| E4740 |
TAK-861 (Oveporexton)
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Oveporexton (TAK-861) is a potent, orally bioavailable agonist of orexin receptor 2 (OX2R), with an EC50 of 2.5 nM in calcium mobilization assays. It induces dose-dependent membrane depolarization in histaminergic neurons within the mouse tuberomammillary nucleus (TMN) with an EC50 of 31.7 nM.
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| S2160 |
Almorexant HCl
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Almorexant HCl (ACT-078573) is an orally active, dual orexin receptor antagonist with IC50 of 6.6 nM and 3.4 nM for OX1 and OX2 receptor, respectively. Phase 3.
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J Adv Res, 2024, S2090-1232(24)00359-X
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bioRxiv, 2024, 2024.07.06.602357
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Cell Rep, 2022, 40(5):111153
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| S7585 |
SB-334867
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SB-334867 is a selective orexin-1 (OX1) receptor antagonist.
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J Pharmacol Exp Ther, 2025, 392(7):103624
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J Neuroinflammation, 2020, 17(1):187
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Med Sci Monit, 2019, 25:2886-2895
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| E0107 |
EMPA
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EMPA is a selective OX2 receptor antagonist and binds to human and rat OX2-HEK293 membranes with Kd values of 1.1 and 1.4 nM respectively.
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Eur Heart J, 2024, 31:ehae472.
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Oxid Med Cell Longev, 2022, 2022:1122494
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| S1545 |
SB408124
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SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively, exhibits 50-fold selectivity over OX2 receptor.
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Nat Chem Biol, 2017, 13(2):235-242
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| S6717 |
TCS-OX2-29
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TCX-OX2-29 is a OX2R antagonist (pKi = 7.5) that exhibits >250-fold selectivity for hOX2R compared with hOX1R (IC50s = 40 nM and >10,000 nM, respectively).
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J Pharmacol Exp Ther, 2025, 392(7):103624
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| S3503New |
Seltorexant
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Seltorexant (JNJ-42847922) is a potent and selective antagonist of the orexin-2 receptor (OX2R) exhibiting strong affinity (pKi ~8.0) for human OX2R. It promotes sleep onset and demonstrates antidepressant effects in major depressive disorder (MDD) patients with insomnia by blocking hyperarousal linked to depression and sleep disturbance.
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| S6726 |
MK1064
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MK1064 is a selective orexin 2 receptor antagonist (2-SORA) with an IC50 of 18 nM.
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