Id |
Subject |
Object |
Predicate |
Lexical cue |
T574 |
0-97 |
Sentence |
denotes |
Previously, isatin (2,3‐dioxoindole) derivatives were observed to inhibit rhinovirus 3C protease. |
T575 |
98-246 |
Sentence |
denotes |
176 Due to the structural similarity between the rhinovirus 3C protease and SARS‐CoV‐1 Mpro, these derivatives were tested against SARS‐CoV‐1 Mpro. |
T576 |
247-386 |
Sentence |
denotes |
Among them, 106 (IC50, 0.95 µM) and 107 (IC50, 0.98 µM) exhibited the best SARS‐CoV‐1 Mpro inhibitory activity in the low micromolar range. |
T577 |
387-545 |
Sentence |
denotes |
176 SAR studies suggested that the inhibition efficiency was mainly reliant on hydrophobic and electronic properties of the isatin core substitution pattern. |
T578 |
546-634 |
Sentence |
denotes |
Docking studies revealed that the molecules fit well in the active site of the protease. |
T579 |
635-739 |
Sentence |
denotes |
Both carbonyl groups of the isatin core engaged in H‐bonds with NH of Gly143, Ser144, Cys145, and His41. |
T580 |
740-962 |
Sentence |
denotes |
Compounds 106 and 107 176 were more selective for SARS‐CoV‐1 Mpro than other proteases like papain (106, 103 µM; 107, 87.24 µM), chymotrypsin (106, ~1 mM; 107, 10.4 µM), and trypsin (106, 362 µM; 107, 243 µM; Figure 28). |