Fluorolintane
Fluorolintane exhibits high affinity for N-methyl-D-aspartate (NMDA) receptors with a Ki of 87.92 nM. Fluorolintane inhibits prepulse inhibition in rats. Fluorolintane also inhibits NMDA receptor-induced field excitatory postsynaptic potentials in rat hippocampal slices[1].
Product Specifications
CAS Number
[2149042-90-8]
UNSPSC
12352005
Target
IGluR
Related Pathways
Membrane Transporter/Ion Channel; Neuronal Signaling
Field of Research
Neurological Disease
Smiles
FC1=CC=CC=C1C(N2CCCC2)CC3=CC=CC=C3
Molecular Formula
C18H20FN
Molecular Weight
269.36
References & Citations
[1]Wallach, J., et al., (2019) . Pharmacological characterizations of the 'legal high' fluorolintane and isomers. European journal of pharmacology, 857, 172427.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Curated Selection
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