Parallel synthesis of a series of subtype-selective NMDA receptor antagonists.
2000
Abstract A series of 1-(heteroarylthioalkyl)-4-benzylpiperidines was rapidly synthesized through the use of parallel synthesis to investigate the binding affinity for the NR1 a /2B receptor subtype.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
3
References
11
Citations
NaN
KQI