Flumexadol is a selective and affinity 5-HT2C receptor agonist with a Ki of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT2A receptor. Flumexadol is an orally active non-narcotic analgesic[1][2].
Molecular Weight:
231.22
Purity:
99.86
CAS Number:
[30914-89-7]
Formula:
C11H12F3NO
Target:
5-HT Receptor
Application Notes:
MCE Product type: Reference compound
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