PubMed:24810734 JSON TXT

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OryzaGP_2021

OryzaGP_2022

{"project":"OryzaGP_2022","denotations":[{"id":"T1","span":{"begin":236,"end":237},"obj":"http://identifiers.org/oryzabase.gene/11216"},{"id":"T2","span":{"begin":248,"end":256},"obj":"http://identifiers.org/oryzabase.gene/14449"},{"id":"T3","span":{"begin":580,"end":588},"obj":"http://identifiers.org/oryzabase.gene/14449"},{"id":"T4","span":{"begin":606,"end":607},"obj":"http://identifiers.org/oryzabase.gene/11216"},{"id":"T5","span":{"begin":618,"end":626},"obj":"http://identifiers.org/oryzabase.gene/14449"}],"text":"Casuarine stereoisomers from achiral substrates: chemoenzymatic synthesis and inhibitory properties.\nA straightforward chemoenzymatic synthesis of four uncovered casuarine stereoisomers is described. The strategy consists of L-fuculose-1-phosphate aldolase F131A-variant-catalyzed aldol addition of dihydroxyacetone phosphate to aldehyde derivatives of 1,4-dideoxy-1,4-imino-D-arabinitol (DAB) and its enantiomer (LAB) and subsequent one-pot catalytic deprotection-reductive amination. DAB and LAB were obtained from dihydroxyacetone and aminoethanol using D-fructose-6-phosphate aldolase and L-rhamnulose-1-phosphate aldolase catalysts, respectively. The new ent-3-epi-casuarine is a strong inhibitor of α-d-glucosidase from rice and of rat intestinal sucrase."}

OryzaGP_2021_FLAIR

{"project":"OryzaGP_2021_FLAIR","denotations":[{"id":"M_0","span":{"begin":593,"end":626},"obj":"hunflair:NA:Gene"},{"id":"M_1","span":{"begin":538,"end":550},"obj":"hunflair:NA:Chemical"},{"id":"M_2","span":{"begin":738,"end":741},"obj":"hunflair:NA:Species"},{"id":"M_3","span":{"begin":0,"end":9},"obj":"hunflair:NA:Chemical"},{"id":"M_4","span":{"begin":557,"end":579},"obj":"hunflair:NA:Chemical"},{"id":"M_5","span":{"begin":225,"end":256},"obj":"hunflair:NA:Gene"},{"id":"M_6","span":{"begin":660,"end":679},"obj":"hunflair:NA:Chemical"},{"id":"M_7","span":{"begin":705,"end":720},"obj":"hunflair:NA:Gene"},{"id":"M_8","span":{"begin":299,"end":315},"obj":"hunflair:NA:Chemical"},{"id":"M_9","span":{"begin":517,"end":533},"obj":"hunflair:NA:Chemical"},{"id":"M_10","span":{"begin":753,"end":760},"obj":"hunflair:NA:Gene"},{"id":"M_11","span":{"begin":726,"end":730},"obj":"hunflair:NA:Species"},{"id":"M_12","span":{"begin":389,"end":392},"obj":"hunflair:NA:Chemical"},{"id":"M_13","span":{"begin":486,"end":489},"obj":"hunflair:NA:Chemical"},{"id":"M_14","span":{"begin":593,"end":617},"obj":"hunflair:NA:Chemical"},{"id":"M_15","span":{"begin":299,"end":325},"obj":"hunflair:NA:Chemical"},{"id":"M_16","span":{"begin":557,"end":588},"obj":"hunflair:NA:Gene"},{"id":"M_17","span":{"begin":225,"end":247},"obj":"hunflair:NA:Chemical"},{"id":"M_18","span":{"begin":281,"end":286},"obj":"hunflair:NA:Chemical"},{"id":"M_19","span":{"begin":162,"end":171},"obj":"hunflair:NA:Chemical"},{"id":"M_20","span":{"begin":670,"end":679},"obj":"hunflair:NA:Chemical"},{"id":"M_21","span":{"begin":353,"end":387},"obj":"hunflair:NA:Chemical"},{"id":"M_22","span":{"begin":329,"end":337},"obj":"hunflair:NA:Chemical"},{"id":"M_23","span":{"begin":414,"end":417},"obj":"hunflair:NA:Chemical"},{"id":"M_24","span":{"begin":494,"end":497},"obj":"hunflair:NA:Chemical"}],"text":"Casuarine stereoisomers from achiral substrates: chemoenzymatic synthesis and inhibitory properties.\nA straightforward chemoenzymatic synthesis of four uncovered casuarine stereoisomers is described. The strategy consists of L-fuculose-1-phosphate aldolase F131A-variant-catalyzed aldol addition of dihydroxyacetone phosphate to aldehyde derivatives of 1,4-dideoxy-1,4-imino-D-arabinitol (DAB) and its enantiomer (LAB) and subsequent one-pot catalytic deprotection-reductive amination. DAB and LAB were obtained from dihydroxyacetone and aminoethanol using D-fructose-6-phosphate aldolase and L-rhamnulose-1-phosphate aldolase catalysts, respectively. The new ent-3-epi-casuarine is a strong inhibitor of α-d-glucosidase from rice and of rat intestinal sucrase."}

Allie

{"project":"Allie","denotations":[{"id":"SS1_24810734_2_0","span":{"begin":353,"end":387},"obj":"expanded"},{"id":"SS2_24810734_2_0","span":{"begin":389,"end":392},"obj":"abbr"}],"relations":[{"id":"AE1_24810734_2_0","pred":"abbreviatedTo","subj":"SS1_24810734_2_0","obj":"SS2_24810734_2_0"}],"text":"Casuarine stereoisomers from achiral substrates: chemoenzymatic synthesis and inhibitory properties.\nA straightforward chemoenzymatic synthesis of four uncovered casuarine stereoisomers is described. The strategy consists of L-fuculose-1-phosphate aldolase F131A-variant-catalyzed aldol addition of dihydroxyacetone phosphate to aldehyde derivatives of 1,4-dideoxy-1,4-imino-D-arabinitol (DAB) and its enantiomer (LAB) and subsequent one-pot catalytic deprotection-reductive amination. DAB and LAB were obtained from dihydroxyacetone and aminoethanol using D-fructose-6-phosphate aldolase and L-rhamnulose-1-phosphate aldolase catalysts, respectively. The new ent-3-epi-casuarine is a strong inhibitor of α-d-glucosidase from rice and of rat intestinal sucrase."}

Oryza_sentences

{"project":"Oryza_sentences","blocks":[{"id":"T1","span":{"begin":0,"end":100},"obj":"Sentence"},{"id":"T2","span":{"begin":101,"end":199},"obj":"Sentence"},{"id":"T3","span":{"begin":200,"end":485},"obj":"Sentence"},{"id":"T4","span":{"begin":486,"end":651},"obj":"Sentence"},{"id":"T5","span":{"begin":652,"end":761},"obj":"Sentence"}],"text":"Casuarine stereoisomers from achiral substrates: chemoenzymatic synthesis and inhibitory properties.\nA straightforward chemoenzymatic synthesis of four uncovered casuarine stereoisomers is described. The strategy consists of L-fuculose-1-phosphate aldolase F131A-variant-catalyzed aldol addition of dihydroxyacetone phosphate to aldehyde derivatives of 1,4-dideoxy-1,4-imino-D-arabinitol (DAB) and its enantiomer (LAB) and subsequent one-pot catalytic deprotection-reductive amination. DAB and LAB were obtained from dihydroxyacetone and aminoethanol using D-fructose-6-phosphate aldolase and L-rhamnulose-1-phosphate aldolase catalysts, respectively. The new ent-3-epi-casuarine is a strong inhibitor of α-d-glucosidase from rice and of rat intestinal sucrase."}