Synthesis and Evaluation of Orexin‑1 Receptor Antagonists with Improved Solubility and CNS Permeability
journal contributionposted on 11.11.2017, 00:00 by David A. Perrey, Ann M. Decker, Yanan Zhang
Orexins are hypothalamic neuropeptides playing important roles in many functions including the motivation of addictive behaviors. Blockade of the orexin-1 receptor has been suggested as a potential strategy for the treatment of drug addiction. We have previously reported OX1 receptor antagonists based on the tetrahydroisoquinoline scaffold with excellent OX1 potency and selectivity; however, these compounds had high lipophilicity (clogP > 5) and low to moderate solubility. In an effort to improve their properties, we have designed and synthesized a series of analogues where the 7-position substituents known to favor OX1 potency and selectivity were retained, and groups of different nature were introduced at the 1-position where substitution was generally tolerated as demonstrated in previous studies. Compound 44 with lower lipophilicity (clogP = 3.07) displayed excellent OX1 potency (Ke = 5.7 nM) and selectivity (>1,760-fold over OX2) in calcium mobilization assays. In preliminary ADME studies, 44 showed excellent kinetic solubility (>200 μM), good CNS permeability (Papp = 14.7 × 10–6 cm/sec in MDCK assay), and low drug efflux (efflux ratio = 3.3).
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CNS Permeability Orexinssolubility7- position substituentsADME studiesselectivityCNS permeabilityP app5.7 nMcalcium mobilization assayslipophilicityOX 1 potencyfavor OX 1 potencyK edrug addictionefflux ratiodrug effluxCompound 44OX 1 receptor antagonistsclogPtetrahydroisoquinoline scaffoldMDCKOX 21- position