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inhibition of control specific binding with 10 Î¼M C1. 5-HT transporter (h) (antagonist radioligand). 5. 5 Î±1 (h) (agonist radioligand). -3. -1. A1 (h) (antagonist ...

Cerep Assay Name 5‐HT transporter (h) (antagonist radioligand) 1 (h) (agonist radioligand) A1 (h) (antagonist radioligand) 1 (non‐selective) (antagonist radioligand) 2 (h) (agonist radioligand) 2 (non‐selective) (antagonist radioligand) A2A (h) (agonist radioligand) A3 (h) (agonist radioligand) AMPA (agonist radioligand) AR (h) (agonist radioligand) AT1 (h) (antagonist radioligand) AT2 (h) (agonist radioligand) B1 (h) (agonist radioligand) B2 (h) (agonist radioligand) BLT1 (LTB4) (h) (agonist radioligand) BZD (central) (agonist radioligand) Ca2+ channel (L, dihydropyridine site) (antagonist radioligand) Ca2+ channel (L, diltiazem site) (benzothiazepines) (antagonist radioligand) Ca2+ channel (L, verapamil site) (phenylalkylamine) (antagonist radioligand) CB1 (h) (agonist radioligand) CB2 (h) (agonist radioligand) CCK1 (CCKA) (h) (agonist radioligand) CCK2 (CCKB) (h) (agonist radioligand) choline transporter (CHT1) (h) (antagonist radioligand) Cl‐channel (GABA‐gated) (antagonist radioligand) CRF1 (h) (agonist radioligand) CysLT1 (LTD4) (h) (agonist radioligand) D1 (h) (antagonist radioligand) D2S (h) (antagonist radioligand) D3 (h) (antagonist radioligand) D4.4 (h) (antagonist radioligand) dopamine transporter (h) (antagonist radioligand) EP2 (h) (agonist radioligand) ER (non‐selective) (h) (agonist radioligand) ETA (h) (agonist radioligand) ETB (h) (agonist radioligand) GABA (non‐selective) (agonist radioligand) GABA transporter (antagonist radioligand) H1 (h) (antagonist radioligand) H2 (h) (antagonist radioligand) H3 (h) (agonist radioligand) I2 (antagonist radioligand) IP (PGI2) (h) (agonist radioligand) kainate (agonist radioligand) KATP channel (antagonist radioligand) KV channel (antagonist radioligand) M (non‐selective) (antagonist radioligand) MC4 (h) (agonist radioligand) Na+ channel (site 2) (antagonist radioligand) NK1 (h) (agonist radioligand) NK2 (h) (agonist radioligand) NK3 (h) (antagonist radioligand) NMDA (antagonist radioligand) NOP (ORL1) (h) (agonist radioligand) norepinephrine transporter (h) (antagonist radioligand)  (non‐selective) (agonist radioligand) opioid (non‐selective) (antagonist radioligand) P2X (agonist radioligand) P2Y (agonist radioligand) PCP (antagonist radioligand) PPAR (h) (agonist radioligand) PR (h) (agonist radioligand) TRH1 (h) (agonist radioligand) V1a (h) (agonist radioligand) V2 (h) (agonist radioligand) Y (non‐selective) (agonist radioligand)

% inhibition of control specific binding with 10 μM 4b 5 ‐3 7 3 2 0 0 8 ‐23 ‐2 ‐18 4 5 ‐1 2 4 ‐4 ‐15 7 7 0 72 0 14 0 0 0 ‐10 3 10 13 2 15 2 ‐19 ‐4 14 ‐12 10 ‐8 0 5 ‐15 ‐9 ‐5 2 13 1 7 7 5 0 1 ‐2 0 26 ‐15 ‐3 ‐4 15 13 0 9 10 6 ‐3

% inhibition of control specific binding with 10 μM C1 5 ‐1 9 5 2 13 9 11 ‐29 3 ‐13 12 ‐2 ‐5 0 22 ‐7 ‐3 19 18 3 68 3 40 0 ‐2 0 27 2 11 31 23 24 4 2 ‐7 5 ‐13 45 ‐11 8 73 ‐19 ‐1 5 3 20 0 41 9 9 4 ‐4 ‐2 30 30 40 5 ‐2 ‐5 13 1 1 11 5 ‐5