PMC:7696151 / 3824-4108 JSONTXT

{"project":"LitCovid-PubTator","denotations":[{"id":"110","span":{"begin":82,"end":87},"obj":"Chemical"},{"id":"111","span":{"begin":142,"end":147},"obj":"Chemical"}],"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":"nd both have enantiomers (R and S isomers). Researches also demonstrated that the R-HCQ is present in the blood at higher concentrations than S-HCQ. These results suggested the stereoselective processes in the metabolism of the molecule [9].\nStudies of structure-activity relationship"}

{"project":"LitCovid-sentences","denotations":[{"id":"T31","span":{"begin":44,"end":148},"obj":"Sentence"},{"id":"T32","span":{"begin":149,"end":241},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"nd both have enantiomers (R and S isomers). Researches also demonstrated that the R-HCQ is present in the blood at higher concentrations than S-HCQ. These results suggested the stereoselective processes in the metabolism of the molecule [9].\nStudies of structure-activity relationship"}