ChemicalBook--->CAS DataBase List--->362665-56-3

362665-56-3

362665-56-3 Structure

362665-56-3 Structure
IdentificationBack Directory
[Name]

Piperidine, 1-[3-[3-(4-chlorophenyl)propoxy]propyl]-
[CAS]

362665-56-3
[Synonyms]

PITOLISANT
Tirolisant
Tiprolisant
Pitolisant (BF2.649)
Tiprolisant Pitolisant
TIPROLISANT;BF-2649;BF 2.649
1-[3-[3-(4-Chlorophenyl)propoxy]propyl]piperidine
3-(4-Chlorophenyl)propyl 3-piperidinopropyl ether
Piperidine, 1-[3-[3-(4-chlorophenyl)propoxy]propyl]-
[Molecular Formula]

C17H26ClNO
[MDL Number]

MFCD18782650
[MOL File]

362665-56-3.mol
[Molecular Weight]

295.85
Chemical PropertiesBack Directory
[Boiling point ]

398.7±32.0 °C(Predicted)
[density ]

1.056
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[solubility ]

DMSO
[form ]

Powder
[pka]

9.41±0.10(Predicted)
[color ]

Colorless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Pitolisant is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor. Pitolisant is also used in the treatment of patients with narcolepsy, excessive daytime sleepiness, cataplexy, disturbed nocturnal sleep, hypnagogic hallucinations and sleep paralysis
[Definition]

ChEBI: Pitolisant is an organochlorine compound.
[in vivo]

The administration of Pitolisantat a single dose of 10 mg/kg 30 min before a single dose of Olanzapine (2 mg/kg b.w.) also significantly affects immobility time in the FST. Subsequent administration of the aforementioned drug sequence in mice statistically significantly increases the duration of immobility in comparison to the time determined in the control group in the FST. It decreased locomotor activity as well. In contrast, the results obtained in subchronic treatment after fifteen administrations of both drugs (Pitolisant 10 mg/kg b.w., and after 30 min Olanzapine 2 mg/kg b.w., and again after 4 h Olanzapine 2 mg/kg b.w.) show that the administration of Pitolisant followed by that of Olanzapine equalized the locomotor activity in mice; in comparison to the level of motility in the control group, to which only Pitolisant is administered. More importantly, this combination of drugs significantly reduces immobility time to the level obtained in the control group in the forced swim test in mice [one-way ANOVA; F (3,20)=4.226,P=0.0181][2]. Rats given Pitolisant (10 mg/kg) during the conditioning phase stayed 502±94 s on the paired texture, a value not statistically different from that of controls, indicating that Pitolisant did not support place preference[3].

Spectrum DetailBack Directory
[Spectrum Detail]

Piperidine, 1-[3-[3-(4-chlorophenyl)propoxy]propyl]-(362665-56-3)1HNMR
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