BB-kb@ldeleger:BB-kb-19004249 JSONTXT

{"project":"bionlp-ost-19-BB-kb-dev","denotations":[{"id":"T1","span":{"begin":0,"end":91},"obj":"Title"},{"id":"T2","span":{"begin":92,"end":618},"obj":"Paragraph"},{"id":"T3","span":{"begin":204,"end":219},"obj":"Phenotype"},{"id":"T4","span":{"begin":204,"end":209},"obj":"Habitat"},{"id":"T5","span":{"begin":221,"end":242},"obj":"Microorganism"},{"id":"T6","span":{"begin":247,"end":263},"obj":"Microorganism"},{"id":"T7","span":{"begin":308,"end":317},"obj":"Microorganism"},{"id":"E1","span":{"begin":221,"end":242},"obj":"Lives_In"},{"id":"E2","span":{"begin":221,"end":242},"obj":"Exhibits"},{"id":"E3","span":{"begin":247,"end":263},"obj":"Lives_In"},{"id":"E4","span":{"begin":247,"end":263},"obj":"Exhibits"}],"relations":[{"id":"R1","pred":"Microorganism","subj":"E1","obj":"T5"},{"id":"R2","pred":"Location","subj":"E1","obj":"T4"},{"id":"R3","pred":"Microorganism","subj":"E2","obj":"T5"},{"id":"R4","pred":"Property","subj":"E2","obj":"T3"},{"id":"R5","pred":"Microorganism","subj":"E3","obj":"T6"},{"id":"R6","pred":"Location","subj":"E3","obj":"T4"},{"id":"R7","pred":"Microorganism","subj":"E4","obj":"T6"},{"id":"R8","pred":"Property","subj":"E4","obj":"T3"}],"attributes":[{"id":"A4","pred":"NCBI_Taxonomy","subj":"T6","obj":"562"},{"id":"A5","pred":"NCBI_Taxonomy","subj":"T7","obj":"1280"},{"id":"A3","pred":"NCBI_Taxonomy","subj":"T5","obj":"1280"},{"id":"A2","pred":"OntoBiotope","subj":"T3","obj":"OBT:002806"},{"id":"A1","pred":"OntoBiotope","subj":"T4","obj":"OBT:002488"}],"text":"Evaluation of antibacterial activity of synthetic aliphatic and aromatic monoacylglycerols.\nThe antibacterial activity of synthetic aliphatic and aromatic monoacylglycerols (MAGs) was studied against two human pathogens: Staphylococcus aureus and Escherichia coli. The active compounds inhibited selectively S. aureus. The most active compounds amongst them were those with medium size aliphatic chain and aromatic MAGs with electron withdrawing substituents at the aryl ring. The introduction of one or two-carbon spacer between the aryl ring and the carboxylic function did not influence antibacterial effectiveness.\n\n"}