(S) -Baclofen (hydrochloride)

(S) -Baclofen hydrochloride is a GABAB receptor agonist that crosses the blood-brain barrier and is orally active, with IC50 values ​​of 1.77 μM for GABAB and 1564 μM for GABAA. (S) -Baclofen hydrochloride can be used in research on muscle disorders such as spasticity[1][2].

63701-56-4

12352005

H302-H315-H319-H335

GABA Receptor

Membrane Transporter/Ion Channel; Neuronal Signaling

Neuroscience-Neuromodulation

Neurological Disease

10 mM in DMSO

OC(C[C@@H](C1=CC=C(C=C1)Cl)CN)=O.Cl

C10H13Cl2NO2

250.12

P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

[1]He Q, et al. Simultaneous Quantitation of S (+) - and R (-) -Baclofen and Its Metabolite in Human Plasma and Cerebrospinal Fluid using LC-APCI-MS/MS: An Application for Clinical Studies. Molecules. 2020 Jan 8;25 (2) :250. |[2]Froestl W, et al. Phosphinic acid analogues of GABA. 1. New potent and selective GABAB agonists. J Med Chem. 1995;38 (17) :3297-3312.

Room temperature

http://file.medchemexpress.com/batch_PDF/HY-B0007A/

Reference compound1

No Development Reported