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PMC:7291971 / 53618-54407 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T1102 85-97 CHEBI:38472;CHEBI:38472 denotes acetonitrile
T1103 261-265 CHEBI:51231;CHEBI:51231 denotes DMSO
T86511 85-97 CHEBI:38472;CHEBI:38472 denotes acetonitrile
T14604 261-265 CHEBI:51231;CHEBI:51231 denotes DMSO

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
919 342-344 Chemical denotes 2H MESH:D003903

LitCovid-PD-CLO

Id Subject Object Predicate Lexical cue
T335 58-59 http://purl.obolibrary.org/obo/CLO_0001020 denotes a
T336 175-176 http://purl.obolibrary.org/obo/CLO_0001020 denotes a

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T17575 85-97 Chemical denotes acetonitrile http://purl.obolibrary.org/obo/CHEBI_38472
T86424 107-113 Chemical denotes buffer http://purl.obolibrary.org/obo/CHEBI_35225
T108 244-246 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T24815 261-265 Chemical denotes DMSO http://purl.obolibrary.org/obo/CHEBI_28262
T20156 282-284 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T65687 296-298 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T8029 310-312 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T2651 324-326 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T5457 386-388 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T115 412-414 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T28173 457-459 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T85971 483-485 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T74956 515-517 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T36399 547-549 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T49547 573-575 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637
T89992 644-646 Chemical denotes 1H http://purl.obolibrary.org/obo/CHEBI_49637

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T381 0-789 Sentence denotes Following method C with 23 (40 mg, 0.45 mol, 1.00 eq) and a 0–50% linear gradient of acetonitrile in TEAAc buffer 50 mM, pH 7 for purification, 5 (20 mg, 72%) was obtained as a white powder with 98% purity determined by HPLC analysis at 260 nm.1H NMR (500 MHz, DMSO‑d 6) δ 8.36 (s, 1H), 8.32 (s, 1H), 8.14 (s, 1H), 8.13 (s, 1H), 7.33 (br. s, 2H), 7.25 (br. s, 2H), 5.97 (d, J = 6.3 Hz, 1H), 5.85 (d, J = 5.2 Hz, 1H), 5.49–5.39 (m, 3H), 5.14 (d, J = 5.3 Hz, 1H), 4.62 (q, J = 5.4 Hz, 1H), 4.52 (dd, J = 6.5, 4.7 Hz, 1H), 4.29 (dd, J = 4.8, 2.8 Hz, 1H), 4.06 (q, J = 4.9 Hz, 1H), 4.00–3.92 (m, 2H), 3.68–3.46 (m, 4H), 2.79 (dd, J = 14.0, 4.6 Hz, 1H), 2.70–2.51 (m, 3H), 2.41–2.30 (m, 2H), 1.22 (q, J = 7.4, 2H), 1.07 (tdd, J = 13.4 Hz, J = 10.5 Hz, J = 6.3 Hz, 2H), 0.73 (t, J = 7.3 Hz, 2H).