ChemicalBook--->CAS DataBase List--->851376-05-1

851376-05-1

851376-05-1 Structure

851376-05-1 Structure
IdentificationBack Directory
[Name]

JNJ-18038683
[CAS]

851376-05-1
[Synonyms]

JNJ-18038683
Inhibitor,JNJ-18038683,5-hydroxytryptamine Receptor,inhibit,JNJ 18038683,JNJ18038683,Serotonin Receptor,5-HT Receptor
[Molecular Formula]

C26H28ClN3O7
[MOL File]

851376-05-1.mol
[Molecular Weight]

529.97
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:200.0(Max Conc. mg/mL);377.38(Max Conc. mM)
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

JNJ-18038683 is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with pKis of 8.19, 8.20 for rat and human 5-HT7 in HEK293 cells, respectively.
[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[1].

[IC 50]

Rat 5-HT7 Receptor: 8.19 (pKi, in HEK293 cells ); Human 5-HT7 Receptor: 8.20 (pKi, in HEK293 cells )
[storage]

Store at -20°C
[References]

[1] Bonaventure P, et al. Translational evaluation of JNJ-18038683, a 5-hydroxytryptamine type 7 receptor antagonist, on rapid eye movement sleep and in major depressive disorder. J Pharmacol Exp Ther. 2012 Aug;342(2):429-40. DOI:10.1124/jpet.112.193995
Spectrum DetailBack Directory
[Spectrum Detail]

JNJ-18038683(851376-05-1)1HNMR
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