Table 32.
Compound | Cyclic CH-Acid 44 in Table 10 |
IC50 (μM) | |||||
---|---|---|---|---|---|---|---|
A549 | PC-3 | MCF-7 | A375 | LNCaP | HDF | ||
45a | 40 | >100 | >100 | 70.7 | 32.1 | >100 | |
45b | >100 | >100 | >100 | >100 | >100 | >100 | |
45c | >100 | >100 | >100 | >100 | >100 | >100 | |
45d | >100 | >100 | >100 | >100 | >100 | >100 | |
45e | >100 | >100 | >100 | >100 | >100 | >100 | |
45f | >100 | >100 | >100 | >100 | >100 | >100 | |
45g | >100 | >100 | >100 | >100 | >100 | >100 | |
45h | >100 | >100 | >100 | >100 | >100 | >100 | |
45i | >100 | >100 | >100 | >100 | >100 | >100 | |
45j | >100 | >100 | >100 | >100 | >100 | >100 | |
Etoposide b | -- | 60 | 40 | 30 | 25.3 | 90 | >100 |
a Reaction conditions: Cyanoacetohydrazide 42 (1 mmol), ninhydrin 43 (1 mmol), malononitrile 2 (1 mmol), cyclic CH-acid 44 (1 mmol), EtOH (10 mL), reflux, 6–12 h. b Standard drug for the study.