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84484-78-6

84484-78-6 Structure

84484-78-6 Structure
IdentificationMore
[Name]

1-[1-(4-Chlorophenyl)cyclobutyl]-3-methylbutylamine hydrochloride
[CAS]

84484-78-6
[Synonyms]

1-[1-(4-CHLOROPHENYL)CYCLOBUTYL]-3-METHYLBUTYLAMINE HCL
1-[1-(4-Chlorophenyl)cyclobutyl]-3-methylbutylamine hydrochloride
1-(4-CHLOROPHENYL)-BETA-(2-METHYLPROPYL)CYCLOBUTANEMETHANAMINE HYDROCHLORIDE
BTS 54-505
N-DI-DESMETHYL SIBUTRAMINE HCL
N-DI-DESMETHYL SIBUTRAMINE HYDROCHLORIDE
1-(4-Chlorophenyl)-alpha-(2-Methylpropyl)Cyclobutane Methanamine Hydrochloride
1-[1-(4-Chlorophenyl)-alpha-(2-methylpropyl)cyclbutanemethan amine hydrochloride
Cyclobutamethamine,1-(4-chlorophenyl)-alpha-(2-methylpropyl)HCl
N-[1-(4-chlorophenyl)cyclobutyl-3-methylbutyl)]hydrochloride
Cyclobutanemethanamine, 1-(4-chlorophenyl)-α-(2-methylpropyl)-, ochloride
CYCLOBUTANEMETHANAMINE, 1-(4-CHLOROPHENYL)-A-(2-METHYLPROPYL)-, OCHLORIDE
[Molecular Formula]

C15H23Cl2N
[MDL Number]

MFCD03411585
[Molecular Weight]

288.26
[MOL File]

84484-78-6.mol
Chemical PropertiesBack Directory
[Melting point ]

160 - 166°C
[storage temp. ]

Desiccate at RT
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
[CAS DataBase Reference]

84484-78-6(CAS DataBase Reference)
Hazard InformationBack Directory
[Uses]

A metabolite of Sibutramine, a serotonin and noradrenaline reuptake inhibitor (SNR). Decreases calorie intake and increases energy expenditure.
[Uses]

A metabolite of Sibutramine, a serotonin and noradrenaline reuptake inhibitor (SNR). Decreases calorie intake and increases energy expenditure.
[Biological Activity]

Potently active primary amine metabolite of sibutramine (1-(4-Chlorophenyl)-N,N-dimethyl-a-(2-methylpropyl)cyclobutanemethanamine hydrochloride ) that exhibits a similar pharmacological profile to the parent compound. Inhibits serotonin and noradrenalin reuptake more potently than sibutramine in vitro . In vivo, reduces food intake in rodents following i.c.v. administration and increases energy expenditure via thermogenesis.
[in vitro]

simultaneous application of bts 54-505 with 5-ht resulted in a prolongation of the recovery time from the 5-ht-mediated suppression of discharge activity. bts 54-505 also prolonged the recovery time from a na-mediated potentiation of firing. these effects on recovery time are attributed to the inhibition of uptake of both 5-ht and na by bts 54-505. the amplitude of the response to 5-ht or na was unaffected by co-ejection of bts 54-505 [1].
[in vivo]

the secondary (bts 54-354) and primary (bts 54-505) amine metabolites of sibutramine hcl exhibit similar in vivo pharmacological activity to the parent compound. thus, each compound displays potent activity in acute behavioural models predictive of antidepressant effects and a comparable ability to inhibit the uptake of monoamines [2].
[IC 50]

0.066 μm for noradrenaline uptake; 5.1 μm for 5-ht uptake; 0.31 μm for dopamine uptake
[storage]

Desiccate at RT
[References]

[1] scott g, luscombe gp, mason r. the effects of bts 54-505, a metabolite of sibutramine, on monoamine and excitatory amino acid-evoked responses in the rat dorsolateral geniculate nucleus in vivo. br j pharmacol. 1994 jan;111(1):97-102.
[2] luscombe gp, hopcroft rh, thomas pc, buckett wr. the contribution of metabolites to the rapid and potent down-regulation of rat cortical beta-adrenoceptors by the putative antidepressant sibutramine hydrochloride. neuropharmacology. 1989 feb;28(2):129-34.
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