Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator. Lumateperone has anticancer activity and can also be used for the study of schizophrenia and bipolar depression[1][2][3].
Molekulargewicht:
393.50
Reinheit:
99.83
CAS Nummer:
[313368-91-1]
Formel:
C24H28FN3O
Target-Kategorie:
5-HT Receptor,Dopamine Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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