GlyT1 Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NFPS | 405225-21-0 | sc-204126 sc-204126A | 10 mg 50 mg | $195.00 $849.00 | ||
NFPS, as a GlyT1 inhibitor, exhibits distinctive molecular interactions characterized by its ability to form stable complexes with glycine transporters. Its unique structural configuration promotes specific binding affinities, influencing transport kinetics and substrate selectivity. The compound's hydrophobic regions enhance membrane permeability, while its polar functionalities facilitate solvation in aqueous environments, allowing for nuanced modulation of glycine uptake pathways. | ||||||
ALX 5407 hydrochloride | 200006-08-2 | sc-361102 sc-361102A | 10 mg 50 mg | $220.00 $900.00 | ||
ALX 5407 hydrochloride, a GlyT1 inhibitor, showcases unique molecular interactions through its selective binding to glycine transporters. Its structural design enables it to engage in specific hydrogen bonding and hydrophobic interactions, which modulate transporter conformation and activity. The compound's dynamic reaction kinetics allow for rapid equilibrium with target sites, while its solubility characteristics enhance its distribution in biological systems, influencing glycine transport regulation. | ||||||
Sarcosine hydrochloride | 637-96-7 | sc-264296 sc-264296A | 10 g 100 g | $50.00 $280.00 | ||
Sarcosine hydrochloride acts as a GlyT1 modulator, exhibiting distinctive interactions with glycine transporters. Its molecular structure facilitates specific electrostatic and van der Waals forces, promoting conformational changes in the transporter. The compound's affinity for the binding site is influenced by its ionic nature, enhancing its solubility in aqueous environments. This solubility plays a crucial role in its diffusion and interaction dynamics within cellular membranes, impacting glycine uptake mechanisms. | ||||||
Sarcosine | 107-97-1 | sc-204262 sc-204262A sc-204262B sc-204262C sc-204262D sc-204262E | 25 g 100 g 250 g 1 kg 2.5 kg 5 kg | $45.00 $106.00 $150.00 $565.00 $819.00 $1450.00 | ||
Sarcosine functions as a GlyT1 inhibitor, showcasing unique binding characteristics that alter transporter kinetics. Its structural conformation allows for selective interactions with the glycine transporter, leading to modulation of substrate affinity. The presence of functional groups enhances its ability to form hydrogen bonds, influencing the stability of the glycine-GlyT1 complex. Additionally, its zwitterionic nature contributes to its reactivity and solubility, facilitating effective cellular transport processes. | ||||||
LY 2365109 hydrochloride | 868265-28-5 | sc-204063 sc-204063A | 10 mg 50 mg | $214.00 $825.00 | ||
LY 2365109 hydrochloride acts as a GlyT1 modulator, exhibiting distinctive molecular interactions that influence transporter dynamics. Its specific stereochemistry enables targeted binding to the glycine transporter, affecting the transporter's conformational states. The compound's unique electronic properties facilitate charge distribution, enhancing its affinity for the binding site. Furthermore, its solubility profile supports efficient diffusion across cellular membranes, impacting overall transport efficacy. | ||||||