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PMC:7291971 / 12306-17424 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T287 210-211 CHEBI:75508;CHEBI:75508 denotes 5
T288 211-212 CHEBI:82321;CHEBI:82321 denotes
T289 212-213 CHEBI:50217;CHEBI:50217 denotes -
T290 213-218 CHEBI:46882;CHEBI:46882 denotes amino
T291 218-219 CHEBI:75508;CHEBI:75508 denotes -
T292 219-220 CHEBI:53233;CHEBI:53233 denotes 2
T293 220-221 CHEBI:52029;CHEBI:52029 denotes
T294 221-222 CHEBI:75508;CHEBI:75508 denotes ,
T295 222-224 CHEBI:52029;CHEBI:52029 denotes 3′
T296 224-239 CHEBI:53250;CHEBI:53250 denotes -isopropylidene
T297 240-249 CHEBI:22260;CHEBI:22260 denotes adenosine
T298 319-334 CHEBI:32863;CHEBI:32863 denotes secondary amine
T299 435-440 CHEBI:32877;CHEBI:32877 denotes amine
T300 512-526 CHEBI:32877;CHEBI:32877 denotes primary amines
T301 553-577 CHEBI:53325;CHEBI:53325 denotes nitrobenzenesulfonamides
T302 582-588 CHEBI:32988;CHEBI:32988 denotes amides
T303 626-631 CHEBI:24433;CHEBI:24433 denotes group
T304 797-822 CHEBI:86228;CHEBI:86228 denotes 2-nitrobenzenesulfonamide
T305 892-907 GO:0006306 denotes DNA methylation
T306 953-962 CHEBI:22260;CHEBI:22260 denotes adenosine
T307 1154-1176 CHEBI:86228;CHEBI:86228 denotes 4-nitrobenzenesulfonyl
T308 1177-1185 CHEBI:17996;CHEBI:17996 denotes chloride
T309 1224-1246 CHEBI:86228;CHEBI:86228 denotes 2-nitrobenzenesulfonyl
T310 1247-1255 CHEBI:17996;CHEBI:17996 denotes chloride
T311 1283-1284 CHEBI:53233;CHEBI:53233 denotes 5
T312 1284-1285 CHEBI:82321;CHEBI:82321 denotes
T313 1285-1286 CHEBI:50217;CHEBI:50217 denotes -
T314 1286-1291 CHEBI:46882;CHEBI:46882 denotes amino
T315 1291-1292 CHEBI:75508;CHEBI:75508 denotes -
T316 1292-1293 CHEBI:53233;CHEBI:53233 denotes 2
T317 1293-1294 CHEBI:52029;CHEBI:52029 denotes
T318 1294-1295 CHEBI:53250;CHEBI:53250 denotes ,
T319 1295-1296 CHEBI:52029;CHEBI:52029 denotes 3
T320 1296-1312 CHEBI:53250;CHEBI:53250 denotes ′-isopropylidene
T321 1313-1322 CHEBI:22260;CHEBI:22260 denotes adenosine
T322 1365-1366 MOP:0002369 denotes -
T323 1419-1424 CHEBI:32031;CHEBI:32031 denotes K2CO3
T324 1480-1492 CHEBI:23447;CHEBI:23447 denotes dinucleoside
T325 1628-1635 CHEBI:60004;CHEBI:60004 denotes mixture
T326 1735-1743 CHEBI:29917;CHEBI:29917 denotes thiolate
T327 1775-1780 CHEBI:32863;CHEBI:32863 denotes amine
T328 1816-1833 CHEBI:51087;CHEBI:51087 denotes protecting groups
T329 1859-1865 CHEBI:37527;CHEBI:37527 denotes acidic
T330 1881-1893 CHEBI:23447;CHEBI:23447 denotes dinucleoside
T331 1924-1930 CHEBI:37527;CHEBI:37527 denotes acidic
T332 1999-2024 CHEBI:86228;CHEBI:86228 denotes 4-nitrobenzenesulfonamide
T333 2120-2128 CHEBI:36357;CHEBI:36357 denotes compound
T334 2163-2171 CHEBI:17478;CHEBI:17478 denotes aldehyde
T335 2224-2228 CHEBI:41865;CHEBI:41865 denotes acid
T336 2277-2286 CHEBI:32952;CHEBI:32952 denotes amination
T337 2320-2326 CHEBI:35607;CHEBI:35607 denotes sodium
T338 2327-2348 CHEBI:28621;CHEBI:28621 denotes triacetoxyborohydride
T339 2353-2364 CHEBI:15366;CHEBI:15366 denotes acetic acid
T340 2463-2472 CHEBI:29191;CHEBI:29191 denotes hydroxyls
T341 2477-2482 CHEBI:32952;CHEBI:32952 denotes amine
T342 2503-2506 CHEBI:17855;CHEBI:17855 denotes TFA
T343 2530-2542 CHEBI:25248;CHEBI:25248 denotes methyl ester
T344 2589-2593 CHEBI:48607;CHEBI:48607 denotes LiOH
T345 2608-2620 CHEBI:25248;CHEBI:25248 denotes methyl ester
T346 2624-2639 CHEBI:33575;CHEBI:33575 denotes carboxylic acid
T347 2784-2799 CHEBI:33575;CHEBI:33575 denotes carboxylic acid
T348 2875-2885 CHEBI:17790;CHEBI:17790 denotes methanolic
T349 2886-2893 CHEBI:16134;CHEBI:16134 denotes ammonia
T350 2894-2902 CHEBI:75958;CHEBI:75958 denotes solution
T351 2963-2973 MOP:0002369 denotes alkylation
T352 2985-2987 CHEBI:86228;CHEBI:86228 denotes 1-
T353 2987-2998 CHEBI:75508;CHEBI:75508 denotes bromobutane
T354 3000-3002 CHEBI:86228;CHEBI:86228 denotes 1-
T355 3002-3007 CHEBI:47265;CHEBI:47265 denotes bromo
T356 3007-3008 CHEBI:86228;CHEBI:86228 denotes -
T357 3008-3023 CHEBI:17824;CHEBI:17824 denotes 3-phenylpropane
T358 3106-3127 CHEBI:50488;CHEBI:50488 denotes diisopropylethylamine
T359 3540-3545 CHEBI:17478;CHEBI:17478 denotes alkyl
T360 3637-3641 CHEBI:48607;CHEBI:48607 denotes LiOH
T361 3674-3686 CHEBI:25248;CHEBI:25248 denotes methyl ester
T362 3703-3718 CHEBI:33575;CHEBI:33575 denotes carboxylic acid
T363 3725-3730 CHEBI:17478;CHEBI:17478 denotes alkyl
T364 3731-3736 CHEBI:50325;CHEBI:50325 denotes chain
T365 3822-3834 CHEBI:23447;CHEBI:23447 denotes dinucleoside
T366 3864-3873 CHEBI:36357;CHEBI:36357 denotes compounds
T367 3896-3901 CHEBI:29337;CHEBI:29337 denotes amide
T368 3969-3970 CHEBI:75508;CHEBI:75508 denotes 5
T369 3970-3971 CHEBI:82321;CHEBI:82321 denotes
T370 3972-3977 CHEBI:46882;CHEBI:46882 denotes amino
T371 3977-3979 CHEBI:75508;CHEBI:75508 denotes -2
T372 3979-3980 CHEBI:52029;CHEBI:52029 denotes
T373 3980-3982 CHEBI:75508;CHEBI:75508 denotes ,3
T374 3982-3983 CHEBI:52029;CHEBI:52029 denotes
T375 3983-3998 CHEBI:53250;CHEBI:53250 denotes -isopropylidene
T376 3999-4008 CHEBI:22260;CHEBI:22260 denotes adenosine
T377 4088-4108 CHEBI:53325;CHEBI:53325 denotes nitrobenzenesulfonyl
T378 4109-4117 CHEBI:17996;CHEBI:17996 denotes chloride
T379 4118-4126 CHEBI:33893;CHEBI:33893 denotes reagents
T380 4162-4172 CHEBI:22260;CHEBI:22260 denotes adenosines
T381 4276-4281 CHEBI:32031;CHEBI:32031 denotes K2CO3
T382 4312-4325 CHEBI:23447;CHEBI:23447 denotes dinucleosides
T383 4421-4428 CHEBI:30832;CHEBI:30832 denotes adenine
T384 4429-4442 CHEBI:23447;CHEBI:23447 denotes dinucleosides
T385 4660-4661 CHEBI:75508;CHEBI:75508 denotes 4
T386 4661-4683 CHEBI:86228;CHEBI:86228 denotes -chlorobenzenesulfonyl
T387 4684-4692 CHEBI:17996;CHEBI:17996 denotes chloride
T388 4798-4800 CHEBI:86228;CHEBI:86228 denotes 4-
T389 4800-4806 CHEBI:47853;CHEBI:47853 denotes chloro
T390 4806-4826 CHEBI:86228;CHEBI:86228 denotes -3-nitrobenzaldehyde
T391 4830-4850 CHEBI:28105;CHEBI:28105 denotes 4-chlorobenzaldehyde
T392 4855-4861 CHEBI:86228;CHEBI:86228 denotes sodium
T393 4862-4883 CHEBI:28621;CHEBI:28621 denotes triacetoxyborohydride
T394 4923-4929 CHEBI:24433;CHEBI:24433 denotes groups
T395 4933-4939 CHEBI:37527;CHEBI:37527 denotes acidic
T396 4963-4976 CHEBI:23447;CHEBI:23447 denotes dinucleosides

LitCovid-PD-FMA-UBERON

Id Subject Object Predicate Lexical cue fma_id
T52 892-895 Body_part denotes DNA http://purl.org/sig/ont/fma/fma74412
T53 933-941 Body_part denotes cytosine http://purl.org/sig/ont/fma/fma82776
T54 1810-1815 Body_part denotes sugar http://purl.org/sig/ont/fma/fma82737
T55 2215-2228 Body_part denotes aspartic acid http://purl.org/sig/ont/fma/fma82760
T56 2457-2462 Body_part denotes sugar http://purl.org/sig/ont/fma/fma82737
T57 2666-2676 Body_part denotes amino acid http://purl.org/sig/ont/fma/fma82739
T58 2805-2815 Body_part denotes amino acid http://purl.org/sig/ont/fma/fma82739
T59 4421-4428 Body_part denotes adenine http://purl.org/sig/ont/fma/fma82774
T60 4556-4563 Body_part denotes adenine http://purl.org/sig/ont/fma/fma82774

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
231 50-62 Chemical denotes dinucleoside
232 210-239 Chemical denotes 5′-amino-2′,3′-isopropylidene
233 240-249 Chemical denotes adenosine MESH:D000241
234 267-268 Chemical denotes N MESH:D009584
235 329-334 Chemical denotes amine MESH:D000588
236 435-440 Chemical denotes amine MESH:D000588
237 520-526 Chemical denotes amines MESH:D000588
238 553-577 Chemical denotes nitrobenzenesulfonamides
239 579-588 Chemical denotes Ns-amides
240 797-822 Chemical denotes 2-nitrobenzenesulfonamide
241 933-941 Chemical denotes cytosine MESH:D003596
242 953-962 Chemical denotes adenosine MESH:D000241
243 1040-1049 Chemical denotes adenosine MESH:D000241
244 1067-1079 Chemical denotes dinucleoside
245 1154-1185 Chemical denotes 4-nitrobenzenesulfonyl chloride MESH:C518227
246 1224-1255 Chemical denotes 2-nitrobenzenesulfonyl chloride MESH:C002732
247 1283-1312 Chemical denotes 5′-amino-2′,3′-isopropylidene
248 1313-1322 Chemical denotes adenosine MESH:D000241
249 1380-1388 Chemical denotes Ns-amide
250 1419-1424 Chemical denotes K2CO3 MESH:C037593
251 1428-1431 Chemical denotes DMF
252 1480-1492 Chemical denotes dinucleoside
253 1735-1743 Chemical denotes thiolate
254 1775-1780 Chemical denotes amine MESH:D000588
255 1810-1815 Chemical denotes sugar MESH:D000073893
256 1881-1893 Chemical denotes dinucleoside
257 1973-1981 Chemical denotes Ns-amide
258 1999-2024 Chemical denotes 4-nitrobenzenesulfonamide
259 2036-2048 Chemical denotes dinucleoside
301 2163-2171 Chemical denotes aldehyde MESH:D000447
302 2213-2228 Chemical denotes l-aspartic acid MESH:D001224
303 2320-2348 Chemical denotes sodium triacetoxyborohydride
304 2353-2364 Chemical denotes acetic acid MESH:D019342
305 2401-2413 Chemical denotes dinucleoside
306 2457-2472 Chemical denotes sugar hydroxyls
307 2477-2482 Chemical denotes amine MESH:D000588
308 2503-2506 Chemical denotes TFA MESH:D014269
309 2530-2542 Chemical denotes methyl ester
310 2589-2593 Chemical denotes LiOH
311 2608-2620 Chemical denotes methyl ester
312 2624-2639 Chemical denotes carboxylic acid MESH:D002264
313 2644-2656 Chemical denotes dinucleoside
314 2664-2676 Chemical denotes α-amino acid MESH:D000596
315 2784-2799 Chemical denotes carboxylic acid MESH:D002264
316 2803-2815 Chemical denotes α-amino acid MESH:D000596
317 2875-2893 Chemical denotes methanolic ammonia
318 2904-2917 Chemical denotes Dinucleosides
319 2985-2998 Chemical denotes 1-bromobutane MESH:C047757
320 3000-3023 Chemical denotes 1-bromo-3-phenylpropane
321 3027-3049 Chemical denotes methyl-4-bromobutyrate
322 3068-3086 Chemical denotes N-methylmorpholine MESH:C038816
323 3106-3127 Chemical denotes diisopropylethylamine
324 3129-3133 Chemical denotes DIEA
325 3514-3517 Chemical denotes TFA MESH:D014269
326 3538-3545 Chemical denotes N-alkyl
327 3637-3641 Chemical denotes LiOH
328 3674-3686 Chemical denotes methyl ester
329 3703-3718 Chemical denotes carboxylic acid MESH:D002264
330 3805-3834 Chemical denotes nosyl-containing dinucleoside
331 3893-3895 Chemical denotes Ns MESH:D009584
332 3896-3901 Chemical denotes amide MESH:D000577
333 3969-3998 Chemical denotes 5′-amino-2′,3′-isopropylidene
334 3999-4008 Chemical denotes adenosine MESH:D000241
335 4052-4055 Chemical denotes CF3
336 4088-4117 Chemical denotes nitrobenzenesulfonyl chloride
337 4154-4172 Chemical denotes N-nosyl adenosines
338 4276-4281 Chemical denotes K2CO3 MESH:C037593
339 4312-4325 Chemical denotes dinucleosides
340 4375-4378 Chemical denotes TFA MESH:D014269
341 4413-4442 Chemical denotes N-nosyl adenine dinucleosides
351 4556-4577 Chemical denotes adenine dinucleosides
352 4606-4628 Chemical denotes NH-linked dinucleoside
353 4660-4692 Chemical denotes 4-chlorobenzenesulfonyl chloride
354 4720-4724 Chemical denotes NEt3
355 4747-4750 Chemical denotes TFA MESH:D014269
356 4798-4826 Chemical denotes 4-chloro-3-nitrobenzaldehyde
357 4830-4850 Chemical denotes 4-chlorobenzaldehyde MESH:C052044
358 4855-4883 Chemical denotes sodium triacetoxyborohydride
359 4963-4976 Chemical denotes dinucleosides

LitCovid-PD-MONDO

Id Subject Object Predicate Lexical cue mondo_id
T33 579-581 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735
T34 1380-1382 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735
T35 1973-1975 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735
T36 3893-3895 Disease denotes Ns http://purl.obolibrary.org/obo/MONDO_0009735

LitCovid-PD-CLO

Id Subject Object Predicate Lexical cue
T114 528-529 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T115 598-599 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T116 615-625 http://purl.obolibrary.org/obo/CLO_0001658 denotes activating
T117 632-635 http://purl.obolibrary.org/obo/CLO_0051582 denotes has
T118 664-666 http://purl.obolibrary.org/obo/CLO_0050507 denotes 22
T119 823-826 http://purl.obolibrary.org/obo/CLO_0051582 denotes has
T120 1050-1052 http://purl.obolibrary.org/obo/CLO_0050510 denotes 18
T121 1113-1115 http://purl.obolibrary.org/obo/CLO_0050510 denotes 18
T122 1187-1189 http://purl.obolibrary.org/obo/CLO_0050507 denotes 22
T123 1196-1199 http://purl.obolibrary.org/obo/CLO_0051582 denotes has
T124 1200-1201 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T125 1389-1391 http://purl.obolibrary.org/obo/CLO_0050510 denotes 18
T126 1587-1588 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T127 1720-1721 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T128 1834-1837 http://purl.obolibrary.org/obo/CLO_0051582 denotes has
T129 2054-2056 http://purl.obolibrary.org/obo/CLO_0001302 denotes 34
T130 2239-2240 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T131 2414-2416 http://purl.obolibrary.org/obo/CLO_0050507 denotes 22
T132 2666-2682 http://purl.obolibrary.org/obo/PR_000018263 denotes amino acid chain
T133 2782-2783 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T134 2805-2821 http://purl.obolibrary.org/obo/PR_000018263 denotes amino acid chain
T135 2840-2842 http://purl.obolibrary.org/obo/CLO_0050507 denotes 22
T136 2848-2849 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T137 3207-3208 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T138 4057-4059 http://purl.obolibrary.org/obo/CLO_0052906 denotes Cl
T139 4199-4201 http://purl.obolibrary.org/obo/CLO_0050509 denotes 27
T140 4362-4364 http://purl.obolibrary.org/obo/CLO_0001407 denotes 52
T141 4367-4368 http://purl.obolibrary.org/obo/CLO_0001020 denotes A
T142 4745-4746 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T143 5092-5094 http://purl.obolibrary.org/obo/CLO_0054055 denotes 71

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T206 213-218 Chemical denotes amino http://purl.obolibrary.org/obo/CHEBI_46882
T207 225-239 Chemical denotes isopropylidene http://purl.obolibrary.org/obo/CHEBI_29858
T208 240-249 Chemical denotes adenosine http://purl.obolibrary.org/obo/CHEBI_16335
T209 319-334 Chemical denotes secondary amine http://purl.obolibrary.org/obo/CHEBI_32863
T210 329-334 Chemical denotes amine http://purl.obolibrary.org/obo/CHEBI_32952
T211 427-440 Chemical denotes primary amine http://purl.obolibrary.org/obo/CHEBI_32877
T212 435-440 Chemical denotes amine http://purl.obolibrary.org/obo/CHEBI_32952
T213 512-526 Chemical denotes primary amines http://purl.obolibrary.org/obo/CHEBI_32877
T214 520-526 Chemical denotes amines http://purl.obolibrary.org/obo/CHEBI_32952
T215 579-581 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T217 582-588 Chemical denotes amides http://purl.obolibrary.org/obo/CHEBI_32988
T218 626-631 Chemical denotes group http://purl.obolibrary.org/obo/CHEBI_24433
T219 892-895 Chemical denotes DNA http://purl.obolibrary.org/obo/CHEBI_16991
T220 933-941 Chemical denotes cytosine http://purl.obolibrary.org/obo/CHEBI_16040
T221 953-962 Chemical denotes adenosine http://purl.obolibrary.org/obo/CHEBI_16335
T222 1040-1049 Chemical denotes adenosine http://purl.obolibrary.org/obo/CHEBI_16335
T223 1177-1185 Chemical denotes chloride http://purl.obolibrary.org/obo/CHEBI_17996
T224 1247-1255 Chemical denotes chloride http://purl.obolibrary.org/obo/CHEBI_17996
T225 1286-1291 Chemical denotes amino http://purl.obolibrary.org/obo/CHEBI_46882
T226 1298-1312 Chemical denotes isopropylidene http://purl.obolibrary.org/obo/CHEBI_29858
T227 1313-1322 Chemical denotes adenosine http://purl.obolibrary.org/obo/CHEBI_16335
T228 1380-1382 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T230 1383-1388 Chemical denotes amide http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988
T232 1419-1424 Chemical denotes K2CO3 http://purl.obolibrary.org/obo/CHEBI_131526
T233 1428-1431 Chemical denotes DMF http://purl.obolibrary.org/obo/CHEBI_17741
T234 1609-1611 Chemical denotes KI http://purl.obolibrary.org/obo/CHEBI_74559|http://purl.obolibrary.org/obo/CHEBI_8346
T236 1628-1635 Chemical denotes mixture http://purl.obolibrary.org/obo/CHEBI_60004
T237 1735-1743 Chemical denotes thiolate http://purl.obolibrary.org/obo/CHEBI_50539
T238 1765-1780 Chemical denotes secondary amine http://purl.obolibrary.org/obo/CHEBI_32863
T239 1775-1780 Chemical denotes amine http://purl.obolibrary.org/obo/CHEBI_32952
T240 1973-1975 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T242 1976-1981 Chemical denotes amide http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988
T244 2163-2171 Chemical denotes aldehyde http://purl.obolibrary.org/obo/CHEBI_17478
T245 2215-2228 Chemical denotes aspartic acid http://purl.obolibrary.org/obo/CHEBI_22660
T246 2224-2228 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T247 2320-2326 Chemical denotes sodium http://purl.obolibrary.org/obo/CHEBI_26708
T248 2353-2364 Chemical denotes acetic acid http://purl.obolibrary.org/obo/CHEBI_15366
T249 2360-2364 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T250 2477-2482 Chemical denotes amine http://purl.obolibrary.org/obo/CHEBI_32952
T251 2503-2506 Chemical denotes TFA http://purl.obolibrary.org/obo/CHEBI_45892
T252 2530-2542 Chemical denotes methyl ester http://purl.obolibrary.org/obo/CHEBI_25248
T253 2530-2536 Chemical denotes methyl http://purl.obolibrary.org/obo/CHEBI_32875|http://purl.obolibrary.org/obo/CHEBI_29309
T255 2537-2542 Chemical denotes ester http://purl.obolibrary.org/obo/CHEBI_35701
T256 2589-2593 Chemical denotes LiOH http://purl.obolibrary.org/obo/CHEBI_33979
T257 2608-2620 Chemical denotes methyl ester http://purl.obolibrary.org/obo/CHEBI_25248
T258 2608-2614 Chemical denotes methyl http://purl.obolibrary.org/obo/CHEBI_32875|http://purl.obolibrary.org/obo/CHEBI_29309
T260 2615-2620 Chemical denotes ester http://purl.obolibrary.org/obo/CHEBI_35701
T261 2624-2639 Chemical denotes carboxylic acid http://purl.obolibrary.org/obo/CHEBI_33575
T262 2635-2639 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T263 2666-2676 Chemical denotes amino acid http://purl.obolibrary.org/obo/CHEBI_33709
T264 2666-2671 Chemical denotes amino http://purl.obolibrary.org/obo/CHEBI_46882
T265 2672-2676 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T266 2702-2705 Chemical denotes SAM http://purl.obolibrary.org/obo/CHEBI_15414|http://purl.obolibrary.org/obo/CHEBI_67040
T268 2733-2736 Chemical denotes SAM http://purl.obolibrary.org/obo/CHEBI_15414|http://purl.obolibrary.org/obo/CHEBI_67040
T270 2737-2747 Chemical denotes analogue 4 http://purl.obolibrary.org/obo/CHEBI_59061
T271 2756-2761 Chemical denotes amide http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988
T273 2784-2799 Chemical denotes carboxylic acid http://purl.obolibrary.org/obo/CHEBI_33575
T274 2795-2799 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T275 2805-2815 Chemical denotes amino acid http://purl.obolibrary.org/obo/CHEBI_33709
T276 2805-2810 Chemical denotes amino http://purl.obolibrary.org/obo/CHEBI_46882
T277 2811-2815 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T278 2886-2902 Chemical denotes ammonia solution http://purl.obolibrary.org/obo/CHEBI_18219
T279 2886-2893 Chemical denotes ammonia http://purl.obolibrary.org/obo/CHEBI_16134
T280 2894-2902 Chemical denotes solution http://purl.obolibrary.org/obo/CHEBI_75958
T281 3002-3007 Chemical denotes bromo http://purl.obolibrary.org/obo/CHEBI_22927|http://purl.obolibrary.org/obo/CHEBI_47265
T283 3027-3033 Chemical denotes methyl http://purl.obolibrary.org/obo/CHEBI_32875|http://purl.obolibrary.org/obo/CHEBI_29309
T285 3514-3517 Chemical denotes TFA http://purl.obolibrary.org/obo/CHEBI_45892
T286 3637-3641 Chemical denotes LiOH http://purl.obolibrary.org/obo/CHEBI_33979
T287 3674-3686 Chemical denotes methyl ester http://purl.obolibrary.org/obo/CHEBI_25248
T288 3674-3680 Chemical denotes methyl http://purl.obolibrary.org/obo/CHEBI_32875|http://purl.obolibrary.org/obo/CHEBI_29309
T290 3681-3686 Chemical denotes ester http://purl.obolibrary.org/obo/CHEBI_35701
T291 3703-3718 Chemical denotes carboxylic acid http://purl.obolibrary.org/obo/CHEBI_33575
T292 3714-3718 Chemical denotes acid http://purl.obolibrary.org/obo/CHEBI_37527
T293 3893-3895 Chemical denotes Ns http://purl.obolibrary.org/obo/CHEBI_33349|http://purl.obolibrary.org/obo/CHEBI_33355
T295 3896-3901 Chemical denotes amide http://purl.obolibrary.org/obo/CHEBI_29337|http://purl.obolibrary.org/obo/CHEBI_32988
T297 3929-3940 Chemical denotes nosyl group http://purl.obolibrary.org/obo/CHEBI_51102
T298 3935-3940 Chemical denotes group http://purl.obolibrary.org/obo/CHEBI_24433
T299 3972-3977 Chemical denotes amino http://purl.obolibrary.org/obo/CHEBI_46882
T300 3984-3998 Chemical denotes isopropylidene http://purl.obolibrary.org/obo/CHEBI_29858
T301 3999-4008 Chemical denotes adenosine http://purl.obolibrary.org/obo/CHEBI_16335
T302 4057-4059 Chemical denotes Cl http://purl.obolibrary.org/obo/CHEBI_23116
T303 4109-4117 Chemical denotes chloride http://purl.obolibrary.org/obo/CHEBI_17996
T304 4118-4126 Chemical denotes reagents http://purl.obolibrary.org/obo/CHEBI_33893
T305 4162-4172 Chemical denotes adenosines http://purl.obolibrary.org/obo/CHEBI_22260
T306 4276-4281 Chemical denotes K2CO3 http://purl.obolibrary.org/obo/CHEBI_131526
T307 4286-4288 Chemical denotes KI http://purl.obolibrary.org/obo/CHEBI_74559|http://purl.obolibrary.org/obo/CHEBI_8346
T309 4375-4378 Chemical denotes TFA http://purl.obolibrary.org/obo/CHEBI_45892
T310 4421-4428 Chemical denotes adenine http://purl.obolibrary.org/obo/CHEBI_16708
T311 4556-4563 Chemical denotes adenine http://purl.obolibrary.org/obo/CHEBI_16708
T312 4606-4608 Chemical denotes NH http://purl.obolibrary.org/obo/CHEBI_29339|http://purl.obolibrary.org/obo/CHEBI_73424
T314 4684-4692 Chemical denotes chloride http://purl.obolibrary.org/obo/CHEBI_17996
T315 4720-4724 Chemical denotes NEt3 http://purl.obolibrary.org/obo/CHEBI_35026
T316 4747-4750 Chemical denotes TFA http://purl.obolibrary.org/obo/CHEBI_45892
T317 4800-4806 Chemical denotes chloro http://purl.obolibrary.org/obo/CHEBI_47853
T318 4830-4850 Chemical denotes 4-chlorobenzaldehyde http://purl.obolibrary.org/obo/CHEBI_28105
T319 4855-4861 Chemical denotes sodium http://purl.obolibrary.org/obo/CHEBI_26708

LitCovid-PD-GO-BP

Id Subject Object Predicate Lexical cue
T29 453-464 http://purl.obolibrary.org/obo/GO_0009056 denotes degradation
T30 892-907 http://purl.obolibrary.org/obo/GO_0006306 denotes DNA methylation
T31 896-907 http://purl.obolibrary.org/obo/GO_0032259 denotes methylation
T32 3220-3229 http://purl.obolibrary.org/obo/GO_0009058 denotes synthesis
T33 4539-4548 http://purl.obolibrary.org/obo/GO_0009058 denotes synthesis

2_test

Id Subject Object Predicate Lexical cue
32563813-21936531-29105576 251-253 21936531 denotes 21
32563813-7086841-29105577 1359-1361 7086841 denotes 23
32563813-28823155-29105578 2262-2264 28823155 denotes 25
32563813-7086841-29105579 4010-4012 7086841 denotes 23
32563813-22424977-29105580 4199-4201 22424977 denotes 27
32563813-30354101-29105581 4205-4207 30354101 denotes 28
32563813-12723945-29105582 4211-4213 12723945 denotes 29
32563813-23335289-29105583 4217-4219 23335289 denotes 30

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T75 0-14 Sentence denotes 2.2 Chemistry
T76 15-255 Sentence denotes The retrosynthetic analysis of the dinucleoside 1 structure suggested the coupling reaction between the tosyl derivative 17 previously described by us (Scheme 2) [14], and the readily accessible 5′-amino-2′,3′-isopropylidene adenosine [21].
T77 256-471 Sentence denotes The direct N-alkylation at room temperature did not afford the secondary amine in satisfactory yields and when increasing the temperature to enhance the reactivity of the primary amine, we noticed degradation of 17.
T78 472-668 Sentence denotes To circumvent the lack of reactivity of primary amines, a synthetic method using nitrobenzenesulfonamides (Ns-amides) as both a protecting and activating group has been developed by Fukuyama [22].
T79 669-782 Sentence denotes The main advantage of this nosyl strategy is that both alkylation and deprotection proceed under mild conditions.
T80 783-968 Sentence denotes Recently, the 2-nitrobenzenesulfonamide has been used successfully to synthetize transition state analogs of DNA methylation based on the coupling of cytosine analogs to adenosine [15].
T81 969-1093 Sentence denotes In the same way, we envisaged the coupling between 17 and the 5′-nosyl adenosine 18 to obtain the dinucleoside 1 (Scheme 2).
T82 1094-1363 Sentence denotes The building block 18 was prepared in 74% yield by reacting 4-nitrobenzenesulfonyl chloride [22] that has a similar reactivity to 2-nitrobenzenesulfonyl chloride as used in Ref. [15], with 5′-amino-2′,3′-isopropylidene adenosine prepared upon published procedures [23].
T83 1364-1522 Sentence denotes N-alkylation of Ns-amide 18 with 17 in the presence of K2CO3 in DMF at room temperature did not afford the expected dinucleoside 19, even at high temperature.
T84 1523-1675 Sentence denotes Nevertheless, according to the literature [24], the addition of a catalytic amount of KI to the reaction mixture was beneficial to give 19 in 74% yield.
T85 1676-1798 Sentence denotes Facile deprotection of 19 by treatment with a nucleophilic thiolate produced the desired secondary amine 20 in high yield.
T86 1799-1909 Sentence denotes Removal of sugar protecting groups has been accomplished in acidic medium to give dinucleoside 1 in 76% yield.
T87 1910-2075 Sentence denotes Likewise, the acidic treatment was applied to the intermediate Ns-amide 19 to afford the 4-nitrobenzenesulfonamide-containing dinucleoside 9 in 34% yield (Scheme 2).
T88 2076-2266 Sentence denotes Compounds 2, 3 and 4 were obtained from key compound 20 via reductive amination of the aldehyde 21 that was prepared in three steps from l-aspartic acid following a published procedure [25].
T89 2267-2370 Sentence denotes Reductive amination was conducted in the presence of sodium triacetoxyborohydride and acetic acid [26].
T90 2371-2450 Sentence denotes The resulting fully protected dinucleoside 22 was isolated in high yield (93%).
T91 2451-2556 Sentence denotes Then, sugar hydroxyls and amine were deprotected by TFA treatment and afforded methyl ester derivative 3.
T92 2557-2719 Sentence denotes Subsequent basic treatment with LiOH converted the methyl ester in carboxylic acid and dinucleoside 2 with α-amino acid chain similar to that of SAM was obtained.
T93 2720-2903 Sentence denotes Finally, the SAM analogue 4 with an amide function instead of a carboxylic acid in α-amino acid chain was prepared from 22 upon a final treatment with 7 M methanolic ammonia solution.
T94 2904-3161 Sentence denotes Dinucleosides 5, 6 and 7 were rather synthesized through N-alkylation of 20 with 1-bromobutane, 1-bromo-3-phenylpropane or methyl-4-bromobutyrate, respectively, in N-methylmorpholine in the presence of diisopropylethylamine (DIEA) at 110 °C under microwave.
T95 3162-3273 Sentence denotes These specific conditions were optimized for a successful synthesis of 23, 24 and 25 with an average 50% yield.
T96 3274-3385 Sentence denotes This moderate yield results from double N-alkylations (observed in mass spectrometry) and incomplete reactions.
T97 3386-3471 Sentence denotes Increasing temperature of the reactions neither did drive the reaction to completion.
T98 3472-3583 Sentence denotes Next, 23, 24 and 25 were deprotected upon TFA treatment to obtain N-alkyl derivatives 5, 6 and 7, respectively.
T99 3584-3751 Sentence denotes Subsequently, an additional basic treatment with 2 M LiOH was applied to 7 to convert the methyl ester moiety into the carboxylic acid-ended alkyl chain of compound 8.
T100 3752-3952 Sentence denotes The same synthetic route used for the preparation of nosyl-containing dinucleoside 9 was followed to synthesize compounds 10–13 with diverse Ns-amide moieties as analogs of the nosyl group (Scheme 3).
T101 3953-4222 Sentence denotes The reaction of 5′-amino-2′,3′-isopropylidene adenosine [23] with four diversely substituted (OMe, CF3, Cl) and commercially available nitrobenzenesulfonyl chloride reagents afforded the corresponding N-nosyl adenosines 26–29 with 40–72% yield [[27], [28], [29], [30]].
T102 4223-4366 Sentence denotes Their subsequent coupling with 17 in the presence of K2CO3 and KI gave the corresponding dinucleosides 30–33 in moderate yields from 43 to 52%.
T103 4367-4517 Sentence denotes A final TFA treatment provided the respective N-nosyl adenine dinucleosides 10–13 which were purified by reversed-phase chromatography (Yield 13–20%).
T104 4518-4643 Sentence denotes Scheme 4 depicts the synthesis of the adenine dinucleosides 14–16 from the intermediate NH-linked dinucleoside 20 (Scheme 2).
T105 4644-4772 Sentence denotes The reaction of 4-chlorobenzenesulfonyl chloride with 20 in the presence of NEt3 [31,32] followed by a TFA treatment yielded 14.
T106 4773-5001 Sentence denotes The treatment of 20 with 4-chloro-3-nitrobenzaldehyde or 4-chlorobenzaldehyde and sodium triacetoxyborohydride, followed by the removal of protective groups in acidic conditions resulted in dinucleosides 15 and 16, respectively.
T107 5002-5118 Sentence denotes It is noteworthy that this reductive amination conducted at 40 °C increased the yields to 71% and 81%, respectively.

MyTest

Id Subject Object Predicate Lexical cue
32563813-21936531-29105576 251-253 21936531 denotes 21
32563813-7086841-29105577 1359-1361 7086841 denotes 23
32563813-28823155-29105578 2262-2264 28823155 denotes 25
32563813-7086841-29105579 4010-4012 7086841 denotes 23
32563813-22424977-29105580 4199-4201 22424977 denotes 27
32563813-30354101-29105581 4205-4207 30354101 denotes 28
32563813-12723945-29105582 4211-4213 12723945 denotes 29
32563813-23335289-29105583 4217-4219 23335289 denotes 30