Baclofen hydrochloride 13C6

Product Name Baclofen hydrochloride 13C6
Alternate Names Baclofen Stable Isotopes, Stable Isotopes of Baclofen
CAT No. CS-EK-01102
CAS No. 28311-31-1 unlabeled
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Baclofen
Canonical Smiles C1=CC(=CC=C1C(CC(=O)O)CN)Cl.Cl
InchIKey WMNUVYYLMCMHLU-UHFFFAOYSA-N
Inchl InChI=1S/C10H12ClNO2.ClH/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14;/h1-4,8H,5-6,12H2,(H,13,14);1H
IUPAC 4-amino-3-(4-chlorophenyl)butanoic acid;hydrochloride
Controlled No
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[13C6]-Baclofen hydrochloride is a labeled form of Baclofen hydrochloride that is used in research and development of drugs. The labeling provides a unique isotopic signature that distinguishes it from other forms of Baclofen hydrochloride. This is useful in drug metabolism and pharmacokinetic studies, as well as in tracing the metabolic pathways of the drug within the body. Baclofen hydrochloride is commonly used as a muscle relaxant and antispasmodic medication. It works by binding to GABA-B receptors in the brain and spinal cord, which inhibits the release of neurotransmitters that cause muscle contractions. This leads to relaxation of the muscles and reduction in muscle spasms. The labeled form, [13C6]-Baclofen hydrochloride, is synthesized by introducing six carbon-13 atoms into the Baclofen molecule. This labeling does not change the pharmacological properties of Baclofen, but it does allow researchers to track the distribution and metabolism of the drug within the body. Overall, [13C6]-Baclofen hydrochloride is a valuable tool in drug development and research, as it provides a unique way to study the pharmacokinetics and metabolism of Baclofen hydrochloride in vivo.

Related Compounds

Baclofen-d5 | Baclofen D4 Hydrochloride | Arbaclofen 13C6 | Baclofen 13C6 | Baclofen D4 (2,2,4,4-D4) | S-Baclofen hydrochloride salt 13C6 | Baclofen-d4,15N |

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