FAAH-like anandamide transporter (FLAT) inhibitor (IC50
= 1.8 μ
M); cytosolic variant of FAAH-1 that binds anandamide. Attenuates anandamide internalization and deactivation in vitro
and in vivo
respectively. Exhibits analgesic effects in rodent models of CB1
-mediated nociceptive and inflammatory pain.
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