PMC:7291971 / 485-995 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T12","span":{"begin":10,"end":20},"obj":"CHEBI:35222;CHEBI:35222"},{"id":"T13","span":{"begin":145,"end":152},"obj":"NCBITaxon:10239"},{"id":"T14","span":{"begin":308,"end":318},"obj":"CHEBI:35222;CHEBI:35222"},{"id":"T15","span":{"begin":384,"end":387},"obj":"GO:0008541"},{"id":"T16","span":{"begin":410,"end":415},"obj":"NCBITaxon:10239"},{"id":"T93340","span":{"begin":10,"end":20},"obj":"CHEBI:35222;CHEBI:35222"},{"id":"T49466","span":{"begin":145,"end":152},"obj":"NCBITaxon:10239"},{"id":"T50627","span":{"begin":308,"end":318},"obj":"CHEBI:35222;CHEBI:35222"},{"id":"T65425","span":{"begin":384,"end":387},"obj":"GO:0008541"},{"id":"T87174","span":{"begin":410,"end":415},"obj":"NCBITaxon:10239"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T5","span":{"begin":175,"end":178},"obj":"Body_part"},{"id":"T6","span":{"begin":388,"end":391},"obj":"Body_part"},{"id":"T7","span":{"begin":471,"end":478},"obj":"Body_part"}],"attributes":[{"id":"A5","pred":"fma_id","subj":"T5","obj":"http://purl.org/sig/ont/fma/fma67095"},{"id":"A6","pred":"fma_id","subj":"T6","obj":"http://purl.org/sig/ont/fma/fma67095"},{"id":"A7","pred":"fma_id","subj":"T7","obj":"http://purl.org/sig/ont/fma/fma82774"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-PubTator","denotations":[{"id":"10","span":{"begin":471,"end":492},"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":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T5","span":{"begin":145,"end":152},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T6","span":{"begin":0,"end":9},"obj":"Chemical"},{"id":"T7","span":{"begin":10,"end":20},"obj":"Chemical"},{"id":"T8","span":{"begin":260,"end":269},"obj":"Chemical"},{"id":"T9","span":{"begin":308,"end":318},"obj":"Chemical"},{"id":"T10","span":{"begin":471,"end":478},"obj":"Chemical"}],"attributes":[{"id":"A6","pred":"chebi_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/CHEBI_22587"},{"id":"A7","pred":"chebi_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/CHEBI_35222"},{"id":"A8","pred":"chebi_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/CHEBI_22587"},{"id":"A9","pred":"chebi_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/CHEBI_35222"},{"id":"A10","pred":"chebi_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CHEBI_16708"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-PD-GO-BP","denotations":[{"id":"T2","span":{"begin":365,"end":376},"obj":"http://purl.obolibrary.org/obo/GO_0032259"},{"id":"T3","span":{"begin":455,"end":464},"obj":"http://purl.obolibrary.org/obo/GO_0009058"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}

{"project":"LitCovid-sentences","denotations":[{"id":"T6","span":{"begin":102,"end":283},"obj":"Sentence"},{"id":"T7","span":{"begin":284,"end":428},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"antiviral inhibitors and/or vaccines to fight these massive outbreaks is an urgent research priority. Enzymes involved in the capping pathway of viruses and more specifically RNA N7- or 2′O-methyltransferases (MTases) are now admitted as potential targets for antiviral chemotherapy. We designed bisubstrate inhibitors by mimicking the transition state of the 2′-O-methylation of the cap RNA in order to block viral 2′-O MTases. This work resulted in the synthesis of 16 adenine dinucleosides with both adenosi"}