Abstract
A series of 5-azaquinoxaline-2,3-dione derivatives were synthesized and evaluated on d-amino acid oxidase (DAAO) inhibition as potential α-hydroxylactam-based inhibitors. The potent inhibitory activities in vitro suggested that 5-nitrogen could significantly enhance the binding affinity by strengthening relevant hydrogen bond interactions. The analgesic effects of intrathecal and systemic injection of 8-chloro-1,4-dihydropyrido[2,3-b]pyrazine-2,3-dione, a representative molecule of 5-azaquinoxaline-2,3-dione, were investigated in rodents. This research not only confirmed the analgesic effect of the DAAO inhibitors but provided a new class of chemical entities with oral application potential for the treatment of chronic pain and morphine analgesic tolerance.
| Original language | English |
|---|---|
| Pages (from-to) | 19-32 |
| Number of pages | 14 |
| Journal | European Journal of Medicinal Chemistry |
| Volume | 117 |
| DOIs | |
| Publication status | Published - 19 Jul 2016 |
| Externally published | Yes |
Keywords
- 5-Azaquinoxaline-2,3-diones
- 8-Chloro-1,4-dihydropyrido[2,3-b]pyrazine-2,3-dione
- Analgesic effects
- D-amino acid oxidase
- DAAO inhibitors
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