PMC:7571312 / 15005-15242 JSONTXT

{"project":"LitCovid-PD-MONDO","denotations":[{"id":"T50","span":{"begin":57,"end":61},"obj":"Disease"}],"attributes":[{"id":"A50","pred":"mondo_id","subj":"T50","obj":"http://purl.obolibrary.org/obo/MONDO_0005091"}],"text":"Molecular modeling of a 2,6-dichlorobenzoate design with SARS CoV-1 3CLpro indicated that a low strain conformation of the ketone carbonyl was aligned in the oxyanion hole and the substituted benzoate is accommodated within the P1′ site."}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T59953","span":{"begin":22,"end":23},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T67520","span":{"begin":90,"end":91},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T69080","span":{"begin":228,"end":230},"obj":"http://purl.obolibrary.org/obo/CLO_0008285"}],"text":"Molecular modeling of a 2,6-dichlorobenzoate design with SARS CoV-1 3CLpro indicated that a low strain conformation of the ketone carbonyl was aligned in the oxyanion hole and the substituted benzoate is accommodated within the P1′ site."}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T241","span":{"begin":24,"end":44},"obj":"Chemical"},{"id":"T242","span":{"begin":123,"end":129},"obj":"Chemical"},{"id":"T243","span":{"begin":130,"end":138},"obj":"Chemical"},{"id":"T244","span":{"begin":192,"end":200},"obj":"Chemical"},{"id":"T245","span":{"begin":228,"end":230},"obj":"Chemical"}],"attributes":[{"id":"A241","pred":"chebi_id","subj":"T241","obj":"http://purl.obolibrary.org/obo/CHEBI_48624"},{"id":"A242","pred":"chebi_id","subj":"T242","obj":"http://purl.obolibrary.org/obo/CHEBI_17087"},{"id":"A243","pred":"chebi_id","subj":"T243","obj":"http://purl.obolibrary.org/obo/CHEBI_23019"},{"id":"A244","pred":"chebi_id","subj":"T244","obj":"http://purl.obolibrary.org/obo/CHEBI_16150"},{"id":"A245","pred":"chebi_id","subj":"T245","obj":"http://purl.obolibrary.org/obo/CHEBI_60949"}],"text":"Molecular modeling of a 2,6-dichlorobenzoate design with SARS CoV-1 3CLpro indicated that a low strain conformation of the ketone carbonyl was aligned in the oxyanion hole and the substituted benzoate is accommodated within the P1′ site."}

{"project":"LitCovid-sentences","denotations":[{"id":"T81","span":{"begin":0,"end":237},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Molecular modeling of a 2,6-dichlorobenzoate design with SARS CoV-1 3CLpro indicated that a low strain conformation of the ketone carbonyl was aligned in the oxyanion hole and the substituted benzoate is accommodated within the P1′ site."}

{"project":"LitCovid-PubTator","denotations":[{"id":"415","span":{"begin":57,"end":65},"obj":"Species"},{"id":"420","span":{"begin":24,"end":44},"obj":"Chemical"},{"id":"421","span":{"begin":123,"end":129},"obj":"Chemical"},{"id":"422","span":{"begin":192,"end":200},"obj":"Chemical"}],"attributes":[{"id":"A415","pred":"tao:has_database_id","subj":"415","obj":"Tax:694009"},{"id":"A421","pred":"tao:has_database_id","subj":"421","obj":"MESH:D007659"},{"id":"A422","pred":"tao:has_database_id","subj":"422","obj":"MESH:D001565"}],"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":"Molecular modeling of a 2,6-dichlorobenzoate design with SARS CoV-1 3CLpro indicated that a low strain conformation of the ketone carbonyl was aligned in the oxyanion hole and the substituted benzoate is accommodated within the P1′ site."}