FP802 is an orally active potent TwinF interface inhibitor that disrupts and detoxifies the NMDAR/TRPM4 death complex. FP802 exerts powerful neuroprotective effects in the 5xFAD mouse model of Alzheimers disease (AD) by preventing cognitive decline, preserving neuronal structural integrity, reducing amyloid-beta plaque formation, and mitigating mitochondrial pathology[1]. FP802 stops loss of motor neurons, reduces serum neurofilament light chain (NfL) levels, improves motor performance, and extends life in a mouse model of amyotrophic lateral sclerosis (ALS)[2]. FP802 can be used for AD and ALS research[1][2].
Molekulargewicht:
212.72
CAS Nummer:
[61694-81-3]
Formel:
C11H17ClN2
Target-Kategorie:
iGluR,TRP Channel
Anwendungsbeschreibung:
MCE Product type: Reference compound1
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