Ron Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
PHA 665752 | 477575-56-7 | sc-203186 sc-203186A sc-203186B sc-203186C | 2 mg 10 mg 50 mg 200 mg | $143.00 $281.00 $714.00 $1510.00 | 24 | |
PHA 665752 is an acid halide that exhibits unique reactivity through its electrophilic carbonyl group, which readily participates in nucleophilic acyl substitution reactions. This compound demonstrates a propensity for forming transient intermediates, leading to diverse reaction pathways. Its steric configuration influences the selectivity of these interactions, while its polar functional groups enhance solubility in organic solvents, facilitating its reactivity in various chemical environments. | ||||||
BMS 777607 | 1025720-94-8 | sc-364438 sc-364438A | 10 mg 50 mg | $400.00 $1269.00 | 1 | |
BMS 777607 is an acid halide characterized by its highly reactive acyl chloride moiety, which engages in rapid nucleophilic attack, generating a range of acylated products. The compound's unique electronic properties allow for selective interactions with nucleophiles, influenced by its steric hindrance. Additionally, its ability to form stable complexes with Lewis bases enhances its reactivity profile, making it a versatile participant in organic synthesis. | ||||||
Foretinib | 849217-64-7 | sc-364492 | 5 mg | $129.00 | 6 | |
Foretinib, an acid halide, exhibits remarkable reactivity due to its electrophilic carbonyl group, which readily undergoes nucleophilic substitution. Its distinct steric environment facilitates selective interactions with various nucleophiles, leading to diverse acylation patterns. The compound's unique electronic characteristics promote rapid reaction kinetics, while its propensity to form transient intermediates allows for intricate reaction pathways, enhancing its utility in synthetic chemistry. | ||||||
Sodium succinate dibasic | 150-90-3 | sc-251053 | 100 g | $40.00 | ||
Sodium succinate dibasic, as an acid halide, showcases unique reactivity through its dual carboxylate groups, which can engage in complex coordination with metal ions. This interaction enhances its solubility in polar solvents and facilitates the formation of stable chelates. The compound's ability to participate in esterification reactions is influenced by its structural symmetry, allowing for efficient energy transfer during molecular interactions, thus impacting reaction rates and pathways in various chemical processes. | ||||||
c-Met/RON Dual Kinase Inhibitor | 913376-84-8 | sc-364532 sc-364532A sc-364532B sc-364532C sc-364532D | 5 mg 50 mg 100 mg 500 mg 1 g | $379.00 $1200.00 $1700.00 $3600.00 $7000.00 | ||
The c-Met/RON Dual Kinase Inhibitor exhibits distinctive molecular behavior through its selective binding to specific kinase domains, influencing downstream signaling pathways. Its unique structural conformation allows for competitive inhibition, altering phosphorylation dynamics. The compound's kinetic profile reveals a rapid association and dissociation with target proteins, enhancing its efficacy in modulating cellular responses. Additionally, its hydrophobic regions contribute to membrane permeability, affecting bioavailability in various environments. | ||||||
4,4′-Bis(4-aminophenoxy)biphenyl | 13080-85-8 | sc-267771 | 5 g | $100.00 | ||
4,4'-Bis(4-aminophenoxy)biphenyl demonstrates intriguing molecular interactions characterized by its ability to form hydrogen bonds and π-π stacking with adjacent aromatic systems. This compound exhibits unique reaction kinetics, facilitating rapid electron transfer processes that enhance its reactivity. Its rigid biphenyl structure contributes to a high degree of planarity, promoting effective stacking in solid-state applications. Furthermore, its solubility properties allow for diverse interactions in various solvents, influencing its behavior in complex mixtures. | ||||||