L-Baclofen (CHEM131470)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-14 18:36:14 UTC | ||||||||
| Update Date | 2026-05-14 19:17:15 UTC | ||||||||
| Accession Number | CHEM131470 | ||||||||
| Identification | |||||||||
| Common Name | L-Baclofen | ||||||||
| Class | Small Molecule | ||||||||
| Description | L-Baclofen is an organic compound with the formula C10H12ClNO2 and an average molecular weight of 213.66 g/mol. L-Baclofen belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. In terms of protein targets, it acts as an agonist of Gamma-aminobutyric acid type B receptor subunit 1 (GABBR1). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C10H12ClNO2 | ||||||||
| Average Molecular Mass | 213.660 g/mol | ||||||||
| Monoisotopic Mass | 213.056 g/mol | ||||||||
| CAS Registry Number | 66514-99-6 | ||||||||
| IUPAC Name | (3S)-4-amino-3-(4-chlorophenyl)butanoic acid | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | NC[C@@H](CC(O)=O)C1=CC=C(Cl)C=C1 | ||||||||
| InChI Identifier | InChI=1S/C10H12ClNO2/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14/h1-4,8H,5-6,12H2,(H,13,14)/t8-/m1/s1 | ||||||||
| InChI Key | KPYSYYIEGFHWSV-MRVPVSSYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
