figure 23B)."}