MK-1064 是一种选择性的、具有口服活性的OX2R拮抗剂 (Ki: 0.5 nM,IC50: 18 nM)。MK-1064 可促进睡眠 (in vivo)。MK-1064 可用于神经相关的研究。
生物活性 | MK-1064 is a selective and orally activeOX2Rantagonist (Ki: 0.5 nM,IC50: 18 nM). MK-1064 promotes sleepin vivo. MK-1064 can be used in the research of insomnia[1][3]. |
IC50& Target[1] | OX2Receptor 18 nM (IC50) | OX1Receptor 1789 nM (IC50) | OX2Receptor 0.5 nM (Ki) | OX1Receptor 1584 nM (Ki) |
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体内研究 (In Vivo) | MK-1064 (30 mg/kg, oral administration) promotes sleep in rodents selectively through OX2R in Wild-type mice[2]. MK-1064 (30 mg/kg, oral administration, 5 days) reverses the struggle behavior induced by CNO pre-treatment in rats[3]. MK-1064 (1-5 mg/kg, intravenous injection/oral administration) shows moderate oral bioavailability and clearance in rat, dog, and rhesus monkey[1].
Animal Model: | Wild-type and OX2R knockout mice[2] | Dosage: | 30 mg/kg | Administration: | Oral administration | Result: | Displayed active wake reduction accompanied by significant increases in SWS (slow-wave sleep) and REM (rapid eye movement) at time points up to 3.5 hours following treatment. |
Animal Model: | Rat, dog, and rhesus monkey (Pharmacokinetics assay)[1] | Dosage: | 1, 2, 3, 5 mg/kg | Administration: | Oral administration (P.O.), intravenous injection (I.V.) | Result: | Pharmacokinetics profile of MK-1064.
Species | Dose (mg/kg) | CL (mL/min/kg) | t1/2(h) | Dose (mg/kg) | Cmax(μM) | F (%) | Rat | 2 (I.V.) | 39 | 0.3 | 5 (P.O.) | 1.5 | 54 | |
Dog | 1 (I.V.) | 16 | 1.0 | 3 (P.O.) | 1.0 | 48 | |
Rhesus | 2 (I.V.) | 12 | 0.8 | 5 (P.O.) | 0.9 | 16 |
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运输条件 | Room temperature in continental US; may vary elsewhere. |
储存方式 | Powder | -20°C | 3 years | | 4°C | 2 years | In solvent | -80°C | 6 months | | -20°C | 1 month |
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溶解性数据 | In Vitro: DMSO : 50 mg/mL(108.25 mM;Need ultrasonic) 配制储备液 1 mM | 2.1650 mL | 10.8249 mL | 21.6497 mL | 5 mM | 0.4330 mL | 2.1650 mL | 4.3299 mL | 10 mM | 0.2165 mL | 1.0825 mL | 2.1650 mL |
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