BAY 1214784 is a potent, selective, and orally active antagonist of the human gonadotropin-releasing hormone receptor (hGnRH-R). BAY 1214784 is a spiroindoline derivative compound. BAY 1214784 effectively lowers plasma luteinizing hormone levels by up to 49%, at the same time being associated with low pharmacokinetic variability and good tolerability. BAY 1214784 has the potential for the research of uterine fibroids[1].
Molekulargewicht:
672.11
Reinheit:
99.8
CAS Nummer:
[1631164-25-4]
Formel:
C29H26ClF4N3O5S2
Target-Kategorie:
GnRH Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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