GlyR Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
SR 95531 Hydrobromide | 104104-50-9 | sc-203701 sc-203701A | 10 mg 50 mg | $205.00 $720.00 | 1 | |
SR 95531 Hydrobromide acts as a potent antagonist of glycine receptors, exhibiting a unique ability to disrupt receptor-mediated chloride ion influx. Its molecular structure allows for specific interactions with the receptor's allosteric sites, effectively inhibiting channel activity. This blockade alters synaptic signaling pathways, leading to significant changes in neuronal communication. The compound's rapid binding kinetics further enhance its efficacy in modulating receptor function. | ||||||
Phenylbenzene ω-phosphono-α-amino acid | sc-301540 | 10 mg | $292.00 | 1 | ||
Phenylbenzene ω-phosphono-α-amino acid exhibits distinctive reactivity as an acid halide, characterized by its ability to form stable covalent bonds with nucleophiles. Its unique phosphonate group enhances electrophilicity, facilitating rapid acylation reactions. The compound's steric properties influence reaction pathways, allowing for selective functionalization. Additionally, its solubility in various solvents promotes diverse reaction conditions, making it a versatile intermediate in synthetic chemistry. | ||||||
Kynurenic acid | 492-27-3 | sc-202683 sc-202683A sc-202683B | 250 mg 1 g 5 g | $26.00 $57.00 $138.00 | 6 | |
Kynurenic acid, as an acid halide, showcases intriguing reactivity through its ability to engage in nucleophilic acyl substitution. The presence of its carboxylic acid moiety enhances its electrophilic character, allowing for efficient interactions with amines and alcohols. Its unique structural features enable selective regio- and stereochemical outcomes in reactions. Furthermore, the compound's solubility profile supports a range of reaction environments, facilitating diverse synthetic applications. | ||||||