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JNJ-18038683,851376-05-1

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  • ¥7950
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-19889
  • 2025年12月05日
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    • 详细信息
    • 技术资料
    • 保存条件

      4°C, sealed storage, away from moisture

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      851376-05-1

    • 规格

      100 mg

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    JNJ-18038683

    CAS No. : 851376-05-1

    MCE 国际站:JNJ-18038683

    产品活性:JNJ-18038683 是 5-羟色胺受体 7 (5-HT7) 的拮抗剂,HEK293 细胞中检测出其对大鼠和人类 5-羟色胺受体 7 的 pKi 值分别为 8.19,8.20。

    研究领域:GPCR/G Protein  |  Neuronal Signaling

    作用靶点:5-HT Receptor

    In Vitro: JNJ-18038683 displaced, with high affinity, specific [3H]5-CT binding sites from rat and human 5-HT7 receptor express in HEK293 cells (pKi=8.19±0.02 and 8.20±0.01, respectively). Similar values are obtained on the native 5-HT7 in membranes from rat thalamus (pKi=8.50±0.20). Hill slope values are close to unity, suggesting one-site competitive binding. Antagonist potency of JNJ-18038683 is determined by the measurement of adenylate cyclase activity in HEK293 cells expressing the human or rat 5-HT7 receptor. 5-HT stimulates adenylyl cyclase activity in rat and human 5-HT7/HEK293 cells with a pEC50 of 8.09 and 8.12, respectively. JNJ-18038683 produces a concentration-dependent decrease of 5-HT (100 nM)-stimulated adenylyl cyclase. The pKB values determined for JNJ-18038683 are in good agreement with the corresponding Ki values determined from [3H]5-CT binding studies.

    In Vivo: JNJ-18038683 dose-dependently suppresses REM sleep mainly during the first 4 h after the treatment. The duration of REM sleep is significantly decreased from the dose of 1 mg/kg onward (P<0.05) during the first 4 h after oral administration. Concomitantly, the REM sleep latency tends to be prolonged in a dose-related manner with a significant increase in REM latency occurring only at the highest dose tested (10 mg/kg; P<0.05). These alterations in REM sleep seem to be state-specific. A separate study is conducted to determine whether repeated administration of JNJ-18038683 for 7 days would result in an adaptation of the EEG sleep response in particular on REM sleep in rats during the course of the treatment and after its discontinuation. JNJ-18038683 is administered for 7 consecutive days (1 mg/kg s.c. per day) at 2 h into the light phase. On the first day of treatment, JNJ-18038683 produces a significant decrease in the time spent in REM sleep during the first 8 h after the injection and a prolongation of the REM sleep latency. The REM sleep latency is increased during the 7-day repeated treatment and is normalized on the first recovery day after cessation of treatment. The significant decrease in REM sleep time is maintained during the 7-day repeated treatment, with a rebound occurring on the first recovery day after treatment discontinuation. The NREM sleep latency and the total NREM sleep time are not affected during the entire treatment.

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