(E/Z)-OT-R antagonist 1 is a mixture of E/Z forms of OT-R antagonist 1 (HY-15015). OT-R antagonist 1 is a novel, potent, selective non-peptide OT-R antagonist that inhibits oxytocin-induced intracellular Ca2+ activation (IC50 = 8 nM)[1][2][3][4].
Molecular Weight:
471.55
CAS Number:
[364076-99-3]
Formula:
C28H29N3O4
Target:
Oxytocin Receptor
Application Notes:
MCE Product type: Reference compound
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