CAS 63701-55-3|(R)-Baclofen (hydrochloride)

Introduction:Basic information about CAS 63701-55-3|(R)-Baclofen (hydrochloride), including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name(R)-Baclofen (hydrochloride)
CAS Number63701-55-3Molecular Weight250.12200
Density/Boiling Point364.3ºC at 760 mmHg
Molecular FormulaC10H13Cl2NO2Melting Point/
MSDSUSAFlash Point174.1ºC

Names

Name(3R)-4-amino-3-(4-chlorophenyl)butanoic acid,hydrochloride
SynonymMore Synonyms

(R)-Baclofen (hydrochloride) BiologicalActivity

Description(R)-Baclofen Hcl(STX-209 Hcl) is a derivative of gamma-aminobutyric acid (GABA) primarily used to treat spasticity and is in the early research stages for use for the treatment of alcoholism.Target: GABABaclofen (brand names Kemstro, Lioresal, Liofen, Gablofen, Beklo and Baclosan) is a derivative of gamma-aminobutyric acid (GABA). It is primarily used to treat spasticity and is in the early research stages for use for the treatment of alcoholism. It is also used by compounding pharmacies in topical pain creams as a muscle relaxant.It is an agonist for the GABAB receptors. Its beneficial effects in spasticity result from actions at spinal and supraspinal sites. Baclofen can also be used to treat hiccups, and has been shown to prevent rises in body temperature induced by the drug MDMA in rats.In addition, research has shown baclofen to be effective in the treatment of alcohol dependence and withdrawal, by inhibiting both withdrawal symptoms andcravings.
Related CatalogSignaling Pathways >>Membrane Transporter/Ion Channel >>GABA ReceptorSignaling Pathways >>Neuronal Signaling >>GABA ReceptorResearch Areas >>Neurological Disease
References

[1]. Mezler M, et al. Cloning and functional expression of GABA(B) receptors from Drosophila. Eur J Neurosci. 2001 Feb;13(3):477-86.

[2]. Dzitoyeva S, et al. Gamma-aminobutyric acid B receptor 1 mediates behavior-impairing actions of alcohol in Drosophila: adult RNA interference and pharmacological evidence. Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5485-90. Epub 2003 Apr 11.

Chemical & Physical Properties

Boiling Point364.3ºC at 760 mmHg
Molecular FormulaC10H13Cl2NO2
Molecular Weight250.12200
Flash Point174.1ºC
Exact Mass249.03200
PSA63.32000
LogP3.35930
InChIKeyWMNUVYYLMCMHLU-QRPNPIFTSA-N
SMILESCl.NCC(CC(=O)O)c1ccc(Cl)cc1

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
MW5084350
CHEMICAL NAME :
Hydrocinnamic acid, beta-(aminomethyl)-p-chloro-, hydrochloride, (R)-
CAS REGISTRY NUMBER :
63701-55-3
LAST UPDATED :
198503
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C10-H12-Cl-N-O2.Cl-H
MOLECULAR WEIGHT :
250.14

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
523 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PJPPAA Polish Journal of Pharmacology and Pharmacy. (ARS Polona, POB 1001, 00-068 Warsaw 1, Poland) V.25- 1973- Volume(issue)/page/year: 32,187,1980

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety PhrasesS24/25
RIDADRUN 2811 6.1/PG 3
RTECSMW5084350

Articles5

More Articles
Effects of phaclofen and the enantiomers of baclofen on cardiovascular responses to intrathecal administration of L- and D-baclofen in the rat.

Eur. J. Pharmacol. 196 , 267, (1991)

In a previous study it was found that i.t. administration of L-baclofen decreased arterial pressure and heart rate while D-baclofen differentially increased arterial pressure. The objective of the pre...

Comparative stereostructure-activity studies on GABAA and GABAB receptor sites and GABA uptake using rat brain membrane preparations.

J. Neurochem. 47 , 898, (1986)

The affinities of a number of analogues of gamma-aminobutyric acid (GABA) for GABAA and GABAB receptor sites and GABA uptake were studied using rat brain membrane preparations. Studies on the (S)-(+)-...

3-(p-Chlorophenyl)-4-aminobutanoic acid--resolution into enantiomers and pharmacological activity.

Pol. J. Pharmacol. Pharm. 32 , 187, (1980)

Racemic 3-(p-chlorophenyl)-4-aminobutanoic acid was resolved into enantiomers and their absolute configuration determined. Pharmacological activity of hydrochlorides of the racemic acid and its enanti...

Synonyms

Arbaclofen HCl
d-Baclofen hydrochloride
MFCD00078579
Arbaclofen hydrochloride
(R)-Baclofen (hydrochloride)
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