Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate)

Modify Date: 2024-01-12 19:03:41

Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate) Structure
Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate) structure
Common Name Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate)
CAS Number 60789-62-0 Molecular Weight 572.010
Density N/A Boiling Point N/A
Molecular Formula C28H41Cl3N4O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Clocapramine hydrochloride hydrate (3-Chlorocarpipramine hydrochloride hydrate)


Clocapramine hydrochloride hydrate is an antagonist of the D2 and 5-HT2A receptors.

 Names

Name Clocapramine hydrochloride hydrate
Synonym More Synonyms

  Biological Activity

Description Clocapramine hydrochloride hydrate is an antagonist of the D2 and 5-HT2A receptors.
Related Catalog
Target

D2 receptor, 5-HT2A receptor[1].

In Vivo Clocapramine shows the lowest potency for D2-occupancy in vivo[1]. An in vivo receptor binding technique is used to evaluate the binding profiles of typical and atypical antipsychotic drugs to striatal dopamine-D2 and frontal serotonin-5-HT2 receptors in a rat brain using more specific ligands. Clocapramine produces ratios of potency in occupying 5-HT2 versus D2 receptors that fall between these two groups (ED50 of 14.5 mg/kg for D2, 4.9 mg/kg for 5-HT2)[2].
Animal Admin Rats[2] Male Wistar rats (210 to 240 g) are housed in a temperature-controlled room with a 12-hour dark/light cycle (lights on at 8:30) and have free access to food and water. For competition studies, rats are pretreated with an intraperitoneal injection of varying doses of antipsychotic drugs or the same volume (0.21 to 0.24 mL) of the corresponding vehicle (DMSO), 10 minutes prior to the injection of [3H]-YM-09151-2 or [3H]-ketanserin[2].
References

[1]. Schotte A, et al. In vitro receptor binding and in vivo receptor occupancy in rat and guinea pig brain: risperidone compared with antipsychotics hitherto used. Jpn J Pharmacol. 1995 Dec;69(4):399-412.

[2]. Sumiyoshi T, et al. Atypicality of several antipsychotics on the basis of in vivo dopamine-D2 and serotonin-5HT2 receptor occupancy. Neuropsychopharmacology. 1995 Feb;12(1):57-64.

 Chemical & Physical Properties

Molecular Formula C28H41Cl3N4O2
Molecular Weight 572.010
Exact Mass 570.229492

 Synonyms

[1,4'-Bipiperidine]-4'-carboxamide, 1'-[3-(3-chloro-10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)propyl]-, hydrochloride, hydrate (1:2:1)
3-Chloro-5-(3-(4-piperidino-4- carbamoylpiperidino)propyl)-10,11-dihydro-5H- dibenz(b,f)azepine dihydrochloride monohydrate
CLOCAPRAMINE DIHYDROCHLORIDE MONOHYDRATE
1'-[3-(3-Chloro-10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)propyl]-1,4'-bipiperidine-4'-carboxamide dihydrochloride hydrate
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