PREP Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Z-Prolyl-prolinal | 86925-97-5 | sc-201285 sc-201285A | 5 mg 25 mg | $87.00 $326.00 | 5 | |
Z-Prolyl-prolinal is a versatile compound that acts as a potent electrophile, engaging in selective nucleophilic attacks due to its unique structural features. Its reactivity is influenced by the presence of the proline moiety, which stabilizes transition states and enhances reaction rates. The compound exhibits distinct stereochemical properties, allowing for specific interactions with various nucleophiles. This specificity can lead to tailored reaction pathways, making it a valuable tool in synthetic chemistry. | ||||||
Baicalein | 491-67-8 | sc-200494 sc-200494A sc-200494B sc-200494C | 10 mg 100 mg 500 mg 1 g | $31.00 $41.00 $159.00 $286.00 | 12 | |
Baicalein is a flavonoid characterized by its ability to form strong hydrogen bonds and engage in π-π stacking interactions, which enhance its stability and solubility in various solvents. Its unique hydroxyl groups facilitate electron donation, making it an effective ligand in coordination chemistry. The compound's planar structure allows for efficient stacking with aromatic systems, influencing reaction kinetics and selectivity in complex organic transformations. | ||||||
Baicalin | 21967-41-9 | sc-204638 sc-204638A sc-204638B sc-204638C | 1 mg 25 mg 1 g 5 g | $55.00 $110.00 $220.00 $260.00 | 4 | |
Baicalin, a flavonoid glycoside, exhibits remarkable solubility due to its hydrophilic sugar moiety, which enhances its interaction with polar solvents. The compound's structural conformation allows for effective intramolecular hydrogen bonding, stabilizing its structure. Additionally, Baicalin's capacity to participate in redox reactions is influenced by its phenolic hydroxyl groups, which can donate electrons, thereby modulating reaction pathways and kinetics in various chemical environments. | ||||||
pramiracetam | 68497-62-1 | sc-280016 | 200 mg | $849.00 | ||
Pramiracetam, a racetam derivative, showcases unique lipophilicity, facilitating its passage through biological membranes. Its molecular structure allows for specific interactions with neurotransmitter receptors, potentially influencing synaptic plasticity. The compound's ability to form stable complexes with metal ions can alter its reactivity and stability in various environments. Furthermore, pramiracetam's kinetic profile suggests a rapid onset of action, driven by its efficient absorption and distribution in lipid-rich tissues. | ||||||
Pikromycin | 19721-56-3 | sc-391096 | 1 mg | $108.00 | ||
Pikromycin, a macrolide antibiotic, exhibits distinctive molecular interactions through its large lactone ring, which enhances its binding affinity to bacterial ribosomes. This interaction disrupts protein synthesis, showcasing a unique mechanism of action. The compound's hydrophobic regions contribute to its solubility in lipid environments, influencing its distribution and bioavailability. Additionally, its reaction kinetics reveal a notable stability under physiological conditions, allowing for prolonged activity against target organisms. | ||||||
Y-29794 oxalate | 129184-48-1 | sc-204408 sc-204408A | 10 mg 50 mg | $203.00 $866.00 | 1 | |
Y-29794 oxalate functions as a potent PREP, characterized by its unique reactivity as an acid halide. It engages in selective acylation reactions, facilitating the formation of stable intermediates. The compound's electron-withdrawing oxalate moiety enhances its electrophilicity, promoting rapid nucleophilic attack. Its distinct steric properties influence reaction pathways, leading to diverse product formation. Furthermore, Y-29794 oxalate demonstrates remarkable solubility in polar solvents, enhancing its reactivity in various chemical environments. | ||||||