| Identification | |
| Name: | ALX 5407 HYDROCHLORIDE |
| Synonyms: | ALX 5407 HYDROCHLORIDE;N-[(3R)-3-([1,1'-BIPHENYL]-4-YLOXY)-3-(4-FLUOROPHENYL)PROPYL]-N-METHYLGLYCINE HYDROCHLORIDE;([(R)-3-(BIPHENYL-4-YLOXY)-3-(4-FLUORO-PHENYL)-PROPYL]-METHYL-AMINO)-ACETIC ACID HYDROCHLORIDE;GLYCINE, N-[(3R)-3-([1,1'-BIPHENYL]-4-YLOXY)-3-(4-FLUOROPHENYL)PROPYL]-N-METHYL-, HYDROCHLORIDE |
| CAS: | 571147-18-7 |
| Molecular Formula: | C24H25ClFNO3 |
| Molecular Weight: | 429.91 |
| Molecular Structure: | ![(C24H25ClFNO3) ALX 5407 HYDROCHLORIDE;N-[(3R)-3-([1,1'-BIPHENYL]-4-YLOXY)-3-(4-FLUOROPHENYL)PROPYL]-N-METHYLGLYCINE...](https://img.guidechem.com/structure/571147-18-7.gif) |
| Properties | |
| Density: | 1.45 (20 ºC) |
| Biological Activity: | Selective non-transportable inhibitor of the glycine transporter GlyT1 (IC 50 values are 3 nM and > 100 mM for human GlyT1c and GlyT2 respectively). Displays no activity at the inhibitory glycine receptor or glycine site of the NMDA receptor (IC 50 > 100 mM). |
| Safety Data | |
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