SR-1D Inhibitors
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Metergoline | 17692-51-2 | sc-204079 sc-204079A | 10 mg 50 mg | $78.00 $286.00 | ||
Metergoline, acting as an SR-1D, showcases intriguing stereochemical properties that facilitate specific molecular interactions. Its unique indole structure allows for effective π-π stacking with aromatic systems, enhancing its stability in various environments. The compound's ability to form transient complexes through hydrogen bonding contributes to its dynamic behavior in solution. Furthermore, its reactivity profile indicates potential for engaging in nucleophilic substitution reactions, broadening its synthetic utility. | ||||||
BRL 15572 hydrochloride | 193611-72-2 | sc-202979 | 5 mg | $100.00 | ||
BRL 15572 hydrochloride, acting as an SR-1D, showcases distinctive reactivity patterns typical of acid halides. Its highly electrophilic nature enables swift acyl transfer processes, engaging with a range of nucleophiles. The compound's specific steric and electronic properties modulate its reactivity, allowing for selective formation of acylated products. Furthermore, its solubility characteristics contribute to its adaptability in diverse chemical environments, facilitating innovative synthetic strategies. | ||||||
Ziprasidone hydrochloride monohydrate | 138982-67-9 | sc-204419 sc-204419A | 10 mg 50 mg | $125.00 $525.00 | ||
Ziprasidone hydrochloride monohydrate, as an SR-1D, exhibits notable reactivity due to its unique structural features. The presence of polar functional groups enhances its interaction with various nucleophiles, promoting rapid acylation reactions. Its crystalline form contributes to stability and influences solvation dynamics, which can affect reaction rates. Additionally, the compound's ability to form hydrogen bonds plays a crucial role in dictating its reactivity and selectivity in synthetic applications. | ||||||
LY 393558 | 271780-64-4 | sc-295369 sc-295369A | 10 mg 50 mg | $185.00 $772.00 | ||
LY 393558, functioning as an SR-1D, showcases distinctive reactivity attributed to its specific electronic configuration and steric properties. The compound's unique arrangement facilitates selective interactions with electrophiles, leading to efficient acylation processes. Its solid-state characteristics influence intermolecular forces, impacting solubility and reactivity profiles. Furthermore, the presence of halogen substituents enhances its electrophilic nature, allowing for diverse synthetic pathways. | ||||||
LY-310,762 hydrochloride | 192927-92-7 | sc-300941 | 10 mg | $179.00 | ||
LY-310,762 hydrochloride, acting as an SR-1D, exhibits remarkable reactivity due to its tailored electronic structure and spatial arrangement. This compound engages in unique molecular interactions, particularly with nucleophiles, promoting rapid acylation reactions. Its crystalline form contributes to distinct thermal stability and solvation dynamics, while the halide component amplifies its electrophilic character, enabling versatile synthetic routes and enhancing reaction kinetics in various environments. | ||||||
GR 127935 hydrochloride | 148642-42-6 | sc-250068 | 10 mg | $209.00 | ||
GR 127935 hydrochloride, functioning as an SR-1D, showcases distinctive reactivity patterns attributed to its specific steric and electronic properties. This compound demonstrates selective interactions with various substrates, facilitating unique acylation pathways. Its solid-state characteristics influence solubility and reactivity, while the presence of the halide enhances its electrophilic nature, allowing for efficient transformations and diverse synthetic applications across different chemical environments. | ||||||