SOAT Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
CI 976 | 114289-47-3 | sc-203892B sc-203892 sc-203892A | 5 mg 10 mg 50 mg | $109.00 $189.00 $774.00 | 4 | |
CI 976 functions as a SOAT by engaging in selective acylation reactions, showcasing its reactivity with nucleophiles through its electrophilic carbonyl group. This compound exhibits unique steric hindrance, which influences its interaction with various substrates, leading to distinct reaction pathways. The kinetics of its acylation processes are characterized by a rapid formation of intermediates, allowing for efficient modulation of target interactions and subsequent downstream effects. | ||||||
TMP-153 | 128831-46-9 | sc-200649 sc-200649A | 20 mg 100 mg | $119.00 $400.00 | 1 | |
TMP-153 acts as a SOAT by facilitating acylation through its highly reactive carbonyl moiety, which is particularly susceptible to nucleophilic attack. Its unique structural features, including specific substituents, enhance its electrophilicity and direct the course of reaction pathways. The compound demonstrates notable selectivity in substrate interactions, resulting in distinct kinetic profiles that favor the formation of stable acylated products, thereby influencing downstream chemical transformations. | ||||||
YM 750 | 138046-43-2 | sc-358844 sc-358844A | 10 mg 50 mg | $138.00 $587.00 | ||
YM 750 functions as a SOAT by exhibiting a pronounced reactivity due to its electrophilic carbonyl group, which readily engages in nucleophilic acyl substitution. Its unique steric and electronic properties promote selective interactions with various nucleophiles, leading to distinct reaction kinetics. The compound's ability to stabilize transition states enhances its efficiency in acylation processes, ultimately shaping the outcome of subsequent chemical reactions and product formation. | ||||||
GERI-BP002-A | 119-47-1 | sc-221667 sc-221667A | 100 mg 1 g | $43.00 $102.00 | ||
GERI-BP002-A acts as a SOAT through its highly reactive acyl chloride functionality, which facilitates rapid nucleophilic attack. The compound's unique electronic configuration allows for selective binding with a range of nucleophiles, influencing the reaction pathways. Its distinctive steric hindrance can modulate the rate of acylation, while the formation of stable intermediates plays a crucial role in determining the overall reaction dynamics and product specificity. | ||||||
Sandoz 58-035 | 78934-83-5 | sc-215839 sc-215839A | 5 mg 25 mg | $202.00 $836.00 | 11 | |
Sandoz 58-035 exhibits remarkable reactivity as an acid halide, characterized by its ability to form transient acyl-enzyme complexes. This compound's electrophilic nature promotes swift interactions with nucleophiles, leading to diverse acylation patterns. Its unique steric environment influences the selectivity of reactions, while the presence of electron-withdrawing groups enhances its reactivity. Additionally, the compound's solubility properties facilitate its integration into various reaction media, impacting kinetics and product formation. | ||||||
VULM 1457 | 228544-65-8 | sc-204390 sc-204390A | 10 mg 50 mg | $185.00 $772.00 | ||
VULM 1457 stands out as a highly reactive acid halide, showcasing a propensity for rapid acyl transfer reactions. Its distinctive electronic configuration allows for enhanced electrophilicity, facilitating interactions with a range of nucleophiles. The compound's unique steric hindrance influences regioselectivity, while its ability to stabilize transition states accelerates reaction kinetics. Furthermore, VULM 1457's solvation characteristics play a crucial role in modulating reaction pathways and product distribution. | ||||||