Table 2. Structures and activities for 4-thiazolidinone analogs 16–32.
| |||
| Compd | R | Inhibitory rate at 10 μM (%) | hDHODH IC50 a (μM) |
| 16 |
|
40.010 | >10 |
| 17 |
|
18.377 | >10 |
| 18 |
|
34.109 | >10 |
| 19 |
|
56.856 | 8.51 |
| 20 |
|
49.438 | 10.64 |
| 21 |
|
68.979 | 2.68 |
| 22 |
|
74.431 | 3.03 |
| 23 |
|
62.932 | 4.41 |
| 24 |
|
52.475 | 9.45 |
| 25 |
|
40.378 | >10 |
| 26 |
|
79.074 | 1.75 |
| 27 |
|
15.064 | >10 |
| 28 |
|
43.738 | >10 |
| 29 |
|
45.360 | >10 |
| 30 |
|
21.886 | >10 |
| 31 |
|
80.327 | 1.12 |
| 32 |
|
25.632 | >10 |
aIC50 values were determined from three independent tests, and attempts to determine IC50 values were made if the inhibition rate at 10 μM was higher than 50%.