Id |
Subject |
Object |
Predicate |
Lexical cue |
T46 |
0-79 |
Sentence |
denotes |
Table 1 Antiviral activity of 16 compounds against SARS-CoV-2 in Vero E6 cells. |
T47 |
80-127 |
Sentence |
denotes |
Compounds Inhibition of SARS-CoV-2 in vitro, μM |
T48 |
128-173 |
Sentence |
denotes |
Name Bioactivity Clinical application CAS No. |
T49 |
174-273 |
Sentence |
denotes |
CC50, μMa CPE inhibitionb Reduction in infectious virusc (EC50) Reduction in viral RNA copyd (EC50) |
T50 |
274-388 |
Sentence |
denotes |
Remdesivir adenosine analogue Phase 4 trials for treatment of Ebola or SARS-CoV-2 1809249-37-3 >100 25 23.15 26.90 |
T51 |
389-513 |
Sentence |
denotes |
Favipiravir guanineanalogue Approved in Japan and China for treatment of influenza infection 259793-96-9 >100 >100 >100 >100 |
T52 |
514-632 |
Sentence |
denotes |
Ribavirin guanosine analogue FDA approved for treatment of chronic hepatitis C infection 36791-04-5 >100 500 >500 >500 |
T53 |
633-741 |
Sentence |
denotes |
Galidesivir adenosine analogue Phase 2 trial for yellow fever virus infection 222631-44-9 >100 100 >100 >100 |
T54 |
742-846 |
Sentence |
denotes |
R-1479 cytidineanalogue Phase 2 trial for treatment of dengue virus infection 478182-28-4 >100 >100 N.D. |
T55 |
847-851 |
Sentence |
denotes |
N.D. |
T56 |
852-951 |
Sentence |
denotes |
Tenofovor adenosine analogue FDA approved for treatment of HIV-1 and HBV 147127-20-6 >100 >100 N.D. |
T57 |
952-956 |
Sentence |
denotes |
N.D. |
T58 |
957-1089 |
Sentence |
denotes |
Fludarabine phosphate adenosine analogue FDA approved for treatment of B-cell chronic lymphocytic leukemia 75607-67-9 >100 >100 N.D. |
T59 |
1090-1094 |
Sentence |
denotes |
N.D. |
T60 |
1095-1232 |
Sentence |
denotes |
Lopinavir protease inhibitor FDA approved for treatment of HIV-1 infection in combination with ritonavir 192725-17-0 49.75 25 26.63 26.10 |
T61 |
1233-1388 |
Sentence |
denotes |
Ritonavir protease inhibitor FDA approved for treatment of HIV-1 infection in combination with other antiretroviral agents 155213-67-5 48.91 >100 >100 >100 |
T62 |
1389-1506 |
Sentence |
denotes |
Emetine hydrochloride anti-protozoal Approved in China for severe invasive amoebiasis 316-42-7 56.46 1.5625 0.46 0.50 |
T63 |
1507-1644 |
Sentence |
denotes |
Oritavancin diphosphate antibiotics FDA approved treatment for skin infection caused by Gram positive bacteria 192564-14-0 N.D. >100 N.D. |
T64 |
1645-1649 |
Sentence |
denotes |
N.D. |
T65 |
1650-1790 |
Sentence |
denotes |
Dalbavancin hydrochloride antibiotics FDA approved treatment for skin infection caused by Gram positive bacteria 2227366-51-8 N.D. >100 N.D. |
T66 |
1791-1795 |
Sentence |
denotes |
N.D. |
T67 |
1796-1910 |
Sentence |
denotes |
Homoharringtonine anti-cancer FDA approved treatment for chronic myeloid leukemia 26833-87-4 59.75 3.125 2.55 2.14 |
T68 |
1911-2048 |
Sentence |
denotes |
Oseltamivir carboxylate antiviral, neuraminidase inhibitor FDA approved treatment for influenza infection 187227-45-8 >100 >100 >100 >100 |
T69 |
2049-2178 |
Sentence |
denotes |
Baloxivir acid antiviral, endonuclease inhibitor FDA approved treatment for influenza infection 1985605-59-1 85.90 >100 >100 >100 |
T70 |
2179-2311 |
Sentence |
denotes |
Chlorpromazine hydrochloride antagonist for post-synaptic receptors FDA approved treatment for schizophrenia 69-09-0 21.29 >100 N.D. |
T71 |
2312-2316 |
Sentence |
denotes |
N.D. |
T72 |
2317-2321 |
Sentence |
denotes |
N.D. |
T73 |
2322-2337 |
Sentence |
denotes |
Not determined. |
T74 |
2338-2497 |
Sentence |
denotes |
a CC50 was determined with serially-diluted compounds in Vero E6 cells at 48 h post-incubation using CellTiter-Glow Luminescent Cell Viability Assay (Promega). |
T75 |
2498-2607 |
Sentence |
denotes |
b Compounds were serially 2-fold or 4-fold diluted from 100 μM, except ribavirin which was started at 500 μM. |
T76 |
2608-2755 |
Sentence |
denotes |
Cytopathic effects (CPE) of SARS-CoV-2 virus in Vero E6 cells under increasing concentration of the compounds were observed at 48 h post-infection. |
T77 |
2756-2892 |
Sentence |
denotes |
The lowest concentration of the compound with 100% CPE inhibition (eg. exhibiting comparable CPE of non-infected controls) was recorded. |
T78 |
2893-3000 |
Sentence |
denotes |
c EC50 determined by infectious virus yield in culture supernatant at 48h post-infection (log10 TCID50/mL). |
T79 |
3001-3112 |
Sentence |
denotes |
d EC50 determined by viral RNA copy numbers in culture supernatant at 48h post-infection (log10 RNA copies/mL). |