LY-178210
| Clinical data | |
|---|---|
| Other names | LY178210; LY-228729; LY228729 | 
| Drug class | Serotonin 5-HT1A receptor partial agonist | 
| Identifiers | |
| 
 | |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C18H25N3O | 
| Molar mass | 299.418 g·mol−1 | 
| 3D model (JSmol) | |
| 
 | |
| 
 | |
LY-178210 is a selective and highly potent serotonin 5-HT1A receptor partial agonist. It has an affinity (Ki) of 0.67 nM for the serotonin 5-HT1A receptor. The drug has high selectivity for this receptor over 12 other assessed targets, including the serotonin 5-HT1D, 5-HT2A, 5-HT2C, and 5-HT3 receptors among others (Ki = ≥380–4,000 nM). LY-178210 is a tricyclic simplified or partial ergoline and is structurally related to LSD. It was described as a potential clinical development candidate but was not further developed and was never marketed. The drug was first reported in the scientific literature by 1990.