|Chemical and physical data|
|Molar mass||333.407 g·mol−1|
|3D model (JSmol)|
KML-010 is a drug derived from spiperone. It functions as a highly selective 5-HT2A receptor antagonist, with negligible affinity for the 5-HT1A or 5-HT2C receptors, and over 400-fold lower affinity for the D2 receptor in comparison to spiperone.
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